Welcome

familiesWelcome to the home of the Walter Sisulu Paediatric Cardiac Foundation.

Did you know that well over 95% of congenital heart disorders are correctable if detected early? The sad reality is, however, that many children are either diagnosed too late, or not at all. They die young and and often don't live into their teen years.

But we're hoping to change that.

This is what led to the establishment of the WSPCF, the sole purpose of which is to raise awareness of these defects, drive skills development amongst Africa's medical fraternity and raise the necessary funds to help those who need life-saving surgery yet cannot afford it.

As you can imagine, we rely heavily on donations and sponsorships in order to raise enough money to fund operations for children who desperately need them, operation that sometimes costs us in the region of R200,000 per child.

Saving children in need is something that Walter Sisulu and his wife, Albertina, held most dear, which is why the WSPCF is such a fitting tribute to one of the most loved and respected citizens of South Africa.

I'm delighted that you've decided to visit our site to see what we're all about, what we do, the lives we've saved and, most importantly, how you can help save even more lives.

Yours in mending broken hearts,

Lynda Bleazard
CEO


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Latest News

January's Newsletter

Dear Walter Sisulu Partners and Friends,

Last year was one of tremendous growth for the Foundation, and it has become so much bigger than any individual person, hospital or organisation. We have been blessed with so much support both from within South Africa and from abroad, and this will stand us in good stead as we continue to grow and spread the benefits of the Foundation's work in public and private hospitals in South Africa and elsewhere on the African continent

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Latest Stories

Michael Marara

The surgery was a great success and Michael was discharged from ICU four days later and officially discharged to the Sheika Al Jalila house on the 29th June 2011 where he stayed to recover before his final examination on the 5th July 2011.
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Waiting list

emily

Mast A Mnyobe

Age: 7 years

Diagnosis: Tetralogy of Fallot

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Founding Partners