Cassie's Home Adaptation Fund
Donation protected
Cassie is a beautiful and cheeky little girl with variety of medical issues and a lot of character!
She has CHARGE Syndrome, Hypotonic Celebral Palsy, Respiratory and ENT Issues, Global Developmental Delay, Severe Mobility and Communication Issues as well as significant problems with her eyesight.
All of the above, don't seem to stop her and although she has her own way and speed of doing things, she is getting there.
As she grows , her other issues seem to be picking up at their own pace, however her mobility is something she really struggles with.
Our house has been now assesed for adaptations and because Cassie's dad works full time, and we are private owners,the council will only provide part of the funding for the adaptations they suggest.
We need to install the Through the floor lift, ramp in tha back as well as the front, widen the paving, install new doors in the back making it wheelchair accesible and install the ceiling hoist track system to help with Cassie's transfers.
This page is to help us get money towards our contribution part for the adaptations or any personal adaptations costs to cover in case council cannot provide them.
Other than the Sick Kids Foundation, when it comes to CHARGE Syndrome related organisations, we would really love to support 3 of them:
Harry's Foundation:
Founded by a mom who lost her beautifus son to Charge Syndrome. Debbie is amazing and all of the donations go towards starter packs which go to parents and families of children who are born with this rare Genetic Disorder. Each pack contains books, toys and a lot of love.
https://www.facebook.com/Harrys-Foundation-755961021163798/?fref=ts&ref=br_tf
The Messy Club:
This absolutely wonderful playgroup for children with special needs was started in Reading by a very close family friend and an amazing mum of 3, of which, the youngest Emmy, has the Charge Syndrome. The group relies on donations and the family members are extraordinary , with the biggest hearts we've ever seen. We love them all so much, and we want to help
https://www.facebook.com/groups/themessyclub/
Help4Joss. Joss and her family are one of the strongest people we've ever met. Jess like Cassie, other than complexity of Charge Syndrome , has plenty of neurological issues. Her mum fights for her every day and we're so proud to know them.
https://www.facebook.com/help4joss-114560415281474/?fref=ts
Pass on the love, share, donate, these children and their families are the rocks. By helping Cassie, other than helping us with equipment, you're building up the amount towards a better future of these affected by CHARGE SYNDROME.
Spread The Word, Spread the love xxxxxx
She has CHARGE Syndrome, Hypotonic Celebral Palsy, Respiratory and ENT Issues, Global Developmental Delay, Severe Mobility and Communication Issues as well as significant problems with her eyesight.
All of the above, don't seem to stop her and although she has her own way and speed of doing things, she is getting there.
As she grows , her other issues seem to be picking up at their own pace, however her mobility is something she really struggles with.
Our house has been now assesed for adaptations and because Cassie's dad works full time, and we are private owners,the council will only provide part of the funding for the adaptations they suggest.
We need to install the Through the floor lift, ramp in tha back as well as the front, widen the paving, install new doors in the back making it wheelchair accesible and install the ceiling hoist track system to help with Cassie's transfers.
This page is to help us get money towards our contribution part for the adaptations or any personal adaptations costs to cover in case council cannot provide them.
Other than the Sick Kids Foundation, when it comes to CHARGE Syndrome related organisations, we would really love to support 3 of them:
Harry's Foundation:
Founded by a mom who lost her beautifus son to Charge Syndrome. Debbie is amazing and all of the donations go towards starter packs which go to parents and families of children who are born with this rare Genetic Disorder. Each pack contains books, toys and a lot of love.
https://www.facebook.com/Harrys-Foundation-755961021163798/?fref=ts&ref=br_tf
The Messy Club:
This absolutely wonderful playgroup for children with special needs was started in Reading by a very close family friend and an amazing mum of 3, of which, the youngest Emmy, has the Charge Syndrome. The group relies on donations and the family members are extraordinary , with the biggest hearts we've ever seen. We love them all so much, and we want to help
https://www.facebook.com/groups/themessyclub/
Help4Joss. Joss and her family are one of the strongest people we've ever met. Jess like Cassie, other than complexity of Charge Syndrome , has plenty of neurological issues. Her mum fights for her every day and we're so proud to know them.
https://www.facebook.com/help4joss-114560415281474/?fref=ts
Pass on the love, share, donate, these children and their families are the rocks. By helping Cassie, other than helping us with equipment, you're building up the amount towards a better future of these affected by CHARGE SYNDROME.
Spread The Word, Spread the love xxxxxx
Organizer
Marta Mansfield
Organizer
