Pred reduction being replaced by azathioprine
Is this the correct forum to be asking if anybody has experience of Myasthenia Gravis, predisolone reduction and starting azathioprine?...
Hi, everyone I haven't posted in a while. Just wanted some advice my azathioprine 50mg has been increased to 75mg this also I was taking the ...
Useful Supplements for Parkinson’s Disease
Useful Supplements for Parkinson’s Disease: Part 3 dose: 800 mg of magnesium citrate Magnesium is involved in a number of crucial bodily func...
Alcohol, sugar, and tremors
Alcohol is associated with decreased incidence of PD, especially beer, which increases uric acid which is also associated with decreased inci...
I agree that I need to cut down on the pred but daily quality of life has to take prioroty....
Feeling fed up needed a moment
This is my first post, iv loved reading everyone elses stories and advice they have received and it is lovely. It has been a horrible year th...
Advice on imuran/azathioprine medication.
Hi. My daughter is now 7....
Increased intolerance to Methotrexate
Hi everyone, I'm just after some advice / experiences from people about intolerance to Methotrexate and what they were switched to ( if it ha...
Was diagnosed with IPF 12 months ago and it is steadily getting worse....
Advice on using Azathioprine
Hi everyone, Can anyone give me any advice on their experience using Azathioprine? Saw my consultant today who has now decided to start me on...
Ulceration in pregnancy
Hi All, I have read some helpful posts and am pleased to have finally joined a group looking at BS. I am 5 months pregnant and suffer from ge...
Pain (what else?)
I have experienced a bad flare up of the PMR over the last 6 weeks - I had got down to 7.5 from 12.5 a day with 100 Azathioprine, just as I s...
Many combinations of drugs & dosages have been tried for the RA....
Hooked on prescription painkillers
I am now concerned that he is trying to reduce my steroid intake for PMR - currently at 13mg after a bad flare at 7.5mg - at any cost but tha...
I'm so grateful for this site b/c I have so many questions about this disease. My fiance was diagnosed about 18 months ago, so we're still le...
Giving up work or reducing hours
Hi there Ive sle and work as a customer service team leader. My job involves long periods on the phones, and long hours sitting at my desk on...
Is there any way that my lupus can get worse while they are investigating on a dosage that suits me?...
Exactly 4 years since a big decision
It's 4 years exactly since I had to stop the Thalidomide treatment for my cerebral vasculitis, because it was causing peripheral nerve damage...
Thank you very much to all who have wished me good luck at the docs today. Well, I have some good news....
I have started on triple therapy mouthwash as recommended by the centre of excellence so am hoping that it will help with my ulcers....
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