← Return to Scleroderma (Systemic Sclerosis): Anyone else?

Discussion
kimberlyf avatar

Scleroderma (Systemic Sclerosis): Anyone else?

Autoimmune Diseases | Last Active: Sep 23 9:04am | Replies (47)

Comment receiving replies
Profile picture for eghclark @eghclark

Hello,I was recently diagnosed with scleroderma and it seems to be progressing rather quickly. Any suggestions or places I can get support? It is very scary.

Jump to this post


Replies to "Hello,I was recently diagnosed with scleroderma and it seems to be progressing rather quickly. Any suggestions..."

I am in the process of being tested for this as well and will definitely follow up with you .

Hi @eghclark and @jennyt23, I moved your messages to this discussion in the Autoimmune Diseases group
- Scleroderma (Systemic Sclerosis): Anyone else? https://connect.mayoclinic.org/discussion/sclerodermasystemic-sclerosis/

I did this so you can easily connect with other members living with scleroderma like @kimberlyf @shiprock @robinlundblade @andielars25 @sonnyforee10 @2beaformerredhead @gila @csmirat and many others.

See all scleroderma-related discussions: https://connect.mayoclinic.org/search/discussions/?search=scleroderma%20

@eghclark, this sounds like a new diagnosis for you. Can you share a bit more? What symptoms led to the diagnosis? How are you doing?

@jennyt23, what testing are you having done? What led to your doctor suspecting scleroderma? I know this is scary.

Me too. There are 2 types I have systemic how about you? What new symptoms are having thinking it’s getting worse? I wish I could tell you more about but I’m still figuring it out too. Keep in touch and let me know about my questions. Thanks