Bio: Hi, I'm Rinah! Healing from Antisynthetase syndrome (includes polymyositis, ild....) since summer '24 🙏🏽🙌🏽

Bio: I’m Tangie I was diagnosed with polymyositis about a year ago and it’s been ruff but I always seem to push through

Bio: Hi! I’m 41 years old and been diagnosed with multiple sclerosis for 21 years

Bio: Diagnosed with polymyositis in 2018, I survived heart failure, a pacemaker, and years of treatment. I’m walking among other things and I’m grateful.

Bio: Grateful for the gift of life

Bio: Scleroderma and Myositis

Bio: Hello 👋 I am Isis 🥰 I'm a Dermatomyositis and a pulmonary fibrosis warrior 💜💜💜

Bio: Im Karina and Im polymyositis warrior

Bio: God bless

Bio: I’m Kimora, diagnosed with Lupus (SLE) and Dermatomyositis autoimmune diseases.

Bio: Hi all! I am a single RN mom, living with Lupus, Myocitis, RA, and Scleroderma. Some days suck, other days don't, EVERY day I try! 💪🏽

Bio: Newly amputee of left leg

Bio: I live in Houston, TX. I am a non profit founder and affinity group leader that is passionate about rare autoimmune diseases.

Bio: Hello, my name is Marsha Bell. I was diagnosed with Polymyositis in November 2010 and I was later diagnosed with NM and ILD in March 2011.

Bio: I was diagnosed with NAM in September 2024. I live in Florida with my husband and two kids. I am working on regaining my strength and independence.

Bio: Polymyositis warrior, waiting patiently for my healing. Appreciating all the progress I’ve seen since diagnosis, celebrating all the little victories.

Bio: New Here 👋🏾🌺

Bio: My name is Simone I’m 36 yrs old & I was diagnosed with Necrotizing Myositis in April of 2025. This has been the hardest thing I’ve ever dealt with💔

Bio: I have polymyositis was diagnosed 12years ago.

Bio: Dermatomyositis warrior

Bio: Living my best life despite living with inclusion body Myositis

Bio: Hello , my name is Stephanie Ridley, I’m 53 I have necrotizing poly myositis , I been battling this disease for 5 years. Now my life is not the same

Bio: Pet Lover