POMOZIMO MARINI DA SE IZBORI SA ALS-om I OSTANE UZ SVOG SINA
Marina Matić (1980) iz Leskovca je samohrana majka petogodišnjeg dječaka i stub svoje male porodice. Živi skromno, u zajedničkom domaćinstvu sa svojim sinom i slijepom sestrom Žaklinom, o kojima se svakodnevno sama brine.
Iako se cijelog života borila sa zdravstvenim izazovima, nedavno joj je dijagnostikovana najteža bolest — amiotrofična lateralna skleroza (ALS), progresivno oboljenje koje postepeno oduzima pokretljivost, govor i osnovne životne funkcije.
Marina već osjeća ozbiljne simptome:
• otežano guta hranu
• slabost u desnoj ruci i nozi
• sve teže obavlja osnovne dnevne aktivnosti
Ako se terapija ne započne uskoro, prijeti joj potpuna paraliza i gubitak govora. Ista bolest odnijela je život njenog oca prije samo nekoliko mjeseci
ŠTA JE MARINI POTREBNO
1️⃣ Edaravone terapija
Ljekari su joj propisali Edaravone injekcije – jednu od rijetkih terapija koja može usporiti napredovanje ALS-a.
Ovaj lijek nije pokriven zdravstvenim osiguranjem, a jedna ampula košta oko 1.000 €, što porodica ne može da priušti.
2️⃣ Terapija matičnim ćelijama – jedina realna šansa
Druga opcija je terapija matičnim ćelijama na klinici Wu Medical, Peking (Kina).
Prema zvaničnom predračunu, tretman u trajanju od 14 dana iznosi:
➡️ 26.000 €
To je naša ciljna suma.
ZAŠTO JE HITNO?
ALS brzo napreduje. Svaki dan bez terapije znači veći rizik od gubitka pokretljivosti i govora.
Marina se najviše plaši da neće moći da brine o svom malom sinu i svojoj slijepoj sestri Žaklini, koji zavise isključivo od nje.
Zato se obraćamo vama — dobrim ljudima koji vjeruju u solidarnost, humanost i snagu zajedništva.
KAKO MOŽETE POMOĆI
Donacijom, dijeljenjem kampanje ili riječju podrške.
Svaki euro približava Marinu neophodnoj terapiji i daje joj šansu da nastavi borbu.
Porodica Mitić vam se od srca zahvaljuje.
Dobro se uvijek vraća. ❤️
HELP MARINA FIGHT ALS AND STAY BY HER SON’S SIDE
Marina Matić (born 1980) from Leskovac, Serbia, is a single mother to a five-year-old boy and the backbone of her small family. She lives modestly, sharing a household with her young son and her blind sister Žaklina, whom she cares for completely on her own.
Although Marina has struggled with health issues her entire life, she recently received the most devastating diagnosis — Amyotrophic Lateral Sclerosis (ALS), a progressive and incurable disease that slowly takes away mobility, speech, and basic life functions.
Marina is already experiencing serious symptoms:
• difficulty swallowing food
• weakness in her right arm and leg
• increasing challenges with everyday tasks
Without timely treatment, she faces the risk of complete paralysis and loss of speech. The same disease took her father’s life just a few months ago.
WHAT MARINA NEEDS
1️⃣ Edaravone Treatment
Marina’s doctors prescribed Edaravone injections — one of the few therapies that can help slow the progression of ALS.
Unfortunately, this medication is not covered by health insurance, and each vial costs around €1,000, which the family cannot afford.
2️⃣ Stem Cell Therapy — Her Only Real Chance
Another treatment option is stem cell therapy at Wu Medical Clinic in Beijing, China.
According to the official estimate, the 14-day treatment costs:
➡️ €26,000
This is our fundraising goal.
WHY IT’S URGENT
ALS progresses rapidly. Every day without treatment increases the risk of losing mobility and speech.
Marina’s greatest fear is that she will no longer be able to care for her young son and her blind sister Žaklina, who depend entirely on her.
This is why we are reaching out to you — to everyone who believes in compassion, solidarity, and the power of helping one another.
HOW YOU CAN HELP
By donating, sharing this campaign, or sending words of support.
Every euro brings Marina closer to the treatment she urgently needs and gives her a fighting chance to stay with her family.
The Matić family thanks you from the bottom of their hearts.
Kindness always comes back. ❤️