Helping Gabez and his family with his everyday care.

If you have come across this page you have likely been linked through family and friends of Gabriel. This is his journey. 😊

Gabriel was born with Severe Refractory seizure disorder a type of Epilepsy that is hard to control under medication. This means that Gabriel has never had a seizureless day in his life. Recently Gabriel traveled to Melbourne Royal Children's Hospital in the hopes of being able to have surgery to remedy his condition. Unfortunately the size of the abnormality was much greater than anticipated. The initial size was that of a 50 cent piece and is now showing through scans the whole right side of his brain to be abnormal (huge difference to what we were first told) leaving the family to seek other avenues due to high risks. Gabriels mobility, sight and speech has been deteriorating the last 3 months and noticably his left side is becoming weaker at the moment. The basics of life for Gabez has completely changed going to the toilet assisted and not being able to feed himself or walk and talk are becoming more of a common occurrence. He has good days but the bad days are becoming more frequent and the constant battle over the 11 years battling the illness is taking its toll on his body. The key is quality of life. Letting Gabriel live and lead a normal as possible life until we find remedy and relief. Gabriel is a very strong and humble boy loved by many. It is always heartbreaking to watch him go through what he does but he has taught us to persevere and what strength truly is. Every little bit will help tremendously on Gabriel journey. We are grateful for everything but most of all Gabriels breath of life.

Xox. Love and light.

#TeamGabez