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Help Master Harsh For Bone Marrow Transplant
I am Sandeep Sudam Bhavsar age 35, stays in Dhule, Maharashtra state. My elder son Harsh Sandeep Bhavsar age 6 years is diagonised with Thalesemmia Major - Genetical disorder in which body will not create blood and hemoglobin levels go down below normal. It was detected at the age of 6 months, from then he is on blood transfusions every month. It is very painful for the kid to undergo blood transfusion every month which started at age of 6 months.
Per Doctor at Narayana Hospitals- Mazumdar Shaw Medical Center, Bangalore, the only solution is bone marrow transplant taking stem cells. The stem cells of parents/sibling did not matched with Harsh. We could found matching German Donor for stem cells.
The cost of carrying this transplant is 24 to 26 lakh ( 8lakh to get stem cell from stem cell bank in GERMAN + 16-18 lakh for BMT) excluding cost of any further complification.
It is very hard to collect 26lakh. I am by profession a farmer and selling milk. I could hardly do any savings due to family burden. As a family we could hardly
manage 10 lakh. We are in process of applying Goverment CM/PM fund for this case and hoping for some aid from Government.
I request your help to take out my kid Harsh out off Thalesemmia major and live him a normal life.
Per Doctor at Narayana Hospitals- Mazumdar Shaw Medical Center, Bangalore, the only solution is bone marrow transplant taking stem cells. The stem cells of parents/sibling did not matched with Harsh. We could found matching German Donor for stem cells.
The cost of carrying this transplant is 24 to 26 lakh ( 8lakh to get stem cell from stem cell bank in GERMAN + 16-18 lakh for BMT) excluding cost of any further complification.
It is very hard to collect 26lakh. I am by profession a farmer and selling milk. I could hardly do any savings due to family burden. As a family we could hardly
manage 10 lakh. We are in process of applying Goverment CM/PM fund for this case and hoping for some aid from Government.
I request your help to take out my kid Harsh out off Thalesemmia major and live him a normal life.
Doctor estimate and test reports
Estimation letter
Ask for an update
25th June 2017
Dear Saviors, Thanks for your wonderful support.
Hard to inform you all that the donor will not be able to give stem cell due to personal reason for at least 6 months. GERMAN registry again activated for donor search.
We had a discussion with doctor and now we have two options.
1. Wait for donor for few months.
2. Haplo process- It is also called as half match- in which stem cell of mother/father can be used for BMT. This procedure will add up another 3 lakhs in estimate since a kit costing 11lakh need to be imported from GERMANY.
It is a bad news for us but beggers are not choosers. Finally we decided to wait for at least 3 to 4 months so that
1. Harsh's Iron overload can reduce.
2. We can get an option of donor from GERMAN or INDIAN-DATRI stem cell bank.
3. If donor option do not work make up our mind to be prepared for Haplo process.
We purchased medicines for next 3 months and sent Harsh back to his native with his mother, so that he can join the school and complete his first term till diwali. Two units blood transfusion to be continued ones 21 days to keep hemoglobin level on higher side.
Harsh will be back at diwali time to fight back Thalesemmia major for permanent cure.
Please pray god to stay with us for Harsh permanent cure. Please do share and support https://milaap.org/fundraisers/Master-Harsh-Bone-Marrow
Bill for 3 months medicine
Regards,
RJ and Vishal
Hard to inform you all that the donor will not be able to give stem cell due to personal reason for at least 6 months. GERMAN registry again activated for donor search.
We had a discussion with doctor and now we have two options.
1. Wait for donor for few months.
2. Haplo process- It is also called as half match- in which stem cell of mother/father can be used for BMT. This procedure will add up another 3 lakhs in estimate since a kit costing 11lakh need to be imported from GERMANY.
It is a bad news for us but beggers are not choosers. Finally we decided to wait for at least 3 to 4 months so that
1. Harsh's Iron overload can reduce.
2. We can get an option of donor from GERMAN or INDIAN-DATRI stem cell bank.
3. If donor option do not work make up our mind to be prepared for Haplo process.
We purchased medicines for next 3 months and sent Harsh back to his native with his mother, so that he can join the school and complete his first term till diwali. Two units blood transfusion to be continued ones 21 days to keep hemoglobin level on higher side.
Harsh will be back at diwali time to fight back Thalesemmia major for permanent cure.
Please pray god to stay with us for Harsh permanent cure. Please do share and support https://milaap.org/fundraisers/Master-Harsh-Bone-Marrow
Bill for 3 months medicine
Regards,
RJ and Vishal
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Beneficiary:
Harsh Sandeep B...
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Supporters (424)
C
Charan
donated Rs.500
mk
murali
donated Rs.1,500
wishing you good health
DS
Dheeraj
donated Rs.2,000
All the best. May God bless you.
K
K
donated Rs.500
AJ
Abhishek
donated Rs.500
PS
Pochareddy
donated Rs.500
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