Comments for CureDuchenne http://www.cureduchenne.org Cure Duchenne Muscular Dystrophy: Giving the Boys a Chance for a Lifetime Fri, 04 Dec 2009 06:52:43 -0600 http://wordpress.org/?v=2.8.5 hourly 1 Comment on CureDuchenne Grants $200,000 to UCLA Duchenne Muscular Dystrophy Research & Clinic by Tommy http://www.cureduchenne.org/2009/11/cureduchenne-grants-200000-to-ucla-duchenne-muscular-dystrophy-research-clinic/comment-page-1/#comment-506 Tommy Fri, 04 Dec 2009 06:52:43 +0000 http://www.cureduchenne.org/?p=1435#comment-506 thank you for all that you are doing to find a cure for DMD and for keeping this site up to date with the latest research information... this site and the information you provide has been invaluable. it took 6 months from when my nephew was first suspected of having DMD (by his primary care physician) to finally getting a DNA test at UCLA... it was very nerve racking waiting. hopefully this donation will help kids/families in the So.Cal area more easily gain access to the research and treatments available. thank you for all that you are doing to find a cure for DMD and for keeping this site up to date with the latest research information… this site and the information you provide has been invaluable. it took 6 months from when my nephew was first suspected of having DMD (by his primary care physician) to finally getting a DNA test at UCLA… it was very nerve racking waiting. hopefully this donation will help kids/families in the So.Cal area more easily gain access to the research and treatments available.

]]> Comment on Meet the 2009 Climb to Cure Duchenne Team! by Bill Burke http://www.cureduchenne.org/2009/06/meet-the-2009-climb-to-cure-duchenne-team/comment-page-1/#comment-158 Bill Burke Wed, 26 Aug 2009 15:16:09 +0000 http://www.cureduchenne.org/?p=886#comment-158 Good luck team. You'll make it to the top. I climb for my grandson who has Angelman's Syndrome. You can see photos of him on my website under "My Training Partner." Sharon and I made a donation. God bless you and your precious sons. Bill & Sharon Burke Costa Mesa, Ca. Good luck team. You’ll make it to the top.

I climb for my grandson who has Angelman’s Syndrome. You can see photos of him on my website under “My Training Partner.”

Sharon and I made a donation.

God bless you and your precious sons.

Bill & Sharon Burke
Costa Mesa, Ca.

]]> Comment on A Touching Video by Maggie Harvey http://www.cureduchenne.org/2009/08/a-touching-video/comment-page-1/#comment-149 Maggie Harvey Thu, 20 Aug 2009 10:07:13 +0000 http://www.cureduchenne.org/?p=1123#comment-149 Thankyou so much for doing this video, Hayley - I hope Dan is doing well and hope to see him at the Avenues in September (if not before) give him my love and best wishes to you all Thankyou so much for doing this video, Hayley – I hope Dan is doing well and hope to see him at the Avenues in September (if not before) give him my love and best wishes to you all

]]>