Rare genetic defect Wrong diagnosis for “Keksi”! Jennifer Saro gives health update on her son

Jennifer Saro's son has Angelman syndrome

“For almost three years I thought I knew what disability my son had”Jennifer Saro begins her most recent Instagram post. In it she now speaks openly about one of the hardest moments of her life as a mother. Since the birth of the boy, whom she publicly calls “Keksi,” granted She gives her community regular insights into her everyday family life – believing that her child is suffering from Prader-Willi syndrome. Jennifer made this diagnosis public at the beginning of 2024 and has continued to give health updates since then.

Now the 30-year-old has surprising news for her 306,000 followers: Because it was obviously a misdiagnosis. After the family moved in the summer of 2025, new genetic examinations were ordered for Cookie, “because there were simply too many points that didn’t apply,” explains Jennifer in an Instagram post. And: “This new genetic test revealed that he has Angelman syndrome.”

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Angelman syndrome is a genetic peculiarity in which the brain works differently. “Many of those affected cannot speak, have motor limitations and need lifelong support. But: They have a joy for life that cannot be explained. Always laughing and with a huge heart,” says Jennifer.

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An injection every day that wasn't necessary

Three years of effort – and suddenly everything is back to square one. A new clinical picture, new therapies, new future perspectives. And lots of question marks. “I really wonder how this can even work. Because these are exactly the differences that were examined back then. And my son has had an injection every day for almost three years that he didn’t actually need.”Jennifer continued.

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The former bachelorette was therefore extremely worried about her child. It is currently not possible to say what effects the incorrect treatment had. You have to wait a few months for that. She really hopes that no lasting damage was done. “The fact that something like this could happen at all shows how little the whole thing has been researched,” says Jennifer.

Apart from the fear for her child, she also has to get used to the new situation first. The influencer now has to read everything again, “because of course I haven’t even dealt with this diagnosis yet”. But despite everything, there is also something positive to report and good news for future planning. “I didn’t inherit the genetic effect, it was just a freak of nature.”

Sources used: Instagram