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Imigran
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90% improvement with STOPPING HORMONAL BIRTH CONTROL
Hi all, I'm an American who's been lurking here since my BD flared up again over a year ago after a nice long time in remission. I'd been diagnosed as a kid so I just needed someone to help me manage things. The past year has been several months of Prednisone, several failed drugs, Imuran keeping things
Hi all, I'm an American who's been lurking here since my BD flared up again over a year ago after a nice long time in remission. I'd been diagnosed as a kid so I just needed someone to help me manage things. The past year has been several months of Prednisone, several failed drugs, Imuran keeping things
LMCharleston
in
Behçet's UK
6 years ago
Newly diagnosed. Needing help please.
Hello everyone. I'm newly diagnosed with chronic idiopathic urticaria, leukocytoclastic urticarial vasculitis and cold urticaria. I'm on Ozalimutab, Lukair, 4 different types of antihistamines, ranitidine for another effect on the urticaria. I'm just starting Imuran on a gradual 2 week increasing
Hello everyone. I'm newly diagnosed with chronic idiopathic urticaria, leukocytoclastic urticarial vasculitis and cold urticaria. I'm on Ozalimutab, Lukair, 4 different types of antihistamines, ranitidine for another effect on the urticaria. I'm just starting Imuran on a gradual 2 week increasing
Bibi77
in
Vasculitis UK
7 years ago
Arava side affects?
Hello, I was reading some posts and had a question. I have active bowel disease UC and undifferentiated connective tissue disease as well as either inflammatory arthritis or symptoms from the above. I was in imuran for a few years and it helped with joint and tendon swelling until I was hospitalized
Hello, I was reading some posts and had a question. I have active bowel disease UC and undifferentiated connective tissue disease as well as either inflammatory arthritis or symptoms from the above. I was in imuran for a few years and it helped with joint and tendon swelling until I was hospitalized
pegboyd
in
Cure Arthritis Community
7 years ago
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Widespread Clotting despite High INR: Adandondment of Warfarin being advised: Begin instead begin IV Cytoxan, Antiplatet, and DOAC -
This is the back of my leg ( just above the bend of my knee ) yesterday. My arms are clotting also. When I clot, I tend to clot “ every where at once.” It’s like my body gets “ rushed “ with antibodies. I have not had any kind of dip in INR to cause this. My INR is set at about 4.0. I am in 16.75 mg
This is the back of my leg ( just above the bend of my knee ) yesterday. My arms are clotting also. When I clot, I tend to clot “ every where at once.” It’s like my body gets “ rushed “ with antibodies. I have not had any kind of dip in INR to cause this. My INR is set at about 4.0. I am in 16.75 mg
KellyInTexas
Administrator
in
Hughes Syndrome APS Forum
7 years ago
AOSD and RA with Atypical Lympho
Hello everyone! I'm a new here. I have AOSD since my childhood with RA since last year. And I got my lab test yeasterday that said I have Atypical Lympho. I took Imuran for 15 days before I got the lab test. I really hope everyone in this community who knows well about the relation of AOSD & RA with
Hello everyone! I'm a new here. I have AOSD since my childhood with RA since last year. And I got my lab test yeasterday that said I have Atypical Lympho. I took Imuran for 15 days before I got the lab test. I really hope everyone in this community who knows well about the relation of AOSD & RA with
Hidden
in
Lymphoma Canada
7 years ago
Atypical lympho
I took a lab test today. I was so thankful to God that my AST & ALT were normal. My ESR and CRP were in normal range after I took Imuran for 14 days. Thank God it finally worked for me. But MCV and MCH were still under the normal. Hb was 11.7, Hematocrit 35.1. BUN and Urea were also under the normal
I took a lab test today. I was so thankful to God that my AST & ALT were normal. My ESR and CRP were in normal range after I took Imuran for 14 days. Thank God it finally worked for me. But MCV and MCH were still under the normal. Hb was 11.7, Hematocrit 35.1. BUN and Urea were also under the normal
Hidden
in
NRAS
7 years ago
Xeljanz vs cimzia
Hi..i may have asked this before but am asking again. I'm at a point with my ra that I need to make medication decisions. My option is between xeljanz or cimzia. I tend to get side effects of medications so am cautious probably over cautious In deciding. I already have high cholesterol, taking prednisone
Hi..i may have asked this before but am asking again. I'm at a point with my ra that I need to make medication decisions. My option is between xeljanz or cimzia. I tend to get side effects of medications so am cautious probably over cautious In deciding. I already have high cholesterol, taking prednisone
Hidden
in
NRAS
7 years ago
Went to Dr today
So, after being diagnosed PBC/AIH overlap syndrome, my GI put me on prednisone (10mg long term) along with the Urso and Atarax. My last blood tests on Monday showed my levels elevated but still dropping. My bilirubin is at 6.9 now. Saw my PC this morning and asked him if he could see my liver biopsy.
So, after being diagnosed PBC/AIH overlap syndrome, my GI put me on prednisone (10mg long term) along with the Urso and Atarax. My last blood tests on Monday showed my levels elevated but still dropping. My bilirubin is at 6.9 now. Saw my PC this morning and asked him if he could see my liver biopsy.
IAmTheGlue
in
PBC Foundation
7 years ago
Need advice on new GP please!
Hello everyone, I just moved to London a month ago and would like to get registered with a GP. My last doctor (back in Mexico City where I was living) sent me here with a lot of Plaquenil and Imuran but I feel like I need to get into the NHS system in case I get a flare up or need to have some blood
Hello everyone, I just moved to London a month ago and would like to get registered with a GP. My last doctor (back in Mexico City where I was living) sent me here with a lot of Plaquenil and Imuran but I feel like I need to get into the NHS system in case I get a flare up or need to have some blood
MerB90
in
LUPUS UK
7 years ago
Dyshidrotic Ezcema, how to manage it?!
Hey all! New to HealthUnlocked but happy to be here from what I've seen so far. The name's Keira, mid twenties female from Australia and I've had Atopic Eczema since I was born practically, and looking to be a life long condition. I swear I've tried everything under the sun for this...and it keeps developing
Hey all! New to HealthUnlocked but happy to be here from what I've seen so far. The name's Keira, mid twenties female from Australia and I've had Atopic Eczema since I was born practically, and looking to be a life long condition. I swear I've tried everything under the sun for this...and it keeps developing
Hidden
in
Eczema Association of Australasia Inc
7 years ago
Thinning hair with PBC? Urso side effects?
This is a random post and my first. After almost 3 years of symptoms, I was FINALLY diagnosed with PBC. I had been on Imuran because they thought it was autoimmune hepatitis, but my livers enzymes actually doubled while I was on it. I’ve also been on Prednisone for almost 5 months and am in the process
This is a random post and my first. After almost 3 years of symptoms, I was FINALLY diagnosed with PBC. I had been on Imuran because they thought it was autoimmune hepatitis, but my livers enzymes actually doubled while I was on it. I’ve also been on Prednisone for almost 5 months and am in the process
Stephanellie
in
PBC Foundation
7 years ago
Waiting
Looks like I might not have GCA. The neurologist here thinks that because I have been on Imuran ( azathiopirine ) for about 20 years that a fungal or bacterial bug is somewhere in my body and may hve been there for a long time. Good news brain looks ok. Bad news I have raised CSF pressure . Good news
Looks like I might not have GCA. The neurologist here thinks that because I have been on Imuran ( azathiopirine ) for about 20 years that a fungal or bacterial bug is somewhere in my body and may hve been there for a long time. Good news brain looks ok. Bad news I have raised CSF pressure . Good news
Rowboat
in
PMRGCAuk
7 years ago
Does anyone know why you can't take Imigran/Sumatriptan while pregnant in the UK?
I know that in the States and in some other countries like Germany you are allowed to take
Imigran
during pregnancy, in the first trimester at least. Apparently there is no data for
imigran
use in the third trimester.
I know that in the States and in some other countries like Germany you are allowed to take
Imigran
during pregnancy, in the first trimester at least. Apparently there is no data for
imigran
use in the third trimester.
Cat00
in
National Migraine Centre
7 years ago
Just coming out of a terrible migraine
This was one of those awful ones where no meds will touch it although it finally seems to have shifted after the last
imigran
this afternoon. Or maybe it was going anyway. Normally the
imigran
work quickly but this one kept coming back and pain excrutiating. Been in bed all day
This was one of those awful ones where no meds will touch it although it finally seems to have shifted after the last
imigran
this afternoon. Or maybe it was going anyway. Normally the
imigran
work quickly but this one kept coming back and pain excrutiating. Been in bed all day
FoggyMoggy
in
Fibromyalgia Action UK
7 years ago
My limbs keep falling asleep?!
Hello everyone, hope you are all having a lovely morning (: So, here's the thing... For the past nights, my limbs, especially my left arm and both legs, have been falling asleep. I often correct my sleeping position, so there shouldn't really be so much tingling and pain (I think). My boyfriend finds
Hello everyone, hope you are all having a lovely morning (: So, here's the thing... For the past nights, my limbs, especially my left arm and both legs, have been falling asleep. I often correct my sleeping position, so there shouldn't really be so much tingling and pain (I think). My boyfriend finds
MerB90
in
LUPUS UK
7 years ago
New with Questions
Hi, Very glad to have found this site. I am in Australia, female and 55. I was admitted to hospital about 18 months ago for over 2 weeks with a severe one sided headache, noise and light sensitivity. After lots of tests scans, mri, blood and whatever else I was released with an undiagnosed headache.
Hi, Very glad to have found this site. I am in Australia, female and 55. I was admitted to hospital about 18 months ago for over 2 weeks with a severe one sided headache, noise and light sensitivity. After lots of tests scans, mri, blood and whatever else I was released with an undiagnosed headache.
Rowboat
in
PMRGCAuk
7 years ago
New member
Hi! I'm new here, from Europe, Hungary. I was diagnosed 20 years ago with overlap syndrom of PBC/AHI . I' ve taken urso from the beginning and I started taking immuran 10 years ago. My itching has disappeared, but the tiredness and headachec occure regularly. My bloodtest is different from time to
Hi! I'm new here, from Europe, Hungary. I was diagnosed 20 years ago with overlap syndrom of PBC/AHI . I' ve taken urso from the beginning and I started taking immuran 10 years ago. My itching has disappeared, but the tiredness and headachec occure regularly. My bloodtest is different from time to
Dodo8
in
PBC Foundation
7 years ago
Medication allergies and lupus
Does anyone have a problem with being allergic to almost every medication? Ever since I've had lupus I've had problems with this. The only reason I can take plaquenil and immuran is because I take prednisone also and I guess it helps with the allergic reaction. Thanks!!!!!!
Does anyone have a problem with being allergic to almost every medication? Ever since I've had lupus I've had problems with this. The only reason I can take plaquenil and immuran is because I take prednisone also and I guess it helps with the allergic reaction. Thanks!!!!!!
Karynbrett
in
LUPUS UK
7 years ago
New here
Hi nice to find this site I was diagnosed last year with sjorens and about 7 or8 other autoimmune diseases I take plaqunil and immuran and gapapentin(2000 mg ) and many more pills I have read up on this disease and all the others I have I feel like a hypercondriact I feel sorry with everyone that has
Hi nice to find this site I was diagnosed last year with sjorens and about 7 or8 other autoimmune diseases I take plaqunil and immuran and gapapentin(2000 mg ) and many more pills I have read up on this disease and all the others I have I feel like a hypercondriact I feel sorry with everyone that has
Fisherman01
in
The Australian Sjögren's Syndrome Association
7 years ago
New to this Community
I am new to this group but have been on other groups regarding vasculitis for a few years helping others with advice and support..... I am 54 years, I had PAN when I was 21 years and went into complete remission after 5 years. In 2013 I was diagnosed with GPA. I relapsed again in 2016 and struggled
I am new to this group but have been on other groups regarding vasculitis for a few years helping others with advice and support..... I am 54 years, I had PAN when I was 21 years and went into complete remission after 5 years. In 2013 I was diagnosed with GPA. I relapsed again in 2016 and struggled
philtw
in
Vasculitis UK
7 years ago
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