<div><strong>Unsere Geschichte</strong>
</div>
<div>Wir sind die Eltern von Dominik und Lukas. Sie sind eineiige Zwillinge, sechs Jahre alt und viel zu früh – in der 28. Schwangerschaftswoche – auf die Welt gekommen. Drei Monate verbrachten sie damals im Spital, mit Beatmung, Magensonde und all den bangen Momenten, die man als Eltern kaum in Worte fassen kann.
</div>
<div>Bei Dominik zeigte sich später, dass er vor der Geburt einen Sauerstoffmangel erlitten hat.
</div>
<div><br />
</div>
<div><strong>Dominiks Diagnose: Zerebralparese</strong>
</div>
<div>Das bedeutet für ihn: Er kann nicht selbstständig laufen oder stehen, bewegt sich teilweise robbend oder krabbelnd fort und braucht im Alltag bei fast allem Hilfe – beim Essen, Trinken, Anziehen, Spielen - in jeder kleinen Handlung.
</div>
<div><br />
</div>
<div>Trotzdem ist Dominik voller Lebensfreude, Neugier und Stärke. Er lacht, er kämpft – und wir alle verfolgen einen großen Traum, den v.a. auch sein Zwillingsbruder Lukas hat: dass Dominik eines Tages selbst stehen und gehen kann.
</div>
<div><br />
</div>
<div><strong>Die große Chance: eine spezielle Stammzellentherapie in den USA</strong>
</div>
<div>Diese Behandlung gibt es nur dort. Sie gibt uns Hoffnung, dass Dominiks Entwicklungsschritte leichter und schneller möglich werden. Wir wünschen uns, dass er dadurch mehr Bewegungsfreiheit gewinnt. Dass er besser kommunizieren kann. Und dass er seine Bedürfnisse spüren und ausdrücken lernt. Doch die Behandlung findet schon sehr bald, Ende Oktober statt und ohne Unterstützung schaffen wir das nicht.
</div>
<div><br />
</div>
<div><br />
</div>
<div><strong>Warum wir eure Hilfe brauchen</strong>
</div>
<div>Diese Behandlung ist mit hohen Kosten verbunden. Allein die erste Reise und die Therapie belaufen sich auf rund 20.000 € – mit hoher Wahrscheinlichkeit, dass mehrere Aufenthalte nötig sein werden.
</div>
<div>Leider übernimmt die Krankenkasse keinerlei Kosten. Und schon Ende Oktober steht die erste Reise bevor.
</div>
<div>Darum bitten wir euch um Unterstützung. Mit eurer Hilfe können wir Dominik die erste Therapie in den USA ermöglichen, die Reisekosten stemmen und begleitende Behandlungen finanzieren.
</div>
<div><br />
</div>
<div>Jeder Beitrag – egal wie groß oder klein – bringt uns dem Ziel näher, Dominik diese Chance auf mehr Selbstständigkeit und Lebensqualität zu ermöglichen. Alles, was über die Therapie hinaus gespendet wird, fließt selbstverständlich in die laufenden Therapien, die Dominik tagtäglich braucht.
</div>
<div><br />
</div>
<div>Wir werden euch mit Updates auf dem Laufenden halten, damit ihr Dominiks Weg miterleben könnt.
</div>
<div><br />
</div>
<div>Bitte helft uns, diesen Traum wahrzumachen – und teilt unsere Geschichte, damit möglichst viele Menschen davon erfahren.
</div>
<div>Von Herzen vielen Dank!
</div>
<div>Marianne + Thomas
</div>
<div><br />
</div>
<div>----------------------------------------------------------
</div>
<div>Englische Version:
</div>
<div><br />
</div>
<div><strong>Donations for a Life-Changing Stem Cell Therapy in the USA</strong>
</div>
<div><br />
</div>
<div><strong>Our Story</strong>
</div>
<div>We are Dominik and Lukas’s parents. They are identical twins, six years old, born much too early – in the 28th week of pregnancy. They spent three months in hospital back then with ventilators, feeding tubes, and countless anxious moments that are hard to put into words as parents. Later it became clear that Dominik had suffered from a lack of oxygen before birth.
</div>
<div><br />
</div>
<div><strong>Dominik’s Diagnosis: Cerebral Palsy</strong>
</div>
<div>This means that Dominik cannot walk or stand on his own. He moves a little by crawling and needs help with almost everything in daily life – eating, drinking, dressing, playing – every little action.
</div>
<div><br />
</div>
<div>Yet Dominik is full of joy, curiosity, and strength. He laughs, he fights – and together we all share a big dream, especially his twin brother Lukas: that one day Dominik will be able to stand and walk on his own.
</div>
<div><br />
</div>
<div><strong>The Big Chance: A Special Stem Cell Therapy in the USA</strong>
</div>
<div>Now there is a unique opportunity: a special stem cell therapy in the USA, available only there. This therapy gives us hope that Dominik’s development will become easier and faster. We dream that he will gain more freedom of movement. That he will be able to communicate better. And that he will learn to feel and express his own needs.
</div>
<div>But the first trip is fast approaching at the end of October and without support, we cannot make it.
</div>
<div><br />
</div>
<div><strong>Why We Need Your Help</strong>
</div>
<div>This treatment comes with very high costs. The first trip and therapy alone amount to around € 20,000 – with more visits likely needed. Unfortunately, health insurance covers none of it.
</div>
<div><br />
</div>
<div>That’s why we are asking for your support. With your help, we can give Dominik access to this therapy in the USA, cover the travel expenses, and finance the additional treatments he urgently needs.
</div>
<div><br />
</div>
<div>Every contribution – no matter how big or small – brings us closer to our goal of giving Dominik this chance for more independence and a better quality of life. Everything raised beyond the therapy costs will, of course, go directly into his ongoing daily therapies.
</div>
<div><br />
</div>
<div>We will keep you updated so that you can follow Dominik’s journey with us.
</div>
<div><br />
</div>
<div>Please help us make this dream come true – and share our story so that as many people as possible can hear about it.
</div>
<div>Thank you from the bottom of our hearts.
</div>
<div>Marianne + Thomas
</div>

Carina Berger

Wolfgang MAYER

Anonymous

Michaela Löwigt

Gina Retschnig

Andreas Steinkellner

Hildegard und Anton Schex

Michaela Hauptmann

Andrea Kulhanek

Gabriele und Erich Köllner

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Doris Helmberger

Carina Charvat

Sean Wagner

Marion Uitz

Andrea Rottensteiner

Spenden für lebensverändernde Stammzellentherapie

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Spenden für lebensverändernde Stammzellentherapie

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