Hi all,
My 1 year old nephew, Thraya, has been diagnosed with a rare genetic disorder known as MPS type 6. This affects 1:250,000 people and is very difficult to treat. Please help us meet the expenses for his treatment by supporting our campaign. Any contribution is appreciated!
The transplant process which Thraya is undergoing is as below:
1. Back-Up - This process was completed in March.
2. Preparation - Thraya was subjected to 3 sessions of preparation where each session lasted for 3 + 1 days, total of 12 days is completed.
3. BMT Line - Currently the doctors have planned to complete this on 9th May.
4. BMT Process - Tentatively the BMT Process is scheduled from 10th May. (We have placed orders for his Depletion KIT which is being sent from Germany)
5. Recovery - the final leg of his treatment where extreme care has to be taken for a minimum period of one year.
1. Back-Up - This process was completed in March.
2. Preparation - Thraya was subjected to 3 sessions of preparation where each session lasted for 3 + 1 days, total of 12 days is completed.
3. BMT Line - Currently the doctors have planned to complete this on 9th May.
4. BMT Process - Tentatively the BMT Process is scheduled from 10th May. (We have placed orders for his Depletion KIT which is being sent from Germany)
5. Recovery - the final leg of his treatment where extreme care has to be taken for a minimum period of one year.
Please share this across your network and help us get him the life saving treatment he needs.