Intro about sickness:
Muscular dystrophy (MD) is a genetic disorder that gradually weakens the body muscles. A child who is diagnosed with MD gradually losses the ability to do things like walk, sit upright, breathe easily and move the arms and hands. This increasing weakness can lead to other health problems.
There is no cure for MD but researches are quickly learning more about to prevent and treat it. Doctors are also working on improving muscle and joint function and slowing muscle deterioration so that those with MD can live as actively and independently as possible.
About Uganesh Rajasegar:
Uganesh is student of SJKT Ladang Ulu Tiram,standard Year 5, 11years boy. He is also like other child loves to play football, swimming and liked to watch discovery channel.
Start to faced this disease :
Uganesh start to fell down oftenly when he was 4 years old. On that time we bring him to hospital sultan Ismail, that time doctor said its seem like nerves problem and give gel n asked to apply in his leg. After that also we never seen any changes so we bringing him to ayurvedic treatment, acupuncture n more places for treat him. But all our actions are failed almost n decided to bring back him to hospital sultan ismail. That time he was 6 years rdy. That day doctor confirm with us that he affected by MD n give us some details about this disease.
As a mother i couldn't take that my child go to die soon because of this disease. So i start to search the details of this disease n study about it. This disease is rare in Malaysia so don't have proper treatment here for him. So i search places that diagnosed this disease but as a mother almost failure. He also 9 years old rdy that time. So I'm give up n leave everything to god. Whatever is happen is all are our fate n karma. And uganesh 2017 after june slowly lost his walking ability. This situation make us more worried. That time i get one whatsup video interview of actor Napoleon. He son also affected with this disease n he decided to diagnosed all kid affected like his son. So he built Mayopathy Kapagam at tirunelveli district in India. Its give us a small light back to diagnosed my son back. We try to contact them 2017-2018 but we couldn't. But lastly 2018 June we get reply to our email. After that we contact Dr Ajay Jeevan Foundation head doctor ask us bring him for check up there to chennai. 2019 January we bring him to check up there n return back to Malaysia. The doctor take 1 month time to verify Uganesh report all. After 1 month they give us positive thought of Uganesh. They said his body still can support for treatment n can make him walk again.
But here our fate play again n we stuck because of my husband lost his work. We started face money problem again and again. Myself also take maximum loan level n couldn't get source of money. This the cause we looking help from helping hand people. Those are share n help us we told thanks in advance.
Hope kind peoples will help us by donating some money. Your small help can make changes in Uganesh health.
State Bank Of India- 20249718973
IFC code- SBIN005591
A/c holder name- Moon Debbarma