In 2016 my family were gathered in a room and told that my survival was between me and Godโฆ๐๐พ I am still here! However, my life after the devastating and crippling effects of the sudden onset of a severe case of Guillain-Barrรฉ Syndrome (AMAN) has not been without complications. The prolonged, full body paralysis and use of life support systems as a result of this rare and serious autoimmune disord
er triggered the onset of a secondary but equally distressing condition called bilateral Neurogenic Heterotopic Ossification (NHO). NHO caused the formation and growth of a significant amount of bone in the soft tissue and muscle surrounding my hip joints resulting in a complete lack of movement at the joints. The corrective surgery is complex and as such, I have been referred for treatment internationally. The treatment plan involves staged surgeries resecting the heterotopic bone, postoperative radiation therapy and intensive rehabilitation therapy estimated at BDS $250,000.00. I wish that I had an alternative to a public appeal, but I was in no way prepared for this level of illness or its life-changing effects, therefore, I am humbly requesting and will be forever grateful for your contributions to The Dawn Drayton Medical Fund Appeal. With your invaluable financial support, there is an option to lifelong wheelchair dependency and chronic, intense pain โ please, lend your support! With love & appreciation
Dawn
P.S. Like, share and follow my journey! Facebook: The Dawn Drayton Medical Fund Appeal
https://www.facebook.com/DawnDrayton.GBS/
Instagram: ๐ I Wear BLUE For GUILLAIN-BARRร SYNDROME Awareness๐
https://www.instagram.com/dawn_medical_fund/
Website: My Journey with Guillain-Barrรฉ Syndrome: Life Altering but not life-defining...
https://www.dawndrayton-gbs.com/hello-world/