Hello, I write with tears in my eyes, because I have a knife in my heart, why I have to do this, why this little angel of mine is going through all this and countless more questions, why... but apparently fate has decided so and we MUST FIGHT !

So,my little beautiful daughter her name is Melissa,now on 27 December she will be 3 years old,but one of our biggest pains is that she is still not walking on her own and for that we are fighting now,but here in Bulgaria we have taken her to all kinds of specialists and nothing... one person gave us hope that in Turkey there is a chance to help us and this ,,flame,, , this ,,light,, in the tunnel is enough to keep fighting and go the long way , even if financially impossible, when you hear that everything can be fixed and the child can walk and be normal, it is GREAT!

Her diagnosis is Methylmalonic Acidemia,her body can't break down protein and she is on a low protein diet,she only eats fruits and vegetables and only a certain amount,12g of protein a day.Maybe that's where the muscle weakness and muscle hypotension comes from,she also doesn't get calcium for her bones,she can't eat cheese,milk,eggs,which are vital for the proper development of a growing child :(

Another problem is also after a trauma to the cerebellum,when she was 9months,then she was in a state of POLUCOMA with a mini stroke in the cerebellum or from the underlying disease we don't know and everyone here says different,but the fact is that there is a disorder in the basal areas of the CEREBRI,which is also responsible for coordination,movements,muscle weakness etc.

Our hope and dream now,what we are fighting for,for this ray of light is to go to Turkey for a consultation and possibly there for treatment and rehabilitation,some procedure for the brain,so that these disorders are cleared and everything will be fine with our beautiful girl ❤

SHE IS WONDERFUL!SWEET!KIND!DEDICATED!JUST AMAZING!

WE CAN'T AFFORD TO STOP FIGHTING AND LET HER STRUGGLE LIKE THIS FOR THE REST OF HER LIFE, KNOWING THAT SHE HAS A CHANCE TO FIX THINGS AND BE A NORMAL CHILD WHO RUNS AND ENJOYS LIFE AND HER CHILDHOOD LIKE THE OTHER KIDS ON THE PLAYGROUND AND NOT STAND BY THE SIDE WHEN WE GO TO THE PARK AND LOOK AT THEM PITIFULLY AND KNOW THAT SHE CAN'T BE LIKE THEM AND LONG FOR IT....... ;( ;( ;(