I was already in touch with Swasti Di (the co-founder of AAS) through social media channels and so became familiar with the NGO. Although I did not personally attend any
I am a patient of FA (Friedreich’s Ataxia), a type of ataxia, which is one of the many rare diseases. It was my mother and other FAer friends who brought
I came across AAS while searching on Google and immediately registered my name on the site. I felt like one with this family, sailing on the same boat. AAS has