Life with Scleroderma: Personal Stories

Life with Scleroderma: Personal Stories

Scleroderma affects everyone differently, as does how each of us manages our disease and responds to treatments.

For this reason, it is important to share many stories. We need to know we are not alone. On Sunday, October 25th, 2020 Scleroderma Atlantic held a webinar; Life with Scleroderma.

Thank you to panelists Kat Briand, Jessie Ferguson, Ken Rozee and Barb Carter for sharing their experiences living with scleroderma. To stay connected contact [email protected].

Scleroderma Atlantic Disclaimer: The Scleroderma Atlantic in no way endorses any drugs or treatments shared within this webinar. Stories shared are meant to share experiences with listeners. Because the manifestations and severity of scleroderma vary among individuals, personalized medical management is essential. Therefore, it is strongly recommended that all drugs and treatments be discussed with the listener’s physician for proper evaluation and treatment.

The Scleroderma Atlantic webinar series is supported by the Government of Canada’s Emergency Community Support Fund and Community Foundation of Nova Scotia.