Help Greg fight MS
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Greg Turnbull:
I was diagnosed with Chronic Progressive Multiple Sclerosis almost 2 decades ago . . . just as I was becoming a father.
Over time, I lost the use of my legs. My energy level dropped to the point that I was unable to work, and I lost my job as a senior sales executive in real estate development, now living on a fixed disability pension.
I do everything I can to fight MS. I financed MRI's, scans and two MS/CCSVI procedures that helped mitigate some symptoms. In order to remain mobile, I purchased a vehicle and added hand controls and a scooter lift.
A home air-cooling system was needed, MS rendered my body unable to deal with extreme heat. I was collapsing in my home, requiring rescuing by the fire department. The cooling and modifications to the bathroom allow me to be safe.
The mounting debt from these and other medical expenses are a financial hardship. I still need to afford a new mobility scooter, repairs to my in home wheelchair, off-label medications and therapies, all not covered by government health insurance. As a fundamentally independent man it's taken a lot for me to ask for help, but I truly need your compassionate financial assistance.
And now for the good part. I founded Hope & Balance, a support group that provides no-cost services to MS patients to improve quality of life such as reflexology, massage therapy and adaptive yoga.
I am blessed to have a beautiful son who was born shortly after my diagnosis. He's an important part of my life, I'm working hard to be the best dad I can.
I am asking for your help with the high medical costs of Chronic Progressive MS so I can continue advocating for others with MS and maintain a high quality of life to be there for my son.
On April 24, 2015 The American Academy of Neurology announced, for the first time, positive results for Progressive MS. Until now MS drug therapies have only been for the most common form, Relapse-Remitting MS. The phase III placebo-controlled trial reported improvements in disability among patients with Progressive MS. The monthly cost is $450-$500. I have the prescription, your generosity will allow me to have it filled. http://www.emaxhealth.com/1275/progressive-multiple-sclerosis-responds-biotin
Please give what you can. Allow your gift to multiply, encourage others to match your generous donation by spreading the word via your social network(s)...............
I can't walk. But I can fight. I'm doing all I can. And I need your help.
Thank you for caring, God bless. ~ Love Greg
I was diagnosed with Chronic Progressive Multiple Sclerosis almost 2 decades ago . . . just as I was becoming a father.
Over time, I lost the use of my legs. My energy level dropped to the point that I was unable to work, and I lost my job as a senior sales executive in real estate development, now living on a fixed disability pension.
I do everything I can to fight MS. I financed MRI's, scans and two MS/CCSVI procedures that helped mitigate some symptoms. In order to remain mobile, I purchased a vehicle and added hand controls and a scooter lift.
A home air-cooling system was needed, MS rendered my body unable to deal with extreme heat. I was collapsing in my home, requiring rescuing by the fire department. The cooling and modifications to the bathroom allow me to be safe.
The mounting debt from these and other medical expenses are a financial hardship. I still need to afford a new mobility scooter, repairs to my in home wheelchair, off-label medications and therapies, all not covered by government health insurance. As a fundamentally independent man it's taken a lot for me to ask for help, but I truly need your compassionate financial assistance.
And now for the good part. I founded Hope & Balance, a support group that provides no-cost services to MS patients to improve quality of life such as reflexology, massage therapy and adaptive yoga.
I am blessed to have a beautiful son who was born shortly after my diagnosis. He's an important part of my life, I'm working hard to be the best dad I can.
I am asking for your help with the high medical costs of Chronic Progressive MS so I can continue advocating for others with MS and maintain a high quality of life to be there for my son.
On April 24, 2015 The American Academy of Neurology announced, for the first time, positive results for Progressive MS. Until now MS drug therapies have only been for the most common form, Relapse-Remitting MS. The phase III placebo-controlled trial reported improvements in disability among patients with Progressive MS. The monthly cost is $450-$500. I have the prescription, your generosity will allow me to have it filled. http://www.emaxhealth.com/1275/progressive-multiple-sclerosis-responds-biotin
Please give what you can. Allow your gift to multiply, encourage others to match your generous donation by spreading the word via your social network(s)...............
I can't walk. But I can fight. I'm doing all I can. And I need your help.
Thank you for caring, God bless. ~ Love Greg
Organizer
Greg Turnbull
Organizer
Maple Ridge, BC