A vicious circle. : I'm sure plenty of us are on this... - NRAS

NRAS

37,316 members46,201 posts

A vicious circle.

Slightly_ginger profile image
3 Replies

I'm sure plenty of us are on this particular treadmill, but I can't seem to see an end to it.

I'm taking fortnightly injections of Humira, which seem to last about ten days, my flare ups seem to get closer together and the good times further apart. So I revert back to Prednisolone for a six week course, titrate the dose down and come off, then the stiffness, fatigue, flu symptoms, chronic pain ramps up and I start the whole process again. I've had two lots of steroids this year. And I know it caused my blood sugar levels to increase, weight gain etc.

I've also been suffering with chronic anaemia.

I have PsA, Fibromyalgia, Kidney and Lymph Node cancer.

Is there anything I can do besides, MST Morphine. Anyone else with PsA + Fibromyalgia, does anything different and live a life not dependent on steroids for normality.

I'm desperate to break this vicious circle and be fitter again.

But after steroids, I can hardly walk, and standing becomes so painful after several minutes

Written by
Slightly_ginger profile image
Slightly_ginger
To view profiles and participate in discussions please or .
Read more about...
3 Replies
Matilda7 profile image
Matilda7

Might be worth considering diet modification if you haven't already?

Ali_H profile image
Ali_H

Hi,

One thing I am finding helps me is getting support beyond family and friends for emotional/stress level support. This may be worth considering as you clearly have a lot going on relight now - your gp can do a referral or your area may do a self referral service ( in the East Midlands it's called 'Let's Talk'.

All the best

Ali

ruth_p profile image
ruth_p

How long have you been on the humira? It doesn't sound like it is working properly. You should call your rheumatology helpline if you have been on it for longer than 3 months. They might need to try a different biologic treatment that isn't anti tnf but works on a different part of your immune system. I'm on tocilizumab which suppresses the IL6 protein. X

Not what you're looking for?

You may also like...

Vicious Circle

So I started Sarilumab (Kevzara) in Mid June it’s a fortnightly injection you do at home. I had my...

Another hospital visit over.

I was at the rheumy clinic today. The good news is i'm not in a flare up. The better news is that i...
sylvi profile image

RA agony, debilitation, biologic not working, pain out of control

Hi all you kind listening ears, Still living with so much chronic pain & agony in so many joints...
Blodynhaul profile image

Biologic or not to biologic

I got diagnosed in January this year with RA. I've was prescribed MTX but unfortunately after 5...
Jaxine profile image

RA and Fibro

Hi guys saw the rheumy yesterday and he says he wont prescribe anything else until I have a scan...
marie66 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.