
I have scleroderma
The Warrior is created by the adversity they’ve faced. Their strength and virtue come from those around them; those who have shown them the way.
Welcome Warriors!

Caregivers/Friends & Family
Empathy, positivity, patience and financial management are just a few of the feelings and responsibilities caregivers face.
Allies lift up Warriors.

Scholarship Program
Promoting secondary education through grant offerings to children and grandchildren of those afflicted is a way for us to establish hope.
Continue to care. Continue to grow.

Places you can interact with the SCW community
Recent News, Articles, and Information
Congratulations to Margaret! – 2024 Scholarship Recipient
Congratulations to Tiffany! – 2024 Scholarship Recipient
Been diagnosed with Pyoderma Gangrenosum?
Congratulations to Morgan! – 2024 Scholarship Recipient
Congratulations to Peter! – 2024 Scholarship Recipient
We are excited to announce that the podcast is now available for access!
About Mogil’s Mobcast- A Scleroderma Chat:
The goal of my podcast is to have a central place for people afflicted with Scleroderma and a place for their families and friends to be informed by specialists in either Scleroderma or autoimmune topics. I will cover a wide range of topics like nutrition, medications, vitamins, and lifestyles. I will also showcase stories from others affected by Scleroderma and how they have dealt with the disease.
For additional information, you can visit my website-Mogilsmobcast.com, or follow me on Instagram-mogilsmob and Facebook-mogilsmob.
Check out ongoing articles from a fellow Warrior!
Chronically Me – Amy Baker
Image credit sclerodermanews.com
Check out Amys’ Column and stay up to date with her posts here: sclerodermanews.com/chronically-me-amy-baker
We are Scleroderma Warriors
Scleroderma | Skleh – ruh – dur – muh |
Scleroderma is a rare, progressive auto-immune disease in which there is currently no cure. The Scleroderma Warriors Project is a program which connects those in need of support and direction with other warriors who are experiencing or have experienced a similar journey.

Thank you to our sponsors.

