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Immunosuppressants
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Alternative Treatment for RA
I was diagnosed with RA in February 8, 2017. This is the most painful experience that I’ve ever been through. October 2016; after two weeks of training for employees to run new machine, I did a lot of heavy lifting at work which I normally don’t do at work. I felt pain on my right shoulder but I told
I was diagnosed with RA in February 8, 2017. This is the most painful experience that I’ve ever been through. October 2016; after two weeks of training for employees to run new machine, I did a lot of heavy lifting at work which I normally don’t do at work. I felt pain on my right shoulder but I told
HDo2010
in
NRAS
7 years ago
Shingles vaccine or not with immunosuppressant
I have chronic sarcoidosis in the lungs and am permanently breathless if I move around. I take prednisone and mycophenalate. The mycophenalate switches off my immune system. L had a flu and pneumonia vaccines last week , but they also have me down for needing the shingles one. I thought I wasn't allowed
I have chronic sarcoidosis in the lungs and am permanently breathless if I move around. I take prednisone and mycophenalate. The mycophenalate switches off my immune system. L had a flu and pneumonia vaccines last week , but they also have me down for needing the shingles one. I thought I wasn't allowed
Jomo46
in
Lung Conditions Community Forum
7 years ago
Insomnia and mycophenalate/ immunosuppressants? Anything anyone's had to help?
Hi, Wondering if anyone is on mycophenalate (cellcept) and has had problems with insomnia from it and if so what helps please? I'm just upping my dosage (still only on half of what I will be on in a month) but really can't sleep. I'm also on prednisolone so that might be affecting it too. I hate taking
Hi, Wondering if anyone is on mycophenalate (cellcept) and has had problems with insomnia from it and if so what helps please? I'm just upping my dosage (still only on half of what I will be on in a month) but really can't sleep. I'm also on prednisolone so that might be affecting it too. I hate taking
Melba1
in
LUPUS UK
7 years ago
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Lupus Survival Much Improved, But Plateaued
Lupus Survival Much Improved, But Plateaued
September 25, 2017 | Lupus By Gregory M. Weiss, M.D.
[i]Survival rates for patients with systemic lupus erythematosus have plateaued since the middle of the 1990s after a period of major improvement starting in the 1950s. [/i]
It has been thought
Lupus Survival Much Improved, But Plateaued
September 25, 2017 | Lupus By Gregory M. Weiss, M.D.
[i]Survival rates for patients with systemic lupus erythematosus have plateaued since the middle of the 1990s after a period of major improvement starting in the 1950s. [/i]
It has been thought
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
7 years ago
A Quick Question About Immunosuppressants and Exposure to Chickenpox.
What I'm not clear about is whether having these antibodies provides
complete
protection against infection with chicken pox when also on
immunosuppressants
?
What I'm not clear about is whether having these antibodies provides
complete
protection against infection with chicken pox when also on
immunosuppressants
?
Foggyme
in
LUPUS UK
7 years ago
10 Weeks post Transplant
Anyway I am now on fortnightly visits to the post tx clinic and steroids have been lowered but still waiting for the
immunosuppressants
to be lowered so I can be relieved of this horrible symptom.
Anyway I am now on fortnightly visits to the post tx clinic and steroids have been lowered but still waiting for the
immunosuppressants
to be lowered so I can be relieved of this horrible symptom.
Bookworm7
in
PBC Foundation
7 years ago
Levothyroxine therapy and impaired clearance are the strongest contributors to small intestinal bacterial overgrowth
Given the prevalence of gut issues reported here, often (but not always) in those taking levothyroxine, I hope the existence of this paper helps. At least it is something to quote! Very interesting to know how adding liothyronine (T3) - or liothyronine-only - would be assessed. [i]World J Gastroenterol
Given the prevalence of gut issues reported here, often (but not always) in those taking levothyroxine, I hope the existence of this paper helps. At least it is something to quote! Very interesting to know how adding liothyronine (T3) - or liothyronine-only - would be assessed. [i]World J Gastroenterol
helvella
Thyroid UK
in
Thyroid UK
7 years ago
What now?
I was diagnosed with Neuro Behçets, treated for the symptoms with gabapentin, metho prednislone,
immunosuppressants
and Diamox Been pretty much left to it by the hospital with no monitoring and as far as they know I am still on full strength meds I stopped the immunosuppressant after a series of illnesses
I was diagnosed with Neuro Behçets, treated for the symptoms with gabapentin, metho prednislone,
immunosuppressants
and Diamox Been pretty much left to it by the hospital with no monitoring and as far as they know I am still on full strength meds I stopped the immunosuppressant after a series of illnesses
Papapickle
in
Behçet's UK
7 years ago
Azathioprine advice?
I'm new to this site, and also
immunosuppressants
. My doctor just prescribed Azathioprine for active Crohn's, and as I am planning to return to Spain (from the US) for another school year, and won't be in the US with my regular doctor, it makes me kind of nervous.
I'm new to this site, and also
immunosuppressants
. My doctor just prescribed Azathioprine for active Crohn's, and as I am planning to return to Spain (from the US) for another school year, and won't be in the US with my regular doctor, it makes me kind of nervous.
viajera
in
Bowel Disease Support
7 years ago
Azathioprine advice?
I'm new to this site, and also
immunosuppressants
. My doctor just prescribed Azathioprine for active Crohn's, and as I am planning to return to Spain (from the US) for another school year, and won't be in the US with my regular doctor, it makes me kind of nervous.
I'm new to this site, and also
immunosuppressants
. My doctor just prescribed Azathioprine for active Crohn's, and as I am planning to return to Spain (from the US) for another school year, and won't be in the US with my regular doctor, it makes me kind of nervous.
viajera
in
Crohn's and Colitis Support
7 years ago
My Big wet walk last week
our coats were waterproof but I had jeans on and they really didn't feel that good when wet, MrRfc had craghopper trousers on, he bought these post transplant as they have uv filter and equivalent to factor 50 and mossie protection as looking after his skin in the sun is top priority when you are on
immunosuppressants
our coats were waterproof but I had jeans on and they really didn't feel that good when wet, MrRfc had craghopper trousers on, he bought these post transplant as they have uv filter and equivalent to factor 50 and mossie protection as looking after his skin in the sun is top priority when you are on
immunosuppressants
Realfoodieclub
in
Active 10
7 years ago
Reprogrammed cells - The promise of 'IP' stem cells
"While treatments exist for the movement disorders caused by Parkinson’s, none of them actually halt progression. Replacing the brain cells destroyed in Parkinson’s holds the promise of actually reversing the disease." "The IPS cells appear to act virtually identically to embryonic stem cells, but
"While treatments exist for the movement disorders caused by Parkinson’s, none of them actually halt progression. Replacing the brain cells destroyed in Parkinson’s holds the promise of actually reversing the disease." "The IPS cells appear to act virtually identically to embryonic stem cells, but
PDConscience
in
Cure Parkinson's
7 years ago
Anyone from Arizona?
Now stable (fingers crossed) and reducing steroids with the help of
immunosuppressants
and an amazing consultant's support.
Now stable (fingers crossed) and reducing steroids with the help of
immunosuppressants
and an amazing consultant's support.
PatMat
in
PMRGCAuk
7 years ago
Septic Shock
My question is, will he have to go back to taking the
immunosuppressants
eventually and also, what do the steroids do on their own - just keep inflammation at bay? Thank you :)
My question is, will he have to go back to taking the
immunosuppressants
eventually and also, what do the steroids do on their own - just keep inflammation at bay? Thank you :)
Hidden
in
Vasculitis UK
7 years ago
Azathioprine advice?
My doctor changed his mind and decided to put me on Azathioprine instead of Humira-at least for the time being-while continuing with Uceris (budesonide tablets) for Crohn's flare. I've never been on an immunosuppressant, and have some concerns about doing so with a cancer history, and while overseas
My doctor changed his mind and decided to put me on Azathioprine instead of Humira-at least for the time being-while continuing with Uceris (budesonide tablets) for Crohn's flare. I've never been on an immunosuppressant, and have some concerns about doing so with a cancer history, and while overseas
viajera
in
NRAS
7 years ago
Aih- unmedicated
I wanted to ask if anybody would share their experiences of living with type 1 aih. Especially if you are not taking any form of immunosuppression. My daughter was diagnosed 3 years ago and decided to stop taking her meds 8months ago, against her consultants advice, She is having fortnightly bloods and
I wanted to ask if anybody would share their experiences of living with type 1 aih. Especially if you are not taking any form of immunosuppression. My daughter was diagnosed 3 years ago and decided to stop taking her meds 8months ago, against her consultants advice, She is having fortnightly bloods and
Blackadder1
in
Children's Liver Disease Foundation
7 years ago
Immunosuppressive?
Hi Everyone, after a mild first time shingles outbreak my dentist is hoping I'm not immunosuppressed. I'm ET jak2+ on HU 500 mg 3x wk Is our immune system suppressed? My heme had said once that HU suppressed the bone marrow. Is that correct and are they the same thing? Now of course I'll worry about
Hi Everyone, after a mild first time shingles outbreak my dentist is hoping I'm not immunosuppressed. I'm ET jak2+ on HU 500 mg 3x wk Is our immune system suppressed? My heme had said once that HU suppressed the bone marrow. Is that correct and are they the same thing? Now of course I'll worry about
DH65
in
MPN Voice
7 years ago
20 Days post transplant
Had a bit of a blip last weekend, spent Fri till Sunday in hospital, I had a terrible headache that just wouldn't go, anyway to cut a long story short it was found my white blood cell count was high so
immunosuppressants
were changed steroids were upped and I am now back on the road to recovery.
Had a bit of a blip last weekend, spent Fri till Sunday in hospital, I had a terrible headache that just wouldn't go, anyway to cut a long story short it was found my white blood cell count was high so
immunosuppressants
were changed steroids were upped and I am now back on the road to recovery.
Bookworm7
in
PBC Foundation
7 years ago
Cancer patients' grey hair unexpectedly darkens in drug study
I know most of the forum discussion about hair centres on loss, rather than greyness, but I am quite sure this somewhat odd story will be of interest to many. It might also be seen to pick up on the mention the other day of using immunosuppressive medicines against Hashimoto's.
[i] Cancer patients
I know most of the forum discussion about hair centres on loss, rather than greyness, but I am quite sure this somewhat odd story will be of interest to many. It might also be seen to pick up on the mention the other day of using immunosuppressive medicines against Hashimoto's.
[i] Cancer patients
helvella
Thyroid UK
in
Thyroid UK
7 years ago
Yoga has helped my mobility and muscular pain
I have tried everything under the sun to ease my pain over the last 7 years. After ending up in hospital with pneumonia last year after starting a new immunosuppressant I decided that was the final straw. I didn't want the toxic side effects of these drugs if they didnt even take all of the pain away
I have tried everything under the sun to ease my pain over the last 7 years. After ending up in hospital with pneumonia last year after starting a new immunosuppressant I decided that was the final straw. I didn't want the toxic side effects of these drugs if they didnt even take all of the pain away
Annalouk
in
Fibromyalgia Action UK
7 years ago
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