"Among the four walls". Story of Katya Nebozhenko. Rett Syndrome.

Rett Syndrome. With this rare hereditary disease 16 years here lives Katya Nebozhenko. The life of this girl and her mother Tatsiana, which alone grows the daughter, is a daily struggle for a survival...

WE RECOMMEND EVERYBODY TO WATCH THIS VIDEO!

We address for the help for Katya to those of you to whom though it is little bit easier in this life and who is not indifferent to sufferings of another's children!!!
Katya constantly needs a SPECIAL MEDICAL PREPARATIONS, DIAPERS, VITAMINS, CLOTHING.
If you are ready to assist the girl, please, CONTACT US by the phones showed on our website thesaviourfund.org, or write, having taken advantage of the inquiry form. Please, do not forget to leave your contact information at filling the inquiry form.

ONCE AGAIN, PLEASE, GO TO OUR WEBSITE WWW.THESAVIOURFUND. ORG FOR DETAILED INFO ABOUT HOW TO HELP TO KATYA NEBOZHENKO.
YOU MAY CALL US +1 718 450-2421, OR SEND US E-MAIL VIA CONTACT FORM ON OUR WEBSITE.

WE THANK ALL RESPONDED!

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• katsiaryna
• foronda
• new
• york
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[TheSaviourFund]

Tatsiana is a really Mother and Women with a big heart! Thank you for your comment on this video.

[TheSaviourFund]

Thank you for comments.

Unfortunately it is :( But it is not necessary will reveal itself in each generation. We spoke with Katya's doctor, and he explained this as well as her mom...

[Rapprochement123]

What a noble and loving mother! Thank u also for the translation!

[karinanjersey]

rett symdrome it not hereditary

[Lavinco]

Shame on the people who told this Mother to give her rett child up. They just don't understand the unbreakable love that a parent can have for their child; no matter what.