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Tiredness - can anyone suggest ways to help with tiredness caused by rheumatoid arthritis?
My drugs are controlling the inflamation caused by RA, but I am still very tired, not able to do the amount I used to do. Any ideas other than pacing myself? Any good vitamins etc? thanks
My drugs are controlling the inflamation caused by RA, but I am still very tired, not able to do the amount I used to do. Any ideas other than pacing myself? Any good vitamins etc? thanks
kormacurry
in
NRAS
10 months ago
b12 injections done but don’t feel better
hi I’ve recently been diagnosed with b12 deficiency, no idea why my if was fine apparently and no sign of coeliac. Dr doesn’t seem to want to look into it any further which is annoying. But I’m finished with my initial injections almost two weeks ago and I don’t feel any better. Is this normal?
hi I’ve recently been diagnosed with b12 deficiency, no idea why my if was fine apparently and no sign of coeliac. Dr doesn’t seem to want to look into it any further which is annoying. But I’m finished with my initial injections almost two weeks ago and I don’t feel any better. Is this normal?
16131613
in
Pernicious Anaemia Society
10 months ago
Help with blood test results please
Hello, I have just recieved the following blood test results and I could do with your thoughts please. I treat my underactive thyroid with a comnination of T4/T3. T4 - 100 mcg 4 x week, 125 mcg 3 x week. I usually take 10 mcg T3 in the morning. FT4 - 14.6 [11.0-22.6] FT3 - 4.4 [3.5-6.5] TSH - 0.06
Hello, I have just recieved the following blood test results and I could do with your thoughts please. I treat my underactive thyroid with a comnination of T4/T3. T4 - 100 mcg 4 x week, 125 mcg 3 x week. I usually take 10 mcg T3 in the morning. FT4 - 14.6 [11.0-22.6] FT3 - 4.4 [3.5-6.5] TSH - 0.06
figster
in
Thyroid UK
10 months ago
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Why do my symptoms feel like Multiple Sclerosis when I taper?
Hi Everyone, I have had to go backwards from 2 years of tapering. I am now at 12 1/4 mg Prednisone today. At times during the day, when I can feel the inflammation inhabiting my body with extreme physical fatigue, extreme tingling extremities and inability to walk as usual. My legs move very slowly
Hi Everyone, I have had to go backwards from 2 years of tapering. I am now at 12 1/4 mg Prednisone today. At times during the day, when I can feel the inflammation inhabiting my body with extreme physical fatigue, extreme tingling extremities and inability to walk as usual. My legs move very slowly
lisbonportugal
in
PMRGCAuk
10 months ago
Water infections
I have been taking Jyselica for rheumatoid for 4 months but been having water infections. Has anybody else been using filgotinib and had water infections.
I have been taking Jyselica for rheumatoid for 4 months but been having water infections. Has anybody else been using filgotinib and had water infections.
Lilahloo
in
NRAS
10 months ago
lupus and cancer
hello to all of you warriors, I haven’t posted in a long time but do read daily posts. I have had lupus for over 30 years but the last few have been particularly difficult. I’ve recently been diagnosed with lung cancer and won’t be able to have radiotherapy or chemotherapy due to the lupus. Has anyone
hello to all of you warriors, I haven’t posted in a long time but do read daily posts. I have had lupus for over 30 years but the last few have been particularly difficult. I’ve recently been diagnosed with lung cancer and won’t be able to have radiotherapy or chemotherapy due to the lupus. Has anyone
sally10
in
LUPUS UK
10 months ago
some advice
swelling in the collarbone I have some swelling in my collarbone which could be linked to rheumatoid arthritis . Is there a link between PMR and rheumatoid arthritis? Can the first lead to the other ? Sorry if I sound so ignorant . This is a new development for me after 3 years of PMR
swelling in the collarbone I have some swelling in my collarbone which could be linked to rheumatoid arthritis . Is there a link between PMR and rheumatoid arthritis? Can the first lead to the other ? Sorry if I sound so ignorant . This is a new development for me after 3 years of PMR
Stanca
in
PMRGCAuk
10 months ago
19 Jul 2023 YOU make the choice, YOU
G'day my Multiple Sclerosis (ms) family. A good day for all so far today, if not WHY not. YOU, not me not your Doctors, nobody else YOU. It may hurt, let me tell YOU about pain. It may be embarrassing Been there done that. All sorts of humilities and embarrassments I have suffered in my 20
G'day my Multiple Sclerosis (ms) family. A good day for all so far today, if not WHY not. YOU, not me not your Doctors, nobody else YOU. It may hurt, let me tell YOU about pain. It may be embarrassing Been there done that. All sorts of humilities and embarrassments I have suffered in my 20
RoyceNewton
in
My MSAA Community
10 months ago
article in the times
One word of caution. A course of high-dose supplements given for at least three months will resolve many deficiencies but, unless diets/medication/underlying conditions change the problem is likely to recur. Many people will require lifelong supplements or, at the very least, future testing to check
One word of caution. A course of high-dose supplements given for at least three months will resolve many deficiencies but, unless diets/medication/underlying conditions change the problem is likely to recur. Many people will require lifelong supplements or, at the very least, future testing to check
Hedgehogs15
in
Pernicious Anaemia Society
10 months ago
NAD+ has anyone tried this supplement?
Hi all, Just had a friend visiting from the States who has battled severe fatigue since having covid, he doesn't have a thyroid condition. He found a supplement called NAD+ really helped him with fatigue. I can't find any info online in relation to this supplement and underactive thyroid, but wondered
Hi all, Just had a friend visiting from the States who has battled severe fatigue since having covid, he doesn't have a thyroid condition. He found a supplement called NAD+ really helped him with fatigue. I can't find any info online in relation to this supplement and underactive thyroid, but wondered
Wrayofsunshine
in
Thyroid UK
10 months ago
Dermaplaning
hi anyone on here had this treatment ? I have lupus tumidus , but contemplating it
hi anyone on here had this treatment ? I have lupus tumidus , but contemplating it
Dressgirl52
in
LUPUS UK
10 months ago
Losing Lupus diagnosis
I was diagnosed in 2010 with lupus, and 2012 with secondary sjogrens, raynauds and antiphospholipid syndrome. I was also badly affected by light photosensitivity. I had in 1978 a pituitary apoplexy and as yet undiagnosed thyroid hormone resistance. There's been a total of 17 different diagnoses
I was diagnosed in 2010 with lupus, and 2012 with secondary sjogrens, raynauds and antiphospholipid syndrome. I was also badly affected by light photosensitivity. I had in 1978 a pituitary apoplexy and as yet undiagnosed thyroid hormone resistance. There's been a total of 17 different diagnoses
linda96
in
LUPUS UK
10 months ago
Historic results
I was diagnosed with Hashimotos in 2014 and because of having one auto immune condition I was consequently tested for others- including Coeliac. I tested negative but as you can see only just & due to a lifetime of IBS caused by wheat I was a low consumer of wheat based foods anyway. I gave up gluten
I was diagnosed with Hashimotos in 2014 and because of having one auto immune condition I was consequently tested for others- including Coeliac. I tested negative but as you can see only just & due to a lifetime of IBS caused by wheat I was a low consumer of wheat based foods anyway. I gave up gluten
Whatnow1973
in
Gluten Free Guerrillas
10 months ago
M.E. or underactive thyroid?
I have a friend who has had an underactive thyroid for many years, she is on 75mcg levo. In recent years she has started suffering from fatigue. She is resistant to the possiblity it may be her thyroid as she has been hypo and on meds for years. Also GP has never suggested it may be her thyroid, because
I have a friend who has had an underactive thyroid for many years, she is on 75mcg levo. In recent years she has started suffering from fatigue. She is resistant to the possiblity it may be her thyroid as she has been hypo and on meds for years. Also GP has never suggested it may be her thyroid, because
AnneEvo
in
Thyroid UK
10 months ago
Research - support
Hello, Im a member of the Pernicious Anaemia Society which hosts this forum. I see from their communications that they are working on a lot of things at the moment including responding to the NICE guidelines on our behalf and funding research into lots of different things relating to pernicious anaemia
Hello, Im a member of the Pernicious Anaemia Society which hosts this forum. I see from their communications that they are working on a lot of things at the moment including responding to the NICE guidelines on our behalf and funding research into lots of different things relating to pernicious anaemia
LadyBothwell
in
Pernicious Anaemia Society
10 months ago
Recent diagnosis of Fibromyalgia
I was diagnosed with Rheumatoid Arthritis in 2021 after nearly two years of pain initially in my left wrist and then progressing to both hands and feet. I’m on so many medications and am awaiting the start of my second biologic as Imraldi only helped for 5 months. I’m wondering if anyone else has both
I was diagnosed with Rheumatoid Arthritis in 2021 after nearly two years of pain initially in my left wrist and then progressing to both hands and feet. I’m on so many medications and am awaiting the start of my second biologic as Imraldi only helped for 5 months. I’m wondering if anyone else has both
Gjbrose
in
NRAS
10 months ago
levothyroxine
I was diagnosed with underactive thyroid in April, i was initially put on 100mg of levothyroxide and dose has been increased steadily and am now on 175mg of levothyroxine, my main question is I have been getting severe joint pains a couple of weeks after taking the medication, the pains are now getting
I was diagnosed with underactive thyroid in April, i was initially put on 100mg of levothyroxide and dose has been increased steadily and am now on 175mg of levothyroxine, my main question is I have been getting severe joint pains a couple of weeks after taking the medication, the pains are now getting
alansing
in
Thyroid UK
10 months ago
Newly diagnosed
Hi All, I've just joined this group looking to educate myself following a recent 2nd positive lupus test. I am waiting for a pheumatology appointment but no idea when that is going to happen so a bit concerned I am losing time on getting a plan in place. 30 years ago I tested positive for Anti Phospholipid
Hi All, I've just joined this group looking to educate myself following a recent 2nd positive lupus test. I am waiting for a pheumatology appointment but no idea when that is going to happen so a bit concerned I am losing time on getting a plan in place. 30 years ago I tested positive for Anti Phospholipid
Autolupus
in
LUPUS UK
10 months ago
False negative ana?
hi, never posted on anything like this before but you all look so nice. I am 39. I developed an unprovoked DVT at the age of 16 had another when I was 19. Have various clotting problems through both my pregnancies too. No underlying cause was found. Ive had psoriasis since I was 8 and was treated for
hi, never posted on anything like this before but you all look so nice. I am 39. I developed an unprovoked DVT at the age of 16 had another when I was 19. Have various clotting problems through both my pregnancies too. No underlying cause was found. Ive had psoriasis since I was 8 and was treated for
Flakeyy
in
LUPUS UK
10 months ago
buprenorphine is not that harmless: sum
. ## KOR and Remyelination In the context of
autoimmune
diseases
like multiple sclerosis, KOR activation has been shown to promote oligodendrocyte-mediated remyelination, alleviating symptoms of experimental autoimmune encephalomyelitis (EAE). ## Conclusion In summary, KOR blockers enhance microglia-mediated
. ## KOR and Remyelination In the context of
autoimmune
diseases
like multiple sclerosis, KOR activation has been shown to promote oligodendrocyte-mediated remyelination, alleviating symptoms of experimental autoimmune encephalomyelitis (EAE). ## Conclusion In summary, KOR blockers enhance microglia-mediated
snoemata
in
Restless Legs Syndrome
1 month ago
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