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Imigran
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Muscle weakness after migraine attack
In the past, after taking
Imigran
, my body has returned back to normal the next day. This is the first time that I still feel very weak, so I'm a little worried now 😩.
In the past, after taking
Imigran
, my body has returned back to normal the next day. This is the first time that I still feel very weak, so I'm a little worried now 😩.
Hidden
in
National Migraine Centre
7 years ago
High B12 levels in a blood test
I feel like I am banging my head against the wall and I have lost confidence in the pediatrician we are seeing, who has treated my son with
Imigran
for his headache, and recomended a psychiatric consult for anxiety, but will not investigate further his overwhelming High B12 levels.
I feel like I am banging my head against the wall and I have lost confidence in the pediatrician we are seeing, who has treated my son with
Imigran
for his headache, and recomended a psychiatric consult for anxiety, but will not investigate further his overwhelming High B12 levels.
lindaand3
in
Pernicious Anaemia Society
8 years ago
Migraines and retracted eardrums?
The doctor has prescribed
Imigran
and then Almotriptan most recently. I had a headache that lasted 13 days, wouldn't go, it wasn't like just a headache but wasn't full blown migraine, until the last day when it was the most horrible one I've ever had.
The doctor has prescribed
Imigran
and then Almotriptan most recently. I had a headache that lasted 13 days, wouldn't go, it wasn't like just a headache but wasn't full blown migraine, until the last day when it was the most horrible one I've ever had.
bluebell37
in
National Migraine Centre
8 years ago
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Huvs
Hello I was diagnosed with hypocomplementemic urticarial vasculitis in 2005 after many years of suffering from burning, painful and itchy hives. I suffered joint pain, extreme bone pain, peripheral neuropathy and foot drop. Through the years the flares have manifested in different ways; uncontrollable
Hello I was diagnosed with hypocomplementemic urticarial vasculitis in 2005 after many years of suffering from burning, painful and itchy hives. I suffered joint pain, extreme bone pain, peripheral neuropathy and foot drop. Through the years the flares have manifested in different ways; uncontrollable
lopiper
in
Vasculitis UK
7 years ago
Otezla for bechets?
Has anyone had success with this medication? I've tried colchicine, Imuran, and methotrexate so far with little to no relief, and a little relief not worth the slew of nasty side effects. I am really optimistic about trying otezla looking for some experiences!
Has anyone had success with this medication? I've tried colchicine, Imuran, and methotrexate so far with little to no relief, and a little relief not worth the slew of nasty side effects. I am really optimistic about trying otezla looking for some experiences!
dani80798
in
Behçet's UK
7 years ago
IPF (and so much more)
Hello to all! My name is Renee from Canada. I have IPF I think maybe stage 4 by now and am on oxygen 24/7 between 4 for sleeping and 15 on exertion. This really sucks having to drag around oxygen tanks. Not to mention that doing so takes even more energy away from me. My IPF apparently was brought
Hello to all! My name is Renee from Canada. I have IPF I think maybe stage 4 by now and am on oxygen 24/7 between 4 for sleeping and 15 on exertion. This really sucks having to drag around oxygen tanks. Not to mention that doing so takes even more energy away from me. My IPF apparently was brought
reneelp
in
Lung Conditions Community Forum
7 years ago
CNS vasculitis - I'm new here
I was diagnosed with retinal vasculitis in 1987 when I was about 20. No one knew much about vasculitis back then. I took high doses of prednisolone over an 18 month period and when I stopped getting more blind patches in my eyes we all thought that I had been cured. The blind patches were small, and
I was diagnosed with retinal vasculitis in 1987 when I was about 20. No one knew much about vasculitis back then. I took high doses of prednisolone over an 18 month period and when I stopped getting more blind patches in my eyes we all thought that I had been cured. The blind patches were small, and
KateB3
in
Vasculitis UK
8 years ago
Recently diagnosed with Autoimmune Hepatitis :(
Hi everyone, I am new here. I have autoimmune disease and I recently have been diagnosed with AIH. I was on prednisone and due to the awful side effects, my doctor switched me to Budesonide--yet I'm still experiencing horrible side effects along with Imuran. These drugs are literally sucking the life
Hi everyone, I am new here. I have autoimmune disease and I recently have been diagnosed with AIH. I was on prednisone and due to the awful side effects, my doctor switched me to Budesonide--yet I'm still experiencing horrible side effects along with Imuran. These drugs are literally sucking the life
CoriCassandra
in
British Liver Trust
8 years ago
An All Meat Diet Cured My Behcets
Hey guys, I've lurked on this forum for years, ever since I was diagnosed but this is the first time I'm compelled to write something and it's good news. My behcets was 'cured' by switching to an all meat diet. What do I mean by 'cured'? I don't get ANY symptoms anymore. I used to have all the symptoms
Hey guys, I've lurked on this forum for years, ever since I was diagnosed but this is the first time I'm compelled to write something and it's good news. My behcets was 'cured' by switching to an all meat diet. What do I mean by 'cured'? I don't get ANY symptoms anymore. I used to have all the symptoms
najeebo
in
Behçet's UK
8 years ago
Imuran (Azathrioprine) and stomach pain.
New to Imura and. I have been taking it for almost a month. Makes me nauseous so I split dose to morning and evening. Started getting sharp stomach pain just below ribs in center of abdomin. Called rheumy to see if I should continue. She told me to take the weekend off and if the pain goes away to go
New to Imura and. I have been taking it for almost a month. Makes me nauseous so I split dose to morning and evening. Started getting sharp stomach pain just below ribs in center of abdomin. Called rheumy to see if I should continue. She told me to take the weekend off and if the pain goes away to go
Lorin
in
NRAS
8 years ago
Hair loss STILL!
Hi All, I have been treated with plaquenil for 6 months now and been on imuran and 5mg prednislone for just over two months. My hair has been falling out for about 4 months but the last couple of months it has happened very quickly. I have 3 massive bald patches and the rest of my hair is very thin
Hi All, I have been treated with plaquenil for 6 months now and been on imuran and 5mg prednislone for just over two months. My hair has been falling out for about 4 months but the last couple of months it has happened very quickly. I have 3 massive bald patches and the rest of my hair is very thin
Emily00
in
LUPUS UK
8 years ago
Bechets and Enbrel
Sorry I haven't posted in a while. So I switched to a different Rhuemtologist. The women I was seeing was very insensitive and rude. We could not agree on a treatment plan for the life of me. She wanted me to be her Ginny pig in all aspects of trying loads of medication. My new dr is amazing! He listens
Sorry I haven't posted in a while. So I switched to a different Rhuemtologist. The women I was seeing was very insensitive and rude. We could not agree on a treatment plan for the life of me. She wanted me to be her Ginny pig in all aspects of trying loads of medication. My new dr is amazing! He listens
Jennifer4284
in
Behçet's UK
8 years ago
Newly dx'd.
Hi I'm 42 live in Arkansas and trying to find assistance to help with Copaxone. I have Medicare so I'm not sure why there is a problem. I am a Registered Nurse disabled from an inflammatory muscle disease called Dermatomyositis or DM for short, MS, Hashimoto, and Fibromyalgia I take Imuran for the DM
Hi I'm 42 live in Arkansas and trying to find assistance to help with Copaxone. I have Medicare so I'm not sure why there is a problem. I am a Registered Nurse disabled from an inflammatory muscle disease called Dermatomyositis or DM for short, MS, Hashimoto, and Fibromyalgia I take Imuran for the DM
laurarogersclark
in
My MSAA Community
8 years ago
Confused - ?RA with no signs of inflammation on hand sono
I have always had intermittent neck and lower back pain from mva in my 20's. Five years ago an mva left me with intermittent hip and shoulder pain and fatigue - all bloodwork negative. Last summer the wrist, hands, ankles, and feet started getting swollen, stiff, and tingling, hip pain with only walking
I have always had intermittent neck and lower back pain from mva in my 20's. Five years ago an mva left me with intermittent hip and shoulder pain and fatigue - all bloodwork negative. Last summer the wrist, hands, ankles, and feet started getting swollen, stiff, and tingling, hip pain with only walking
NY65
in
NRAS
8 years ago
Immuran (Azathioprine )50 mg twice or Myfortic 360 mg twice daily (mycophenolate sodium )
Immuran (Azathioprine )50 mg twice OR Myfortic 360 mg twice daily (mycophenolate sodium ) is better for MCTD or lupus and Sjogren?? any experience? i have to choose between them !
Immuran (Azathioprine )50 mg twice OR Myfortic 360 mg twice daily (mycophenolate sodium ) is better for MCTD or lupus and Sjogren?? any experience? i have to choose between them !
Samaka
in
LUPUS UK
8 years ago
help!
If I catch it in time with
imigran
I get relief but if I'm too late it will go on for hours but rarely goes on longer than a 24 hour period. Seems to be driven by hormones and stress. The other headaches are the ones that are causing me more of an issue in terms of frequency.
If I catch it in time with
imigran
I get relief but if I'm too late it will go on for hours but rarely goes on longer than a 24 hour period. Seems to be driven by hormones and stress. The other headaches are the ones that are causing me more of an issue in terms of frequency.
Shapark
in
National Migraine Centre
8 years ago
Fighting this Lung disease
I have systemic Lupus along with interstitial lung disease im now on oxygen 24/7 and now on immuran i was taken off prednisone and had hemmoraged in my Lungs. I pray it gets better and then i can prayfully get off oxygen. Im also having my kidneys looked out the dr says im spilling protein in my urine
I have systemic Lupus along with interstitial lung disease im now on oxygen 24/7 and now on immuran i was taken off prednisone and had hemmoraged in my Lungs. I pray it gets better and then i can prayfully get off oxygen. Im also having my kidneys looked out the dr says im spilling protein in my urine
Ginatay4t
in
LUPUS UK
8 years ago
Having iTP Since 6 months i want to get rid steriod
Hi, I diagnose ITP 6 months ago when i go for blood test and all this released i am on steriod DELTACORTAL 15mg/day with immuran bla bla my doctor and I want to get rid steriod as this has lots of side effects my count is in between 30 to 50 but as i lowdown the dosage of DELTACORTAL it get down near
Hi, I diagnose ITP 6 months ago when i go for blood test and all this released i am on steriod DELTACORTAL 15mg/day with immuran bla bla my doctor and I want to get rid steriod as this has lots of side effects my count is in between 30 to 50 but as i lowdown the dosage of DELTACORTAL it get down near
akhurram
in
ITP Support Association
8 years ago
I'm now CCH free !!!!
It took him about 6 appointments before he prescribed
IMIGRAN
SUBJECT INJECTIONS, the only relief medicine I know! It can take effect within minutes or it did with me.
It took him about 6 appointments before he prescribed
IMIGRAN
SUBJECT INJECTIONS, the only relief medicine I know! It can take effect within minutes or it did with me.
jockeye1
in
National Migraine Centre
8 years ago
Crohn's Disease for over 35 years
I have had Crohn's Disease for over 35 years. I have tried Asacol, Sulfasalazine, Entocort, Imuran, Remicade and of course Prednisone. I have only been hospitalized once, 3 years ago, with a partial bowel obstruction and was put on Remicade which ended up to be a horrible experience. I developed such
I have had Crohn's Disease for over 35 years. I have tried Asacol, Sulfasalazine, Entocort, Imuran, Remicade and of course Prednisone. I have only been hospitalized once, 3 years ago, with a partial bowel obstruction and was put on Remicade which ended up to be a horrible experience. I developed such
Cbeckwall
in
Crohn's and Colitis Support
8 years ago
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