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@bonstonker said:condolences to his family and friends.it's going to take a very long time for them to heal.
i'm thinking he had hypertrophic cardiomyopathy,the reason i say this is because close friends of ours lost their 14 year old last year.
he also was a gentle giant at 14 6'4" and 215 lbs.
it is believed to exist in 1 out of every 500 and approximately one case of sudden cardiac death occurs every three days in organized youth sports across the United States.
i'm not sure what the rate is in australia.
since we started doing screenings 4 showed abnormalities and another friend of ours was screened last week and found a hole in her heart and goes in for surgery next week.
for parents out there check out what an Echocardiogram Ultrasounds and Electrocardiograms would cost for your child.they are not usually covered by insurance over here,so the foundation was set up to help.not sure what you have to go through in australia for tests.
sorry to hijack the thread but this is a subject i feel needs to be highlighted more.
with each child that is diagnosed through the living4burke foundation,it has helped his family heal.
i hope the same can happen for the Fotuaika family if this was in fact the cause of his death .
R.I.P Mosese
@bonstonker said:condolences to his family and friends.it's going to take a very long time for them to heal.
i'm thinking he had hypertrophic cardiomyopathy,the reason i say this is because close friends of ours lost their 14 year old last year.
he also was a gentle giant at 14 6'4" and 215 lbs.
it is believed to exist in 1 out of every 500 and approximately one case of sudden cardiac death occurs every three days in organized youth sports across the United States.
i'm not sure what the rate is in australia.
since we started doing screenings 4 showed abnormalities and another friend of ours was screened last week and found a hole in her heart and goes in for surgery next week.
for parents out there check out what an Echocardiogram Ultrasounds and Electrocardiograms would cost for your child.they are not usually covered by insurance over here,so the foundation was set up to help.not sure what you have to go through in australia for tests.
sorry to hijack the thread but this is a subject i feel needs to be highlighted more.
with each child that is diagnosed through the living4burke foundation,it has helped his family heal.
i hope the same can happen for the Fotuaika family if this was in fact the cause of his death .
R.I.P Mosese