Headache and fatigue

Migraine

2009.01.10 13:43 Migraine

A community of headache disease sufferers. Whether migraines, cluster headaches, or whatever head pain you experience. We support each other, and spread knowledge about our various conditions.
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2009.08.11 14:07 dkesh Chronic Fatigue Syndrome / Myalgic Encephalomyelitis

For research, treatments, and personal stories regarding Chronic Fatigue Syndrome (CFS)/Myalgic Encephalomyelitis (ME). ME/CFS is a multi-systemic neurological disease, distinct from chronic fatigue as a symptom. For more information, please see our FAQ.
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2020.07.24 20:58 lvl0rg4n covidlonghaulers

A community for individuals suffering from the effects of COVID-19 longer than the estimated 4 weeks, also known as PACS, PASC, and Long Covid.
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2024.05.15 14:46 SaltyWindigo Possible endometriosis symptoms. Seeking help!

Sorry in advance for the length of this post. Ihave been struggling with a variety of symptoms off and on for the last couple of years. This last flare up has been the worst by far and I am miserable and desperately seeking answers. I have been to my OBGYN, GI doctor, mental health doctors, my general practitioner and multiple ER's and specialists and have gotten zero answers. All of my CT scans, MRIs, lab work, upper and lower endoscopy, etc always come back perfect and show nothing. The only abnormal test results I have had are abnormal pap smears for cervical dysplasia and severe inflammation in my stomach and intestine lining. I have also struggled with SIBO but these particular flares seem different and don't fully fit and I have noticed that these flare ups seem to start about 2 to 2 and a half weeks before my periods begin. It has just been hard to notice the pattern because I have very irregular periods. The symptoms for each flare up are: Severe gas pain and burping Constipation Severe bloating/ stomach distension to where I look pregnant Nausea Stomach cramps Lower abdominal and pelvic pain that resemble contraction pain and bad period cramps Bad lower back pain that radiates into hips, butt (like sciatica) and thighs Sharp pain that radiates into right shoulder A cramp or sharp pain in both flanks under ribs that is worse on the right side Headaches Extreme fatigue (I exercise daily and couldn't for nearly 2 weeks) Zero appetite Weight loss (6lbs in 2 weeks) Feeling of extreme fullness after eating just a bite or two of food (doesn't matter what the food is. I tried the blandest and easiest foods on the stomach) Irritability and very emotional (which I am normally not) but I contributed this to being malnourished and exhausted)
All of these symptoms get bad enough to where my daily functioning is severely impaired. I can barely work, sleep, anything. The reason I ask if it could be endometriosis or something similar is because the day my period starts, nearly all of these symptoms disappear it go way down to a very tolerable level. Once I start menstruating the only symptoms I am left with are bad period cramps and the lower back pain. All GI symptoms seem to vanish and the horrible pain in my back/hips/sides goes way down. Any help is appreciated
submitted by SaltyWindigo to endometriosis [link] [comments]


2024.05.15 14:17 MundaneSource8380 Help finding answers ):

just as the title says i just want some help finding answers if i can. ive been dealing with health issues since i was about 12 years old, it started as stomach issues and progressed to daily headaches. im turning 24 this year and within the last 5 years my overall symptoms have gotten worse. my skin itches all the times and has for years, its sometimes so bad i make myself bleed and have constant scab on my legs and arms/ scars from scratching all the time. i have really intense brain fog/fatigue constantly as well where i cant even go up amd dowm stairs or take a shower without needing a break. my arms and shoulders hurt so bad i can barely sleep, i used to sleep on my side but hurts my arms, even when on my back. i get so unbalanced just walking or standing that sometimes i almost fall over and have to catch myself. i get really bad stabbing pains all over my body but mostly my shoulder and this one spot on my back near my neck, that spot near my neck on my back is also completely numb most days that when its itchy back there i cant even feel myself scratching it and its frustrating. i barely sleep because my body is in so much pain. i get bad brain fog, i get really bad muscle spasms and my muscles hurt so bad sometimes i cant sit still. i have eye problems, my eyes hurt so bad sometimes i cant look around or blink and my eye will be completely blood shot plus i get really bad headaches. my joints and body just hurt all the time. ive been diagnosed with fibromyalgia and endometriosis but sometimes i worry it could be more and sometimes i just want it to be so i can find a treatment plan. most doctors are clueless though and dont know why my pain is so bad. im currently being tested for MS and EDS but just wondering if anyone who has fibro or MS can let me know how your experience was and your symptoms? i just want to know whats wrong with me so bad and just feel better.. im so tired after 12 years
submitted by MundaneSource8380 to ChronicIllness [link] [comments]


2024.05.15 09:14 Electrical-Owl-5853 Symptoms in this order

Symptoms in this order
In this order
Pre illness I thought I was starting my period tingles in my thighs Bubbles guts for over a week Thick white vaginal discharge(no smell) slight barely noticeable cramps Everything started to hit me Sunday, May 5 (I only remember this because I thought all of this was due to the ice cream we got I ate it after leaving it out) Early symptoms- Tuesday Sore throat with no drastic pain, only when swallowing Dry cough Minor dull Headache Since Friday, May 10 Minor dull lower back ache( maybe because of standing in heels ate concert) Mucus started breaking up and coming out Itchy Rash from the mid back to my upper butt(the most alarming symptoms,maybe due to washing with an old rag Friday) Diarrhea (not continuously or painful) Very Fatigue
Tuesday, May 14
All other symptoms have subsided
My gums are bleeding (but I haven’t brushed my teeth in over a week from anxiety of this condition) I can barely bite down with it a shifting pain
Two small barely noticeable bumps on left hand
As far as timeline tho this would be considered way past, the average is 2-6 weeks but all started week 10
submitted by Electrical-Owl-5853 to hivsymptoms [link] [comments]


2024.05.15 09:07 fjall_risk vomiting after having a cold for 6 days

hi :)
im really sick :(.
i'm 25F, 5'4, 125lbs, no existing issues... except unexplained peripheral neuropathy on and off (currently off) & ADHD, currently taking adderall (XR daily 25mg, IR 10mg as needed), lamotrigine(daily 150mg) and guanfacine(daily 1mg) , i drink socially 1-2 drinks a night on the weekend and have stopped smoking weed and nicotine, but was never a big participant. have had 1 white claw since i became ill.
i've had a nasty nasty virus where i've been out of work since thursday (it's the end of tuesday, so 6 days). i've been incredibly congested, incredibly fatigued, whole body hurts, headache, and dizziness when i stand for too long or walk. i took 2 at home covid tests on sun and mon, both neg.
my chest started hurting yesterday really badly and i couldnt take a deep breath, so i went to the urgent care today and they gave me a steroid shot and a breathing treatment and prescribed albuterol. i haven't picked it up bc i took a nap instead. this was at like 3pm
i ate dinner at 11pm (im so tired :((( ) and then ive been on my bathroom floor puking since. my boyfriend had the same meal and is fine, so it's not food poisoning.
is it just the steroid shot? should i go back? is there a secondary infection that needs to be addressed? what should i be considering?
lmk any relevant thoughts or experiences :) thank you so much!
submitted by fjall_risk to AskDocs [link] [comments]


2024.05.15 08:52 EvilItrovert Strange symptoms during a flare.

So shit had been pretty good for quite a while. After a year of being totally out of commission, I have been at about a solid 75-80% for the last year.
I live a pretty stress free life, by design. And recently have been pissed off about a couple of things. I don’t usually indulge in anger, so when it arises, it def is a shock to my system. So here we are, flaring like a MF.
Which brings me to question…
Periorbital edema (like slits for eyes) severe hives. I was a runner and had a knee replacement at 40, my knee swells up and I swear I can feel the implant itching. Followed by all the usual PEM, overwhelming fatigue, RLS, acne (which I had never had in my life) headaches…the list goes one. These are all the “normal” things I expect now.
Today I had this weird sensation like I had tennis balls in the arches of my feet. No visible swelling. I don’t even know another way to describe it.
Has anyone had this?
submitted by EvilItrovert to covidlonghaulers [link] [comments]


2024.05.15 08:22 Ultra_Care_PRO MOI Plus: The Future of Period Pain Relief

MOI Plus: The Future of Period Pain Relief
Hey there, womanhood warriors! We get you, and we especially get you on those days of the month. Period cramps are a real problem for women out there, and there is no way you can escape its clutches!
Period pain affects more than 80% of women in India, mild or adverse; it doesn’t matter. The sad reality is that it “affects” women, and it affects them in the negative. Abdominal pain, namely cramps, comes in conjunction with headaches, fatigue, loss of appetite, and bloating. Women are born multitaskers, and a cramping sensation in parts of their bodies knocking in every time they are out to ace a task is unacceptable!
But women, if you think there is no way out of this debilitating circle of period pain, you are mistaken! Once more, UltraCare PRO is here to rescue you! In December 2022, we launched MOI, an Instant Period Pain Relief Device. A combination of TENS and heating therapy, MOI successfully provided period pain relief to more than 2,00,000+ women.
Working on the love you have showered our way with MOI and pondering on a mission to make pain-free menstrual health accessible to all, we are back with something advanced for you!
https://preview.redd.it/iufv74kt9j0d1.png?width=833&format=png&auto=webp&s=afca9a35255ae72f50b1badbc527e9504d942ac1
The wait is finally over. Meet MOI Plus the advanced period pain relief device that will make your cramps run at that time of the month.
Curious to know more about MOI Plus? Click the link below to read the entire blog - it tells you everything about this advanced and amazing period pain relief device!
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submitted by Ultra_Care_PRO to u/Ultra_Care_PRO [link] [comments]


2024.05.15 06:32 kmpxo 7 months since my POTS diagnosis and I still feel terrible

I was diagnosed with POTS in November of 2023 after having COVID. I always had minor symptoms of POTS but it escalated drastically after being sick. I have a cardiologist who just told me to increase my salt intake, water intake, get good sleep and wear compression socks. I try to do all of that and nothing is helping. I have dizzy spells throughout the day, sometimes seeing stars and almost collapsing. Headaches almost everyday, weakness, fatigue. I never get a full nights rest - I’ll wake up several times in the night either from overheating or my heart pounding. My temperature regulation is horrible - I’m either freezing or so hot to the point where I’m sweating and need ice packs to cool me down. I don’t know what to do and am hoping for some advice on how to navigate this new way of life. It’s becoming increasingly more difficult to function throughout the day. Any advice is greatly appreciated ❤️
submitted by kmpxo to POTS [link] [comments]


2024.05.15 05:35 Sad-Statistician-598 Am I slowly dying?

(18F/65.5kg/163cm) I have had chronic pain and fatigue for 2 years with no answers, at first I focused on it too much and wouldn’t stop googling but recently I have been just giving up and trying to push through it every day. Recently I have been getting these symptoms that are concerning to me: Worsening blurry/cloudy vision, constant bad headaches, ear discomfort, random jolts of stinging pain, aggression, shoulder and back pain, clear fluid leaking out of left nostril, decreased libido, visible veins in palms, face pain. I also have persistent chest and rib cage pain + discomfort but I don’t think it’s related. I feel like I’m getting confused and it’s so hard to do daily activities like cleaning and walking. I’m scared of seeing a doctor as I’ve just been ridiculed in the past, but if I really need to see one I will. I feel like my life is slipping away and I have no one to go to.
submitted by Sad-Statistician-598 to AskDocs [link] [comments]


2024.05.15 05:20 classyhornythrowaway Actual unsent letter by my ex-wife I found in a recipe book a few weeks after she moved out. Date unknown.

"I'm so tired. I have headaches almost all the time, fatigue, and my flare ups [eczema] are so hard to deal with. I need help. My depression is getting worse. I wish it was easy to end my life. I know my family will be a bit sad about it, but they will be relieved. I also know my husband will get over it once he finds another one. He'll probably never mention me again. My problem is I'm so scared of the pain. I'm worried."
Nothing I say can describe the pain I feel whenever I read this, and that pales in comparison with what you were going through. I'm so sorry you felt that way, and I'm so sorry I let you down, I'm sorry I didn't hug you and squeeze you, I'm sorry I disrespected you and us.
It's been two years, and I'm still trying to heal from your loss. I'm still trying to accept that there will never be anyone as cool, as smart, as strong, as captivating as you. I'm still trying to find joy or meaning in anything I do. Hell, if you clone yourself and kept the exact same memories, I would still want you. There's no "another one" to find, because there's only one you. In two years, I haven't been able to be in a relationship with anyone. You might be the one who moved on from me a long time ago. You deserve all the contentedness, love and serenity your fluttering 90-bpm-ass-resting-heart-rate heart can handle. I'm sorry this post-script isn't as eloquent and poetic as you'd expect from me.
You've ruined all women for me. I love you, eternally
“للأبد؟
ـ ماذا؟
ـ ستظل تحبني للأبد؟
ـ حتى تحترق النجوم وحتى تفنى العوالم حتى تتصادم الكواكب، وتذبل الشموس وحتى ينطفئ القمر، وتجف البِحار والأنهار
حتى أشيخ فتتآكل ذكرياتي حتى يعجز لساني عن لفظ اسمك حتى ينبض قلبي للمرة الأخيرة
فقط عند ذلك ربما أتوقف.. ربما...”
submitted by classyhornythrowaway to UnsentLetters [link] [comments]


2024.05.15 04:12 Enough-Future-7002 22F Endocrinologist recommending Irish Sea Moss and Gaia Herbs to lower DHEA-S levels?

Hi guys. My DHEAS levels have been almost 700 the last two times I got tested. I don't have a stressful life, and I don't have PCOS according to the ultrasound attached, and am experiencing symptoms like acne, suuuuper itchy skin, extreme tiredness and fatigue, frequent panic attacks, muscle cramps, pain on my left side, severe headaches(migraines so severe multiple doctors thought I was having seizures), lactation even though I'm not pregnant, severe heat intolerance, unexplained weight gain, etc.
These are my recent labs. My endocrinologist wants me to get a CT scan of my adrenals, but not until I've tried 3 months of taking Irish Sea Moss and Gaia Herb supplements. He says he's doing this because my test results for my testosterone weren't elevated and he thinks this will bring down my DHEA-S levels, but I'm a bit skeptical. I just don't understand why or how this would help them. Can someone explain?
He also ordered repeat testing again in 3 months and marked the diagnostic code as PCOS, which I find strange because I was told I didn't have PCOS and that my ovaries/uterus looked perfect.
I'm a 5'7 female who weighs about 155 lbs. I take Adderall, Risperidone, Xanax, Metformin, and combination birth control pills.
Should I be concerned? Should I find a new endocrinologist, or does this approach make sense? My dad also has multiple endocrine neoplasia.
submitted by Enough-Future-7002 to AskDocs [link] [comments]


2024.05.15 03:54 Enough-Future-7002 Endocrinologist recommending Irish Sea Moss and Gaia Herbs to reduce DHEA-S?

Endocrinologist recommending Irish Sea Moss and Gaia Herbs to reduce DHEA-S?
Hi Reddit. This sub looks kind of dead but if anyone can help me out here it would be much appreciated. My DHEAS levels have been almost 700 the last two times I got tested. I don't have a stressful life, and I don't have PCOS according to the ultrasound attached, and am experiencing symptoms like acne, suuuuper itchy skin, extreme tiredness and fatigue, frequent panic attacks, muscle cramps, pain on my left side, severe headaches(migraines so severe multiple doctors thought I was having seizures), lactation even though I'm not pregnant, severe heat intolerance, unexplained weight gain, etc.
These are my recent labs. My endocrinologist wants me to get a CT scan of my adrenals, but not until I've tried 3 months of taking Irish Sea Moss and Gaia Herb supplements. He says he's doing this because my test results for my testosterone weren't elevated and he thinks this will bring down my DHEA-S levels, but I'm a bit skeptical. I just don't understand why or how this would help them. Can someone explain?
He also ordered repeat testing again in 3 months and marked the diagnostic code as PCOS, which I find strange because I was told I didn't have PCOS and that my ovaries/uterus looked perfect.
I'm a 5'7 female who weighs about 155 lbs. I take Adderall, Risperidone, Xanax, Metformin, and combination birth control pills.
Should I be concerned? Should I find a new endocrinologist, or does this approach make sense? My dad also has multiple endocrine neoplasia.
submitted by Enough-Future-7002 to endocrinology [link] [comments]


2024.05.15 03:46 Palpateenieweenie New to diagnosis and medication (Focalin XR), feeling very discouraged... maybe I don't have ADHD. Advice?

I was recently diagnosed with ADHD at age 27 and started on Focalin XR about a month ago. I have been diagnosed with generalized anxiety disorder since middle school and have been on antidepressants for about as long.
My experience with Focalin has been pretty negative so far. At 10mg I experienced all the side effects that I had heard that I might - headaches, tunnel vision, bouts of fatigue, irritability, initial euphoria, etc. Now that I've been on 20mg XR for about a week, I'm not having those side effects but things just... aren't what I was expecting. The euphoric, energetic, motivational effect that I get 45 minutes after taking it is great, but that lasts for only 2-4 hours. After that I crash and often have to take a nap. Even while I am having the positive effects, I don't get much done, it just feels like a mood booster more than anything, and I really don't want to feel like I'm using a drug recreationally. I very much want to feel what I've heard people talk about - The peaceful, quieted thought process, the clear thinking, the focus, and an easier path to achieve things that I've never felt like I could...
Anyway, all this is to say, my response to the medication makes me think that maybe I don't have ADHD after all. Has anyone had this experience? What did you do?
submitted by Palpateenieweenie to ADHDers [link] [comments]


2024.05.15 03:41 UtenaMage Playing chicken with Adrenal Crisis

Hey y'all, I'm not sure if I'm looking for advice on how to survive the summer or if I need motivation to keep going, or any thoughts on what might be ahead if anyone has any similar experience
I thought I was getting close to figuring it out with my dose in March but at the end of April as it got warmer what I'd been figuring out went out the window. My last crisis and ER visit were in February and since it's been so long some of the symptoms that eased up I'm having again full force and I recognize them as a warning sign
I'm not sure if I should go to the ER yet since I'm not in a crisis right now, but I'm in what I remember the days/week leading up to one feeling like. And it's an awful game of chicken that I can't win either way by having a crisis or not
Brain fog and feeling detached mentally and emotionally, severe fatigue and feeling tired all the time, dull temple headaches, freezing and can't control my body temperature, huge joint and bone pains (my lower right ribs are absolutely screaming as I type this lol) massive shouldeback pain, muscle weakness, insane insomnia despite being worn down or after sleeping 14+ hours, can't eat and haven't felt hungry to even try for days... the usual I think, for what most severe lows in cortisol feel like here (maybe?)
Not sure what changed but here's my dosing; 0.1mg fludrocortisone 6:30am 2.5mg prednisone 6:30am 1.5mg prednisone 2pm 2mg Rayos (delay release pred) 9pm
My endocrinologist wants me to try to stay around 6mg total prednisone including Rayos as best I can to avoid going too over, and said not to double the fludrocortisone for now because we are working out what my labwork is doing
My last labs showed my TSH was extremely low at 0.301 but my T3, T4 and the reverses were normal. He did a Thyroid antibody and it came back normal/negative, so it's impacted by something but unclear why only the TSH ACTH level was 14.2 (normal range said 7.6-64.2) Vitamin E Gamma, K1 and K2 were all low Food allergy panels showed nothing, negative for celiacs
Despite having Primary AI I had a second very high IGF-1 level in a row. First one was 320, this one was 350 (normal range is labeled as 91-300) so he will be doing a second MRI to scan for a pituitary tumor the first one might have missed. If anyone has any familiarity with that labwork or maybe growth hormone issues too?
But... yeah. I did double my pred doses today or I would have been nonfunctional like the last day or two. I feel like I'm barely scraping by on replacing cortisol and the summer isn't helping, fludro had the salt wasting and night sweating under control until this month. Without much else I can do but wait and see both on a crisis and MRI does anyone have any tips on how I might be able to tip it back away from a potential crisis? Or how to survive summer?
Thoughts on anything above always welcome, especially if you had similar experiences before treating something more. Or just how you got through, because 13 months later I'm losing my endurance on surviving this all. especially if what I thought I figured out in March was really that fragile
submitted by UtenaMage to AddisonsDisease [link] [comments]


2024.05.15 03:18 tw4lyfee Anyone else without shakiness/sweating?

At a recent check up I tested low for blood sugar. (60 mg/dL, I was not fasting). A follow up two weeks later had similar results.
I have felt fatigued, had occasional headaches, had bouts of racing pulse/breathlessness/lightheadedness, and just felt generally off the last several weeks. I really don't want to deal with this day-to-day.
My doctor seems pretty unconcerned because I haven't had any shakiness or sweating, which he considers the tell-tale signs. I'm really thinking this might be the answer to why I've been feeling off, but he's giving me doubts.
Is it unlikely that I have hypoglycemia? Do any of y'all have hypoglycemia without shakes and sweats?
I am getting set up with an endocrinologist, and planning to make some diet adjustments to see of that helps. Thank in advance for sharing your thoughts and experiences!
submitted by tw4lyfee to Hypoglycemia [link] [comments]


2024.05.15 01:20 LORD_BYRON_OF_RIVIA How has marijuana affected your symptoms in the long term or at all for that matter?

I smoked weed all my life but quit for the most part since getting this shitty disease. Sometimes made my anxiety go off the rails and sometimes neuro stuff worse. Sometimes it was great and just made me laugh at the absurdity of this fucking sickness.
Thinking about starting again. Not like I used to but just a puff here and there to take the edge off.
Background: I've been hauling for 2.5 years and anxiety and neuro stuff is the worst for me. Fatigue comes and goes but ok 80% of the time. No headaches but definitely brain numbness and fog.
I don't really expect anyone to recommend smoking with my symptoms but let's be honest I've been half a human for 2.5 years now and I don't see it getting better. I'm more just seeing how others have experienced pot since they had theirife stolen
submitted by LORD_BYRON_OF_RIVIA to covidlonghaulers [link] [comments]


2024.05.15 01:02 Relevant-Honeydew958 Very High ANA and nothing else positive?!

Hi all. I am a 20 year old female and my health has been declining for a while. I got my ANA tested in Feb and it was >=1:1280 with a homogenous and speckled pattern. I just repeated it last week and it was the same exact thing. I have had all of the following tests come back negative: -Smith antibody -Sjorgen antibodies (SSA and SSB) -Scleroderma antibody -ENA -Cyclic citrullinated peptide -Complement C4 and C3 -ESR -Creatine kinase -Rheumatoid factor -Anti-double stranded DNA My symptoms include: Generalized body and muscle weakness, fatigue, muscle spasms, dizziness, chest pain, headaches everyday and occasional joint pain in my hips.
Im going to see another rheumatologist for a second opinion. I am just very very concerned about how high my ANA is and am looking for any ideas on more tests we could do to figure this out! I know some people can be healthy with a positive ANA but its hard to think I’m on of them with how high it is and i feel horrible all of the time.
submitted by Relevant-Honeydew958 to Autoimmune [link] [comments]


2024.05.14 23:50 Ok-Reflection1005 Should I be looking for any other tests or specialists?

Hi! What other diagnostic testing should be requested? I’m having a very hard time being taken seriously by my last few PCPs and am trying to push for further specialist referrals and tests. I have been very dismissed and feeling crazy. I even sought a psychiatrist thinking maybe all this was in my head after all and they have supported me in continuing to push for answers because I am in fact not crazy lol.
I’ve had the following done and come back normal, but wondering if there is anything else my PCP should check before ruling out lupus definitively.
Came back normal-
CBC, metabolic panels repeated 2021-2024
2022- ANA
2024- rheumatoid factor Cyclic certificates peptide DNA DS antibody Chromatin neucleosomal antibody Complement components c3c and c4c Sed rate by modified westergren Complete abdomenal ultrasound Vitamin D, B12, Iron, Ferritin
Came back abnormal- 2022-2024 antiphospholipid antibodies B2 glycoprotein IGM high
2024- head mri with/ without contrast- few white matter lesions and scarring
2023- HLA- DQ8 genetic variant confirmed
I’ve got a whole host of symptoms that are both lupus and other auto immune specific. These include: Brain fog Extreme fatigue Memory issues Intermittent Butterfly and raised skin rash Feeling like I’m sunburnt even after only a few minutes outside Intermittent hearing issues Intermittent balance/ coordination issues Severe skin breakouts, digestive issues Constant illness Joint pain Swollen sore hands Numbness and tingling hands and feet Bladder retention and emptying issues Choking/ swallowing issues, chronic cough Pinpoint burning or itching sensation Since I was young, but now increasing again: “aura” like migraine or seizure aura without any headache or obvious seizure activity. Only other way I can explain this is “Alice in wonderland syndrome” (see fastfeeling)
My doctor has questioned SLE, MS but not really super conclusively. I also have wondered if celiac could be a factor but was informed after ANA testing that I may not have been eating gluten in my diet long enough for it to show other than the genetic test (usually avoid gluten by chance). I also have not yet heard back from my PCP on the results of the MRI- these findings were taken directly from the report uploaded in my patient portal. My family history is questionable as my mom was adopted, no one in my family really goes to the dr. Only Cancers and brain tumors have been confirmed. The most troublesome issues as of late are the cognitive issues and my hearing going out. It’s a few minutes or a few hours one ear at a time, pressure and muffled hearing. Any thoughts are appreciated, as I am exhausted
submitted by Ok-Reflection1005 to Autoimmune [link] [comments]


2024.05.14 23:42 Epoche-Ataraxia Mild chronic hypophosphatemia, going for genetic tests

Hi all- I was diagnosed with mild hypophosphatemia a little over two years ago. After two years of blood tests my phosphate levels have been a little below the reference range at 0.60-0.75 mmol/L (not sure in mg/dL).
After blood and urine tests doc has decided it’s probably a genetic cause as I also have phosphaturia and am being prescribed alfacalcidol.
The trouble I’m having is trying to sensibly work out what experiences I’m having that could be hypophosphatemia related or are just the struggles of life! Are my mental and physical fatigue and headaches just stress related? Are my funny looking knees the onset of rickets or just funny looking knees? Is there a proper test for bow-leggedness? How did you work out what was what?
Has anyone experienced long term alfacalcidol use?
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2024.05.14 23:19 Dependent-Aspect3902 Anybody else have Seronegative RA?

December 2023, started getting brain fog, off and on, several days per week. I thought I might need a change in the supplements I usually take, so I ditched Quercetin, Astaxanthin, and Krill Oil, and just kept taking the usual vitamins. No improvement in brain fog.
In late February 2024, I started feeling weak in the legs, with oddly stiff knees, when getting out of bed in the morning. It was hard to walk and my feet hurt. The brain fog also increased, and I started getting horribly fatigued, sometimes all day long. During the day and in the evening, my hands/knuckles/fingers started throbbing, sometimes severely. No fever, no swollen glands. I went to my primary doctor on March 19, and she ordered blood tests and xrays. Xrays showed no joint damage, and my inflammatory markers were pretty good, but my Rheumatoid Factor test was positive. She referred me to a Rheumatologist.
In mid-April, Rheumatologist took history and ordered a gazillion blood tests and urine test. Inflammatory markers looked good, except for IgA, which was elevated to 435. RF was negative though, after being positive the month before. FANA test was also negative (positive, with speckled pattern, but an insignificant titer....so, negative). Meanwhile, symptoms persist...brain fog, headaches, fatigue, joint pain (including wrists, now), weak/stiff/wobbly legs in the morning for about 45 minutes (but they come back if I sit or lie down for too long). At a recent follow up appointment, my primary doc ordered a brain MRI (haven't had it yet) and told me she still thinks I'm dealing with RA, but the Seronegative version.
Has anyone else experienced the same things? How did your Seronegative RA get diagnosed?
submitted by Dependent-Aspect3902 to rheumatoid [link] [comments]


2024.05.14 22:59 Flashy-Lawfulness127 Treatment Advice Needed

I was diagnosed with FND less than 2 weeks ago after months of feeling extremely fatigued and having pains all around my body, shortness of breath,headaches, difficulty concentrating, eye strain, sensitivity to light, chest palpitations, and probably some more I am forgetting. But the fatigue is the only thing preventing me from living my life. I am a male aged 22 and this all started a little less than 6 months ago. I only saw a neurologist once for about 45 minutes and he said he has no doubt in his mind that fnd is what I have. There was no event that occurred that caused me extreme stress or trauma so the cause of all this is unknown still.
I’ve done a lot of research on FND, people with FND, and treatments. The treatments recommended which I have seen are occupational therapy, physiotherapy, psychotherapy, and maybe some medication. After doing a lot of research on a lot of you people who have experience with fnd and have experienced things such as difficulty walking or difficulty operating particular limbs, and those of you who have went through difficult times of stress or trauma, I can see how those treatments I stated can benefit you but for me I don’t see how as I have no difficulty operating/ using my legs arms, whole body basically and I cannot say I went through trauma or extreme stress to cause FND. Because of this I am unsure of how to go about treating this and don’t see how physiotherapy, occupational therapy, and psychotherapy, would help me. I am currently trying to address my problems as if it were chronic fatigue syndrome, such as implementing a lot of vitamins into my diet and trying to consume foods which will give me energy rather than make me more fatigued.
PS: this is not very relevant but I do worry about my future a lot now since this has come on. I wonder if I’ll ever be able to live a normal life again, whether I will ever able to to get a partner as I have never had a girlfriend and this is only going to make that more difficult, whether I will be able to manage financially as I have had to quit work because of this. There are so many things I want to do in my life and if I carry on like this I can’t see myself being able to peruse any of them.
Any advice is greatly appreciated. I hope you all get better, this isn’t easy.
Edit: I have had countless blood tests and scans to rule out everything else basically.
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2024.05.14 22:02 Strawberry_Ice_Pop Iron deficiency

Those of you with iron deficiency is the low blood count so to HS, or PCOS? Is it difficult to prove what it's caused by? Is it possible to use iron deficiency to aid in getting potential disability benefits if it's long term or reoccurring? Edit: I've been diagnosed with iron deficient anemia multiple times and it leads to headaches, and chronic fatigue so that's why it feels so disabling to me. I'm constantly exhausted and feel like I can't get anything done.
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2024.05.14 21:55 SeeCrew106 [Debunk] Ivermectin is effective against COVID-19 and otherwise caused no harm

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 Pharmatm 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
submitted by SeeCrew106 to JamiePullDatUp [link] [comments]


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