Hi there hope you all are well😊 I was a very very active person, I was working hard and still going to the gym and do my weight lifting 6 days a week, but now since I’ve been diagnosed with hypo and hashimotos ( my antibody’s just recently got negative so I don’t understand why I’m still feeling sometimes like s**t, probably testing again privately since my endo hasn’t been doing anything to help me ) my endurance has declined quite a bit, last year I’ve been very unwell so I wasn’t able to do my workouts or be much active, so now I’m starting to go back but I’m starting very gently and even like that what I feel is like an intolerance to it and it’s sad for me because the gym has been a massive help with my mental health and now I can’t even use it as I want( but I understand it has to be one step at time and that I need to be patient ) but it’s so hard because I’ve been loosing weight, so far probably lost 6 kilos in muscle ( sibo and diets and treatment doesn’t help either ) ( I went from 71kg to 61 kg from last year to present and it scares me ) so is there anything I could do that would help me with this ??? Kind regards Miss V

My almost month old son was in the NICU for his first 20 days and has only been home about a week. We have not have much luck with breastfeeding - I had to exclusively pump for most of his NICU stay and he hasn’t latched well since. We maybe try 1-2 times a day and he either won’t do it, will refuse without a nipple shield, or when he does latch he only gets a tiny amount out. He takes a bottle well but my production is only about half of what he eats in a day, so we are supplementing with formula. I am essentially attached to a pump 7-8 hours a day and there’s no way I can continue to do that when my husband goes back to work in a week - I am basically useless during pumping times but am fighting constant engorgement so I can’t go way off the schedule either.
I think I’ve realized that this just isn’t going to work for us. Has anyone been in a similar boat, and if so, how have you wound down from BF/pumping? Did you slowly decrease pumping sessions each day? Has anyone been able to keep one or two pumps per day to have enough to give baby for some antibodies? I’d be open to that if it’s an option but am also content with just fully switching to formula if needed.

Been on infliximab for over 2 years now; it doesn’t work, it never worked, but by doctor thinks otherwise. According to her, the biological is doing something… this purely because my blood tests say so? They do this kinda test to see if you have any antibodies developing against the medicine. Don’t know exactly how it works, but my blood results come out perfect every time and show that the infliximab is doing something? My entire colon is inflamed and mainly the last part. The only thing that works for my CU/Crohn’s, are two different types of enemas that I started using not long ago. Before using the enemas I was really sick and couldn’t go without prednisone. Mind you, back then I already was on Infliximab for more than a year. It’s the enemas that made me go into remission, because once I stop using them for a while and not regularly, I instantly start to flare. Massive pain and bleeding… I think I don’t have to explain :”)
Using Enema’s twice a day isn’t sustainable for me, because of my irregular work schedule. I at least tried 5 different kinds of biologicals already and not one has worked for me yet… did you go thru the same thing? Failing almost all biologicals :”)? It’s frustrating… atm I’m losing big amounts of blood and just feel so shit. It’s pretty obvious infliximab is inflixi-shit for me :”)

Hi everyone, I first wanted to preface this by saying that I will of course be consulting by with my rhuemotologist about this result. I am posting on here because I am 21 and still see a pediatric rhuemotologist, so I’d like to hear other adult’s experiences.
I was recently re-tested for other autoimmune diseases, and I got my results back today. My anti-dsDNA (commonly seen in lupus) result was high, at 28.4IU/mL. On the description of ranges, it said that this range is “borderline positive”, which is a gray area. My question is: does anyone else with Bechet’s have high levels of this antibody and it ISNT lupus? Also, if it is borderline lupus, has your Bechet’s treatment helped with your borderline lupus? I am hoping that if it is a borderline lupus diagnosis, the Humira I am about to start will help it, too.
Please let me know and thanks!

Blood tests can be used when a person has no visible symptoms but has concerns about having herpes. Blood tests do not actually detect the virus; instead, they look for antibodies (the body’s immune response) in the blood.
IgM vs. IgG
When an individual contracts herpes, the immune system responds by developing antibodies to fight the virus: IgG and IgM. Blood tests can look for and detect these antibodies—not the virus itself. IgG appears soon after infection and stays in the blood for life. IgM is actually the first antibody that appears after infection, but it may disappear thereafter.
IgM tests are not recommended because of three serious problems:
Many assume that if a test discovers IgM, they have recently acquired herpes. However, research shows that IgM can reappear in blood tests in up to a third of people during recurrences, while it will be negative in up to half of persons who recently acquired herpes but have culture-document first episodes. Therefore, IgM tests can lead to deceptive test results, as well as false assumptions about how and when a person actually acquired HSV. For this reason, we do not recommend using blood tests as a way to determine how long a person has had herpes. Unfortunately, most people who are diagnosed will not be able to determine how long they have had the infection. In addition, IgM tests cannot accurately distinguish between HSV-1 and HSV-2 antibodies, and thus very easily provide a false positive result for HSV-2. This is important in that most of the adult population in the U.S. already has antibodies to HSV-1, the primary cause of oral herpes. A person who only has HSV-1 may receive a false positive for HSV-2. IgM tests sometimes cross-react with other viruses in the same family, such as varicella zoster virus (VZV) which causes chickenpox or cytomegalovirus (CMV) which causes mono, meaning that positive results may be misleading. The accurate herpes blood tests detect IgG antibodies. Unlike IgM, IgG antibodies can be accurately broken down to either HSV-1 or HSV-2. The challenge here is that the time it takes for IgG antibodies to reach detectable levels can vary from person to person. For one person, it could take just a few weeks, while it could take a few months for another. So even with the accurate tests, a person could receive a false negative if the test is taken too soon after contracting the virus.
For the most accurate test result, it is recommended to wait 12 – 16 weeks from the last possible date of exposure before getting an accurate, type-specific blood test in order to allow enough time for antibodies to reach detectable levels.
https://www.ashasexualhealth.org/herpes-testing/

I feel tired and sluggish at around 3pm every single day. I don’t have any other hypo symptoms.
Free thyroxine is just above the upper limit of 20.
My TSH has been around 3.5 for my last few blood tests.
I tested negative for antibodies back in 2017, but haven’t done the test again since.
Other values are “normal and in range”. Would you start 25mcg daily?

Sorry, I just need a moment to blow steam off about my little guy and his tummy troubles 😭.
So, I was on nutramigen as a baby for an intolerance to milk, as was my first child, a daughter, and now my second child, a little boy, is also on nutramigen for the same reason. Very obviously there's a genetic component 🫠
Both of my children were born early, my daughter at 36 weeks and my son at 34 weeks, who had to have a 12-day NICU stay before he could come home. He's gained weight beautifully thankfully, but coming to the realization that he had issues with dairy and would need even more special attention to his diet has left me a little depressed after the Insanity of his feeding tube and triple feeding at the hospital and just struggling to get him to learn how to eat and put on weight.
With my daughter I did my best to cut out dairy while I combo fed her, and as a vegetarian that was a really tough on me as it eliminated a lot of the foods I ate (I have an issue with soy so it's not like I can replace it with that). Now that I also have a toddler at home, who has outgrown her intolerance like I did and is now eating and drinking lots of dairy, finding time to eat, let alone eat food without dairy in it, is so so hard. I thought that since my boy's symptoms are less severe than my girl's was, I could maybe just still have cheese in my diet. But I noticed that he would get flare-ups of his little baby rash / acne and more gas so I did my best to cut out the cheese.
I didn't even think about it this morning and totally messed up so bad! I stopped at McDonald's for a small iced coffee, a rare treat for myself, and completely forgot that there is milk in it. Milk! The thing that hurts his tummy the most! I am so upset, and he's cluster feeding right now and really wants to nurse. I'm nursing him, and just so sad at the thought of him with gas pains and even more of this baby acne / rash in the coming hours 😭 I could pump, but I have no idea how long it's going to be in my system and all he wants right now is booby. This just sucks. I wish I could stop breastfeeding entirely and just give him straight formula, but him being a preemie has made me so invested in him getting breast milk each day for the antibodies, and my husband is very firm that he wants our second breastfed for a full year like our first was. I'm just so done with all of this.

Understanding inflammation and its impact on health

Before we delve into the specific effects of red meat on inflammation, it's important to understand the broader context of inflammation and its implications for our health.
Inflammation is a natural immune response that helps the body defend against infection, injury, and other threats. However, when inflammation becomes chronic or excessive, it can lead to a range of health problems, including cardiovascular disease, type 2 diabetes, and certain types of cancer.
The facts of our modern diets and lifestyles, characterized by inflammatory grains, sugars, and seed “vegetable” oils, keep our inflammation simmering at a chronic level. Our bodies experience these substances as harmful “antigens.” And it responds by constantly producing antibodies that damage healthy tissues and organs.
The importance of reducing inflammation cannot be overstated.
And at least 60% of the American population have at least one chronic inflammatory condition.
Understanding inflammation and its impact on health
Before we delve into the specific effects of red meat on inflammation, it's important to understand the broader context of inflammation and its implications for our health.
Inflammation is a natural immune response that helps the body defend against infection, injury, and other threats. However, when inflammation becomes chronic or excessive, it can lead to a range of health problems, including cardiovascular disease, type 2 diabetes, and certain types of cancer.
The facts of our modern diets and lifestyles, characterized by inflammatory grains, sugars, and seed “vegetable” oils, keep our inflammation simmering at a chronic level. Our bodies experience these substances as harmful “antigens.” And it responds by constantly producing antibodies that damage healthy tissues and organs.
The importance of reducing inflammation cannot be overstated.
And at least 60% of the American population have at least one chronic inflammatory condition.

The role of nutrients in red meat and their impact on inflammation

One of the key factors in understanding the relationship between red meat and inflammation is the nutrient profile of red meat.
Red meat is an excellent source of high-quality protein, as well as a rich source of essential vitamins and minerals, such as iron, zinc, and vitamin B12. These nutrients play a crucial role in supporting the body's immune function and reducing inflammatory processes.
There is one other survey study that may provide a more reliable insight into the effects of meat on inflammation. It was conducted by Harvard researchers in 2021 and collected responses from 2029 people on the carnivore diet.
This more restrictive version of the ketogenic diet calls for consuming only animal products, is centered around fatty red meat, and eliminates all plant foods. The researchers found that 89% improved or resolved autoimmune conditions.
Taken together, the preponderance of evidence tells us that red meat is not more inflammatory than non-red meat and oily fish. And that it is likely less inflammatory than carbs.

Fresh red meat is also no longer believed to cause cancer, stroke, or heart disease. Our modern diets and lifestyles, characterized by inflammatory grains, sugars, and seed "vegetable" oils, keep our inflammation simmering at a chronic level. A study from 2007 where participants replaced carbohydrates with red meat showed significant reductions in inflammatory markers.

Cheers Carnivores !

It's very rare for a lab to offer this test. My country doesn't do this at all. I found one lab in Germany where I'll hopefully send my sample through some local lab. These antibodies are still under research from what I'm reading but it looks like they correlate specifically with neurological symptoms. If anybody has done them, what was your level (and the lab reference)? And how it correlates with other factors such as symptoms/other antibodies/time after going GF? It's very interesting.

What does this mean? This is being very poorly explained to my primary and I. She doesn’t know what to do, and thinks the rheumatologist should address it. I’m not sure if it’s the rheumatologist’s department. The rheum that ran the test was for a second opinion, because my current one keeps saying my symptoms aren’t from lupus. I’m just curious what other people experienced with this. I’ve got the APS antibodies too. I just don’t get why a test like this would be run due to the symptoms I’m having, it be positive, then the doctor not address it. Is a hematologist I should see? She suspects I have capillary leak syndrome too, but that’s not the rheumatologists department either

Finally am getting more testing done since I don’t fit the Type 2 profile. I’m 32, fluctuate about 18-20 BMI, active, eat relatively healthy (100-125 g carbs a day because I’m breastfeeding and need calories). I’ve had gestational diabetes 3x, each pregnancy making my carb tolerance significantly worse. Can’t eat 50 g carbs without hitting over 200 and staying above 140 for a few hours.
Never issues with fasting, just post meals. Even with being on metformin 1000 mg, my A1C was 5.6– partly could be hormonal and sleep deprived but still. I asked for cpeptide and antibody testing to see what’s going on.
My cpeptide came back at 1.07 when the range is .8- 3.85. Now just waiting on GAD panel to come back which will take a few more days. It doesn’t really change my treatment plan (Metformin, diet and exercise) but it gives me answers.
Yall don’t be afraid to ask for further testing!

...then I spoke to my PCP :')
So apparently a TSH of 10.5 is high enough for them to finally concede there may be a thyroid problem (ignoring the high antibodies but whatever), but still they can't accept that it's the thyroid causing my symptoms and insist it's probably something else.
I understand they want to cover their bases by ruling out other health issues, but I feel so unheard in all this. I asked if they'll consider medicating for hypothyroidism if the other tests come out normal, and they said no. Wah.
EDIT to fix dumb typo, brain fog bad day

TW: Pregnancy
Longtime lurker, first time poster. Apologies for the length but this is a complicated story. I had an ER in 2013 at the age of 30, prior to an allogenic stem cell transplant for leukemia. I got 8 eggs (6 mature) that were frozen. A few months after the transplant I had not gotten my period, so my gyno put me on BC as a form of HRT, assuming that I had been put into premature menopause due to the chemotherapy. I was later diagnosed with Hodgkin’s Lymphoma in 2018 and went through another round of chemotherapy. Free of disease since. All this time, I had not gotten a period and remained on BC. After 7 year, out of nowhere I got a period in March 2020 and continued to have a monthly cycle (still on the BC). In 2022, my husband and I consulted with REI, planning to fertilize and transfer the frozen eggs. We did all the preliminary testing and were ready to go with my next cycle in 2/2023 when I get a call to tell me that they had missed that I was sensitizes for the D antigen and had antibodies. The plan shifted to have a PGT-M probe created to possibly select an Rh- embryo. My husband’s blood type is A+. I was born with B+ blood but after SCT, my Blood type is O-. Everyone initially assumed I was sensitized due to the SCT, but review of my medical records showed that I had been sensitive prior to the SCT. Turns out I have an inherited D variant so while a normal B+ blood type would not create D antibodies, mine did, which would likely result in the antibodies attacking the red blood cells of any Rh+ fetus I carried. The problem was that due to the SCT, Cooper Genomic could not get sufficient isolated DNA from me to create the probe. Ultimately, we were only able to because Dana Farber, where I have my SCT, had my frozen retained DNA from 2013 that could be used. Thank god I consented to allow them to use my DNA for research. But all of this took forever, and the probe wasn’t ready until 2/2024.
On 4/12/2024 we moved forward to fertilize. 6 out of 8 survived the thaw, 3 fertilized and none made it to blast. I always knew that could happen, but I am so angry that every medical professional involved made it seem like only a minute possibility and that no one ever even mentioned that it might be a good idea to see if we could get any additional eggs first seeing as how I was 40+ and been through chemo. I am angry that my gyno just assumed I was infertile and never investigated at all. I am angry at myself for only now being informed enough to know that I could have done more and now it might be too later. We are moving forward with egg retrieval and are just waiting on insurance clearance. When they last checked my AMH in 10/2022 it was 0.2. Last FSH in 4/2023 was 4.28 but prior to that on 9/2022 it was 30. No idea what my AFC is yet but assume low.
Not sure if I am looking for advise or just ranting but I knew that those in this group could empathize. With all I have been through medically I have never been one to feel “why me” or “life’s not fair” but this has really taken me down in a way I have never experienced.
Ironically, during all this I spontaneously got pregnant in 9/2023 but we ended up having to TFMR around 13 weeks to due chromosomal abnormalities. It took 12 weeks afterwards, but my period did come back.

I gave it the prompt: "write a super long essay on why the lobotomy trend is the funniest thing to happen in the Geometry Dash community (lobotomy in this case mostly consists of people using the Geometry Dash level editor to make distorted versions of Geometry Dash levels, and having the difficulty face icons yell short sentences like "fire in the hole", "water on the hill", "shadows from the grave", "rock on the ground", "air detected", "area confirmed" etc. With "fire in the hole" being the most popular one. This happened after RobTop Games taking 7 years to release the long awaited 2.2 update for Geometry Dash.)"
It responded with this nonsense: "Title: The Hilarity of Lobotomy: A Humorous Analysis of the Geometry Dash Community's Response to the Long-Awaited 2.2 Update
Introduction:
In the dynamic and ever-evolving world of gaming, communities often find unique and unexpected ways to express their excitement, frustration, and creativity. The Geometry Dash community, renowned for its passionate and inventive player base, experienced a particularly amusing phenomenon following the release of the long-awaited 2.2 update by RobTop Games. This phenomenon, dubbed "lobotomy," involves players utilizing the game's level editor to create distorted versions of Geometry Dash levels, accompanied by hilariously absurd difficulty face icons uttering short, nonsensical phrases. This essay aims to delve into why the lobotomy trend became one of the funniest occurrences in the Geometry Dash community, examining its origins, characteristics, and the underlying humor that captivated players worldwide.
Origins of Lobotomy:
The genesis of the lobotomy trend can be traced back to the anticipation and subsequent release of the 2.2 update for Geometry Dash. RobTop Games, the developer behind the wildly popular rhythm-based platformer, kept fans waiting for seven long years before unveiling the much-awaited update. As excitement reached a fever pitch within the community, players eagerly anticipated new features, levels, and enhancements promised by the developer.
However, the prolonged wait and heightened expectations inevitably led to a mix of emotions among players upon the update's release. While many were thrilled with the new content and improvements, others found themselves grappling with a sense of surrealism and absurdity surrounding the update's delayed arrival. It was within this climate of anticipation and catharsis that the lobotomy trend emerged as a humorous outlet for expressing both jubilation and bemusement.
Characteristics of Lobotomy:
Lobotomy levels within Geometry Dash exhibit distinct characteristics that set them apart from traditional gameplay experiences. These levels are characterized by their distorted layouts, unconventional design elements, and, most notably, the inclusion of difficulty face icons that emit short, nonsensical phrases. The phrases, ranging from the absurdly comical ("fire in the hole") to the downright bizarre ("shadows from the grave"), serve as a whimsical commentary on the heightened emotions and anticipation surrounding the 2.2 update.
Furthermore, lobotomy levels often incorporate elements of surrealism and randomness, challenging players' expectations and subverting traditional gameplay conventions. This departure from the norm contributes to the overall humor and absurdity of the lobotomy trend, as players navigate through levels filled with unexpected obstacles and nonsensical audio cues.
Humor in Lobotomy:
The humor inherent in lobotomy levels stems from a combination of factors, including their absurdity, unpredictability, and satirical commentary on the gaming community's collective experience. By juxtaposing familiar gameplay mechanics with nonsensical phrases and distorted visuals, lobotomy levels subvert players' expectations and invite them to embrace the absurdity of the gaming experience.
Moreover, the widespread popularity of the lobotomy trend within the Geometry Dash community speaks to the universal appeal of humor as a means of coping with anticipation, disappointment, and frustration. In a gaming landscape often characterized by intense competition and high stakes, lobotomy levels offer players a lighthearted respite from the pressures of achieving high scores and completing challenging levels.
Conclusion:
In conclusion, the lobotomy trend represents a humorous and inventive response to the long-awaited 2.2 update for Geometry Dash. By distorting traditional gameplay elements and incorporating nonsensical phrases, lobotomy levels capture the absurdity and excitement surrounding the gaming community's collective experience. Through their surrealism and unpredictability, lobotomy levels invite players to embrace the humor inherent in the gaming experience and find joy in the unexpected. As players continue to create and share lobotomy levels within the Geometry Dash community, the legacy of this hilarious phenomenon is sure to endure, serving as a testament to the creativity and camaraderie that define the world of gaming."
God it's so terrible. I'm sorry.

Short background: vegan, male, 34yo, at the lower end of adipositas, always on coffeine to not be tired, working out hard with no real benefits.
I went 4 months ago to get tested: 5,56TSH, T3 and T4 normal, Thyroid size and look normal, testosterone at higher end.
I just got my results from my new blood test, after taking 200mcg iodine daily for 3 weeks: 3,78 TSH, T3 and T4 normal. TPO-Ak 54U/ml
My doc says I'm fine. To make sure, I will get tested in a week again, while dropping any biotin and St John's wort .
Is it plausible that I just had an iodine defciancy? My TPO-Antibodies look like a slight hashimoto?

"The Crimes of Dorian Gray" by Arvind Ethan David is a compelling story that reimagines Oscar Wilde's famous figure, Dorian Gray, in a contemporary environment. Set in modern-day London, the plot follows Dorian Gray, a wealthy and intriguing character with a dark secret - he remains eternally youthful while a portrait of him ages and wears the marks of his transgressions.
As Dorian navigates the complications of his everlasting existence, he becomes engaged in a series of crimes that threaten to disclose his actual identity to the world. With the help of his devoted friend, Basil Hallward, and the mysterious detective, Rose Aveling, Dorian sets out to discover the mystery behind the crimes while addressing his own inner demons.
David's prose is descriptive and atmospheric, preserving the essence of Wilde's original work while adding a contemporary spin. The tale is loaded with suspense, intrigue, and moral ambiguity, as Dorian grapples with the implications of his deeds and the endless conflict between good and evil.
What sets "The Crimes of Dorian Gray" different is its treatment of eternal themes such as vanity, depravity, and the search of immortality. Through Dorian's character development, the story delves into the nature of sin and forgiveness, allowing readers to think on the intricacies of human nature.
Overall, "The Crimes of Dorian Gray" is an intriguing and thought-provoking read that will appeal to aficionados of mystery, suspense, and literary fiction. With its thoroughly realized characters, dramatic setting, and captivating storyline, it gives a novel twist on a classic tale that is likely to capture readers until the very end.
Free Audiobook with a free trial of Audible at freeaudiobookstrial .com

import os, cv2, numpy as np os.system('cls') cap = cv2.VideoCapture('vid/3.mp4', 0) while True: success, img = cap.read() img = cv2.cvtColor(img, cv2.COLOR_BGR2GRAY) img = cv2.Canny(img, 30, 30) kernel = np.ones((1, 1), np.uint8) img = cv2.dilate(img, kernel, iterations=1) img = cv2.erode(img, kernel, iterations=1) cars = cv2.CascadeClassifier('haarcascade_car.xml') results = cars.detectMultiScale(img, scaleFactor=1.1, minNeighbors=3) for (x,y,w,h) in cars: cv2.rectangle(img,(x,y),(x+w,y+h),(0,255,0),2) cv2.imshow('Result', img) if cv2.waitKey(25) & 0xFF == ord('q'): break 

Here's the error

results = cars.detectMultiScale(img, scaleFactor=1.1, minNeighbors=3) ^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^ cv2.error: OpenCV(4.9.0) D:\a\opencv-python\opencv-python\opencv\modules\objdetect\src\cascadedetect.cpp:1689: error: (-215:Assertion failed) !empty() in function 'cv::CascadeClassifier::detectMultiScale' 

36 year old dude here whos been going through hair loss since early 20s. Ive had success with dermarolling and minoxidil but terrible heart palpitations so I had to stop. I wont touch finasteride. Ive also had alot of success with dermarolling and coffee/water spray. Once I went on the keto diet I was also intermittent fasting and lost nearly half of my hair. This was depressing to say the least as I was starting to recover almost all my hair before. Im not sure if I tiggered bad telogen effluvium but ita been over a year and im trying to tackle anything else involved it could be. At this point not sure if im having telogen effluvium or a result of some vitamin deficiency. Most of my vitamin b levels are high or in the middle range with niacin looking a little on the low side. I attached all my results labs that included every b vitamin, zinc, magnesium, iron, and vitamin d. My tsh is within normal levels, im getting my t3 and t4 and tyroid antibodies tested next to rule out if I have hypothyroidism. My iron binding capacity seem low too not sure if that has a correlation. Ive attached all my results from my recent labs. If anyone has any useful information on this id greatly appreciate it 🤘

Have any of you experienced a 'rough' second anatomy screening when the tech was digging in your belly too much and then you felt sore afterwards? It's painful to walk or sit. My actual question is: did this rough 'treatment' cause you to produce antibodies later on???? I haven't had my rhogam yet.