Systemic sclerosis: I have limited... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

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Systemic sclerosis

Lo1234 profile image
8 Replies

I have limited cutaneous systemic sclerosis, but my doctor told me that my condition is overlapping and would progress to diffuse systemic sclerosis. My pheripheral veins in both hands and feet are damaged. It's difficult to get veins open and extract blood. My right foot was recently operated on, and my toe was amputated. The right foot has a severe ulcer and osteomyelitis. Due of the acute ulcer and osteomyelitis, some toes are amputated and others are lost. I'm taking injections of mythylprednisolone and cyclophosphamide, but they don't seem to be working. My doctor recommends that I start using biological medications, specifically ritixumab or illoprost infusion. Is anyone on illoprost infusion? Also, what is the price?

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Lo1234 profile image
Lo1234
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8 Replies
fairy56 profile image
fairy56

Hi, I have Iloprost infusions every 6 months, I find it helps with my Raynauds. It is free on the NHS, I was prescribed it by my Doctor at my local hospital, hope this helps. Take care x

Lo1234 profile image
Lo1234 in reply tofairy56

NHS? Sorry I'm not getting

fairy56 profile image
fairy56 in reply toLo1234

Hi Lo, have just read your reply to another reply, and noticed you live in Nepal, I live in the UK, and we have a National Health Service. Hope you get the help you need. Take care x

trunchalobesity profile image
trunchalobesity

So sorry to hear of your problems.I almost lost a finger tip this summer, I take Sildenafil (viagra) 3 times a day. I had a weeks long infusion of flolan at the QE, as they no longer recommend Illiprost.

I had two course of cyclophosphamide, each one infusion every month for 6 months. This was to arrest my lung disease.

I’m on a maintenance dose of prednisone but the game changer for me has been mycophenolate for my lungs.

My RA overlap has caused joint pain and swelling and it is now recommended that I have Rituximab but I have been hesitant but will probably start shortly.

Are you in the UK? Treatment is free on the NHS.

Best wishes and kindest regards

Lo1234 profile image
Lo1234 in reply totrunchalobesity

Not UK but I'm from Nepal

trunchalobesity profile image
trunchalobesity in reply toLo1234

I hope you get all the help and support you need. X

kimbalina profile image
kimbalina

Ask your doctor about Botox injections. I was referred to a plastic surgeon who advised they are having lots of success with Botox to open arteries. Fortunately mine had nearly healed when I spoke to the plastic surgeon. But he advised me to get back to them if I had further problems.

Sanmateogirl107 profile image
Sanmateogirl107

WHY DIDN'T YOUR DOCTOR TELL YOU ABOUT (PRAZOSIN 1 MG) OR WILD LETTUCE EXTRACT FOR PAIN. I TAKE IT WORKS GREAT 10 DROPS UNDER THE TONMGUE MORNING AND NIGHT FOR PAIN. EBAY, MT ROSE HERBS HAS IT. 4OZ 18.00 AND UP LOVE JULIE

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