I'm Shereen, I don't have MS but I like volunteering, and I volunteered before with a renowned organization. I knew about from a close friend. She is like a sister to me. We grew up together. She told me about MS care, which let me know about her socially unclear illness (MS), so I wanted to go with her to MS educational session held by MS Care Society. Then, I felt like I wanted to know more about MS, so I subscribed in MS care group on Facebook, and I started to deliver free siring to patients who can't afford it and accompany patients to their clinics and Physiotherapy. 
Accordingly, I decided to participate in all of their activities and join all committees such as patient committee, World MS Day and social trips committees. Amazingly, I felt something in MS care that I didn't feel before, despite I volunteered for a renowned organization, which is the real care, love, family essence and warmth. It’s not just an association that started for the patients to support them, help them to live along side with MS and to be present in the society again, but also it is a big family guided by a group of people. I consider them angels in the shape of humans. In fact, I found sisters and friends that I’m proud of.  All I can say is I'm proud to be a member of MS care Society.