Ellies scleroderma morphea fund

Hi everyone..  I would like to fund raise for my daughter Who is suffering from a rare skin disease/disorder which is called scleraderma Morphea.. that is twisting and hardening her skin to the point of her bones being dislocated.. She is currently on chemotherapy and a few other treatments but it is not  Stopping the twisting and hardening of the skin.. She is also haveing physiotherapy.. I have also bought her a big pool so that she can take the weight of her body and relax for a hour or 2 a day, we have been referred to alder hay in liverpool.. Please if you could find it to spear a few penny's every little helps.. i don't want to wait so long that her symptoms and twisted and dislocated bones are to far gone to treat I would like to get her fast tracked and see my little 9 year old girl grow up into



a beautiful young lady and to be able to walk in her prom dress and be whatever she wants to be, not end up having to rely on people to push her around and do things for her because I don't think it would be something she would want either.. I am totally heart broken, I will do anything to raise the funds she needs to make her better.. but it would also be a little quicker if people would be able to  help my child live a normal life.. To be so kind to donate I would be forever grateful and would take it to my grave how everyone pulled together to help my child.. Please do not feel pressured into donating but if you have a few extra pennies and are able to help I will be forever grateful..



.. Many many thanks to you in advance... Xxx xxx xxx xxx xxx