Tasha's electric wheelchair fund

Hi,
My name is Tasha and I am from north Wales. I have a rare genetic  collagen disorder called ehlers danlos syndrome type 3.  This is a painful debilitating disorder of the protein called collagen, basicslly all my collagen is floppy and I'm so bendy that my joints dislocate, they dislocate between 2-10 times per day, each one is very painful. EDS causes other issues such as postural orhtostatic tachycardia syndrome, this means  my heart races and the blood pools in my legs, this means I can get very dizzy and have problems with any temperature changes . EDS also effects my gatro system and my skin.

I am becoming more and more  isolated as I am only entitled to the self propelled , I cannot use thus due to recurrent shoulder dislocations , so I would need someone to  push me.

so I am in desperate need of an electric wheelchair, to keep me mobile and regain my independence, although on really good days I can walk a little bit with my stick, the u predictability of my eds means I need an electric wheelchair, one minute I could be fine the next I could have a major dislocation.


if you would like to know more please like my Facebook page 

http://www.facebook,com/bendyzebra

Please donate and help me regain my life and finally be able do the things normal people take for granted.

i am also in the daily post here's the link 

http://www.dailypost.co.uk/news/north-wales-news/denbighshire-woman-rare-condition-dislocates-9672202

every penney counts please give what you can all of the money will be going to get my electric wheelchair.

Thank you 

Tasha