ENGLISH VERSION
Need help to collect means for treatment of my son Daniel!
Ivanchuk Daniel
born 09.08.2009
The diagnosis: lymphangiome of the left axillary area between a vein and an artery.
Removal is required.
About illness
The kid was born on time, despite of 4 multiple wrapping umbilical cords round a neck, 8 mark on a scale of Apgar. I was unbelievably happy to become mum at last, and it seemed everything was all right with the kid. So we went home. During the pediatrician survey it appeared that Daniel had a small strange swelling in his left armpit – the lymphangiome. I have read on the Internet that it was a tumor of lymphatic vessels. My mind refused to admit it. But it has turned out to be true, and there was no way but to submit.
In September 2009 the diagnosis - lymfangiome of axillary area for our month-old son had been confirmed by the experts of our Republic Tatarstan DRKB. We were told by the surgeons that it was necessary to operate before the child reaches a year age. We were warned by the medical staff against any possible illness, as the tumor will start to grow and squeeze the next bodies, disturbing their work.
Everyday we pray, for our child didn’t caught a cold or picked up an infection...
About the treatment:
Why do I hope to treat my little son in Germany?
I have made decision to raise money for treatment of the child in Germany as the method used there to remove the tumor is the most safeguard and effective. It is a laser and the preparation ok-432 or "phicibanyl" which are not certificated in Russia.
Nowadays the successful result of operating lymphangiome in Russia is 12 %, in Germany it is 80 %.
My every free minute I’ve been searching for the information on the methods of treating this kind of tumor. After many days of discussing the problem with parents of children with the same illness on forums, writing on medical web-sites, I have come to the conclusion that the method of treatment used in Germany was the most reasonable.
I have sent letters to the German Clinics which are engaged in given illness to learn the detailed description of their method of treatment and their prices.
The clinics in Luebeck, the University Centre of Schleswig-Holstein, has consented to accept the child and to practice a non-surgical tumor removal, a method of sclerosing a method of sclerosing the tumor by picibanyl or "ok-432".
The calculation exposed by the clinics is 18.489 Euros for the treatment and after-treatment supervision and 2.400 Euros for the road and residing expenses.
A few words about us:
Daniel is a very long-waited child. For 7 years I had a diagnosis of barrenness. So it was the greatest miracle I got pregnant. Pregnancy proceeded very hard and for 3 times I’d been admitted to hospital with abortion threat for preservation. But the kid have kept, thanks God for His Miracle.
What to tell?Danja is a very smiling boy, his smile is so light and laughter is so fervent... His is 5 month already, and he is so curious, interested in all around. The child is growing fast and even doctors say he is very big boy for his age, a real athlete. When Daniel sits at mum’s arms his tiny hands are trying to investigate all around. And there is so much interesting and new for him in this world… Our family, determined that we would find a better option than watching Daniel be consumed by this disease.
From the moment of his birth Danja became everything for me. He is a part of my life, a part of my soul…
My husband works hard, but the money he earns in our town is not enough.
I am on the maternity leave now and engaged with my child. Therefore our family cannot collect such a sum.Fund-raising
Danja has a chance
to live the healthy child!
HOW YOU CAN HELP?
If you have no means to donate, please send this referrense http://daniyl.ru/ to your friends or people you think could be of financial help.
We would be very grateful for any help you can offer!
Web-site & blogs codes:
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