Scleroderma Stories: Glorie Shares Her Journey

Wendy Henderson avatar

by Wendy Henderson |

Share this article:

Share article via email

In this video from the Scleroderma Foundation, Glorie Ann Jaramillo shares that she was diagnosed with scleroderma in February 2014 after experiencing symptoms for two years.

MORE: Four tips to help navigate a scleroderma diagnosis.

Scleroderma is an autoimmune disease that affects different parts and organs in the body. Glorie’s skin and lungs are affected by the disease; in fact, the skin has tightened so much on her hands that she now struggles to grip and hold things. She also suffers from scleroderma-related fatigue.

Glorie explains that she felt relief when she was finally diagnosed with scleroderma, since she could be proactive in her treatment and seek out support. However, she also says the disease has stolen her identity as she is no longer able to work or be as active as she used to be.

MORE: How to manage scleroderma fatigue.

Scleroderma News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.