Fighting Mitochondrial disease
All donations to be made to [email protected]
Say hello to five year old Evie.
Evie has mitochondria, she loves to play, she loves to explore, she loves to have fun like any other child her age. Most of all she loves her life! But that's the very thing that is being taken away from her!
Evie has a terminal condition that is being ignored by the NHS. To the NHS Evie is just a case number,A statistic. BUT, to her loved ones a Daughter, a sister, a granddaughter, a cousin, a niece but most of all, Evie is a human being !!
Evie & her family are all helpless! all the love in the world cannot cure her of this condition. there is NO cure The NHS have given up on her, leaving her to die, a five year old child, Where is the compassion?
there is hope thought, fellow compassionate human beings like me & you reading this right now can help prolong this little girls life & make it as comfortable as possible, for as long as possible.
There is treatment available in Canada, Oxford & 2 other places within the UK. But the people in the health profession who you would expect to want to help, simply won't! so we have to do what we can to get this little girl to either one of these specialist hospitals to give her a glimmer of hope, a chance of life, a chance to be as normal child as possible. We can do this for her, we can JOIN together. There is NO CURE but, there is HOPE!!
It's a shame that this poor little girl's life comes down to how much it;s worth financially.
Thankfully Evie knows no different, She doesn't know her life has a price tag. Let us show those who should help what can be done when we pull together and show some care.
Please don't think of this as you giving money, Think of it as you giving life, quality of life to Evie.
From Evie& Family xxxxxxxxxxxxxxx
Evie has mitochondria, she loves to play, she loves to explore, she loves to have fun like any other child her age. Most of all she loves her life! But that's the very thing that is being taken away from her!
Evie has a terminal condition that is being ignored by the NHS. To the NHS Evie is just a case number,A statistic. BUT, to her loved ones a Daughter, a sister, a granddaughter, a cousin, a niece but most of all, Evie is a human being !!
Evie & her family are all helpless! all the love in the world cannot cure her of this condition. there is NO cure The NHS have given up on her, leaving her to die, a five year old child, Where is the compassion?
there is hope thought, fellow compassionate human beings like me & you reading this right now can help prolong this little girls life & make it as comfortable as possible, for as long as possible.
There is treatment available in Canada, Oxford & 2 other places within the UK. But the people in the health profession who you would expect to want to help, simply won't! so we have to do what we can to get this little girl to either one of these specialist hospitals to give her a glimmer of hope, a chance of life, a chance to be as normal child as possible. We can do this for her, we can JOIN together. There is NO CURE but, there is HOPE!!
It's a shame that this poor little girl's life comes down to how much it;s worth financially.
Thankfully Evie knows no different, She doesn't know her life has a price tag. Let us show those who should help what can be done when we pull together and show some care.
Please don't think of this as you giving money, Think of it as you giving life, quality of life to Evie.
From Evie& Family xxxxxxxxxxxxxxx
Here are a few Mitochondrial videos,xx
|