Sushma was diagnosed with juvenile dermatomyositis, and was at the brink of death with how severely the rare autoimmune disorder had attacked her respiratory system and kidneys. Sushma’s poor parents had tried all they could, but had run out of ways to support her treatment. They felt defeated in terms of arranging the money they would require to save their daughter’s life. 

That is when you became their beacon of hope, and shined your light on young Sushma. With your abundant blessings and support, her treatment continued without a hitch, and she was soon able to make a full recovery. Today, Sushma is enjoying a new lease of life and back on track, working towards her dream of becoming a lecturer.

Charvi, Sushma, and Vikas' parents were fortunate that their prayers were answered right in time, and that your help arrived before something bad could happen to them. But the bitter truth is that many children born with rare disorders do not receive the same help. Millions of innocent kids suffer from cruel symptoms such as underdevelopment, weakness, localised pain, etc, due to which their life becomes a living nightmare. 

If these little ones do not get treated within a specific period of time, the quality of life suffers, and eventually they face the risk of death. Funds stand between them and their healthy, bright futures. You can help avoid these complications, by donating to Milaap Kids’ Rare Disease Fund, which will ensure that no child suffering from rare diseases is left behind.