Tips or advice to help calm autoimmune flare ups at h... - NRAS

NRAS

37,276 members46,139 posts

Tips or advice to help calm autoimmune flare ups at home??

Jj01994 profile image
6 Replies

I have had a few flare ups with this new medicine which is not unexpected but as much as I like Prednisone my doctor does not. Prednisone is the current treatment for flare ups but she does not do a standing order just case by case and her appointments book week to months in advance so hard to always get it from her. So any tips or advice on how to lessen or decrease symptoms or duration of a flare would be very helpful. I hope everyone has their own good day.

Written by
Jj01994 profile image
Jj01994
To view profiles and participate in discussions please or .
Read more about...
6 Replies
Rosie-NRAS profile image
Rosie-NRASPartnerNRAS

Hi Ji01994, sorry to hear that you are experiencing a flare at the moment. I have included some links below from our website that offer some tips on managing flares at home. Also our SMILE-RA programme has a module on managing pain and flares which may be of interest to you. Hope you feel better soon. Kind regards, Rosie @ NRAS.

nras.org.uk/resource/managi...

nras.org.uk/smile/

Ompie profile image
Ompie

Gosh I wish I was in your boat. Every time I go on a course of prednisone combined with a course of mesalazine, the rebound is horrific. I bleed so much more after the course tapers off and I have very very loose stools. I absolutely also hate that I can’t sleep during the course, and my temperament is up there with the demons!

Gitaga profile image
Gitaga

I only use prednisone when I have a flare up. I take 1 daily for 7 days and stop.

Normally my flare up happens every 6 to 8 weeks.

Hope this helps

AgedCrone profile image
AgedCrone

You have a Good Doctor…..the less Pred you are prescribed the better.The longer you take it, the more you are hooked on it and if you read back here you will see how those who are hooked on it wish they weren’t!

I highly recommend an anti-inflammatory diet. It's worked for me. I've had rheumatoid (seropositive) for almost 5 years and I've never been on medication. If I do get a flare up, it's very mild. Not using meds has been a bonus during covid. Diet combined with exercise, especially cardio, could offer you tremendous relief

Raynes profile image
Raynes

Ask for the injection instead of the oral script. It works faster, better and longer that the pills. And the side affects are far less than with the pills

Not what you're looking for?

You may also like...

Enbrel not working

I've been on enbrel ever since it was marketed but now it seems my flare ups are almost on going ,...
harcourt2 profile image

So I am understanding what RA and a Flare is at last...or not???

Ok so following on from a post I wrote yesterday, and apologies if I sound a little stupid but I...
Beelady profile image

Any Advice please!!?

Hello, My wife was recently in hospital with septic arthritis in her shoulder. She's was discharged...
Binkyboy profile image

prednisone

I had a call from my GP surgery yesterday, Doctor has refused to give me prednisone for my flare up...
Bagpuss2021 profile image

Itchy flare ups?

Hi Random question but does anyone get itchy flare ups? wherever I get a bad flare up it's just...
Tara26186 profile image

Moderation team

See all
KateL-NRAS profile image
KateL-NRASAdministrator
Donagh-NRAS profile image
Donagh-NRASAdministrator
Nicola-NRAS profile image
Nicola-NRASAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.