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levothyroxine induced lupus erythematosus?
Hiya, I am fairly new to all this, I have been on Levothryroxine for Hypothyroid (Hashimoto’s disease.) since June. My initial symptoms started after my first covid infection. All was going well until November time when I started to develop a Malar rash in the classic butterfly shape on my face. I don
Hiya, I am fairly new to all this, I have been on Levothryroxine for Hypothyroid (Hashimoto’s disease.) since June. My initial symptoms started after my first covid infection. All was going well until November time when I started to develop a Malar rash in the classic butterfly shape on my face. I don
Baker16
in
Thyroid UK
4 months ago
Rapid Onset of Symptoms
Hello, I was wondering if anyone can help me…. My dad has been diagnosed with PSP only a few months ago but has had symptoms for about 18months. His recent symptoms were textbook stage 2 but quite independent ….. this past Sunday morning he woke up feeling a bit off and then suddenly lost feeling in
Hello, I was wondering if anyone can help me…. My dad has been diagnosed with PSP only a few months ago but has had symptoms for about 18months. His recent symptoms were textbook stage 2 but quite independent ….. this past Sunday morning he woke up feeling a bit off and then suddenly lost feeling in
IPinkie
in
PSP Association
2 months ago
IBS and wind
I have had IBS for years and I am really suffering at the moment not only with the unpredictability of BMs but also terrible bloating and wind. It seems to be worse as soon as I go out shopping or to social events. I wonder if anxiety is partly to blame. I keep a food diary and am really careful
I have had IBS for years and I am really suffering at the moment not only with the unpredictability of BMs but also terrible bloating and wind. It seems to be worse as soon as I go out shopping or to social events. I wonder if anxiety is partly to blame. I keep a food diary and am really careful
Starry56
in
IBS Network
6 months ago
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Brain, ears, sleep. How can I make sense of tinnitus?
Hi all! I have tinnitus that comes and goes. Ig is a buzzing sound that fluctuates in volume. I don't have it when I am well rested and sleep deeply but as soon as I have a night where my dreams are uneasy in events..not nightmares just worries, I wake up with it or when I work late and become tired
Hi all! I have tinnitus that comes and goes. Ig is a buzzing sound that fluctuates in volume. I don't have it when I am well rested and sleep deeply but as soon as I have a night where my dreams are uneasy in events..not nightmares just worries, I wake up with it or when I work late and become tired
Peacely
in
Tinnitus UK
2 months ago
Pain in Left Eye
Hi Kind Friends, I am currently on 12.5 mg prednisone (tapering from 60 in Oct.) and weekly Actemra injections (about 4 months) Double vision from high prednisone has resolved as I have tapered. Occasionally I feel pain in my left eye, in the outer lower corner. It will hurt when I move my eye,
Hi Kind Friends, I am currently on 12.5 mg prednisone (tapering from 60 in Oct.) and weekly Actemra injections (about 4 months) Double vision from high prednisone has resolved as I have tapered. Occasionally I feel pain in my left eye, in the outer lower corner. It will hurt when I move my eye,
Lenore58
in
PMRGCAuk
2 months ago
Ibs symptoms
I was told I had IBS 29 years ago after having an ultrasound. It all started just after I was diagnosed with thyroid problems. Not a day has gone by where my stomach doesn't bother me, it always feels as if full of wind, bloated, tight and I often have diarrhea especially in the mornings. Anyone else
I was told I had IBS 29 years ago after having an ultrasound. It all started just after I was diagnosed with thyroid problems. Not a day has gone by where my stomach doesn't bother me, it always feels as if full of wind, bloated, tight and I often have diarrhea especially in the mornings. Anyone else
Harveyhound
in
IBS Network
8 months ago
does anyone use pepto-bismol?
interesting article in the New York Times today about a man with Parkinson’s who suddenly deteriorated and it was eventually found to be caused by the Bismuth containing meds he was taking. https://www.nytimes.com/2024/03/07/magazine/bismuth-toxicity-pepto-bismol.html ”DiCenso was also struck by the
interesting article in the New York Times today about a man with Parkinson’s who suddenly deteriorated and it was eventually found to be caused by the Bismuth containing meds he was taking. https://www.nytimes.com/2024/03/07/magazine/bismuth-toxicity-pepto-bismol.html ”DiCenso was also struck by the
LAJ12345
in
Cure Parkinson's
2 months ago
feeling a bit overwhelmed and lost
In September 2023 I found out by chance that I had apparently been diagnosed with lupus 15-20 years ago. I haven’t been told at any point in this time by a doctor - I found out almost by accident from my GP physio. Since then my current GP has been initially verbally supportive although said they knew
In September 2023 I found out by chance that I had apparently been diagnosed with lupus 15-20 years ago. I haven’t been told at any point in this time by a doctor - I found out almost by accident from my GP physio. Since then my current GP has been initially verbally supportive although said they knew
opalescenthope
in
LUPUS UK
4 months ago
a newby to Lupus
Hello folks, I was only diagnosed with lupus a few days ago, after six months of being told I have stage4 CKD, currently at 21% .Eight years ago I was diagnosed with severe anaemia by my GP, which with retrospect I think was a symptom of Lupus and the cause wasn’t looked into. I don’t have the energy
Hello folks, I was only diagnosed with lupus a few days ago, after six months of being told I have stage4 CKD, currently at 21% .Eight years ago I was diagnosed with severe anaemia by my GP, which with retrospect I think was a symptom of Lupus and the cause wasn’t looked into. I don’t have the energy
C0rnflakes
in
LUPUS UK
4 months ago
possible recurrence…
Hi ladies, I am stage 4 and have had 2 lines of carbo/taxol/avastin I am having an MRI scan today and have had a CT scan, my symptoms are a little bit of bloating and pain in my tummy and other areas since September last year when my ca-125 started increasing from 66, going up and up and now at 650
Hi ladies, I am stage 4 and have had 2 lines of carbo/taxol/avastin I am having an MRI scan today and have had a CT scan, my symptoms are a little bit of bloating and pain in my tummy and other areas since September last year when my ca-125 started increasing from 66, going up and up and now at 650
sarah040866
in
My Ovacome
5 months ago
Fibro medication and alcahol
Diagnosed a few years ago but decided not to take medication. The only meds I take are for my underactive Thyroid,i also have Ostioarthritis and Scoliosis but finding my pain is gradually feeling worse. What medication would you recommend? I am sociable and enjoy a sociable beer so is there anything
Diagnosed a few years ago but decided not to take medication. The only meds I take are for my underactive Thyroid,i also have Ostioarthritis and Scoliosis but finding my pain is gradually feeling worse. What medication would you recommend? I am sociable and enjoy a sociable beer so is there anything
henrythewasp
in
Fibromyalgia Action UK
4 months ago
Lanzoprazole and side effects
Hello, I am over 2 years past Ivor Lewis oesophagectomy and have been taking Lanzoprazole 15mg once a day, then Gavison at night. I’ve found that my folate and ferritin are low , probably caused by ppi use and wonder if anyone has managed to come off them. I know they have lots of potential bad effects
Hello, I am over 2 years past Ivor Lewis oesophagectomy and have been taking Lanzoprazole 15mg once a day, then Gavison at night. I’ve found that my folate and ferritin are low , probably caused by ppi use and wonder if anyone has managed to come off them. I know they have lots of potential bad effects
PopandMo
in
Oesophageal & Gastric Cancer
2 months ago
pain upper right side
I started with a terrible pain in my upper right side into my back with a gnawing sensation to the upper right front about 4 weeks ago. Liver function tests were not normal but an ultrasound concluded no gallstones and liver, gallbladder, spleen all looked normal. Still in pain, which starts in the evening
I started with a terrible pain in my upper right side into my back with a gnawing sensation to the upper right front about 4 weeks ago. Liver function tests were not normal but an ultrasound concluded no gallstones and liver, gallbladder, spleen all looked normal. Still in pain, which starts in the evening
Mrssmmf
in
British Liver Trust
7 months ago
Autoimmune Diseases
Saw this news article today and found it interesting. https://www.ctvnews.ca/health/lupus-and-other-autoimmune-diseases-strike-far-more-women-than-men-now-there-s-a-clue-why-1.6751469 Really found this part interesting. “Scientists have long thought it takes a combination of genetic susceptibility
Saw this news article today and found it interesting. https://www.ctvnews.ca/health/lupus-and-other-autoimmune-diseases-strike-far-more-women-than-men-now-there-s-a-clue-why-1.6751469 Really found this part interesting. “Scientists have long thought it takes a combination of genetic susceptibility
Swift20
in
Pernicious Anaemia Society
4 months ago
Laser iridiridotomy
Hi all, I am a glaucoma suspect and on the list for LI. I need to make a decision whether or not to go ahead with this procedure. I was wondering if anyone (suspect) had it and what was the difference you felt post-procedure. I am suffering from dry eye and dull and occasional sharp pain at the
Hi all, I am a glaucoma suspect and on the list for LI. I need to make a decision whether or not to go ahead with this procedure. I was wondering if anyone (suspect) had it and what was the difference you felt post-procedure. I am suffering from dry eye and dull and occasional sharp pain at the
btsg09
in
Glaucoma UK
2 months ago
Worst flare up to date.
Hi everyone I guess I'm just needing to vent as I feel so scared and alone. I have suspected Endometriosis but I'm 90 percent certain I have it. So yesterday morning when I woke up and my bladder was full I was feeling very sore round my pelvic region so went for a pee then after I went everything just
Hi everyone I guess I'm just needing to vent as I feel so scared and alone. I have suspected Endometriosis but I'm 90 percent certain I have it. So yesterday morning when I woke up and my bladder was full I was feeling very sore round my pelvic region so went for a pee then after I went everything just
KB1987
in
Endometriosis UK
2 months ago
Sjogren's Syndrome
Was diagnosed with PMR 3 years ago. Under control at moment and injections down to monthly. Has anyone on this site gone on to develop Sjogren's Syndrone with PMR?
Was diagnosed with PMR 3 years ago. Under control at moment and injections down to monthly. Has anyone on this site gone on to develop Sjogren's Syndrone with PMR?
Bothan
in
PMRGCAuk
3 months ago
Article: Why autoimmune disease is more common in women
I thought people might be interested in this article from Nature about why autoimmune diseases are more common in women: https://www.nature.com/articles/d41586-024-00267-6 "A new explanation for the discrepancy has emerged: a molecular coating typically found on half of a woman’s X chromosomes — but
I thought people might be interested in this article from Nature about why autoimmune diseases are more common in women: https://www.nature.com/articles/d41586-024-00267-6 "A new explanation for the discrepancy has emerged: a molecular coating typically found on half of a woman’s X chromosomes — but
cyberbarn
in
NRAS
4 months ago
Virus affecting IBS-D
I recently had a mild virus (headache, stomach pains and bad taste in mouth), which made me feel very tired. However, I was still able to go about my daily life whilst taking paracetamol to keep me going. The virus also affected my stomach causing loose bowel movements and occasional diarrhoea after
I recently had a mild virus (headache, stomach pains and bad taste in mouth), which made me feel very tired. However, I was still able to go about my daily life whilst taking paracetamol to keep me going. The virus also affected my stomach causing loose bowel movements and occasional diarrhoea after
laurajn087
in
IBS Network
8 months ago
Some new science on why women are more prone to autoimmune disease
This is an interesting read that suggests the preponderance of systemic autoimmune conditions in women is linked to incomplete X chromosome inactivation. Sadly, it doesnt have any immediate practical implications for us lot, but may be a pointer for the future. https://www.nature.com/articles/d41586
This is an interesting read that suggests the preponderance of systemic autoimmune conditions in women is linked to incomplete X chromosome inactivation. Sadly, it doesnt have any immediate practical implications for us lot, but may be a pointer for the future. https://www.nature.com/articles/d41586
whisperit
in
LUPUS UK
4 months ago
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