Systemic sclerosis/Scleroderma
Options
naila_007
Community member Posts: 37 Connected
Hi,
Just wondering how Systemic sclerosis/Scleroderma affects any one else.
Its a rare autoimmune condition. It has affected my skin and joints.
regards,
Naila
Comments
-
@naila_007 hi is that a type of lupus I have lupus and have similar symptoms
I have joint pain and skin problems but not severe skin problems -
Yes it falls under the same umbrella. Its been a long journey but couldnt have managed without the meds. So at the moment am in the vulnerable category.
-
How long have you had it i was diagnosed when I was 26 but said I probably started with it when I was 18 after my first baby
Do you cope well with it or do you struggle alot lupus has different effects on people I went to pain management for pain because slot of medications affect my lupus and so does food
Hope thst you gave an understanding dr that helps -
It has been 4 years now. At the beginning i struggled so much had physio, OT and various tests every week. Tried different meds and last resort was to go on immune suppressants. With SS there is no pattern it’s different for each person. I couldnt even pick up a 2 pint milk bottle or bend down. My skin were so stiff and swollen. But now i just have to remember i can do it but just
different to everyone else. ?
Everyday is a learning curve! -
@naila_007 same with me I have learnt to do things differently i also have the blood clotting side of lupus my skin used to becresly bad if I had gone into remission once I came out it was worse
I dont go into remmision anymore I know it sounds mad but I can cope better now -
@lisathomas50 just wondering if you have had the Covid Jab?
-
@naila_007 hi my specialist and my doctor advised me not to have it have you had yours yet
-
Hi - i have been invited to have my jab and all booked in. I have emailed my specialist nurse waiting to hear back. I feel my GP may not know enough about the condition. I am on immune suppressants and touch wood not in a flare up. I have been reading the vacacine is not a live one. My appointment is for the 24th Feb - i been doing a lot of reading too but still non the wiser
-
@naila_007 my dr is good she got in touch with my specialist they got in touch with the St Thomas hospital in London and they said I couldn't have any of them you may be ok let me know how you get on
Brightness
Categories
- All Categories
- 13K Start here and say hello!
- 6.6K Coffee lounge
- 103 Games lounge
- 416 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 199 Community updates
- 9.3K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 776 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 615 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 737 Transport and travel
- 31.5K Talk about money
- 4.3K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17K PIP, DLA, and AA
- 4.9K Universal Credit (UC)
- 6.3K Talk about your impairment
- 1.8K Cerebral palsy
- 868 Chronic pain and pain management
- 180 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 319 Sensory impairments
- 824 Rare, invisible, and undiagnosed conditions