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Imigran
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Imuran
Anyone doing well on this?
Anyone doing well on this?
Funnygirl64
in
NRAS
4 years ago
Intermittent fasting for crohns?
Has anyone tried intermittent fasting to assist with the symptoms of crohns? Currently on methotrexate injections once a week after little success with mercaptopurine tablets daily and intolerant to imuran. Looking at the fasting to try and manage pain mainly but also to rest the gut between 2000hrs-
Has anyone tried intermittent fasting to assist with the symptoms of crohns? Currently on methotrexate injections once a week after little success with mercaptopurine tablets daily and intolerant to imuran. Looking at the fasting to try and manage pain mainly but also to rest the gut between 2000hrs-
Levradoll
in
Crohn's and Colitis Support
4 years ago
Feeling awful update
Well my Rheumatologist called and let me know that he wanted me to go ahead increase my imuran to 100mg a day. Also he wants me to get a PFT as soon as they open up elective testing for the shortness of breath. Since I’m not sick and have no fever it’s not emergent. I am going also for a chest X-ray
Well my Rheumatologist called and let me know that he wanted me to go ahead increase my imuran to 100mg a day. Also he wants me to get a PFT as soon as they open up elective testing for the shortness of breath. Since I’m not sick and have no fever it’s not emergent. I am going also for a chest X-ray
precious123
in
NRAS
4 years ago
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Just feel awful
I have been on imuran 50mg for approx 3 weeks now. I was taken off of methotrexate as it had stopped working for me. I am very concerned as every time my meds stop working I usually have extreme fatigue pain and shortness of breath. This time I have not got the quick relief I usually have in the past
I have been on imuran 50mg for approx 3 weeks now. I was taken off of methotrexate as it had stopped working for me. I am very concerned as every time my meds stop working I usually have extreme fatigue pain and shortness of breath. This time I have not got the quick relief I usually have in the past
precious123
in
NRAS
4 years ago
Acthar Gel injections
Anyone ever took these injections before and if so how did you do with them? Did they help? I just got put on them after I had a video appt with my RA doctor. My sed rate is very high and he also had previously put me on imuran. So just wondering how things went for any of you that may have taken it
Anyone ever took these injections before and if so how did you do with them? Did they help? I just got put on them after I had a video appt with my RA doctor. My sed rate is very high and he also had previously put me on imuran. So just wondering how things went for any of you that may have taken it
precious123
in
NRAS
4 years ago
Imuran
Have any of you been on imuran for your RA before? I just started it I am on day 3 or 4 of it. Tonight I feel bad. Like so weak and hurting pretty bad. That being said I have been like this anyway but tonight it feels worse. I was just wondering if maybe the medicine is just getting into my system
Have any of you been on imuran for your RA before? I just started it I am on day 3 or 4 of it. Tonight I feel bad. Like so weak and hurting pretty bad. That being said I have been like this anyway but tonight it feels worse. I was just wondering if maybe the medicine is just getting into my system
precious123
in
NRAS
4 years ago
Ohh the pain today
Pain today man it’s been rough. My back is hurting and has drained me. I have failed yet another Med methotrexate so now my RA doc is keeping me on the orencia but adding imuran. I have also take. Orencia and imuran before. Orencia just quit working and I had to come off of imuran before due being
Pain today man it’s been rough. My back is hurting and has drained me. I have failed yet another Med methotrexate so now my RA doc is keeping me on the orencia but adding imuran. I have also take. Orencia and imuran before. Orencia just quit working and I had to come off of imuran before due being
precious123
in
NRAS
4 years ago
Hair loss
Over the last year I've been losing hair and texture has changed.... I've tried a strengtheners, Biotin and so on. I am on Prednisone, Plaquenil, and Imuran; which can cause loss of hair but at this point a necessity. Are there any hair remedies???
Over the last year I've been losing hair and texture has changed.... I've tried a strengtheners, Biotin and so on. I am on Prednisone, Plaquenil, and Imuran; which can cause loss of hair but at this point a necessity. Are there any hair remedies???
randa_lupie
in
LUPUS UK
4 years ago
Coronavirus: PAS Advice - PA Diagnosis Does Not Fulfil High Risk Criteria. Follow Current NHS and Government Guidance - Links Here
Hi All We are getting an increasing number of posts about coronavirus and questions about whether those with PA are in the high risk category. The PAS have issued the following advice... [i]As far as we know patients with the diagnosis PA do not fulfil the criteria of high risk. PA is an autoimmune disease
Hi All We are getting an increasing number of posts about coronavirus and questions about whether those with PA are in the high risk category. The PAS have issued the following advice... [i]As far as we know patients with the diagnosis PA do not fulfil the criteria of high risk. PA is an autoimmune disease
Foggyme
Administrator
in
Pernicious Anaemia Society
4 years ago
Managing joint pains
Hi everyone I'm new to the group. I'm so glad to have joined because I feel like I'm alone dealing with lupus!. I am currently having a bad flare with joint pain being my worst symptoms. I usually take imuran daily for the last 10 years and was doing well on it. This has come on out of the blue. Iam
Hi everyone I'm new to the group. I'm so glad to have joined because I feel like I'm alone dealing with lupus!. I am currently having a bad flare with joint pain being my worst symptoms. I usually take imuran daily for the last 10 years and was doing well on it. This has come on out of the blue. Iam
Lioness42
in
LUPUS UK
4 years ago
Lupus and Nursing
Hey all, anyone here a nurse on Imuran ( immunosuppressant ) and working? How do you cope / manage with no immune system and the fact you are with infectious patients ? Thanks !
Hey all, anyone here a nurse on Imuran ( immunosuppressant ) and working? How do you cope / manage with no immune system and the fact you are with infectious patients ? Thanks !
Hannalow
in
LUPUS UK
4 years ago
Otezla
Hi! Has anyone been put on Otezla? How did it help with your symptoms and management of them? Currently on imuran and getting toxic affects so this is the next one they want to try!
Hi! Has anyone been put on Otezla? How did it help with your symptoms and management of them? Currently on imuran and getting toxic affects so this is the next one they want to try!
Camp1997
in
Behçet's UK
5 years ago
Feeling Im losing Hope :(
So I've been sick for many years with inflammatory RA , Osteo, Behcet's, connective tissuue disease & others. It has gotten worse. These past 2 years are so so hard. For 3 weeks I cannot barely walk, sit down, stand, it's pretty awful & I'm afraid.. I'm taking colchacine, imuran & have iv remicade
So I've been sick for many years with inflammatory RA , Osteo, Behcet's, connective tissuue disease & others. It has gotten worse. These past 2 years are so so hard. For 3 weeks I cannot barely walk, sit down, stand, it's pretty awful & I'm afraid.. I'm taking colchacine, imuran & have iv remicade
Ang4upmich
in
ABDA
5 years ago
The Dreaded Itch
Hi All - Please I need help about the Dreaded Itch... I was diagnosed 1 month ago with PBC (and AIH overlap), For about a year beforehand, the only real symptom I had was the itch which would come and go all over or on legs, palms, and scalp. For the past 2 months I have had no itching at all. I began
Hi All - Please I need help about the Dreaded Itch... I was diagnosed 1 month ago with PBC (and AIH overlap), For about a year beforehand, the only real symptom I had was the itch which would come and go all over or on legs, palms, and scalp. For the past 2 months I have had no itching at all. I began
positivethoughts03
in
PBC Foundation
5 years ago
is it a risk to stay on imuran when i have had 4 skin cancer surgeries in the last 8 month's
i have GPA Valastitis for 3 years have been in remission for 1 year. i take imuran 150ml a day. i have had 4 skin cancer surgeries in the last 8 months. My Dr. says yes Imuran can be the cause of many cancers. My question is do i stop taking Imuran and hope my valastitis stays in remission, or do
i have GPA Valastitis for 3 years have been in remission for 1 year. i take imuran 150ml a day. i have had 4 skin cancer surgeries in the last 8 months. My Dr. says yes Imuran can be the cause of many cancers. My question is do i stop taking Imuran and hope my valastitis stays in remission, or do
1943bonnie
in
Vasculitis UK
5 years ago
NEWBIE
At present was treated for 6 months with chronic sinusitis and constant antibiotics and codeine with paracetamol, had terrible migraines, went to private E.N.T, no chronic sinusitis but maybe migraines but see a neurologist, told GP outcome and he said he treat me with
imigran
and propranolol.
At present was treated for 6 months with chronic sinusitis and constant antibiotics and codeine with paracetamol, had terrible migraines, went to private E.N.T, no chronic sinusitis but maybe migraines but see a neurologist, told GP outcome and he said he treat me with
imigran
and propranolol.
phobicgirl
in
Thyroid UK
5 years ago
Iv remicade question
A nurse is flying up here on Friday to give me home IV treatment. I am on imuran, colchacine & TRIED Humera shot every other week. I have severe joint pain , when I sit, my tendon or joints feel that they grow together then i recrack them, anyway I am so hopeful as someone here suggested iv remicade
A nurse is flying up here on Friday to give me home IV treatment. I am on imuran, colchacine & TRIED Humera shot every other week. I have severe joint pain , when I sit, my tendon or joints feel that they grow together then i recrack them, anyway I am so hopeful as someone here suggested iv remicade
Ang4upmich
in
Partners for Behcet's
5 years ago
Cellcept V Imuran and Side Effects
So the time has come for me to go on cellcept or Imuran. I was doing well on 20 mg prednisone but symptoms started to come back as I tapered. So a few questions Which do you like better Cellcept or Imuran? Side Effects - I have a phobia of nausea and vomiting so want to know how common Is anyone worried
So the time has come for me to go on cellcept or Imuran. I was doing well on 20 mg prednisone but symptoms started to come back as I tapered. So a few questions Which do you like better Cellcept or Imuran? Side Effects - I have a phobia of nausea and vomiting so want to know how common Is anyone worried
rottiro1
in
Lung Conditions Community Forum
5 years ago
Imuran for Itp
Did any one took imuran to increase the platelets count?
Did any one took imuran to increase the platelets count?
Entelaela
in
ITP Support Association
5 years ago
Pregnancy Questions
Hi everyone, I’m provisionally diagnosed with Behçet’s and being treated with Imuran 100mg twice a day. Not feeling much benefit as of yet but it’s only been 3 months. I was previously on colchicine but I had awful side effects so had to stop that. On top of Behçet’s I also have hashimotos and no thyroid
Hi everyone, I’m provisionally diagnosed with Behçet’s and being treated with Imuran 100mg twice a day. Not feeling much benefit as of yet but it’s only been 3 months. I was previously on colchicine but I had awful side effects so had to stop that. On top of Behçet’s I also have hashimotos and no thyroid
Jacbar
in
Behçet's UK
5 years ago
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