5-year-old Affected With One of The Rarest Diseases Needs | Milaap
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5-year-old Affected With One of The Rarest Diseases Needs Urgent Help
  • BM

    Created by

    Bharath Mohan
  • L

    This fundraiser will benefit

    Likhit

    from Bangalore, Karnataka



It all started when Likhit was just 2 years old. His parents saw that his pillow was covered in blood and baby Likhit kept gargling. He had started bleeding from the gums. Likhit is 4 years old now, but the bleeding hasn’t stopped. He has a disease that is so rare that there are only 500 diagnosed cases in the world. His parents cannot afford the cure, and they have gone as far as writing to PM Modi for help.

“There is never any pain or any other kind of irritation, he just bleeds every 10 days. You know what happens when we lose that much blood.” - Bharath (Father)

Likhit is brave, but it is not enough to save him from this struggle
Likhit suffers from a very rare genetic disorder, LAD Type III & Glanzman Thrombasthenia which causes him to bleed profusely until he gets blood transfusions. Every 15 days, they run to the hospital with Likhit holding his hands over his mouth, trying to stop the blood from oozing out. He does not like the taste of it. He is not able to spit it out. He is scared that his teeth may all fall out. 

"Likhit knows that it is hospital time when he bleeds, and he knows the entire drill, but he never cries, neither is he cranky. He goes around smiling and making friends in the ward, talking to everyone. Due to his thin veins, nurses insert the injection in his neck, a painful procedure, but he is very brave."

Over the last 2 years of treatment, Bharath has already spent 8 lakhs in treatment, and he needs 40 lakhs more
The only permanent cure for Likhit is a Bone Marrow Transplant(BMT). The bleeding has increased, and so have the visits to the hospital. While the financial strain can be managed, Likhit's tiny body cannot handle the iron buildup from transfusions. It is likely that his organs will get damaged from frequent transfusions. This could be fatal.

“I am paying more than 30k a month because the frequency of the bleeding has gone up. Only last week, he got the platelets transfusion, and now again within a week we had to admit him for another platelet transfusion. Can you imagine what this does to a child, struggling with this disease for years?"
Bharath who works with payroll management company earns Rs. 27000 a month, exhausting more than that for Likhit's treatment. He is the only earning member of his family, looking after his son, wife and aged father. He sometimes works on Loss of Pay, as he has exhausted all his leaves trying to reach out to friends, acquaintances, government officials, support groups to ask for help for Likhit, but those contributions have not been sufficient. Likhit's bone marrow transplant itself would cost him 40 lakhs. Bharath knows that he will not able to arrange for such a large amount on his own. Sometimes, he loses hope that he would ever be able to save his son.

"It is Likhit's smiling face, that keeps me and my wife keep up the struggle," says Bharath.

He will grow up to be a linguist if he survives this disease
Likhit is a talented kid, and he already knows to speak in 4 languages, including, English, Telegu, Kannada, Tamil, and now wants to learn Malayalam from Youtube. He also loves to have ice-cream, since it is soft and melts right away in his mouth. Biting anything hard makes his gums bleed. If his condition deteriorates further, it would be very hard to save him.

Your contribution can help Bharat save his son.

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