[Sg] 3-month-old baby needs S$2.4 million medicine to treat rare genetic disorder, parents appealing for donations

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https://mothership.sg/2023/07/3-mon...tic-disorder-parents-appealing-for-donations/
 
Isn't it better to let him go ? He is not going to live for long.
 
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<<As of Jul. 16, S$1,753,934 has been raised by 14,235 donors>>

That’s why Sinkies are well known for being suckers. Can sell them $70 a tub ice cream from asshole preparing it from his hdb too. Haha
 
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Just let the little bugger live out the rest of his life and let him repay his karmic debts. :cool:
 
Wat happens after the 2.4 million treatment? Will the baby become an economically productive adult or an economic social parasite? Than who pays?
 
The state, if they want to encourage more babies, should shoulder the health burden. Its like a insurance for those unlucky to get unhealthy kids. 99% will be healthy and contribute to society and help pay for the 1%.
Some kids are born healthy, but became mentally ill after a fever. If gomen leave the risk to parents guarantee cannot achieve their target birth rate.
 
Wat happens after the 2.4 million treatment? Will the baby become an economically productive adult or an economic social parasite? Than who pays?
highly doubt any “medicine” will “treat” or undo genetic disorders. it may ease the ailment or pain temporarily but not treat it to the point of curing from it. after $2.4m will need another $3.69m and then another $6.9m. complete scam. if genetic disorder is true, couple should have done genetic tests on themselves and the embryo before going into 6.9 weeks of pregnancy. genetic tests are highly recommended in obgyn clinics in sk, us, jp, and european cuntries. almost mandatory with health insurance. sg so advanced in medicine how cum not recommended. in fact with so many hereditary diseases, gene pool issues, plus inherited mental cases in sg, it should be mandatory.
 
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highly doubt any “medicine” will “treat” or undo genetic disorders. it may ease the ailment or pain temporarily but not treat it to the point of curing from it. after $2.4m will need another $3.69m and then another $6.9m. complete scam. if genetic disorder is true, couple should have done genetic tests on themselves and the embryo before going into 6.9 weeks of pregnancy. genetic tests are highly recommended in obgyn clinics in sk, us, jp, and european cuntries. almost mandatory with health insurance. sg so advanced in medicine how cum not recommended. in fact with so many hereditary diseases, gene pool issues, plus inherited mental cases in sg, it should be mandatory.
Gahman should just Soylent Green the baby... Let the baby move on in peace
 
highly doubt any “medicine” will “treat” or undo genetic disorders. it may ease the ailment or pain temporarily but not treat it to the point of curing from it. after $2.4m will need another $3.69m and then another $6.9m. complete scam. if genetic disorder is true, couple should have done genetic tests on themselves and the embryo before going into 6.9 weeks of pregnancy. genetic tests are highly recommended in obgyn clinics in sk, us, jp, and european cuntries. almost mandatory with health insurance. sg so advanced in medicine how cum not recommended. in fact with so many hereditary diseases, gene pool issues, plus inherited mental cases in sg, it should be mandatory.
As stated in the article the Medicine is to stopped the progression rather than curing it.
Uncle also doesn't know how effective it can be but since they dare to charge so high price something must be very powerful about this Medicine.
 
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