Mollie's Wheelchair Fund

I'm raising money for an electric wheelchair to enable me to regain some independence, despite M.E and Hypermobility cramping my style!

Project aim

I'm raising money for an electric wheelchair to enable me to regain some independence, despite M.E and Hypermobility cramping my style!

About the project

I have recently become very ill with M.E and Hypermobility (more info below), which left me bedidden for a period of months, unable to study and at times even eat and drink. I began to improve with lots of support from family and friends, however recent problems with my mental health and pain from endometriosis have knocked me back to a stage where just standing is incredibly difficult and not safe due to the risk of fainting and falls. 

I am therefore using savings and raising money to purchase an electric wheelchair such as the one shown below, to enable me to get around both within the house (so I will never again need to be caried to the toilet!) and out, so I can enjoy the great outdoors once again, as my current very basic travel chair cannot be pushed on uneven griund, grass or in the wet. It would be brilliant to be able to enjoy the sunshine in the garden with my family, and have days out without further significant pain from an unnsupportive chair. I am also hopeful that this will enable me to get back into studying and/or working again which I miss dearly, so I can begin to regain some independence. 

As I am 18, funding has proved difficult as I'm too old to recieve various charity grants for children, but too young for others. I am therefore relying on the generosity of friends and family in this, as well as doing what I can to fundraise the money independently.

I really really do appreicate any help, as every little it really does add up. If recent events have taught me anything, it is that life can change in an instant, and the only thing that truly matters are the friends and family who are brave enough to stick with you through that journey. Thank you so very much. 

 

Information on M.E/CFS and Hypermobility:

-90% of people with M.E have been forced to stop or drastically reduce paid work and social contact, while half have reduced or lost capacity to drive and a quarter being no longer able to leave their home independently, often remaining bed ridden. (Action for M.E)

-M.E is a chronic condition of which the vast majority of people never recover from, categorised by extreme fatigue, digestive problems and constant flu-like symptoms.

-Hypermobility weakens the collagen in my body, causing pain and stiffness, fainting/falls, and increases the risk of injury.

 

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