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Immunosuppressants
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Happy Holidays! Holidaying abroad?...... or not....(as the case may be)........please consider your Hepatitis A and Hepatitis B vaccinations
Hi there! With the thought of overseas Summer holidays, please bear in mind your immunisations. (You may need full courses, or possibly some booster doses). Anyone with a compromised liver function must make sure that they are vaccinated against the relevant diseases where appropriate, and even if you
Hi there! With the thought of overseas Summer holidays, please bear in mind your immunisations. (You may need full courses, or possibly some booster doses). Anyone with a compromised liver function must make sure that they are vaccinated against the relevant diseases where appropriate, and even if you
L4LSarah
in
Liver4Life
10 years ago
[Blog] Sweet's syndrome triggered by azathioprine.
LJBentley27 developed Sweet's syndrome as a result of taking the immunosuppressant drug azathioprine for ulcerative colitis. Read her blog 'My IBD Story: I Almost Died This Year' @ http://lisatalksabout.com/2014/05/19/my-ibd-story-i-almost-died-this-year/
LJBentley27 developed Sweet's syndrome as a result of taking the immunosuppressant drug azathioprine for ulcerative colitis. Read her blog 'My IBD Story: I Almost Died This Year' @ http://lisatalksabout.com/2014/05/19/my-ibd-story-i-almost-died-this-year/
Shell567
Sweet's Syndrome UK
in
Sweet's Syndrome UK
10 years ago
latest results, do they look ''fine' to those of you with more knowledge/experience?
signed me off, says I can see the doctor from now on for 3 monthly reviews, says I am not hypothyroid, my levels are "fine"but keeping me on 25mg of levothyroxine a day because of the TED, she cannot explain the lethargy/exhaustion but says it's nothing to do with my thyroid, and thinks maybe its the
immunosuppressants
signed me off, says I can see the doctor from now on for 3 monthly reviews, says I am not hypothyroid, my levels are "fine"but keeping me on 25mg of levothyroxine a day because of the TED, she cannot explain the lethargy/exhaustion but says it's nothing to do with my thyroid, and thinks maybe its the
immunosuppressants
catalonia
in
Thyroid UK
10 years ago
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I have SLE, diagnosed in April 2000. I have no-one looking after me for my Lupus. What blood tests should I be having if any, and how often?
I have a kidney transplant, this is due to Lupus 'killing off' my kidneys, eye troubles - light sensitivity and multiple episodes over many years of scleritis, rarely iritis too. I have highly sensitive, itchy skin, and quite fatigued mostly, often feel completely rubbish, systemically just not right
I have a kidney transplant, this is due to Lupus 'killing off' my kidneys, eye troubles - light sensitivity and multiple episodes over many years of scleritis, rarely iritis too. I have highly sensitive, itchy skin, and quite fatigued mostly, often feel completely rubbish, systemically just not right
MandaM
in
LUPUS UK
10 years ago
Gas exchange low end of normal on lung function test
I guess being on
immunosuppressants
it will take a while to get over. I asked the technician if that would affect the results and he said no the machine was top of the range. Surely no matter how good the machine is if you arent fully functioning as normal it will affect the results.
I guess being on
immunosuppressants
it will take a while to get over. I asked the technician if that would affect the results and he said no the machine was top of the range. Surely no matter how good the machine is if you arent fully functioning as normal it will affect the results.
lollipop
in
Scleroderma & Raynaud's UK (SRUK)
10 years ago
Has anyone out there with PBC/AIH had to have a blood test done for TB I am waiting results for mine before I can start immunosuppressants?
MrsworryGuts
in
PBC Foundation
10 years ago
I have been denied IVIG by NHS England . I have been prescribed immunosuppressant medication instead .
I feel bad on them after only three days of taking them. I am dragging myself about feeling lethargic. Dizzy: low mood: and tearful. I wonder if anybody else has had experience of a similar drug to suppress the immune system ? Thanks in advance.
I feel bad on them after only three days of taking them. I am dragging myself about feeling lethargic. Dizzy: low mood: and tearful. I wonder if anybody else has had experience of a similar drug to suppress the immune system ? Thanks in advance.
Hidden
in
Scleroderma & Raynaud's UK (SRUK)
10 years ago
2 weeks ago I stopped taking Methotrexate 25mg by s/c injection ( it was wearing off after 5 days ) and have switched to mycophenolate.
Has anyone else changed
immunosuppressants
and how did you manage your symptoms until your new drug started working? I don't have a definitive diagnosis other than auto immune inflamatory.
Has anyone else changed
immunosuppressants
and how did you manage your symptoms until your new drug started working? I don't have a definitive diagnosis other than auto immune inflamatory.
Hidden
in
Vasculitis UK
10 years ago
Has anyone used DermaSilk theraputic socks and clothing for itching and skin abrasions?
Like many others who suffer from liver disease I suffer from itching and needless to say I am aware of and have tried many of the anti itch topical creams and gels with some being more effective than others . However being a fairly active individual I also suffer from frequent scratches,bruises and
Like many others who suffer from liver disease I suffer from itching and needless to say I am aware of and have tried many of the anti itch topical creams and gels with some being more effective than others . However being a fairly active individual I also suffer from frequent scratches,bruises and
findasolution
in
British Liver Trust
10 years ago
TED - dental work, awful dentist, now terrified
Hi everyone, I'm currently on
immunosuppressants
for the TED, had a tooth infection 10 days ago, walk-in clinic gave me 7 days of antibiotics, pain and swelling all now gone, went to see new dentist yesterday (old one retired) and am now feeling absolutely devastated. aside from he said he won't be
Hi everyone, I'm currently on
immunosuppressants
for the TED, had a tooth infection 10 days ago, walk-in clinic gave me 7 days of antibiotics, pain and swelling all now gone, went to see new dentist yesterday (old one retired) and am now feeling absolutely devastated. aside from he said he won't be
catalonia
in
Thyroid UK
10 years ago
Worried after visit to doctor today
My GP weighed me and said I had put on a stone in 3 months. Then he tested my blood via finger prick and found my glucose levels were pre-diabetic. Next, my blood pressure had gone up. He said I had been reducing the steroids much too slowly, which I disagree with as I don't think from 20 mg to 12.5
My GP weighed me and said I had put on a stone in 3 months. Then he tested my blood via finger prick and found my glucose levels were pre-diabetic. Next, my blood pressure had gone up. He said I had been reducing the steroids much too slowly, which I disagree with as I don't think from 20 mg to 12.5
Badgergirl
in
PMRGCAuk
10 years ago
Advice please at my wits end here so low have RA
I have Rheumatoid, Psoriatic and osteo arthritis. I am currently on these medications Sertraline 100mg 1 Bedranolol 160mg, Cyclizine 50mg twice daily, Folic acid 5mg, Tramadol 50mg 8 caps daily, sulfasalazine 500mg 6 tablets daily, Leflunomide 10mg, Lansoprazole 30mg, Methotrexate 15mg, Golimumab 2
I have Rheumatoid, Psoriatic and osteo arthritis. I am currently on these medications Sertraline 100mg 1 Bedranolol 160mg, Cyclizine 50mg twice daily, Folic acid 5mg, Tramadol 50mg 8 caps daily, sulfasalazine 500mg 6 tablets daily, Leflunomide 10mg, Lansoprazole 30mg, Methotrexate 15mg, Golimumab 2
stiffenlady
in
NRAS
10 years ago
Drugs refused funding...
Six years after diagnosis of Takayasu's Arteritis I seem to have gone through all the
immunosuppressants
(aza, mycophenolate, cyclo, MTX) all of which I've either not tolerated or haven't satisfactorily kept it under control.
Six years after diagnosis of Takayasu's Arteritis I seem to have gone through all the
immunosuppressants
(aza, mycophenolate, cyclo, MTX) all of which I've either not tolerated or haven't satisfactorily kept it under control.
JElsom
in
Vasculitis UK
10 years ago
Long term medication?
I have been on a number of different
immunosuppressants
over the years and either I haven't been able to tolerate them or they haven't controlled the disease progression.
I have been on a number of different
immunosuppressants
over the years and either I haven't been able to tolerate them or they haven't controlled the disease progression.
JElsom
in
Vasculitis UK
10 years ago
Is Behcets related to the foods we eat?
I was diagnosed with Behcets about 3 years ago and I was prescribe a large dose of immunosuppressant's and steroids. Late last year (2013) I went for a food intolerance test. This test showed that I have an intolerance to diary and wheat. Since I cut both of these from my diet I have noticed a massive
I was diagnosed with Behcets about 3 years ago and I was prescribe a large dose of immunosuppressant's and steroids. Late last year (2013) I went for a food intolerance test. This test showed that I have an intolerance to diary and wheat. Since I cut both of these from my diet I have noticed a massive
Wicker
in
Behçet's UK
10 years ago
Please say someone feels like I do....
Hi everyone, I'm asthmatic and always have been I seemed to grow out of it as a teen and since having my little boy two years ago it has come back. I was admitted to hospital in Feb 2013 for an exacerbation of asthma and to be honest never been 100% well since. In June I was re admitted for hospital
Hi everyone, I'm asthmatic and always have been I seemed to grow out of it as a teen and since having my little boy two years ago it has come back. I was admitted to hospital in Feb 2013 for an exacerbation of asthma and to be honest never been 100% well since. In June I was re admitted for hospital
Hidden
in
Asthma Community Forum
10 years ago
Rash on right arm.....it's shingles. Any advice welcome.
Does anyone have any experience of this when on steroids and
immunosuppressants
? The leaflet with the aciclovir is not very helpful and just gives warnings about seeing your doctor if your immune system is poor.
Does anyone have any experience of this when on steroids and
immunosuppressants
? The leaflet with the aciclovir is not very helpful and just gives warnings about seeing your doctor if your immune system is poor.
BronteM
in
Vasculitis UK
10 years ago
Prednisilone: 5mg per day = Good or Bad?
I do not take any
immunosuppressants
, apart from the Pred and haven't done for almost a year (on the advice of my consultant) because all of the
immunosuppressants
I've tried in the past I either cannot tolerate or they stop working for me.
I do not take any
immunosuppressants
, apart from the Pred and haven't done for almost a year (on the advice of my consultant) because all of the
immunosuppressants
I've tried in the past I either cannot tolerate or they stop working for me.
HiveMind
in
Vasculitis UK
10 years ago
Can I make a plea that all of us who are coeliac stop saying that we are allergic to or intolerant of gluten.
We have an autoimmune disease which we are lucky in that it can be controlled by diet alone. But if it is untreated or not treated well it has serious consequences not just in our gut but in our bones, vitamin levels, brain, blood etc. I think we sometimes are our own worst enemies because we underplay
We have an autoimmune disease which we are lucky in that it can be controlled by diet alone. But if it is untreated or not treated well it has serious consequences not just in our gut but in our bones, vitamin levels, brain, blood etc. I think we sometimes are our own worst enemies because we underplay
Mia1057
in
Gluten Free Guerrillas
10 years ago
Is most everyone with Behcet's on some type of an immunosuppressant long-term? What is your experience? Thanks
(One doctor wants me on azathioprine for two years to settle down my system and put things into remission hopefully and my "second opinion" doctor doesn't feel the need at this point.)
(One doctor wants me on azathioprine for two years to settle down my system and put things into remission hopefully and my "second opinion" doctor doesn't feel the need at this point.)
Rose138
in
Behçet's UK
10 years ago
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