Aidake Ketteril võidelda Wilsoni tõvega!

Aidake Ketteril võidelda Wilsoni tõve vastu!

Wilsoni tõbi on harvaesinev pärilik haigus, mis põhjustab vase kogunemist teie maksa, ajju ja muudesse elutähtsatesse organitesse. Lisaks sellistele sümptomitele nagu käte ja sõrmede värisemine on Ketter ainus Eestis, kes ei saa korralikult rääkida. Ta vajab personaal treenereid, logopeedi tunde ja peab oma tervise stabiilsena hoidmiseks pidevalt kulutama raha kallitele ravimitele. Ma arvan, et me kõik koos saaksime teda ja tema perekonda aidata katta põhilukusid ,et hetkel Ketteril seisundit stabiilsena hoida. kuniks neil on võimalusi saada uusimaid ravimeetodeid.

Help Ketter Fight Wilsons desease !

Wilson's disease is a rare inherited disorder that causes copper to accumulate in your liver, brain and other vital organs. It was about a year ago when she got diagnosed with the condition. Besides symptoms like shivering hands and fingers, Ketter is the only one in Estonia who can´t speak. She needs persoanl trainers, speech therapist classes and has to constantly spend money on expensive medicine to keep her going. I think we could all help her familily to keep finding new treatments and cover medicine costs for Ketter. This donation would help Ketter pay for her basic treatment expences next year. Their family is also in touch with Wilsons Desease Association and are searching for their new goal in treatment opportunities!