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Imuran
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Help! Headaches ruining my life
Hi, I was diagnosed with Hughes in 1998 after suffering a stroke. I have suffered with the most horrendous migraines since 1993. I am now getting desperate for some help/advise as my migraine headaches are now almost constant - I NEVER have a day without pain. I live in South Africa and almost feel
Hi, I was diagnosed with Hughes in 1998 after suffering a stroke. I have suffered with the most horrendous migraines since 1993. I am now getting desperate for some help/advise as my migraine headaches are now almost constant - I NEVER have a day without pain. I live in South Africa and almost feel
Hidden
in
Hughes Syndrome APS Forum
11 years ago
Optical Migraines
My friend has just been dignosied with migraine (it's the optical one) and she has been given imirgran and that's it. She would like to know what alternatives are avaialbe as the first sign of her migrianes are a dibilitating aura (changing aura, very, very bright, vision distortion, both eyes and peripheral
My friend has just been dignosied with migraine (it's the optical one) and she has been given imirgran and that's it. She would like to know what alternatives are avaialbe as the first sign of her migrianes are a dibilitating aura (changing aura, very, very bright, vision distortion, both eyes and peripheral
Puzzled
in
National Migraine Centre
12 years ago
i had severe migraines as a child, i had imigran injections, my son whos 22 has them now, is there no new remedies
andreana
in
National Migraine Centre
12 years ago
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neuro behcet's in Ireland
Hi, I have been suffering from bad headaches since christmas and have leisons on my brain but by neuro is not familiar with behcet's - i am the only patient he has with it! I dont feel he is taking this seriously enough and am very frustrated. i have been on sibilium, epilim, amnytriptline and asprin
Hi, I have been suffering from bad headaches since christmas and have leisons on my brain but by neuro is not familiar with behcet's - i am the only patient he has with it! I dont feel he is taking this seriously enough and am very frustrated. i have been on sibilium, epilim, amnytriptline and asprin
cailin
in
Behçet's UK
12 years ago
just got email saying I have PBC, scared and confused
After an initial few years of seroius illness taking steroids and
Imuran
I was able to remain in remission for many years. I spent my whole life trying not to be defined by this illness. Studied Chinese, lived in China, traveled, got 2 MA degrees, etc.
After an initial few years of seroius illness taking steroids and
Imuran
I was able to remain in remission for many years. I spent my whole life trying not to be defined by this illness. Studied Chinese, lived in China, traveled, got 2 MA degrees, etc.
Maddieroo
in
PBC Foundation
12 years ago
Left Headed Migraines?
I have always had right headed migraines since i was about 18 (now 32), then about 4 years ago i started getting left headed one - which were really severe and would basically keep me in bed for 2 days. It took about 2 yrs before the doctor realised and told me i was experiencing a migraine. I don't
I have always had right headed migraines since i was about 18 (now 32), then about 4 years ago i started getting left headed one - which were really severe and would basically keep me in bed for 2 days. It took about 2 yrs before the doctor realised and told me i was experiencing a migraine. I don't
Puzzled
in
National Migraine Centre
12 years ago
Migraine had reverted to those of 2 yrs ago, anyone had the same problem? - more details below.
Just over 2 years ago i used to get left headed migraines that would be so bad that if i stood up for any short or long period of time they i would be sick, and not be any to keep any food or liquid down, the imigran and anti-sickness medician that i was on didn't work, and i would quite literally spend
Just over 2 years ago i used to get left headed migraines that would be so bad that if i stood up for any short or long period of time they i would be sick, and not be any to keep any food or liquid down, the imigran and anti-sickness medician that i was on didn't work, and i would quite literally spend
Puzzled
in
National Migraine Centre
12 years ago
Just need to vent
So last week I started MMF 500mg a day- I used to take 100mg of
Imuran
. Well went back in to flare and feel terrible.And now I am on 15mg of prednisone instead of 10. I am so angry cause I wanted to go and see my family and enjoy my holiday now I dont know how I will feel.
So last week I started MMF 500mg a day- I used to take 100mg of
Imuran
. Well went back in to flare and feel terrible.And now I am on 15mg of prednisone instead of 10. I am so angry cause I wanted to go and see my family and enjoy my holiday now I dont know how I will feel.
TonyaM868
in
LUPUS UK
12 years ago
headaches
i seem to constantly have a headache these days its beggining to get me down now .only my imigran will take it away and thats taking couple of hours to kick in. love to all have a happy sunday xx
i seem to constantly have a headache these days its beggining to get me down now .only my imigran will take it away and thats taking couple of hours to kick in. love to all have a happy sunday xx
tofty
in
Fibromyalgia Action UK
12 years ago
Seen this on the internet - positive as it Highlights Lupus. Men may find this useful with Lupus SLE
Immunosuppressive drugs may also be used (with or in place of steroid treatments), such as cyclophosphamide (Cytoxan®), azathioprine (
Imuran
®), cyclosporin A, and mycophenolate mofetil (CellCept®).
Immunosuppressive drugs may also be used (with or in place of steroid treatments), such as cyclophosphamide (Cytoxan®), azathioprine (
Imuran
®), cyclosporin A, and mycophenolate mofetil (CellCept®).
Lulabelle
in
LUPUS UK
12 years ago
Yucky
I currently take Plaquenil 200mg 2X daily and
Imuran
100mg 2X daily...Lortab 7.5 as needed (I rarely take them because I hate masking pain) anyway nothing seems to help and I feel yucky all the time now...not a feeling I want to keep so I am looking for suggestions.
I currently take Plaquenil 200mg 2X daily and
Imuran
100mg 2X daily...Lortab 7.5 as needed (I rarely take them because I hate masking pain) anyway nothing seems to help and I feel yucky all the time now...not a feeling I want to keep so I am looking for suggestions.
smilanatu
in
LUPUS UK
13 years ago
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