Some people still swear up and down that ivermectin is actually effective against COVID-19. This is false. They also insist ivermectin has far fewer side-effecs than the Coronavirus vaccine. This is also false. I'm going to prove it to you, but whether you are capable of accepting evidence such as listed below is something I obviously have no control over. I can try, and you can keep an open mind.
First of all, ivermectin has many side-effects, ranging from innocuous to severe.^[1]
To wit:

General

Ivermectin is well tolerated compared to other microfilaricidal agents (i.e., thiabendazole, diethylcarbamazine). Adverse reactions (i.e., pruritus, fever, rash, myalgia, headache) occur commonly during the first 3 days after treatment and appear to be related to the extent of parasitic infection and systemic mobilization and killing of microfilariae. The majority of reactions can usually be treated with aspirin, acetaminophen and/or antihistamines. Adverse effects tend to occur with lesser frequency during periods of retreatment.

Ocular

Ocular side effects have included eyelid edema, anterior uveitis, blurred vision, conjunctivitis, limbitis, punctate opacity, keratitis, abnormal sensation in the eyes, and chorioretinitis/choroiditis; however, these effects are also associated with the disease onchocerciasis. Loss of vision has occurred rarely but usually resolved without corticosteroid treatment. Conjunctival hemorrhage has been reported during postmarketing experience in patients treated for onchocerciasis.

Other

Worsening of Mazzotti reactions, including arthralgia, synovitis, lymph node enlargement and tenderness, pruritus, skin involvement (including edema, papular and pustular or frank urticarial rash), and fever, has been reported during the first 4 days following treatment for onchocerciasis.

Nervous system

Nervous system side effects have included dizziness, headache, somnolence, vertigo, and tremor. Serious or fatal encephalopathy has been reported rarely in patients with onchocerciases, and heavily infected with Loa loa, either spontaneously or after treatment with ivermectin. Seizures have been reported during postmarketing experience.

Gastrointestinal

Gastrointestinal side effects have included anorexia, constipation, diarrhea, nausea, vomiting, and abdominal distention.

Other

Other side effects have included asthenia, fatigue, abdominal pain, chest discomfort, facial edema, and peripheral edema.

Hematologic

Hematologic side effects have included decreased leukocyte count (3%), eosinophilia (3%), and increased hemoglobin (1%). Hematomatous swellings associated with prolonged prothrombin times have been reported, but the clinical significance is unknown. Leukopenia and anemia have been reported in at least one patient.

Hepatic

Hepatic side effects have included elevated ALT and/or AST. Elevated liver enzymes, elevated bilirubin, and hepatitis have been reported during postmarketing experience.

Cardiovascular

Cardiovascular side effects have included tachycardia and orthostatic hypotension. EKG changes, including prolonged PR interval, flattened T waves and peaked T waves, have been reported in single cases. Hypotension (primarily orthostatic hypotension) has been reported during postmarketing experience.

Dermatologic

Dermatologic side effects have included pruritus, rash, and urticaria. Toxic epidermal necrolysis and Stevens-Johnson syndrome have been reported during postmarketing experience.

Respiratory

Respiratory side effects have included worsening bronchial asthma, laryngeal edema, and dyspnea.

Musculoskeletal

Musculoskeletal side effects have included myalgia.

Renal

Renal side effects have included rare transient proteinuria.
I tried to get incidence rates for these side-effects, but in some if not most instances, the answer given for these side-effects is either simply "unknown" or they're just not shown. Imagine telling this to anti-vaxers: if they have at least a consistent set of beliefs, this should deeply alarm them, shouldn't it?
Some people actually did take the horse dewormer version out of sheer desperation and got really sick, were hospitalized or worse: they died.

1. In New Mexico, two people died after taking a deworming drug for horses and other livestock to treat COVID-19.^[2]
2. The FDA received multiple reports of patients who required medical support and hospitalization after self-medicating with Ivermectin intended for horses.^[3]
3. There was a significant increase in calls to poison control centers due to misuse of Ivermectin. Texas saw a 550% spike in poison control calls due to people ingesting horse and cow dewormer.^[4]
4. People poisoned themselves with the horse-deworming version to thwart COVID-19, resulting in an uptick in calls to poison control centers.^[5]

Ivermectin was consistently found to be ineffective in treating COVID-19:

1. A systematic review and meta-analysis published in the Virology Journal evaluated the efficacy of Ivermectin for COVID-19 patients based on current peer-reviewed RCTs. The study concluded that Ivermectin did not have any significant effect on outcomes of COVID-19 patients.^[6]
2. A Cochrane meta-analysis of 11 eligible trials examining the efficacy of Ivermectin for the treatment of COVID-19 published through April 2022 concluded that Ivermectin has no beneficial effect for people with COVID-19.^[7]
3. An article published in the Journal of the American Medical Association (JAMA) concluded that taking 400 mcg/kg Ivermectin for three days, when compared with a placebo, did not significantly improve the chances for a patient with mild to moderate symptoms of COVID-19 to avoid hospitalization.^[8]
4. A study published on News Medical concluded that in COVID-19 outpatients with mild or moderate illness, Ivermectin use for three days at a dose of 400 μg/kg showed no significant improvement in the time to sustained recovery compared to those who received placebos.^[9]

The unwarranted hype surrounding ivermectin can be traced back to its promotion on the Joe Rogan Experience.^[10]

Public interest in ivermectin ballooned following Joe Rogan’s podcasts. “On a national level Rogan’s podcast was a tipping point,” said Keenan Chen, an investigative researcher with First Draft News, an organization that tracks misinformation. (Rogan, who has previously expressed hesitancy to vaccines, announced in September he had contracted Covid-19. He claimed to be taking ivermectin among several other treatments.)

Joe Rogan took a cocktail of Big Pharma^tm meds which, with the exception of monoclonal antibodies, were not indicated for his situation. In fact, some of the medication he took could have made things worse.^[11] Rogan probably didn't get seriously ill because he's fit and without significant comorbidities. The one thing that would have actually been the most effective was the vaccine, which he refused to take.
Many others weren't as lucky as Joe was. I suggest you follow the footnotes and see for yourself. Especially the first one.^[12][13]
Other than ivermectin, coronavirus vaccines are also a subject both Joe Rogan and his guests have shamelessly lied about numerous times, which could have caused medical harm to people who bought into it, and probably did. The most prominent guest which comes to mind is RFK Jr.
RFK Jr.'s influence is so odious, I am comfortable saying he probably contributed to thousands of unnecessary deaths in total. One incident in which 83 people (mostly children) died is particularly disgusting:^[14]

In June 2019, Kennedy and his wife, the actress Cheryl Hines, visited Samoa, a trip Kennedy later wrote was arranged by Edwin Tamasese, a Samoan local anti-vaccine influencer.
Vaccine rates had plummeted after two children died in 2018 from a measles vaccine that a nurse had incorrectly mixed with a muscle relaxant. The government suspended the vaccine program for months. By the time Kennedy arrived, health authorities were trying to get back on track.
He was treated as a distinguished guest, traveling in a government vehicle, meeting with the prime minister and, according to Kennedy, many health officials and the health minister.
He also met with anti-vaccine activists, including Tamasese and another well-known influencer, Taylor Winterstein, who posted a photograph of herself and Kennedy on her Instagram.
“The past few days have been profoundly monumental for me, my family and for this movement to date,” she wrote, adding hashtags including #investigatebeforeyouvaccinate.
A few months later, a measles epidemic broke out in Samoa, killing 83 people, mostly infants and children in a population of about 200,000.
Public health officials said at the time that anti-vaccine misinformation had made the nation vulnerable.
The crisis of low vaccination rates and skepticism created an environment that was “ripe for the picking for someone like RFK to come in and in assist with the promotion of those views,” said Helen Petousis-Harris, a vaccinologist from New Zealand who worked on the effort to build back trust in the measles vaccine in Samoa.
Petousis-Harris recalled that local and regional anti-vaccine activists took their cues from Kennedy, whom she said “sits at the top of the food chain as a disinformation source.”
“They amplified the fear and mistrust, which resulted in the amplification of the epidemic and an increased number of children dying. Children were being brought for care too late,” she said.

The pandemic is over. Ivermectin wasn't effective. On the one hand we should move on, on the other hand, there should be some accountability for people who pushed this lie, especially those who benefited from it financially.^[10][15]
[1] Drugs.com - Ivermectin Side Effects
[2] USA Today - 'A serious issue': New Mexico health officials suspect two people dead from ivermectin poisoning
[3] Global News - FDA warns Americans to stop taking horse dewormer for COVID-19: ‘You are not a horse’ (Some anti-vaxers counter that the FDA lost a court battle about ivermectin, proving that it works - this is false)
[4] USA Today - Fact check: 590% jump in poison control calls about ivermectin seen in Texas
[5] Ars Technica - More people are poisoning themselves with horse-deworming drug to thwart COVID
[6] Virology Journal - Ivermectin under scrutiny: a systematic review and meta-analysis of efficacy and possible sources of controversies in COVID-19 patients
[7] JAMA Network - At a Higher Dose and Longer Duration, Ivermectin Still Not Effective Against COVID-19
[8] KU Medical Center - Ivermectin shown ineffective in treating COVID-19, according to multi-site study including KU Medical Center
[9] News Medical - Ivermectin is ineffective in non-severe COVID-19 patients according to new study
[10] The Guardian - Ivermectin frenzy: the advocates, anti-vaxxers and telehealth companies driving demand
[11] Doctor Mike - Here's Why Joe Rogan's COVID Treatment Is Problematic
[12] /JamiePullDatUp - "I made a terrible mistake" vs. "I'm still not a 100% sold on the inoculation" - videos of unvaccinated COVID-19 patients in the hospital
[13] /HermanCainAward
[14] AP - RFK Jr. spent years stoking fear and mistrust of vaccines. These people were hurt by his work
[15] Time - ‘What Price Was My Father’s Life Worth?’ Right-Wing Doctors Are Still Peddling Dubious COVID Drugs

reddit
Hello everyone, I am a 22/F and work at an early childhood education center. The place I work at is privately owned by a man, but is a corporation, if that makes sense. There have been a lot of issues since working here. First off, they encourage sick children and workers to come here. If one of my kids is throwing up, running a fever, or obviously very ill, they do not make them go home. They just tell us to give the parents a courtesy call and let them know the child does not have to go home. For workers, they do not let us go home if we get sick at work. We have a stomach bug going around and 3 of my coworkers are vomiting in the classroom bathrooms or trash cans. Our directors will not let them go home because they are fever free. One time, I was running a 102.8°F temperature and vomiting. I sent them a picture of the thermometer and said I would not make it in as I was sick. They responded saying they were understaffed and needed me to come in or it could possibly result in a write up. I got a doctor’s note so they couldn’t write me up. I was out a few days. The issue is, not everyone here has a backbone and they come to work sick when the directors tell them they can’t call off. There is always something going around at work. There was another time I contracted hand foot and mouth disease. I saw the doctor on my lunch break and confirmed it. I went to my boss’s office after my break, gave her my doctor’s note and let her know I had to go home as I was contagious. She said no and made me stay the whole day. I did not know how to advocate for myself. They would not let me go. This is a major issue here. Everyone here is always sick because of it. I’m sick at least once a month. I am sick today and my boss went off on me stating that people calling off here has become normal and she is tired of it. She told me she feels like I don’t even want to be here and that I am faking sick to get out of work. She told me if I stay home today, regardless of a doctor’s note, she will write me up and I am at risk for being fired. Every time I’ve been sick I have provided a doctor’s note. I have never not provided one. My call outs have always been valid. If I am not contagious, I am here. I am here today despite being in pain and contagious, though. Another example, 4 months ago, a 13 month old girl went to the doctor. She tested positive for RSV and came back. The mother said the doctor said she needs to be out until she is fever free, but she works here and had no one to take her child, so her and her child were here. The whole school broke out in RSV, and one girl was hospitalized for a few days.
Another issue is the directors play favoritism. The directors and 9 of the teachers here always go out and party together. All of their kids are best friends. The directors let these teachers they are besties with get away with anything and everything. It took one of them smoking weed in the bathroom to get fired, despite neglecting kids. I went into her class once and her kids had not had diaper changes in 5 hours. One of the kids’ diaper was split in half. Parents were complaining about their kids having severe diaper rashes. She would also scream in their faces and chase them with a hose outside. Again, it took her smoking weed in the bathroom to get fired. But I’m at risk for being fired because I get sick a lot. I was never sick a lot before working here, by the way.
They are also really rude with the way they talk to people. One of the teachers was concerned because we were out of ratio so she called the director asking for help. The director came outside and yelled at her, saying she knows ratio and knows how to do her job and does not need help because she’s been doing it for years. Also, this school is never following QA unless QA is here.
There is probably more I’m not even thinking about right now that has happened. There is more I didn’t mention just because this is already so long. I’m just stumped at what to do, who to call? Do I just quit? I’ve been here a little over a year and I’m tired of it.
We also signed contracts stating that we have to give 60 days notice before quitting, or they can keep our last paycheck due to trauma from lack of staffing. They said they can even ask us to give more money than the last paycheck if deemed necessary. These contracts, to my knowledge, aren’t actually legal contracts since they aren’t notarized.

(sorry this is long, I just started and couldn’t stop)
I'm a 57F professional working as a Contracts Specialist for a large Tech Company. I discovered I have total Aphantasia about 2 months ago. I hate saying it that way, I "have" Aphantasia. It sounds like a disease or something. Still working on a way to word that when I share this with people who have never heard of it.
I have spent the months doing as much reading and self-searching as possible. I immediately felt relief when I discovered what Aphantasia is and have never had the feeling that I am missing out by not seeing the images, but I can sure understand why some would feel that way. For me it was the answer to questions I have been asking myself all my life. I just found out "I'm not crazy" AND "I'm not alone". I've never posted anything like this before, but when I joined, reading things like this from others when they first find out they are an Aphant was very helpful.
Some things I have thought about since learning this about myself.
Psychology Profession and Memory Loss - I have known I have a bad memory since I was a kid, I never understood why I couldn't remember things until someone "triggered" the memory. Once triggered, I can remember things fairly well. As many young adults, I had some issues adjusting to college life and chose to seek help with a professional. This was my first experience with being told I must be repressing a traumatic experience from my childhood. We spent many months/years and many tears trying to determine what that could be. Now I should add I was abused as a child and had remembered and dealt with that. My parents ended up shipping me off to my Grandparents to get away from her influence. But answer me this, if I remembered it and dealt with it and no longer had negative consequences from it, why didn’t my memory get better? Over the years I have seen a couple other therapists that wanted to concentrate on repressed memories because of my memory. I went along for a while but finally became convinced that there were no other memories to find. But that profession took a lot of my money, time and emotional wellbeing - yet nothing was ever discovered. I doubted people in my life that I never should have. Now I believe Aphantasia should be a part of all professional training for mental health wellness. I'm old, so maybe it is now??
Fake Memories - After experiencing this kind of high pressure "therapy" I can totally understand how people create fake memories. So many thoughts and details were provided during these sessions, I could have easily started to "make" things up and that leads to believing it happened in that environment. As a woman, I am always looking to please people, I tried to please my therapists. Aphantasia or not, false memories are not as hard to plant as you might think especially when that person is trying to make you happy.
Being Present - This has been a big thing the last few years. People pushing for you to be present in your life. Professionals have also mentioned that my memory issues may be due to the fact that I have never "been present" in my life. It took a few sessions to understand what the hell they meant and then spent much time trying to "be present" and I the only thing I determined is that I have always "been present" as best I can! I stopped going to therapists after this one.
Objects & Memories - I now understand why I have been holding on to things that most people would have let go of by now. For instance I have a large stuffed animal collection and have always told my husband I could not get rid of any of them as each one is a trigger for a good memory. I am afraid if I get rid of it, that memory will be lost forever. If the memory really does go away, then I can get rid of that object. If there is no memory trigger, it's pretty easy to let go. Same with taking photos, I have a better understanding of why I always had my camera out. Without a picture, did it really happen? Not in my memory!
Deep Connections - Aphantasia may be a factor in my perception as to why I cannot make deep connections with people. Because my brain does not pepper me with visions and thoughts of loved ones, I don't think about other people very often. I don't know what people mean when they say "I miss you". I truly am an OUT OF SIGHT OUT OF MIND lifer. When I have expressed to others that I feel that way, I have been told they feel a deep connection and don't know what I would mean by deeper. Now I believe since I don't think about others often, I've just convinced myself over the years that my feelings must not be deep. If it were deep, wouldn’t I be on their minds like I am on theirs? I am starting to understand things a bit differently now, I love and care DEEPLY for the people in my life, I'm just not triggered to remember them.
Learning/Training - I have always had issues with classroom learning. I have trouble concentrating on what is being presented unless there is some kind of hands-on activity associated with the training. I recently moved to a new position at work, I used to be a corporate trainer. To start my new position there was a large learning curve. I found when someone one told me something about the job I needed to see it or even better perform the task myself. That is not always available in training situations. It has taken a while to get up to speed in this position and I was doing a great job of beating myself up about not catching on quickly. I must be getting old, I thought. I was usually frustrated as a trainer when I had to train people my age, they just didn't seem to "get it" when others did. Well here's my payback, now I have to learn and I'm the one not "getting it". I do really wish I had known about Aphantasia/Hypophantasia/Hyperphantasia while I was a trainer. I think about all the improvements I could make on the material if I knew how the student's memory worked. I never really used much visual assistance, other than performing the task in front of them, and now I think that would have been helpful for "normal" memory types. The good thing about my memory is that once I understand WHY something is done, I've got it, it's in the vault. I actually do better than most others once that lightbulb goes off. Sometimes it just takes a while to really have that understanding. I am very detail oriented and technical; I can pick up computer operating systems quickly, they make sense.
Face/People Recognition - I have a hard time identifying characters in a movie, especially if they are wearing similar clothing or haricuts. I even have difficulty remembering my waitperson after talking to them directly. I usually remember if they were Female or Male, but not always. If I need something from them, I am awful at locating my wait person. I usually end up asking some random employee. Once I am familiar with the person, I will recognize them, but there has to be some kind of connection made. This has proven to cause quite a bit of embarrassment when I run into someone I have met and have zero recollection of who they are or where I met them. Unfortunately, this has happened more than a handful of times. It makes the other person feel bad and that's the last thing I want to do.
Another thing I noticed that I believe fits in this section, is how people can imitate others. I now understand how they can do that; they actually have a mental image of that person doing something. They can see them moving, hear them talking and then interpret that to an imitation. That was one of the many lightbulbs that went off in my head while researching Aphantasia. I mean how does someone tell a sketch artist what someone looked like after a crime? Not only face blindness but adrenaline flowing as well. But some people can remember down to the angle of their eyes and shape of the mouth. That has always been such a mystery to me, how can people do that? Now I understand, they actually SEE the face.
Processing Information - One thing I have been wondering is if Aphantasia has anything to do with how fast my brain processes information on the regular. I have been called a fast thinker when I come to a conclusion quickly and process what is in front of me quicker than others. I notice this when playing games, learning and putting things together during a conversation. I have the ability to see the big picture which allows me to put things in place and make decisions quickly. It drives me crazy when it takes my mom 5 mins to make a move in a game. I can understand that a bit better now, so learning this about myself has also helped me understand others. Others have all kinds of images they are needing to process to decide. And after sharing my findings with my family I have determined that my mom is a Hyperphantasic. Her memory is amazing, she remembers everything from her childhood from 4yrs on. I've always been jealous of that kind of memory.
I even understand how Chess works and what they mean by look ahead 5 moves.
Psychedelics - In the Aphantasia community, I have FINALLY found kindred spirits when it comes to experimenting with certain drugs. Aspirin, Antihistamines, pain killers and other prescribed drugs work just fine. But when I have taken any illicit psychedelics, nothing happens. The first time I noticed I was not as affected as others was in college. I just figured everyone else was really exaggerating and I wasn't interested in trying again. But I have since tried experimenting again with my husband who has gotten into Microdosing. We thought it would be interesting to take a recreational dose. He had an awesome time with lots of visuals and motion. For me, nothing. I could make the grass or a picture on the wall get "movement" but nothing like what he was experiencing. Decided to try again, this time with my sister and husband. I took a double dose this time just to make sure I would feel something. Nope, nothing. I have tried up to 10g at a time with nothing (DO NOT TRY THIS AT HOME, DONE BY A PROFESSIONAL). I have never heard of anyone else having this kind of experience until I joined this group. There have been several people indicate they have similar experiences including one who even called out that they don't feel anything more than a minor wavey feeling.
Now I think it is probably for the same reason we don't have a "minds eye". Some synapses somewhere are not sparking normally. I do believe for some Aphants, this does actually lead to some visual or other sensory experiences they have not had before. But for some of us, we don't have the ability to "Trip". This is probably the only thing I have found that I don't like about Aphantasia. I have been able to put a positive spin on most of what I have found, but I do wish I could experience that feeling others have while taking a "Trip".
Where do you see yourself in 10 years? – This is a question that I have had to answer many times in my career, it is one of the favorite questions asked during an interview. I’ve never been good at answering that question. Others would provide great details on where they see themselves going, but I have never had the ability to look that far ahead. I don’t see myself anywhere specifically, I tend to follow the opportunities that come my way.
In conclusion (yes finally almost done) I've gone 57 years telling myself I can improve my memory, "I'll remember that if I really think hard" but I never do. Or I try to make sure I am "Present" so I can remember, nope, doesn’t help either. Now that I have an answer that explains my brain is acting differently than most people, I don't kid myself anymore. I'm just not going to remember and that's OK, that's how my brain works and part of who I am. There is nothing I can do about it, no more wasted time working on my memory!!
I can honestly say I am grateful to learn about this memory process and for the ability to move on from difficult situations. There are many more things I could get into, but that would be an even bigger book. My sister can get stuck on something that is difficult for her to get past, the images of bad things “haunt” her. For me, as soon as the actual event is over, it may take a few days depending on the severity, it is buried and does not "pop in" and bring me back. If only I had known this when I was younger, I can only imagine what I could have accomplished! I imagine my self-doubt/hate could have been less with this information as well as the therapist bills that could have been saved. This is such important knowledge, I am so happy to see research being done!! I only hope the information continues to spread so more people are aware. I don’t know if all the things above are in direct relation to Aphantasia, but my eyes have been open to these differences.

Broke no contact after one year and now I feel like I’m dying
I(M19) broke up with my ex(F19) one year ago. I broke up with her because I was in a very toxic relationship and we had long distance (she used to live 500km from my city). She used to always be rough with me because I didn’t have enough money to spend on her. For example( one day when i went to her and didn’t buy her flowers she told me to send her the money for the flowers 30£ on PayPal). She used to stay on tinder (she didn’t know that I had access to her phone and saw it) and even went to the club with her uni group and a week later got “the kissing disease”. She was always telling that she didn’t kiss anybody even if doctors say that you can get this disease only by kissing someone. During the winter break she had to come to my city and told me to buy her the ticket(60£). After I told her many times that I don’t have the money, she told me “if you’ll want me near, you’ll find the money” and she was right, even though I was in the last year of high school, I used to work on Saturdays and payed her train ticket. Every time when I went to her, I had to pay both the train ticket and the hotel room because her sister wouldn’t let me sleep in their apartment even though they had 2 bedrooms. At the same time, my family let her sleep in our apartment when she came to my city. So I broke up with her before summer, when she didn’t want to pay 40%(she didn’t even want to ask her family if they can or cannot pay it) of the total sum of our trip to Spain. She told me that she regrets being in a relationship with me, blocked me and I thought at the moment that she broke up with me. The next day, she called me and I asked her who will initiate (I thought it was a call to break up officially). She started screaming through the phone that I m a psycho and that it was me the one who wanted to breakup. I felt so guilty that the next month I was everyday crying. Finally I decided to call her to have a normal conversation about what happened, we clarified everything. One month later, after a terrorist attack near my city, she texted me and asked how am I doing and sent a picture with us, telling that we’re so cute together. I said that it was true. She didn’t apologize, didn’t even say anything that she would like to get back together.
After this we didn’t talk for the entire year but I was feeling very sad the whole year because when I broke up with her, I didn’t tell her about tinder(saw 2 chats with 2 dudes in her phone) or about what happened in the club that night.
After one year, I called her and very respectfully said that I really needed answers in order to obtain closure. She told me that she was only “communicating” on tinder (I think it’s a lie) and totally refused to recognize that she cheated on me that night in the club. After this, she told me that she has to go and that if I want to continue talking, we can talk in the evening . 20 minutes after this short call I wrote her that I was thankful for her answers but I didn’t think it would be right for us to continue talking. She responded that I shall never get in touch with her ever again in order to accuse her of something that happened a year ago. One week later I called her again in order to excuse myself for the fact that I reached out to her. She didn’t respond and at that moment I understood that she restricted me on insta . I sent her the message that I was sorry. My friends told me that I was a piece of shit for doing this.
NOW I FEEL LIKE MY HEART WILL EXPLODE BEACUSE I FEEL SO STUPID AND ASHAMED . I even though maybe buying a train ticket and go to her city to visit her, but idk if it’s right. My family doesn’t want even to hear about my ex and is tired of hearing me talk about her. What should I do, please HELP
Ps we were dating during a year and a half and I was traveling to her every 3 weeks

Chronic leukemias - does normal bloodwork exclude it?
Most recent bloodwork:
https://ibb.co/Msr6GpH
https://ibb.co/kSRmN53
https://ibb.co/99VFjTw
https://ibb.co/bzH9V7F
Previous bloodwork showing some abnormalities:
https://ibb.co/VT7CHcG
https://ibb.co/GdYSFXy
29 female living in England, on duloxetine 90mg for 3 years, no other medications
Have had symptoms for 2 years, started as bowel problems and weight loss with no findings in tests (colonoscopy/gastroscopy/mri) and my weight levelled out.
Now I get bone pain and what feels like joint pain too, maybe a bit arthritic feeling.
More recently, I also get rashes that come and go alongside recurrent staph boils. I sometimes wake up at night sweaty, usually when having vivid dreams. I’ve had night sweats on & off since 2018.
I’m a very anxious person and have OCD. I had a normal full blood count and protein electrophoresis. I had an incident of raised total protein, globulin, liver enzymes and lowered egfr but after a week my bloods were normal again. My WBC, platelets have always been in range and for the past 2 years have been between 6-8. Platelets are around 310.
Can I exclude any type of leukemia as causing my symptoms? I’m worried I could have chronic type that is not showing in bloods. This would explain all my symptoms I think so I’m worried sick.
Thank you

So the past two-ish months I have been noticing really different things about me and my body. I know I need to go to the doctor and am currently looking for one, but until then can someone tell me what these things mean?
To start, I have random bruises everywhere. Now, as a female I know this is normal and I am also anemic, so makes sense. However, this has been a very recent issue. Only about two months ago this started. I got blood work done a couple of weeks ago which proved anemia, and the things I am low on are blood urea nitrogen, B12, and Vitamin D. I have been taking vitamin d supplements now, but when googling (I know..) the low blood urea nitrogen can be a sign of kidney failure or liver damage. Keep this in mind.
TMI: A new and more scary issue is bleeding when I shit. It is a lot of blood too. For a while, like I would bleed a little bit and just thought it was normal. Now it is really bad and seeing blood clots when I wipe. This could also be why I am anemic but idk.
I am extremely exhausted, more so than usual and again started about two months ago. I thought it was because of my Adderall, but I do not think so anymore. I have noticed that I am more fatigued when I take my adderall which can be an underlying issue. I also have not been eating but I think that is because of the Adderall. I started losing my appetite when I started taking the medication four months ago, but I am wondering now if I destroyed my intestines by doing this lmao.
Now this may just be because i have dermatillomania, but I have these red bumps showing up all over my legs. This has been for a while too and I didn't think it to be an issue before, but idk anymore. Basically, all I can think of is cancer.
I never thought I was a hypochondriac until like last year when I realized I google every single issue I have and just hope that I do have one of the issues I look up so that my body can make sense to me. Overall, my stupid brain thinks kidney disease, liver disease, colon cancer, leukemia, any other random health issue so help lol

Having an issue adding pictures. I had a 1 night stand 3 weeks ago and left feeling not confident in my partners truth about cleaning. I was tested before and all came back clean. 2 days after I had a sore throat went to the dr. and they said it wasn’t strep. I gave a sore throat to 2 other friends so I figured that wasn’t from an std. however, it’s been 3 weeks since the meeting and my throat is no longer sore but I still have a cough. My tongue now almost looks like small cuts are appearing. Every time I look up a symptom I feel like I have it. Might be in my head but idk anymore.
I performed fellatio, didn’t not swallow, doesn’t seem like that matters though when it comes to diseases. I know I have to get tested just feel like it’s to soon.
I guess my question is can anyone please tell me some symptoms they would worry the most about.

N64 Pictures: https://imgur.com/a/n64-games-n64-console-sCri6E3
Let me know if you need pictures of any of the items listed below. Shipping is $5 flat for anything under one pound. I've got 400+ transactions on this board and accept payment via PayPal (F&F) or Venmo (F&F) only.
Consoles
GBA Indigo - $80 shipped
GBA SP (Silver CIB) - $120 shipped
Nintendo 2DS w/ charger - $85 shipped
Nintendo 3DS XL Pokemon X & Y Edition Console - $225 shipped
Nintendo 64 Console w/ hookups + OEM Controller - $90 shipped
Nintendo Wii Console (gamecube compatible) w/ hookups + Wii remote & numb chuck - $75 shipped
PS2 w/ hookups, OEM controller, OEM memory card - $100 shipped
Retron 5 Hyperkin (GBA/GBC/SNES/NES/Genesis) unused CIB - $120 shipped
Super Nintendo w/ hookups & OEM controller - $95 shipped
Xbox OG Console w/ hookups & OEM controller + Project Gotham Racing (CIB) - $100 Shipped
Controllers/Accessories
Gameboy OEM Clam Shells (lot of 32) - $75 shipped
Gamecube OEM Controller (Indigo) - $30 shipped
Gamecube OEM Wavebird Controller w/ receiver- $95 shipped
NES OEM 10-Cart Storage Case (3x avail) - $20 + shipping each
N64 OEM Expansion Pak - $50 shipped
N64 OEM Green Controller - $30 shipped
N64 Memory Card - $14 shipped
PS2 Logitech Wireless Controller (w/ dongle) - $35 shipped
PS2 OEM Memory Card- $14 shipped
Sega GameGear Super Wide Gear - $20 shipped
Wii U Wireless Controller (WUP-005) & charging cable - $35 shipped (2x avail)
N64 Games
007 GoldenEye - $25
007 World is Not Enough - $14
Army Men Sarge's Heroes - $15
Automobil Lamborghini - $8
Backstage Assault - $12
Banjo Kazooie - $25
Bass Hunter 64 - $8
Beetle Adventure Racing - $17
Charlies Blasts - $40
Diddy Kong Racing - $25
Doom 64 - $30
Extreme G Racing - $10
Forsaken 64 - $10
Gex 64 - $16
Iggy's Reckin' Balls - $20
Killer Instinct Gold - $30
Knockout Kings 2000 - $6
Magical Tetris Challenge - $20
Mario Kart - $40
Monster Truck Madness - $15
MRC Multi Championship Racing - $10
Namco Museum 64 - $12
Nascar 99 - $7
Nascar 2000 - $7
NBA In the Zone 98 - $5
NBA Live 99 (CIB) - $20
NBA Showtime - $12
Polaris Sno-Cross -$30
Pokemon Snap - $20
Quest 64 - $25
Ready 2 Rumble Boxing - $12
Ridge Racer 64 - $15
San Francisco Rush - $15
Starfox 64 - $25
Star Wars Episode 1 Racer - $10
South Park Chef's Luv Shack - $25
Supercross 2000 - $7
Super Mario 64 - $35
Super Smash Bros. - $40
Tetrisphere - $12
Top Gear Rally - $10
Turok Dinosaur Hunter - $12
Turok 2 Seeds of Evil - $12
Vigilante 8 - $21
Virtual Pool - $13
Waialae Country Club - $6
War Gods - $10
Wave Race (Player's Choice) - $15
WCW Backstage Assault - $11
WCW NWO Revenge - $11
Wheel of Fortune - $11
Zelda Ocarina of Time (label wear) - $30
N64 Manuals
1080 Snowboarding - $7
Duke Nukem Manual - $10
Flying Dragon Manual - $40
Rush Extreme Racing - $8
Silicon Valley Space Station Manual - $40
Supercross 2000 - $6
Tony Hawk Pro Skater - $6
Nintendo Gamecube Games (CIB unless noted)
ATV Quad Power Racing 2 - $10
The Hobbit - $24
Enter the Matrix - $13
Eternal Darkness - $90
Fifa 2003 - $6
Fifa Street 2 - $25
Finding Nemo - $8
F-Zero GX - $90
Gun (missing manual) - $10
Harry Potter Chambers of Secret - $12
Killer 7 - $65
Luigi's Mansion - $60
Madden 2003 - $5
Madden 2007 - $8
Mario Golf Toadstool Tour - $27
Mario Kart Double Dash - $75
Monopoly Party - $10
Monsters, Inc. Scream Arena - $7
Nascar Thunder 2003 - $7
Pikmin - $50
Power Rangers Dino Thunder - $8
Resident Evil - $25
Resident Evil 2 - $100
Resident Evil 4 - $30
Resident Evil Zero - $18
The Sims Bustin Out - $12
Smuggler's Run (missing manual) - $12
Sonic Adventure Battle 2 (missing manual) - $45
Spiderman 2 - $15
Spyro A Hero's Tail (missing manual) - $15
SSX Tricky - $28
Starfox Assault - $45 (CIB; some wear to cover art)
Super Mario Sunshine (missing manual) -$35
Super Smash Brothers Melee - $60
Ty the Tasmanian Tiger (missing manual) - $12
WWE Crush Hour - $27
WWE Day of Reckoning 2 (missing manual) - $25
Nintendo DS Games (cart only unless CIB noted)
Avatar The Game - $6
Bionicle Matoran Adventures - $6
Build-A-Bear Workshop (CIB) - $6
Carnival (CIB) - $6
Deal or No Deal - $5
Guitar Hero On Tour Bundle (CIB) - $25
Happy Feet - $4
Horsez (CIB) - $6
Hot Wheels Beat That - $6
Kung Fu Panda (CIB) - $6
Mario Party DS - $13
Mario Kart DS (loose) - $15
Mario Kart DS (CIB) - $18
Mario & Sonic at the Olympic Games (CIB) - $10
Mario & Sonic at the Olympic Winter Games (CIB) - $10
Megaman Starforce Dragon - $85 shipped
Metroid Hunters First Hunt - $6
Nacho Libre - $15
Namco Museum DS - $8
Naruto Ninja Council 3 - $6
New Super Mario Bros. (CIB) -$22
Nickelodeon Team Umizoomi - $6
Phoenix Wright Ace Attorney - $20
Picross 3D - $9
Ping Pals - $3
Planet Puzzle League - $10
Pokemon Mystery Dungeon: Explorers of Sky (case & manual only, no game) - $55
Pokemon Ranger Shadows of Almia (cart only) - $30
Ratatouille - $5
Rayman DS - $10
Ridge Racer DS - $8
Shrek Superslam - $5
Spiderman 3 - $8
Star Wars II The Original Trilogy (LEGO) - $6
Super Money Ball Touch & Roll - $6
Transformers Animated - $11
Tron Evolution - $4
Zhu Zhu Pets - $3
Nintendo 3DS (cart only unless noted)
Animal Crossing: New Leaf (CIB) - $20
Lego Marvel Superheroes: Universe in Peril - $5
Mario Kart 7 - $12
Minecraft New Nintendo 3DS Edition - $18
Pilotwings Resort - $10
Pokemon X (CIB) - $30
Skylander Giants - $6
Skylander Swap Force - $16
Skylander Trap Team - $12
Super Mario Maker - $10
Super Smash Bros (CIB) - $15
Teenage Mutant Ninja Turtles - $9
Wipeout: Create & Cash - $5
Wreck-it Ralph - $6
Yo-Kai Watch - $15
NES Games (cart only; unless noted)
8 Eyes - $11
A Boy and His Blob (cart, box, manual) - $40
Blades of Steel - $8
Bubble Bobble - $16
Burgertime - $15
Castlevania II Simon's Quest - $15
Castlevania III Dracula's Curse - $45
Chip & Dale Rescue Rangers (CIB) - $125
Contra - $40
Dick Tracy - $7
Double Dragon - $13
Donkey Kong 3 - $20
Dr. Mario - $10
Duck Tales - (cart & box) - $100
Excite Bike - $11
Faxanadu - $11
GI Joe: A Real American Hero - $75
Golf - $3
Legend of Zelda - $30
Mickey Mousecapade - $7
Mike Tyson's Punch-out - $40
Paperboy - $16
Punch-Out - $20
Rad Racer - $6
RBI Baseball 3 (cart & box) - $25
Robocop - $10
Rollerball - $8
Skate or Die 2 (cart & box) - $65
Spy Hunter - $5
Street Fighter 2010 - $15
Super Glove Ball - $7
Super Mario Bros. 2 - $20
Super Off-Road - $12
Super Team Games - $7
Teenage Mutant Ninja Turtles II - The Arcade Game (cart & box) - $80
Tiger Heli - $8
Wall Street Kid (cart, box, registration card, poster) - $45
WWF Wrestlemania - $6
SNES Games (cart only)
Aladdin - $15
Castlevania IV - $45
Clue - $5
Earthbound - $350
F-Zero (Player's Choice) - $20
Jungle Strike - $9
Ken Griffey Jr Major League Baseball - $11
Kirby's Avalanche - $15
Lion King - $11
Mario Paint - $6
Mega Man X - $32
Mickey Mania - $13
Mortal Kombat - $13
Ms. Pacman - $9
NBA All-Star Challenge - $5
Pilot Wings - $10
Scooby Doo Mystery - $11
Starfox - $15
Super Adventure Island - $16
Super Baseball 2020 - $13
Super Ghouls N Ghosts - $23
Super Mario All-Stars - $25
Super Mario Kart - $40
Super Mario World - $20
Super Punch Out - $28
Top Player Tennis - $8
WWF Raw - $13
Zombies Ate My Neighbors - $30
GBA (cart only unless noted)
Aggravation/Sorry/Scrabble - $5
Barnyard - $8
Bratz - $4
Care Bears Care Quest (CIB) - $28
Cars - $5
Cars (CIB) - $16
Castlevania Double Pack - $85
Cho Makaimura R Super Ghouls N Ghost ( Japanese Import) - $95 Shipped
Crash Bandicoot 2 N-tranced - $10
Crash Huge Adventure - $11
Curious George (CIB) - $28
Dave Mirra Freestyle BMX 2 - $4
Disney Party - $10
Disney Princess (CIB) - $12
Donkey Kong Country (GBC/CIB) - $56
Dora Explorer's Pirate Pig's Treasure - $4
Dragon Ball Z Supersonic Warriors - $20
Elf - $10
ESPN Great Outdoor Games Bass 2002 - $5
F-14 Tomcat - $7
Finding Nemo - $5
Green Eggs & Ham (CIB) - $20
Incredibles (CIB) - $14
Kong 8th Wonder of the World - $5
Lost Vikings - $25
Madden 2005 - $5
Mario Kart Super Circuit (torn label) - $20
Metroid Zero Mission - $60
Monsters Inc - $4
Monster Jam Maximum Destruction - $6
Namco Museum - $6
Oddworld Munch's Oddysee - $12
Pirates of the Caribbean - The Curse of the Black Pearl - $5
Pong Asterios Yar's Revenge - $4
Sonic Advance 3 - $25
Quad Desert Furty - $3
Shaun Palmers Pro Snowboarding (GBC/CIB) - $10
Shrek Swamp Kart Speedway - $5
Spirit Stallion of the Cimarron - $5
SpongeBob Battle for Bikini Bottom - $7
Spongebob Squarepants Super Sponge - $6
SSX 3 - $7
The Incredibles - $3
Thunder Alley - $5
Top Gear GT Championship - $10
Sony PSP (all CIB)
Crisis Core: Final Fantasy VII - $15
Gurumin A Monstrous Adventure - $42
LocoRoco - $10
Mega Man Powered Up - $38
Parappa the Rapper - $27
Sega Genesis Collection - $17
PS1 Games (CIB unless noted)
007 Tomorrow Never Dies - $7
Action Bass - $6
Andretti Racing (GH) - $5
Ball Breakers (sealed) - $10
Bass Championship - $7
Battle Arena Toshinden (GH) - $14
Bust A-Move 4 - $17
Driver 2 (GH) - $10
Fighting Force - $20
IHRA Drag Racing - $5
Missile Command - $6
MLB 2001 - $9
MLB 2003 - $9
Nascar Heat (CIB) - $7
NBA Live 2000 - $8
NBA Shootout 98 - $9
NHL 98 - $8
NHL Faceoff 97 (GH) - $5
PlayStation Underground Jampack Fall 2001 - $9
Resident Evil 2 (DualShock Edition) - $65
Rocket Power Team Rocket Rescue - $7
Rugrats in Paris: The Movie - $12
Spongebob SquarePants Super Pants - $7
Syphon Filter 2 (GH) - $10
Tecmo Super Bowl - $20
Tiger Woods 99 - $8
Tony Hawk Pro Skater 3 - $12
Twisted Metal 2 (Greatest Hits) - $32
Toy Story 2 - $22
Walt Disney World Quest: Magical Racing Tour - $20
World Cup 98 - $12
PS2 Games (CIB unless noted)
All-Star Baseball 2005 - $5
Ape Escape 2 - $48
Ape Escape 3 - $43
ATV Offroad Fury 2 - $6
Avatar the Last Airbender - $8
Batman Begins - $13
Batman Vengeance - $19
Buffy the Vampire Slayer Chaos Bleeds - $28
Burnout Revenge - $11
Burnout 3 Takedown - $13
Buzz the Mega Quiz - $12
Capcom Classics Collection Volume 2 - $13
Castlevania Lament of Innocence -$25
Corvette - $5
Crash Bandicoot The Wrath of the Cortex - $12
Crash Nitro Kart (GH) - $9
Crazy Taxi - $10
Dance Dance Revolution Extreme 2 - $7
Dead to Rights - $6
Devil May Cry (GH) - $7
Enter the Matrix - $10
Eragon - $6
Family Feud - $5
Finding Nemo - $6
Fire Pro Wrestling Returns - $10
Ford Racing 3 - $5
Frogger the Great Quest - $7
Golden Compass - $5
GTA 3- $10
Gran Turismo 3 - $5
Godfather the Game - $14
Guitar Hero - $10
Guitar Hero Aerosmith - $7
Guitar Hero II - $7
Guitar Hero III Legends of Rock - $9
High Heat Major League Baseball 2004 - $5
Hot Wheels Velocity - $10
Hot Wheels World Race (missing manual) - $12
Hobbit - $10
Ice Age 2 The Meltdown - $7
Ironman - $6
Karaoke Revolution Party - $8
Karaoke Revolution Presents: American Idol - $5
Legends of Wrestling II - $12
Lego Star Wars The Original Trilogy - $6
Lego Star Wars The Video Game - $7
Lord of the Rings Fellowship of the Ring - $10
Madden 2003 - $5
Madden 2004 - $5
Madden 2005 -$5
Madden 2007 - $5
Matt Hoffman's Pro BMX 2 - $10
Max Payne - $10
Metal Arms Glitch in the System - $16
Midway Arcade Treasures (1) - $12
Midway Arcade Treasures (2) - $12
MLB 07 the Show - $5
MLB Slugfest 2003 - $10
MLB Slugfest 2004 - $13
Namco Museum (GH) - $8
Nascar 2001 - $5
Nascar Thunder 2003 - $7
NBA Street - $12
Need for Speed Underground 2 (missing manual) - $20
NFL Blitz Pro - $10
NFL Street - $17
NFL Street 3 (missing manual) - $20
Onimusha 3 Demon Siege - $21
Pinball Hall of Fame - $5
Pirates - The Legend of Black Kat - $12
Power Rangers: Dino Thunder - $8
Reel Fishing III - $7
Resident Evil Code Veronica X - $13
Rise of Kasai - $8
Rocky - $11
Scarface the World is Yours - $45
Scooby Doo First Frights - $13
Sega Superstars - $10
Sega Superstar Tennis - $10
Shrek Superslam - $8
Simpson's Hit & Run (Greatest Hits) -$50
Spiderman - $10
Sprint Cars Road to Knoxville - $6
Spy Hunter - $7
Spy Hunter 2 (missing manual) - $7
Starsky & Hutch - $7
SSX - $7
SSX 3 - $9
SSX On Tour - $8
Superman Shadow of Apokolips - $14
Super Monkey Ball Adventure - $10
Summoner - $10
Taito Legends - $15
Teenage Mutant Ninja Turtles 2: Battlenexus (missing manual) - $17
Teen Titans - $22
Theme Park Roller Coaster - $8
Tiger Woods PGA Tour 2004 - $6
Thrillville - $6
Thrillville Off the Rails - $10
Time Crisis 3 - $23
Ty the Tasmanian Tiger - $11
Wheel of Fortune - $6
Virtua Fighter 4 (missing manual) - $6
Warriors of Might & Magic - $10
WWE Smackdown vs Raw - $11
WWE Smackdown vs Raw 2007 (Sealed) - $45
WWE Smackdown vs Raw 2007 - $17
WWE Smackdown vs Raw 2009 - $10
WWE Smackdown Shut Your Mouth - $15
PS3
Band Hero - $6
Batman Arkham Asylum - $7
Battlefield 3 - $6
Call of Duty Advanced Warfare - $6
Call of Duty Ghosts - $6
Call of Duty Mordern Warfare 3 - $6
Call of Duty 4 Modern Warfare - $7
Call of Juarez Bound in Blood - $9
Crysis 2 - $7
Dirt 2 - $12
Dirt 3 - $10
Driver San Francisco - $25
Enemy Territory Quake Wars - $9
Fifa Soccer 11 - $5
Fight Night Champion - $13
GTA IV Complete Edition - $25
Gran Turismo 5 Prologue - $8
Gran Turismo XL Edition - $11
Gran Turismo 6 - $19
Heavy Fire: Afghanistan - $10
Infamous - $6
Infamous 2 - $8
Killzone 2- $7
Killzone 3 - $7
Lego 3: Beyond Batman - $8
Lego Harry Potter Years 5-7 - $7
Lego The Hobbit - $9
LittleBigPlanet - $9
Madden 2011 - $5
Metro: Last Night - $8
Mortal Kombat Komplete Edition - $12
MLB the Show 10 - $4
MLB the Show 11 - $4
Monster Jam Path of Destruction - $20
NCAA Football 11 - $9
Sports Champions - $5
Tiger Woods PGA Tour 14 [Masters Historic Edition] - $23
Transformers Fall of Cybertron - $35
Transformers Rise of the Dark Spark - $13
Virtua Tennis 3 - $6
WWE 2K16 - $12
PS Vita
Lumines Electronic Symphony - $16
Need for Speed Most Wanted - $20
Sly Cooper Collection - $50
Sega 32X (all cart only)
Primal Rage - $50
Virtua Fighter - $24
Virtua Racing - $20
Sega Dreamcast Games (disc & manual only***; do not have original cases unless noted CIB)
Centipede - $7
Plasma Sword Night of Bilstein - $50
Psychic Force 2012 - $25
Ready 2 Rumble Boxing - $12
Resident Evil Code Veronica (CIB) - $40
Rippin Riders - $5
Sega Bass Fishing - $8
Sega Rally 2 Championship - $12
Speed Devils - $15
Sword of Berserk: Gut's Rage (game only) - $65
Trick Style - $7
Zombie Revenge - $30
Sega Genesis (**CIB unless noted)
Aladdin (cart + manual) - $10
Double Dragon (cart & box) - $45
Game Genie (loose + booklet) - $20
Hard Drivin' (Missing Manual) - $15
John Madden Football (cart + manual) - $20
Lemmings (CIB) - $30
MERCS (cart & box) - $35
NBA Jam T.E. (CIB) - $20
Prime Time NFL Football starring Deon Sanders (cart +manual) - $9
Ren & Stimpy Show: Stimpy's Intervention (CIB) - $20
Road Rash II (CIB) - $22
Robocop 3 (CIB) - $40
Streets of Rage (cart only) - $22
Super Off-Road (CIB) - $30
WWF Super Wrestlemania (CIB) - $20
X-Men (cart + manual) - $15
Zero Tolerance (CIB) - $35
Sega Master System (CIB unless noted)
Alex Kidd: The Lost Stars - $28
California Games (missing manual) - $20
Choplifter - $18
Ghostbusters - $25
Great Baseball - $10
Monopoly - $10
Parlour Games - $10
Pro Wrestling - $14
Rocky - $17
Space Harrier (missing manual) - $18
Shinobi (includes map; missing manual) - $30
Xbox (all CIB)
MechAssault 2 Lone Wolf (Limited Edition) - $8
Project Gotham Racing - $6
Xbox 360 (CIB)
Assassin's Creed - $6
Assasin's Creed II - $6
Asssasin's Creed III - $6
Battlefield Hardline Deluxe Edition - $10
Battlefield 3 Limited Edition - $6
Bioshock - $7
Bioshock Infinite - $5
Call of Duty World at War - $9
Call of Juarez: Blood Bound - $10
Civilization Revolution - $6
CSI Hard Evidence - $9
Fifa Soccer 10 - $5
Fifa Work Cup South Africa 2010 - $5
Game of Thrones - $11
Gears of War - $9
Halo 4 - $5
Injustice Gods Among Us - $5
L.A. Noire - $7
Mass Effect - $5
Mass Effect 2 - $5
N3 Ninety-Nine Nights - $20
NBA 2K12 - $5
NHL 10 - $3
NHL 14 - $6
Saints Row 2 - $10
Saints Row The Third - $5
Skate 3 - $6
Star Trek Legacy - $18
Star Wars Kinect - $7
Tiger Woods PGA Tour 2007 - $5
Tiger Woods PGA Tour 2008 - $5
Top Spin 3 - $6
Walking Dead Survival Instinct - $8
Wheel of Fortune - $14
Who Wants to Be a Millionaire -$5
Nintendo Wii (all CIB unless noted)
Animal Crossing City Folk - $20 (includes inserts but missing manual)
Celebrity Sports Showdown - $6
Guitar Hero World Tour - $18
Little League World Series Baseball 2008 - $10
Madden 2013 - $14
Mario Kart Wii - $35
Mario Super Sluggers (disc only) - $25
Mario Strikers Charged (disc only) - $10
NBA Live 09 All-Play - $5
New Super Mario Bros - $25
Super Monkey Ball Banana Blitz - $6
Super Smash Bros. Brawl - $20
Tony Hawk Downhill Jam - $5
Tony Hawk Shred Big Air - $5
Warioware Smooth Moves - $22
Wii Sports - $22
Wii Sports Resort - $30
Wheel of Fortune - $6
WWE Smackdown vs Raw 2009 - $7

Mast cell activation syndrome (MCAS) is the subject of heated debate. How are mast cell activation syndromes defined? Which diseases are included? What is the diagnosis and treatment of mast cell activation syndrome? Prof. Dr. Knut Brockow, Clinic and Polyclinic for Dermatology and Allergology at the Biederstein, Technical University of Munich answers these questions in an interview with MeinAllergiePortal.
Mast cell activation syndrome: The most important facts!
-The prototype of mast cell activation syndrome is recurrent anaphylaxis
-Other forms of idiopathic mast cell activation syndrome are being sought; however, there are mainly symptom descriptions where the diagnosis cannot be made
-Clinical suspicion of MCAS is based on recurring allergy-like symptoms on the skin, nose, respiratory tract, gastrointestinal tract and circulation
-The diagnosis of MCAS is made according to recognized international criteria based on three criteria
-MCAS is often suspected even when symptoms are inappropriate and the diagnosis is unclear; the suspicion is then not helpful for patients
-The same medications are used to treat MCAS as are used to treat allergies, in particular antihistamines and cromoglicic acid
Prof. Brockow, what kind of disease is MCAS?
Mast cell activation syndrome is not an established diagnosis, but rather a concept. Historically, this concept arose because an increasing number of patients came to the doctor's office with complaints that gave the impression of having been triggered by mast cells. These patients sometimes showed symptoms similar to those of allergic reactions, anaphylaxis or mastocytosis, but a clear diagnosis for these diseases could not be made. Nevertheless, it was suspected that there could at least be a connection with mast cell diseases. Unfortunately, the term MCAS created more uncertainty than understanding. This is because MCAS is now thrown around as a diagnosis for many patients with many symptoms and an unclear diagnosis. This is not helpful for patients and fuels short-term hope of diagnosis and cure, which cannot be fulfilled later.
Is MCAS an autoimmune disease?
No, in autoimmune diseases mast cells are not primarily involved and not as lead cells, but lymphocytes that attack the body's own structures, in some cases by forming antibodies.
Is there a connection between mast cell activation syndrome and autoimmune diseases?
No, there is no known connection between MCAS and autoimmune diseases. It has also been claimed by specific authors that other diseases, such as Ehlers-Danlos syndrome, postural orthostatic tachycardia syndrome (POTS) and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) are related to mast cell activation syndrome. However, there are no good arguments for this. Unfortunately, such claims are easy to make and difficult to refute.
What is the cause of mast cell activation syndrome?
Mast cell activation syndrome is actually more of a symptom description than a diagnosis in its own right. Mast cell activation syndrome is fully applicable to recurrent anaphylaxis (severe allergic reactions in several organ systems such as the skin, respiratory tract, digestive tract and circulatory system), for example due to insect bites. All the criteria for mast cell activation syndrome are met here. Severe allergic reactions are the most common cause of MCAS. However, although the term MCAS is correct in this context, it does not provide any additional information, as patients with such events are better described as patients with a diagnosis of anaphylaxis or allergy, and the term MCAS is somewhat confusing.
Is mast cell activation syndrome genetic?
MCAS itself is not genetic, but patients with the genetic disease mastocytosis often suffer from anaphylaxis, particularly to insect venom, and therefore MCAS. In addition, it is currently being investigated whether people with genetically determined hereditary alpha-tryptasemia suffer more frequently from MCAS.
How did the term mast cell activation syndrome come about?
There were many patients without a clear diagnosis, some of whom predominantly showed the symptoms typical of mast cell diseases. Accordingly, the experts dealing with mast cell diseases saw the need to develop a concept that took into account the “undiagnosable” symptoms of the patients. In the course of this, the terms “mast cell activation” and “mast cell activation syndrome” were defined. In addition, an attempt was made to sort all mast cell diseases into a classification with regard to mast cell activation. However, the difficulty in classifying these complaints is that many of the complaints described by patients are subjective, relatively non-specific and can be both organic and psychosomatic.
How have you defined mast cell diseases and which diseases do they include?
Mast cell diseases are defined as recurring chronic symptoms that are compatible with mast cell activation.
Mast cell activation is classified on the basis of three criteria:
Recurrent typical clinical symptoms in at least two organ systems
An increase in mast cell mediators can be detected in the blood, most frequently by determining the serum tryptase level during an acute attack
Good response of symptoms to anti-mast cell mediator-directed therapy, especially H1 antihistamines
What types of mast cell disease are there?
The classification of mast cell diseases associated with mast cell activation syndromes defines three groups:
1. primary mast cell activation syndrome
Primary mast cell activation syndrome is explained by a clonal expansion of mutated overactive mast cells. It manifests as systemic or cutaneous mastocytosis. If these criteria are not completely fulfilled, but clonal mast cells have been detected, it is referred to as monoclonal mast cell activation syndrome.
2 Secondary mast cell activation syndrome
Secondary mast cell activation syndrome is present when clear triggers of mast cell activation are known. There are established terms for secondary mast cell activation syndrome that we are more familiar with, such as “anaphylaxis” to a known trigger. The classification in the second group of mast cell diseases is therefore merely a reclassification. Examples of mast cell activation are physical urticaria or cold urticaria. Allergies such as pollen allergies are also secondary mast cell activations, as hay fever also causes symptoms typical of mast cell diseases. In pollen allergies, mast cell mediators are found in the blood serum and drugs directed against mast cells have a good effect. If the symptoms recur in several organ systems, this is referred to as mast cell activation syndrome.
3. tertiary or idiopathic mast cell activation syndrome
Tertiary or idiopathic mast cell activation syndrome refers to mast cell diseases whose triggers are unknown. This group would include, for example, chronic spontaneous urticaria, which has additional symptoms in other organs. Here we know that mast cells are activated, but not by what. This group of idiopathic mast cell activation syndromes would also include patients with as yet undescribed clinical pictures who do not fulfill the diagnostic criteria of known mast cell diseases, e.g. allergy, anaphylaxis, but in whom the disease is triggered by mast cells. In these patients, however, the connection between the symptoms and the activities of the mast cells must be proven.
Does this mean that tertiary or idiopathic mast cell activation syndrome is a diagnosis of exclusion?
Idiopathic mast cell activation syndrome can be described as a diagnosis of exclusion insofar as the prerequisite for the diagnosis is that there is no other disease causing the symptoms. However, the symptoms described are often very, very unspecific and could also be caused by a variety of other diseases. However, there are the three criteria for mast cell activation syndrome already mentioned. If these are not all fulfilled, this diagnosis cannot be made.
How common is mast cell activation syndrome?
Anaphylaxis and severe recurrent allergies are not uncommon and represent the vast majority of appropriate cases for MCAS. In addition, mastocytosis patients often have multiple anaphylaxis and therefore also MCAS. However, our initial idea of finding a new disease, idiopathic mast cell activation syndrome, has not yet been confirmed. There are many patients with many symptoms for whom a clear organic diagnosis cannot yet be made. However, it is almost never possible to prove that a defect in the mast cells is primarily responsible for the symptoms. Many of these patients describe symptoms that could fit, and in some patients anti-allergic drugs also have a positive effect. But in only very few patients can an increase in mast cell mediators be detected during an acute attack. I now believe that somatic stress disorders could play a significant role in many of the patients examined.
Histamine intolerance is also a diagnosis of exclusion, is there a connection with mast cell activation syndrome?
Histamine intolerance can cause similar symptoms, but is not a mast cell disorder and has nothing to do with MCAS. When mast cells are activated, the messenger substance histamine is released, which in turn can cause symptoms. In histamine intolerance, the mast cell is not activated - it is not involved in any way. Rather, histamine intolerance describes patients with an increased sensitivity to histamine, which is supplied, for example, via the diet. This can lead to similar symptoms, but in contrast to mast cell activation syndrome, histamine intolerance has a clear trigger, histamine. As a result, the symptoms occur after eating histamine-rich foods, but disappear again if the patient follows a low-histamine diet. A test is also available to diagnose histamine intolerance.
So there are also patients with suspected mast cell activation syndrome who cannot be assigned to a classification group, even though they have corresponding symptoms?
There are many patients in whom no mast cell activation syndrome can be detected despite suspicion. They do not fit into one of the three groups. However, this also used to include monoclonal mast cell activation syndrome. These patients showed anaphylaxis and a KIT mutation, but not the full criteria for mastocytosis. In the meantime, a separate disease diagnosis has been created for these patients. The independent accepted disease of these patients therefore lies between mastocytosis and normal findings.
We thought that there might be other forms of idiopathic MCAS with clinical pictures that have not yet been described. However, this is not supported by the findings to date. There are patients who show symptoms but do not meet the necessary criteria for idiopathic mast cell activation syndrome. In these patients, the diagnosis remains unclear. In how many of these patients functional physical complaints play a role still needs to be investigated.
Are there risk factors that favor mast cell activation syndrome?
There are hardly any recognized studies on this. In a study conducted by Cem Akin in the USA, patients were examined who met the three criteria for idiopathic mast cell activation syndrome. They had the right symptoms, there was an increase in mediators and their symptoms improved with treatment. It was shown that many of these patients suffered from urticaria factitia, a scratch-induced urticaria, abdominal pain and flushing.
Recently, a genetic trait was discovered, hereditary alpha-tryptasemia with elevated basal serum tryptase levels. In patients with this trait and insect venom allergy, the severity of the allergic reaction appears to be increased. It is also discussed that the frequency of mast cell activation syndrome is increased in patients with this genetic trait. However, the published studies are not yet unanimous in this respect.
What symptoms can occur with MCAS?
The following symptoms could be signs of mast cell activation syndrome:
MCAS symptoms on the skin:
Appearance of sudden intense redness (flushing)
itching
wheal formation
Deep wheal formation (angioedema or Quincke's edema)
MCAS symptoms on the nose:
Nasal congestion
Nasal itching
MCAS symptoms in the airways:
Swelling of the upper airways
Wheezing
Shortness of breath
MCAS symptoms of the digestive tract:
Vomiting
abdominal pain
diarrhea
Systemic MCAS symptoms:
Syncope - where you suddenly lose consciousness, but only for a short time
Sudden drop in blood pressure
Allergic shock
These symptoms can occur together or individually. In principle, symptoms must occur in two or more organ systems for MCAS. These symptoms, together with the typical skin changes and anaphylaxis, are also typical of mastocytosis.
Are muscle pain and hair loss also symptoms of MCAS?
No, why would anyone think that these symptoms are primarily caused by a malfunction of mast cells? Mast cells are not important cells for muscle pain and hair loss.
How is MCAS diagnosed?
MCAS is a diagnosis of exclusion, i.e. there is no mast cell activation syndrome test. However, this does not mean that all other diseases must be ruled out before a diagnosis of MCAS can be made.
When testing directly for mast cell activation syndrome, three criteria would be examined, all of which must be met, not just two:
First, there must be a matching of symptoms to see if the above symptoms are leading, recurrent and occur in at least two organ systems.
Is there a substantial or complete improvement in the clinical symptoms when taking anti-allergic medication, antihistamines or cromoglicic acid? Then this criterion would apply.
The blood levels of tryptase in the serum can now be examined at two different points in time. This would check whether there is an increase in mast cell mediators or tryptase in the blood serum in a highly symptomatic phase or during a seizure compared to a time when there are no symptoms.
What does the tryptase level in the blood mean in the diagnosis of mast cell activation syndrome?
If the mast cell mediator tryptase rises by 20 percent of the basal value, i.e. the initial value, + 2 ng/ml during such an episode, the diagnosis of mast cell activation syndrome has been made without the need to rule out other diseases beforehand. However, taking blood samples to determine the tryptase levels is very time-consuming, because a blood sample should be taken in the normal state and then another blood sample should be taken during a seizure or a highly symptomatic episode. This means that the patient must see a doctor in good time for a blood test during the acute phase. If these tests are negative, mast cell activation syndrome cannot be confirmed.
Elevated tryptase levels also play a role in anaphylaxis, is there a connection with mast cell activation syndrome?
Anaphylaxis is an extremely strong mast cell activation, the “prototype” of mast cell activation, so to speak. The tryptase level rises, so that it is considered an indicator of anaphylaxis. Here too, the basal value is measured and compared with the value during an episode. The relevant factor is the resulting increase in the tryptase value. The therapy against mast cells is effective in this case. In this respect, anaphylaxis is the classic form of mast cell activation syndrome.
The tryptase value also plays a role in the diagnosis of mastocytosis, what are the correlations here?
Mastocytosis patients also have an elevated baseline tryptase level. This is therefore an indication of mastocytosis and an indication for a final diagnosis by means of a bone marrow biopsy. However, there is also a mastocytosis-independent correlation between tryptase and anaphylaxis. People who have a higher number of mast cells often develop more severe anaphylaxis than people with fewer mast cells. The tryptase basal value is therefore considered a kind of indicator for the total mast cells in the body. For example, insect venom anaphylactic patients with elevated basal mast cell tryptase levels in the blood are at increased risk of severe anaphylaxis.
What can be done against MCAS and which medications help?
The aim of treatment for mast cell activation syndrome is to slow down the effect of the overactivated mast cells and to calm the mast cells. In particular, the avoidance of allergic triggers is available for this purpose.
Histamine receptor blockers are tried as medication to block the effects of mast cell activation by histamine. Mast cell stabilizers or blockers of mast cell release, cromoglicic acid, can also calm the mast cells. Cromoglicic acid is also used in mastocytosis patients. It is important to know that the use of cromoglicic acid is not advisable if the attack has already run its course. On the other hand, many patients achieve a significant improvement in symptoms if cromoglicic acid is taken continuously as a preventive measure and in a sufficiently high dose. This has also been shown to be the case with antihistamines.
Another option would be leukotriene receptor antagonists and corticosteroids in the short term, but never over a longer period of time.
Unfortunately, many patients with previously unexplained complaints are given a suspected diagnosis of MCAS in the hope that this knowledge will lead to better treatment or perhaps a cure. However, apart from the drugs mentioned, which can also be used on a trial basis in cases of suspected MCAS, there are no other useful drugs available. In this respect, the suspicion of MCAS unfortunately does not offer patients any additional treatment options.
Are there foods that activate or deactivate mast cells?
No such foods are known in humans. Of course, it is possible to bombard mast cells in a test tube with high concentrations of food and measure whether the natural activation of mast cells is increased or reduced. However, such tests are generally not meaningful for humans when consumed.
Can naturopathy help with mast cell activation syndrome?
I don't know how it could help. Naturopathy is the attempt to achieve a positive effect through naturally occurring active substances. Is the avoidance of allergens in our natural environment already naturopathy?
Could certain vitamins, for example vitamin C, be beneficial for MCAS?
This is claimed by a few doctors without any convincing results. Vitamin C is also said to help against seasickness. After all, vitamin C, taken in normal amounts, is not harmful and is beneficial. Sometimes the conviction that a substance is good for you also helps. That's why the experiment doesn't bother me.
Is it possible to prevent mast cell activation syndrome?
Yes, by avoiding MCAS with a known trigger. This is the case with allergies. In the case of allergies and recurrent anaphylaxis as a form of MCAS, omalizumab, an antibody against immunoglobulin E, can also be used in individual patients.
Prof. Brockow, thank you very much for this interview!
https://www.mein-allergie-portal.com/mastozytose-mastzellaktivierungssyndrom-mcas/925-idiopathisches-mastzellenaktivierungssyndrom-ein-neues-krankheitsbild.html

https://www.uniklinikum-leipzig.de/einrichtungen/lica/Seiten/mastzell-aktivierungs-ayndrom-mcas.aspx
More and more patients are contacting us because they suspect that they have mast cell activation syndrome (MCAS). We would therefore like to provide some basic information on this clinical picture based on a recent publication (Weiler et al. J Allergy Clin Immunol. 2019 Aug 30).
Some publications and the lay press define the diagnostic criteria for MCAS very broadly. In some cases, findings of non-validated laboratory tests are associated with atypical symptoms in order to diagnose MCAS. This sometimes leads to great confusion among patients and medical professionals. This becomes critical when underlying diseases that are not mediated by mast cells remain undiagnosed.
Clinical symptoms for which there is no evidence of a connection with MCAS, but which are nevertheless frequently associated with it, are
Tiredness / fatigue, Feeling ill, Fibromyalgia-like pain, dermographism, oedema, Various skin rashes, Tinnitus, Lymph node swelling, constipation, Prostatitis, Chronic back pain, Headache, Mood swings, Anxiety, Post-traumatic stress, Weight changes, Hypothyroidism / hyperthyroidism, Polycythemia, Psychiatric/neurological complaints. Anemia Electrolyte disorders, Increased or decreased blood protein levels
Complaints or symptoms may also not be used for diagnosis if they are present in isolation, e.g. abdominal pain, diarrhea or reddening of the skin, or if they occur chronically rather than in attacks.
Affected organs and associated symptoms that are of diagnostic value for making a diagnosis (at least two of four organ systems must be affected, typically in an attack-like manner):
-Cardiovascular: drop in blood pressure, palpitations, dizziness / loss of consciousness / collapse
-Respiratory tract: wheezing, shortness of breath, stridor when inhaling
-Skin: paroxysmal redness, urticaria, itching, angioedema
-Gastrointestinal tract: diarrhea, nausea, abdominal cramps
Another characteristic feature is the detection of elevated blood levels of transmitter substances originating from the mast cell, such as tryptase. If the tryptase level is significantly elevated, mastocytosis of the skin and other organs must be ruled out (presentation to outpatient dermatology and hematology). The diamine oxidase measurement in serum has no diagnostic value with regard to MCAS. If you notice that certain foods or medications trigger or intensify your symptoms, these must be avoided.
With MCAS, the symptoms typically respond to treatment with antihistamines; only rarely will other medications (e.g. glucocorticosteroids, omalizumab) be used.
The prescription of emergency medication may be useful.
If underlying allergies are suspected, we advise you to consult an allergy specialist near your home. If they are in favor of a referral, we will be happy to make appointments. Last but not least, MCAS is a diagnosis of exclusion.
We are not the right contact for complaints of isolated organ systems or non-specific general symptoms.

My dad and grandfather had a disease related to legs which is genetical and it got passed down to me. So, today I was in the metro and saw this guy offering the seat to an old lady. My legs were hurting because I am not able to stand for more than an hour. I saw the empty seat and sat there, I acted when I saw the opportunity.
But this guy, who was sitting there before me. Damn he was ugly af.
So yeah he started yelling at me. I am introverted and I read Fredpicklerick neitchze also so I couldnt bring myself to say anything to him.
While he was burning me with his sour language I saw this girl taling pictures or maybe recording video of him yelling and cussing me.
It was very embarassing.

This is not medical advice. I am not suggesting you take these. I am, however, suggesting you perhaps ask your doctor about these supplements and whether it would be okay to take them. You could even present the studies.
Now I can't promise these will be the golden bullet to stop NAFLD or reverse it, but what I can promise is that these supplements are well tolerated, have few side effects when taken as directed, and are generally helpful to very helpful. I don't have NAFLD however I do have genetic liver issues, and have seen positive results from these supplements. I therefore feel like this information is too important not to share. There's also a lot of research backing up weight loss as a result of these supplements, especially NAC - look into it on google scholar, or ask in the comments and i'll provide some.
N-Acetyl L-Cysteine (NAC) is a supplement and medication derived from the amino acid L-cysteine. It acts as a precursor to glutathione, a powerful antioxidant that helps protect cells from damage caused by free radicals and toxins.
It is a well tolerated supplement that shows excellent promise in preventing and treating liver disease, to me it looks to be a miracle supplement as it helps so many conditions.

1. NAC shows an enhanced effect to improve liver function by reducing the levels of oxidative stress and pro-inflammatory markers such as IL-6, TNF-α and IL-1β, NF-κB, TGFβ-1, and MDA levels. This is a review/meta analysis that looks into many studies and found that the results are very promising, even predicting a large increase in demand for NAC because it's so promising.
2. Long-term administration of NAC significantly reduced liver steatosis and triglyceride levels in mice fed a high-fat diet. The researchers suggested that NAC's ability to alleviate endoplasmic reticulum stress and improve fatty acid oxidation contributed to these beneficial effects​
3. NAC treatment in mice leads to a reduction in Liver Fat Accumulation, reduces oxidative stress, improved liver function and concluded it shows potential as a therepeutic agent
4. https://www.sciencedirect.com/science/article/abs/pii/S2213434423000154 - it significantly increased albumin (ALB) and decreased bilirubin levels, a positive change for both measures. The meta analysis suggested larger trials are necessary assessing dose.

Zinc is an essential mineral that plays a crucial role in various biological functions, including those related to liver health

1. Zinc supplementation for three months improved insulin resistance and oxidative stress status in overweight/obese NAFLD patients
2. The Effect of Zinc Supplementation on Steatosis Severity and Liver Function Enzymes in Overweight/Obese Patients with Mild to Moderate Non-alcoholic Fatty Liver Following Calorie-Restricted Diet: a Double-Blind, Randomized Placebo-Controlled Trial

Why I'm posting both together: Zinc acts as a cofactor for a variety of enzymes, including those involved in the metabolism of amino acids like cysteine. For example, the enzyme zinc metalloproteinase relies on zinc to maintain its structural integrity and catalytic function, which can affect the processing of cysteine and related compounds. Zinc is crucial for the storage and secretion of insulin in the pancreas. Insulin contains cysteine residues that form disulfide bonds, essential for its proper structure and function.
Co-administration of zinc and n-acetylcysteine prevents arsenic-induced tissue oxidative stress in male rats. This study doesn't look into liver disease, but it shows remarkable protection against oxidative stress, which is a cause of liver damage.
The combination showed remarkable protection against blood delta-aminolevulinic acid dehydratase (ALAD) activity as well as providing protection to hepatic biochemical variables indicative of oxidative stress
Good luck everyone!

Apologies if I do anything wrong, this is my first time posting here.
I get this strange recurring rash, almost always on my thighs/butt, but sometimes on the inner arms as well. The area will suddenly get hot and itchy, and after I scratch it (not especially hard) the skin will break and bleed and the area will become covered in small red dots and ugly red streaks for a few days. Doesn't feel any different after the initial scratching. Eventually goes away after a few days. Most of the time when I scratch the same areas nothing happens.
I don't think it's environmental, since I've gotten them before and after moving around throughout the years. I don't think it's clothing related, since I've gotten them while wearing full pants and shorts. Really confused as to what it could be.
Pictures here.

2.3.5 Controversial views and perceptions of the clinical picture of MCAS
2.3.5.1 Alternative diagnostic criteria ("Consensus-2")
In 2011, the group of authors led by Gerald Molderings from the Institute for Human Genetics at the University Hospital Bonn and Lawrence Afrin published their own approach to the diagnosis of MCAS (51). In contrast to the diagnostic criteria of Valent et al. (1), the focus here is more on clinical symptoms. In 2016, Afrin et al. published a list of the most common symptoms that could indicate MCAS (52). Furthermore a questionnaire was developed and published on a website (53), after the answers to which the suspected diagnosis of MCAS could be supported or ruled out depending on the scores obtained. In a recently published publication, the working group referred to their diagnostic criteria as "Consensus-2" and compared and discussed them with the criteria of Valent et al. from 2016 (so-called "Consensus-1") (51). An important difference to the criteria Valent et al. 2016, the authors consider the symptoms not only as the main criterion, but also a much wider range of previously unexplained symptoms (111 unexplained symptoms(44)) as the most important indication of a a mast cell-mediated cause (14 symptoms in Valent et al. (1)). As The diagnosis of MCAS is considered confirmed if the main criterion is present together with a secondary criterion and possible alternative diagnoses have been excluded. The secondary criteria, in turn, are based on observations made at the time of the 500 people with suspected MCAS at the time of the first publication (44). Further differences between the two consensuses can be found in the laboratory parameters to be determined. For example, the researchers from different disciplines, which according to their own statements can draw on a wealth of experience of of over 10,000 MCAS patients (diagnosed according to their own criteria, nota bene), consider CgA to be specific for mast cells in addition to tryptase, among other things (44). The counterargument of the lower specificity compared to serum tryptase is granted a certain validity in the addendum to the "Consensus-2" published in 2020 (44), however the differential diagnoses with elevated CgA values should be easy to rule out and other markers are also never 100% specific. However, another group was already able to show in 2017 that CgA should not be used as a marker for mast cell disease(49). Furthermore the group of authors of the "Consensus-2" counts heparin as an important marker for MCAS, which should be determined after venous congestion using a blood pressure cuff (54). This maneuver was reported to cause irritation of excessively activatable mast cells with release of heparin in the congested area. Interestingly, the following section mentions markers such as IL-6 or tumor necrosis factor (TNF) which, due to their lack of specificity, are not used in diagnostics, but only in the evaluation of a successful therapy. The authors of "Consensus-2" criticize "Consensus-1" for, among other things the lack of definitions for a treatment response, whereby the "Consensus-2 does not provide any concrete proposals for evaluating or monitoring the response to therapy. Another point of criticism is the lack of exclusion of other comorbidities or differential diagnoses, such as CFS, EDS and irritable bowel syndrome, as clinical indications of MCAS. [...] In return, the AAAAI expressly points out that there is no evidence to date of a connection between CFS or EDS and MCAS. Overall, the clinical picture of MCAS is so complex and heterogeneous that a precise definition of a diagnostic algorithm is not possible at the present time. Molderings et al. therefore propose the acceptance of both the "Consensus1" according to Valent et al. and their "Consensus-2" until more precise findings are available through research. The resulting disadvantages, such as the the poorer comparability of patient populations in scientific studies would weigh less heavily than those resulting from the rejection of "Consensus-2" (an underdiagnosis due to criteria that are too restrictive according to the authors). On the other hand, the large number of non-specific complaints that are supposedly associated with MCAS harbors the risk of inflationary diagnosis.
2.3.5.2 Presentation in the lay press
An expansion of the MCAS definition with the use of non-validated clinical and laboratory chemical parameters for diagnosis is frequently found in the lay media, above all on websites, but also in the specialist literature. Increasingly, patients with (suspected) MCAS are organizing themselves with commitment and are increasingly organizing themselves into interest groups such as MCAS Hope e.V., which campaigns for the recognition of MCAS "as an independent disease". In addition They also network those affected and their relatives and carry out public relations work, which aims to make the clinical picture known to a broader public. This expansion of the diagnostic criteria described above increases the risk of a misdiagnosis of MCAS and overlooking the underlying disease, which may be easily treatable. On the other hand, such an erroneous diagnosis can also lead to the use of unnecessary or potentially harmful therapies for MCAS and supposed comorbidities (20). Shortly after publication of the review paper "Doctor, I Think I Am Suffering from MCAS: Differential Diagnosis and Separating Facts from Fiction" by Valent et al. a self claimed affected person started an online petition in which she demands the authors and the publishing Journal of Allergy and Clinical Immunology to remove the article (55). Among other things, they criticize the criterion of the tryptase increase, which is too harsh and would therefore prevent many patients from being diagnosed. The clinic also does not typically manifest as anaphylaxis, contrary to what is described in the paper, since mediator release in anaphylactic degranulation differs from that in piecemeal degranulation. Finally, the author of the petition, who sees herself as a "patient spokesperson", reports on personal experiences of frustration and feelings of frustration and rejection that were conveyed to her by doctors in the course of her medical history. The petition has so far reached just under 3,000 of the targeted 5,000 digital signatures (as of December 2020) and shows in particular how emotional the issue of the topic of MCAS is being observed and discussed not only in professional circles, but also among patients. Apparently, some patients find the diagnosis of MCAS to be the last explanation for their multiple non-specific symptoms and hope for more acceptance in scientific circles.
2.3.5.3 Difficulties in making a diagnosis
In recent years, despite the existence of consensus criteria, a (suspected) diagnosis is often made in practice, even though these criteria are insufficiently fulfilled. In some cases, the MCAS diagnosis is also increasingly used for otherwise inexplicable conditions that cannot otherwise be explained. The evaluation of symptoms without a known direct connection with the release of mast cell mediators, for example from the neurological or psychiatric spectrum, as a manifestation of the disease leads to a further dilution of the MCAS diagnosis (43). In the "Bonn" questionnaire, the vast majority of the items asked are not based on the consensus criteria formulated by Valent et al. for example they see the sonographic evidence of an enlarged liver as an indication of the disease (53). The measurement of a tryptase elevation in acute relapse, as required by the diagnostic criteria is difficult to implement in practice, whether for reasons of time, capacity or billing. Targeted therapy trials with maximum specificity with regard to all possible decisive mediators are not possible without prior measurement of urinary metabolites and, in the absence of criteria or measuring instruments often do not produce satisfactory results (43). Last but not least, the wide range of possible differential diagnoses, such as for example from the endocrinological, neurological, psychiatric or cardiovascular area, further complicates the diagnosis (43).
Translated with deep.l
https://refubium.fu-berlin.de/bitstream/handle/fub188/32749/diss_s.gu.pdf;jsessionid=A575C43E11977D2F576404BF69D6469C?sequence=3

I was reading a bug subreddit earlier this week, and someone mentioned getting bitten by a tick, and said something about a bullseye rash. I realized a mysterious rash I got about 3 years ago looks exactly like a bullseye rash associated with Lyme disease.
I don’t think I have been symptomatic? I have some random joint/muscle pain here and there, but mostly attribute it to exercise, since I am pretty active.
I can’t attach pictures of the rash (located back of leg), but it started as a red circle about 5cm in diameter and turned into a bullseye-like shape with a red bump in the middle, and was about 8 cm total diameter. I never saw the tick (if that’s what bit me)…
EDIT: photos in comments
Should I/can I still be tested for Lyme? Is it possible my body fought off infection on its own? I’ve seen so much conflicting info online.
Located in Utah.
Thanks!

Hi!
I am a 32F , 5’7” tall, about 130lbs, Caucasian, live in Canada. Current medications include tylenol/ibuprofen, prucalopride (for GI motility) and birth control. Attending regular physiotherapy for multiple conditions. Symptoms began around 2016 and have progressed since.
I have a pretty intolerable combination of symptoms at the moment - I’m seeing different specialists for each condition, but I’m wondering if there might be something connecting my symptoms that’s being missed. I really would welcome any ideas, because this absolutely sucks - life is coming to a standstill at this point.

• trigeminal nerve pain and numbness along the trigeminal distribution - this comes and goes but sticks around for days or weeks once it starts. Right side only…wildly painful
• increased migraine frequency - about 1-2 per month, used to get 1-2 per year
• chronic pelvic pain, more recently confirmed involvement of the pudendal nerve. Pain and periodic numbness along the PN distribution, mostly left side…also wildly painful!
• burning left shoulder / upper back pain, L side
• random numbness / tingling in lower limbs, both sides, not following any specific distribution that I can tell
• periods of mild urinary incontinence or retention
• chronic constipation, treatment resistant
• potentially endometriosis, adenomyosis - waiting for laparoscopy
• maxillary and mandibular recession and cant, tmj disorder both sides
• quite severe silent reflux
• waves of severe fatigue, flu like symptoms, systemic joint pain (elbows, wrists, knees hot, red, and painful) - was happening once per month and now less frequently, maybe once every 3 months
• Thygeson’s disease diagnosed in R eye

I had a brain mri without contrast that was normal except for a “T2 and FLAIR hyperintense focus within the right peritrigonal region measuring 9mm”. My understanding was that this wasn’t anything really notable. LumbaSacral MRI also normal, except for some wearing of the facet joints. Blood work is generally normal.
I realize I could definitely just be unlucky to have multiple things happening here (and I get that the stress of being sick with one condition could exacerbate another). But I don’t really have anyone who is looking at the big picture - is there any sign that there could be something going on connecting these symptoms?
Thanks for your insight!

Nursing assignment writers cover a wide range of topics to help nursing students understand different aspects of healthcare. These topics are like pieces of a puzzle that come together to create a bigger picture of nursing practice. Let's explore some of these topics in more detail:

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3. Medical Conditions: Nursing assignment writers also cover various medical conditions, such as diabetes, heart disease, and mental health disorders. They help students understand the causes, symptoms, and treatment options for different illnesses.
4. Nursing Ethics: Ethics is a crucial aspect of nursing practice, and writers often delve into topics related to ethical decision-making, patient confidentiality, and professional conduct. They help students navigate complex ethical dilemmas they may encounter in their careers.
5. Evidence-Based Practice: Nursing assignment writers emphasize the importance of evidence-based practice, which involves using research findings to inform clinical decisions. They teach students how to critically evaluate research studies and apply evidence-based interventions in patient care.
6. Nursing Theory: Understanding nursing theory is essential for students to develop a solid foundation in nursing practice. Writers explain different nursing theories and their applications in clinical settings, helping students understand the underlying principles of nursing care.
7. Leadership and Management: Nursing assignment writers also cover topics related to leadership and management in healthcare settings. This may include discussions on delegation, conflict resolution, and quality improvement initiatives.
8. Cultural Competence: In today's diverse healthcare environment, cultural competence is essential for providing patient-centered care. Writers discuss topics related to cultural awareness, sensitivity, and competence, helping students learn how to effectively communicate and collaborate with patients from diverse backgrounds.
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In summary, nursing assignment writers cover a diverse range of topics to provide comprehensive support to nursing students. By addressing these topics in their assignments, writers help students develop the knowledge, skills, and competencies needed to excel in their future nursing careers.

DAY: MAY 13, 2024

• 5-13-2024BIKING REVEALED TO BE ASSOCIATED WITH LESS KNEE PAIN LATER IN LIFE A study reveals that people who participated in regular bicycling over their lifetime had a lower prevalence of frequent knee pain, radiographic osteoarthritis (ROA) and symptomatic radiographic osteoarthritis (SOA). Rheumatologists often encourage regular physical activity for the prevention of osteoarthritis, the most common form of arthritis. However, some exercises are more effective than others.
• 5-13-2024STRESSFUL LIFE EVENTS CAN INCREASE YOUR RISK OF ALZHEIMER’S Stressful life events, such as the death of a loved one or divorce, put a person at greater risk of developing dementia in later life, a recent study has found. But only if the stressful event happened in childhood or midlife. The study included 1,290 people at increased risk of developing Alzheimer’s disease. The researchers looked at 18 stressful life events and when in people’s lives they happened.
• 5-13-2024TIPS FOR LOWERING STROKE RISK May is National Stroke Awareness Month, and as part of everyday awareness, Mayo Clinic health care professionals suggest reducing stroke risk and knowing the signs. A stroke happens every 40 seconds in the U.S., and the likelihood of stroke increases with age, according to the National Institutes of Health. Preventing a stroke is a crucial aspect of health care, as about 80% of all strokes are preventable. The focus is on managing risk factors to reduce the long-term risk of stroke.
• 5-13-2024IT’S TIME TO USE TIKTOK TO TALK TO YOUNG PEOPLE ABOUT OBESITY, SAYS RESEARCHER There is an urgent need to harness the potential of TikTok and other social media channels to provide scientific information about obesity to young people in engaging and accessible way . The popularity and broad reach of such platforms provides the opportunity to reach diverse audiences, including teenagers and young adults, explains lead researcher Dr. Antonella Franceschelli, of Unicamillus International Medical University, Rome, Italy.
• 5-13-2024WHY YOU SHOULD NEVER TAKE NUTRITION ADVICE FROM A CENTENARIAN It’s a cliche of reporting on people who reach 100 years of age, or even 110, to ask them some variation of the question: “What did you do to live this long?” Inevitably, some interesting and unexpected answer is highlighted. Fish and chips every Friday. Drinking a glass of strong liquor every day. Bacon for breakfast every morning. Wine and chocolate. While a popular news story, this is a relatively meaningless question that doesn’t help us understand why certain people have lived so long.
• 5-13-2024JUNK FOOD MARKETING ON VIDEOGAME LIVESTREAMING PLATFORMS INCREASES PURCHASES AND CONSUMPTION AMONG TEENS, STUDY FINDS Food and drink advertisements on videogame livestreaming platforms (VGLSPs) like Twitch are associated with more positive attitudes towards, and purchases and intake of, unhealthy foods that are high in fat, salt and/or sugar (HFSS) like energy drinks among adolescents aged 18 or younger. The concerning findings prompt researchers to call for stronger regulations on digital marketing of unhealthy foods to young people on these platforms, where there is currently no effective regulation
• 5-13-2024HIGHER BLOOD SUGAR LEVEL AT GESTATIONAL DIABETES DIAGNOSIS LINKED TO HARMFUL OUTCOMES FOR MOTHERS AND BABIES The higher the blood sugar level in pregnant women when first diagnosed with diabetes, the higher the risk of complications around and after birth
• 5-13-2024ASKING ADULTS WITH OBESITY ABOUT THEIR WEIGHT DURING CHILDHOOD COULD HELP DETERMINE THEIR MORTALITY RISK Being asked whether you considered yourself a normal weight, plumper or thinner as a child when attending a doctor’s appointment as an adult might appear like a very strange question to ask, but new research suggests that such questions can help identify increased mortality risk in adults living with obesity.
• 5-13-2024ENERGY DRINKS CAN LEAD TO SERIOUS HEART ISSUES IN KIDS AND TEENS, HEALTH EXPERTS SAY Hennessy Sepulveda thought she was going to die. “I began dissociating as I was driving. I was 10 minutes away from my house. My vision started warping and the lights were hitting me really bright,” she said. “I felt my chest pounding, I felt a wave of panic hit me—I knew something was wrong.” Sepulveda, a Florida International University student who was 19 at the time, was admitted to the hospital, and was surprised by the cause of her symptoms
• 5-13-2024A BLOOD TEST TO HELP DETECT LUNG CANCER? NEW TEST OFFERED AT 18 LOCATIONS Julie Harris had never been tested for lung cancer. A low-dose CT scan, the only recommended screening for adults at risk of developing lung cancer, was not something she’d ever found time to do. But when her primary care doctor recently suggested a new blood test to help look for signs of the disease, Harris was intrigued. She had her blood drawn the same day, in the same building as her doctor’s appointment.
• 5-13-2024STUDY SHOWS EXERCISING SLOWS OUR PERCEPTION OF TIME results of a new study show for the first time that individuals tend to experience time as moving slower when they are exercising compared to when they are resting or after completing their exercise.
• 5-13-2024BREAKTHROUGH THERAPIES ARE SAVING LIVES, BUT CAN WE AFFORD THEM? Harnessing the body’s own cells to fight disease, long a medical dream, is finally a reality. Now comes the bill. Last month, Stanford became the first hospital in the nation to use a new $515,000 cell therapy to treat a patient with advanced melanoma. A related approach, costing $420,000 to $475,000, is offering hope to patients with lethal blood cancers. Meanwhile, cells fixed by gene therapy can slow, even stop, the progression of intractable diseases like sickle cell or beta thalassemia—
• 5-13-2024RESEARCH FINDS DAYLIGHT SAVING TIME SPELLS BAD NEWS FOR HEALTHY HABITS
• 5-13-2024HOW READING HELPS YOUNG CHILDREN LEARN ABOUT THE CONCEPT OF PAIN
• 5-13-2024HEART FAILURE PATIENTS WHO DO YOGA HAVE STRONGER HEARTS AND CAN BE MORE ACTIVE, RESEARCH SUGGESTS
• 5-13-2024ITALIAN STUDY FINDS EVIDENCE OF BODY DYSMORPHIA IN PROFILE PICTURES OF PEOPLE LIVING WITH OBESITY
• 5-13-2024UNDERSTANDING AND PREVENTING BLADDER CANCER
• 5-13-2024OUR BRAINS TRICK US INTO THINKING CONSCIOUSNESS CAN RESIDE OUTSIDE THE BODY, RESEARCH ARGUES
• 5-13-2024YOGA SHOWS ‘MOST IMPROVEMENT’ IN RESTORING BRAIN HEALTH IN LONG-TERM CANCER SURVIVORS, RESEARCHER SAYS
• 5-13-2024DISTURBING NEW TRENDS ARE DRIVING UP THE NUMBERS
• 5-13-2024SUPPORTING WEIGHT-LOSS MEDICATIONS WITH ADEQUATE, TAILORED NUTRITION
• 5-13-2024WHAT HAPPENS INSIDE A SLEEPWALKER’S BRAIN?
• 5-13-2024COMING OFF OZEMPIC SLOWLY COULD PREVENT WEIGHT GAIN, STUDY SHOWS
• 5-13-2024STUDY SHOWS ALARMING RISE OF ELECTRONIC VAPING USE IN US ADOLESCENTS
• 5-13-2024UK SURVEY FINDS ‘DISGUST FACTOR’ NEEDS TO BE OVERCOME IF EATING INSECTS IS TO BECOME TRULY MAINSTREAM
• 5-13-2024SEMAGLUTIDE CAN YIELD WEIGHT LOSS, LOWER HEART ISSUES FOR AT LEAST FOUR YEARS IN NON-DIABETIC ADULTS WITH OVERWEIGHT
• 5-13-2024BETTER NUTRITION CAN HELP FIREFIGHTERS FIGHT CANCER
• 5-13-2024EXPLORING THE BIOLOGICAL BASIS FOR RESILIENCE
• 5-13-2024REMOTE HEART FAILURE MONITORING DEVICE COULD PREVENT HOSPITALIZATIONS
• 5-13-2024IDENTICAL ODORS SEEM DIFFERENT WHEN GIVEN DIFFERENT NAMES
• 5-13-2024HOW CANNABIS AND PSILOCYBIN MIGHT HELP SOME OF THE 50 MILLION AMERICANS WHO ARE EXPERIENCING CHRONIC PAIN
• 5-13-2024AUTISTIC CHILDREN COULD BE THE REAL WINNERS FROM ONLINE GAMES
• 5-13-2024TEENAGE USERS OF HIGH-THC CANNABIS VARIETIES TWICE AS LIKELY TO EXPERIENCE PSYCHOTIC EPISODES
• 5-13-2024PEPTIDE-BASED HYDROGEL SHOWS PROMISE FOR A WIDE RANGE OF TISSUE AND ORGAN REPAIR
• 5-13-2024TO AVENGE OR NOT TO AVENGE? PSYCHOLOGISTS DIG DEEPER INTO HOW PEOPLE SEE REVENGE AND THOSE WHO DO IT
• 5-13-2024TRANSGENDER PRETEENS REPORT 13 HOURS OF DAILY SCREEN TIME
• 5-13-2024STUDY FINDINGS DEMONSTRATE BENEFIT TO PEDIATRIC CELIAC DISEASE MASS SCREENING
• 5-13-2024COMMONLY USED ANTIBIOTIC BRINGS MORE COMPLICATIONS, DEATH IN THE SICKEST PATIENTS
• 5-13-2024NEW PAPER EXAMINES POTENTIAL POWER AND PITFALLS OF HARNESSING ARTIFICIAL INTELLIGENCE FOR SLEEP MEDICINE
• 5-13-2024VARIATIONS IN TELOMERE LENGTHENING GENES MAY PREDISPOSE SOME PEOPLE TO PAPILLARY THYROID CANCER
• 5-13-2024WHAT IS THE PROCESS OF AN ATHLETE BEING ‘MEDICALLY RETIRED’ DUE TO CONCUSSION?
• 5-13-2024NOT SURE ABOUT VACCINES? HOW MESSAGING IS FRAMED MAKES A DIFFERENCE, NEW RESEARCH SHOWS
• 5-13-2024NEW STUDY REVEALS THE KEY ROLE OF MITOCHONDRIAL PROTEINS IN CARDIAC REGENERATION
• 5-13-2024NEW SYNTHETIC BIOMARKER TECHNOLOGY DIFFERENTIATES BETWEEN PRIOR ZIKA AND DENGUE INFECTIONS
• 5-13-2024IN SEARCH OF THE BEST TEST FOR HEPATIC ENCEPHALOPATHY
• 5-13-2024ORGANIZATIONS PUBLISH JOINT GUIDELINE ON GLUCOCORTICOID-INDUCED ADRENAL INSUFFICIENCY
• 5-13-2024CLINICAL TRIAL INVESTIGATING AFICAMTEN MEETS PRIMARY ENDPOINT IN OBSTRUCTIVE HYPERTROPHIC CARDIOMYOPATHY
• 5-13-2024RESEARCH INVESTIGATES LIMITED EFFICACY OF COMMON LOCAL ANESTHETIC
• 5-13-2024HOW SCIENCE CLEARED THE AIR OVER INHALED HEALTH RISKS
• 5-13-2024WHAT’S KEEPING THE US FROM ALLOWING BETTER SUNSCREENS?
• 5-13-2024PATIENTS CAN NOW STAY CONNECTED BY WEARING ONE
• 5-13-2024THERAPEUTIC OPPORTUNITIES FOR HYPERMUTATED UROTHELIAL CARCINOMAS BEYOND IMMUNOTHERAPY
• 5-13-2024RESEARCHERS REVEAL THE DOUBLE-EDGED-SWORD EFFECT OF OVERCONFIDENCE ON GAMBLING
• 5-13-2024TEAM STUDIES FACTORS RELATED TO A SENSE OF ECONOMIC INSECURITY IN OLDER ADULTS
• 5-13-2024PEDIATRICIAN OFFERS TIPS ON HOW TO SUPPORT HEALTHY MENTAL AND EMOTIONAL DEVELOPMENT IN YOUR CHILD
• 5-13-2024NEW DEVICE COULD IDENTIFY WHICH BABIES WILL STRUGGLE WITH BREASTFEEDING
• 5-13-2024COULD FLIRT LEAD TO A SUMMER UPTICK?
• 5-13-2024RESEARCH HIGHLIGHTS DRAMATIC INCREASE IN FENTANYL SEIZED BY AUTHORITIES IN LAST SIX YEARS
• 5-13-2024CHILD MEASLES CASE AT SACRAMENTO HOSPITAL MAY HAVE EXPOSED 200 PEOPLE, HEALTH OFFICIALS SAY
• 5-13-2024AN AUXILIARY CHD DIAGNOSTIC SYSTEM BASED ON MULTI-VIEW AND MULTI-MODAL TRANSTHORACIC ECHOCARDIOGRAMS
• 5-13-2024PROJECTED ESTIMATES OF CANCER IN CANADA IN 2024: STUDY
• 5-13-2024REPORT FINDS PRIVATE HEALTH PLANS PAID HOSPITALS 254% OF WHAT MEDICARE WOULD PAY DURING 2022
• 5-13-2024HOW OBESITY AND METABOLIC SYNDROME AFFECTS WOMEN’S RISKS OF BREAST CANCER AND CANCER-RELATED DEATH
• 5-13-2024CANCER AND COVID DROVE PATIENT TO DOUBLE-LUNG TRANSPLANT
• 5-13-2024CHOLERA OUTBREAK INTENSIFYING IN YEMEN, UN WARNS
• 5-13-2024RESEARCH TAKES ELECTRORETINOGRAPHY TO THE NEXT LEVEL WITH A SOFT MULTI-ELECTRODE SYSTEM
• 5-13-2024NEW STUDY SHOWS CERTAIN COMBINATIONS OF ANTIVIRAL PROTEINS ARE RESPONSIBLE FOR LUPUS SYMPTOMS
• 5-13-2024DID A WORM REALLY EAT PART OF ROBERT F. KENNEDY JR.’S BRAIN?
• 5-13-2024REINING IN ROGUE OBAMACARE AGENTS WITHOUT SLOWING ENROLLMENT
• 5-13-2024IS ‘HERD IMMUNITY’ IN INTENSIVE CARE DOING MORE HARM THAN GOOD?
• 5-13-2024TOO MANY AUSTRALIANS AREN’T GETTING A FLU VACCINE—WHY, AND WHAT CAN WE DO ABOUT IT?
• 5-13-2024RESEARCHERS FIND 13% REDUCTION IN ASTHMA IN CHILDREN BORN IN AN URBAN LOW EMISSION ZONE
• 5-13-2024RESEARCHERS USE DUAL DRUG STRATEGY TO ADVANCE MELANOMA TREATMENT AGAINST RESISTANCE
• 5-13-2024ENGINEERING MINI HUMAN HEARTS TO STUDY PREGNANCY COMPLICATIONS AND BIRTH DEFECTS
• 5-13-2024FOR TREATING RETINOPATHY OF PREMATURITY, RESEARCH PROVES THAT RANIBIZUMAB IS SAFE
• 5-13-2024STUDY FINDS SENSE OF SHARED SIMULTANEITY INCREASES WITH GROUP SIZE
• 5-13-2024WHAT YOU NEED TO KNOW
• 5-13-2024ATTACKING BIRTH CONTROL PILLS, US INFLUENCERS PUSH MISINFORMATION
• 5-13-2024UN NEARS LANDMARK DEAL ON COMBATING BIOPIRACY
• 5-13-2024VARIATIONS IN ‘ANCIENT’ IMMUNE CELLS LINKED TO PATIENTS’ SURVIVAL IN CANCER
• 5-13-2024SOURCE OF SUGAR MAY BE MORE IMPORTANT THAN AMOUNT WHEN IT COMES TO THE DEVELOPMENT OF OBESITY IN CHILDREN
• 5-13-2024UK STUDY INVOLVING OVER 80,000 ADULTS FINDS SMOKERS TEND TO EAT LESS AND HAVE A LESS HEALTHY DIET THAN NON-SMOKERS
• 5-13-2024TRIAL REVEALS ANTI-INFLAMMATORY POWER OF AEROBIC EXERCISE IN ADULTS WITH OBESITY
• 5-13-2024LARGE-SCALE FINNISH STUDY DISCOVERS LINK BETWEEN PREMATURE MENOPAUSE AND MORTALITY RISK
• 5-13-2024SOCIODEMOGRAPHICS TIED TO REHAB USE DURING CRITICAL ILLNESS HOSPITALIZATION
• 5-13-2024AVOID OVERHEATING DANGERS WHEN RECHARGING MEDICAL DEVICES
• 5-13-2024LOWER PREVALENCE OF EMPLOYMENT SEEN FOR SURVIVORS OF CHILDHOOD CANCER
• 5-13-2024BLOOD PRESSURE DOWN WITH SELF-MONITORING, SELF-TITRATION OF MEDICATIONS
• 5-13-2024PSILOCYBIN MAY REVERSE ANOREXIA’S COGNITIVE RIGIDITY
• 5-13-2024STUDY HIGHLIGHTS NEED FOR CELL-TYPE-SPECIFIC THERAPIES IN TREATMENT OF HIV
• 5-13-2024INTENSE ULTRASOUND EXTRACTS GENETIC INFO FOR LESS INVASIVE CANCER BIOPSIES
• 5-13-2024WEIGHT LOSS DRUG LINKED WITH REDUCED NEED FOR DIURETICS IN HEART FAILURE PATIENTS
• 5-13-2024EVIDENCE OF A TRAVEL DIRECTION SIGNAL THAT IS INDEPENDENT FROM HEAD DIRECTION IN HUMANS
• 5-13-2024STUDY SHOWS CHATGPT CAN ACCURATELY ANALYZE MEDICAL CHARTS FOR CLINICAL RESEARCH, OTHER APPLICATIONS
• 5-13-2024WHAT MAKES A MEMORY? IT MAY BE RELATED TO HOW HARD YOUR BRAIN HAD TO WORK
• 5-13-2024BIRTH BY C-SECTION MORE THAN DOUBLES ODDS OF MEASLES VACCINE FAILURE, STUDY FINDS
• 5-13-2024SCIENTISTS FIND SLEEP MAY NOT CLEAR BRAIN TOXINS