Little Fighter
Fundraising campaign by
Erilda Sulaj
-
€1,323.00raised of €5,000.00 goal goal
No more donations are being accepted at this time. Please contact the campaign owner if you would like to discuss further funding opportunities
Campaign Story
Dimitri is a very happy 4 year old boy with a positive attitude to life.He was diagnosed with an extremely rare form of congenital muscular dystrophy, called (CMD LMNA) is a life-limiting muscle wasting disease due to an unavoidable geneticc mutation.The muscles in his body get weaker and this will have an effect on his heart an also his lungs, which is why children with LCMD have a shorter life expectancy than normal, statistically 18 years or less.There is no cure for LCMD but there are researches.
He requires regular visits with a cardiologist, pulmonologist, orthopedic and neurologist every six months, which are done at MDA HELLAS.
We visit a rehabilitation center twice a week for physical and occupational therapy.He also takes many supplements every day.
Additionally, we insist on going abroad for a second opinion or other methods which can be helpful.
Please show your support and join us in raising money for Dimitri's physical therapy and his supplements.
Thank you in advance
Erilda and Giannis Skarlis
Dimitri's parents
Ο Δημητρης ειναι ενα χαρουμενο αγορι 4 ετων με ορεξη για ζωη.Εχει διαγνωσθει με μια πολυ σπανια μορφη μυικης δυστροφιας cmd lmna, η οποια εχει περιορισμο οριου ζωης και καταστρεφει τους μυες του εξαιτιας μιας γονιδιακης μεταλλαξης.Οι μυες στο σωμα του γινονται πιο αδυναμοι και αυτο εχει επιδραση στην καρδια και στα πνευμονια του.Αυτος ειναι και ο λογος που το οριο ζωης των παιδιων με lcmd ειναι κατωτερο του φυσιολογικου, στατιστικα ειναι γυρω στα 18 τους η και λιγοτερο.Δεν υπαρχει θεραπεια για την lcmd αλλα γινονται πολλες ερευνες.
Ο Δημητρης επισκεπτεται τακτικα καρδιολογο,πνευμονολογο,ορθοπαιδικο και νευρολογο καθε εξι μηνες στην MDA HELLAS.
Επισκεπτομαστε δυο φορες την εβδομαδα ενα κεντρο αποκαταστασης για τις θεραπειες του και λαμβανει καποια σκευασματα τα οποια δινουν ενεργεια και μειωνουν την φλεγμονη στους μυες του.
Επιπλεον, επιμενουμε στο να ταξιδεψουμε στο εξωτερικο για μια δευτερη γνωμη η και μεθοδους που μπορει να βοηθησουν.
Προσπαθουμε να συγκεντρωσουμε το 50% για το ταξιδι ,τις θεραπειες του Δημητρη και τα συμπληρωματα 2 μηνων .
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Log.ethnikis
Ευχαριστουμε εκ των προτερων,
Organizer
- Erilda Sulaj
Donors
- Stella
- Donated on Sep 04, 2019
Kouragio! Makari kamia manoula na mi zouse tetoia agwnia...
- Tolis
- Donated on Aug 31, 2019
Raising money for Dimitris occupational therapy
Update posted by Erilda Sulaj at 10:19 pmDimitri is a very happy 4 year old boy with a positive attitude to life.He was diagnosed with an extremely rare form of congenital muscular dystrophy, called (CMD LMNA) is a life-limiting muscle wasting disease due to an unavoidable geneticc mutation.The muscles in his body get weaker and this will. . . . .
Donors & Comments
- Anonymous
- Donated on Sep 06, 2019
<3
- Stella
- Donated on Sep 04, 2019
Kouragio! Makari kamia manoula na mi zouse tetoia agwnia...
- Tolis
- Donated on Aug 31, 2019
- Guest
- Donated on Aug 27, 2019
- Iljonka Begollari
- Donated on Aug 23, 2019
- Margarita Vasiliou
- Donated on Aug 22, 2019
- Magda Peleka
- Donated on Aug 21, 2019
- Stamatis Chatzichristodoulou
- Donated on Aug 20, 2019
koyragio kai filia sto mpompira
- Anonymous
- Donated on Aug 20, 2019
- Ryan
- Donated on Aug 20, 2019
<3