Fibromyalgia.

[1whitestar]

I was diagnosed with fibromyalgia last April. Things have got worse more severe. Parts of the body any part hans arm feet trees etc started to swell red puffy itch and was so painful. After my bloods were done again my rumertied has gone up they can rule out gout. But said something is brewing up towards the arthritis side . So the consultant is starting me on low dose of sulfasalazine. Does anyone have any advise about this medication.

[jackaboo]

Hi, I`ve been on sulpha for many years with no problems i also take it alongside other meds as i also lupus. I get no side effects except for bright yellow wee! If you also have any stomach problems it`s given to people with colitis/crohns as it`s a good med. xx

[1whitestar in reply to jackaboo]

Thank you for the reply 🙏. That gives me some peace of mind.

[Daffodil63]

1whitestar- Hi, I've been taking Sulfasalazine for several years and as already mentioned the only obvious side effect is bright yellow wee! You will probably need regular blood tests to monitor any (rare) more serious side effects. If you don't see any improvement after about 6/8 weeks they may increase your dose. I wish you luck and hope you start to feel better soon x

[Hidden]

Hi Whitestar.Hope you are ok. This med helps with redness&swelling.(inflammation) RA. You should be monitored whilst taking it. You have to drink plenty water. Dose will be lowered if your symphons improve. I read this medication is often withdrawn. (Have a check on this info) 👍Take Care

[1whitestar in reply to Hidden]

Thank you for the reply . 🙏