Family Holiday For Lacey-Mae
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I am starting this page on behalf of a VERY brave little girl and her incredible family who live in Cheshire, U.K. This is a little of their story.
Lacey-Mae is a beautiful little 2 year old girl with a smile that would melt any heart.
When Lacey-Mae was just 22 months old she was rushed into hospital with suspected Pneumonia, this was early February of 2014, it was Valentines day her parents were told the devastating news that their little princess had been disagnosed with Metastasis Embryonal Rhabdomyosarcoma type 2, it was affecting her Lungs. Her family were naturally destraught but somehow managed to carry on and do everything they could for their beautiful baby girl. Lacey-Mae was kept in hospital until the April and has had many sessions of Chemotherapy and even though doctors were not convinced of her surivial rate she fought through it and was showing great signs, the Cancer seemed to have shrunk alot. The family were starting to feel some relief.....
This was until further testing revealed that Lacey-Mae's Cancer had spread, secondary Cancer in her bones. This little princess is currently undergoing more intensive chemotherapy and Radiotherapy. Her parents have been given only a 10% chance of this treatment being successful.
While all this was going on the family were blessed with a bonny baby boy, so you can imagine how difficult a time it must be for them trying to juggle a young family and taking care of Lacey-Mae, who requires (sometimes daily) trips to Alder Hey for her treatment, and she has spent many days in Chester hospital while fighting this awful illness.
So, as you can see they have been through hell and back and back to hell all over again in a year. This young family deserve a break, something they could remember forever and get some proper quality family time with both of their children.
This is where you come in to the equation. I would be very greatful of any donations given to help me send this family to Disneyland Paris (thats the wish) but if we cant get enough money together, the best we can get them for what we can raise.
Please join us on Facebook and follow Lacey-Mae's progress and more details about her condition.
https://www.facebook.com/groups/1478773252401989/
Please dig deep if you can, every penny really will make a difference to a wonderful family. Thank you for reading our story and helping if you can x
Lacey-Mae is a beautiful little 2 year old girl with a smile that would melt any heart.
When Lacey-Mae was just 22 months old she was rushed into hospital with suspected Pneumonia, this was early February of 2014, it was Valentines day her parents were told the devastating news that their little princess had been disagnosed with Metastasis Embryonal Rhabdomyosarcoma type 2, it was affecting her Lungs. Her family were naturally destraught but somehow managed to carry on and do everything they could for their beautiful baby girl. Lacey-Mae was kept in hospital until the April and has had many sessions of Chemotherapy and even though doctors were not convinced of her surivial rate she fought through it and was showing great signs, the Cancer seemed to have shrunk alot. The family were starting to feel some relief.....
This was until further testing revealed that Lacey-Mae's Cancer had spread, secondary Cancer in her bones. This little princess is currently undergoing more intensive chemotherapy and Radiotherapy. Her parents have been given only a 10% chance of this treatment being successful.
While all this was going on the family were blessed with a bonny baby boy, so you can imagine how difficult a time it must be for them trying to juggle a young family and taking care of Lacey-Mae, who requires (sometimes daily) trips to Alder Hey for her treatment, and she has spent many days in Chester hospital while fighting this awful illness.
So, as you can see they have been through hell and back and back to hell all over again in a year. This young family deserve a break, something they could remember forever and get some proper quality family time with both of their children.
This is where you come in to the equation. I would be very greatful of any donations given to help me send this family to Disneyland Paris (thats the wish) but if we cant get enough money together, the best we can get them for what we can raise.
Please join us on Facebook and follow Lacey-Mae's progress and more details about her condition.
https://www.facebook.com/groups/1478773252401989/
Please dig deep if you can, every penny really will make a difference to a wonderful family. Thank you for reading our story and helping if you can x
Organisateur
Carrie Barrett
Organisateur
England