Tadgh's Medical Trip Fund
Donation protected
Tadgh's Medical Trip Fund An appeal from a mothers heart to give her boy the best chance of a normal life can only be achieved through your generosity to enable the medical world to investigate the rarest of genetic abnormalities.
Mum has come to a dead end in Ireland medically and is reaching out to specialists in the USA who would consider taking a look at Tadgh
Tadgh is a true fighter born flat lying at 28 weeks weighing 1.kg. He has suffered with his health and has had many difficult paths in his short life. Recently Tadgh was diagnosed with a rare chromosome disorder. He has a dulpicate of 984kb on the short arm of chromosome 7 at band 7p14.3 He has multiple problems and is very complex. He will need 24/7 full time care for the rest of his life. As nobody else in the world has been registered with the same condition the doctors can not tell us if all his diagnosis and problems are down to his genetic condition. I have set up this page to spread awareness and hopefully to find someone in the world with the same issues. At the moment I am looking into research for very rare diseases all over the world and hope somebody can help him.
Tadgh has an older brother Paul who also has mutiple diagnosis so his Mammy can't work.
This page is for awareness and to help with funding for costs of services and hopefully to get him to the States for research and possible help.
Mum has come to a dead end in Ireland medically and is reaching out to specialists in the USA who would consider taking a look at Tadgh
Tadgh is a true fighter born flat lying at 28 weeks weighing 1.kg. He has suffered with his health and has had many difficult paths in his short life. Recently Tadgh was diagnosed with a rare chromosome disorder. He has a dulpicate of 984kb on the short arm of chromosome 7 at band 7p14.3 He has multiple problems and is very complex. He will need 24/7 full time care for the rest of his life. As nobody else in the world has been registered with the same condition the doctors can not tell us if all his diagnosis and problems are down to his genetic condition. I have set up this page to spread awareness and hopefully to find someone in the world with the same issues. At the moment I am looking into research for very rare diseases all over the world and hope somebody can help him.
Tadgh has an older brother Paul who also has mutiple diagnosis so his Mammy can't work.
This page is for awareness and to help with funding for costs of services and hopefully to get him to the States for research and possible help.
Organizer
Melissa Magee
Organizer
County Dublin
