Marek Sálus

Volám sa Marek, narodil som sa ako zdravý chlapec. No v období nástupu do školy som nepriazňou osudu prestal rozumieť a rozprávať. V 6 rokoch mi lekári naordinovali medikamentóznu liečbu a diagnostikovali Landau – Kleffnerov syndróm (LKS), a tak som začal bojovať so vzácnou chorobou – vývinová afázia.

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Volám sa Marek, narodil som sa ako zdravý chlapec. No v období nástupu do školy som nepriazňou osudu prestal rozumieť a rozprávať. V 6 rokoch mi lekári naordinovali medikamentóznu liečbu a diagnostikovali Landau – Kleffnerov syndróm (LKS), a tak som začal bojovať so vzácnou chorobou – vývinová afázia.

Po malých krôčikoch sa môj stav zlepšuje. Chcel by som byť čo najviac samostatný, opäť rozprávať aj čítať ako ostatné deti.

Verím, že ak budem pravidelne absolvovať rehabilitačné pobyty, môj zdravotný stav sa bude zlepšovať. Jediný problém je, že na finančne náročný pobyt zdravotná poisťovňa neprispieva. Veľká vďaka patrí nadáciám a ľudom, ktorým môj osud nie je ľahostajný a podporujú ma v nádeji, že raz budem žiť plnohodnotný život. Za každé venované euro, ktoré pribudne na mojom účte v Nadácii ADELI vopred zo srdca ďakujem.

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At the ADELI Foundation, we help people with neurological conditions. To get back on your feet

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It works closely with the non-state healthcare facility ADELI Medical Center in Piešťany, which is the only one in Slovakia to provide comprehensive, unique neurorehabilitation with 20 therapies „under one roof“.“
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Winner of the Made by ADELI extra prize for sharing: Katarína Sikora

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