hopeforgus.blogspot.com
Hope for Gus - Searching for a Cure for DMD
Hope for Gus - Searching for a Cure for DMD. Sunday, January 2, 2011. The Year for DMD - The Year for Hope for Gus - Part 1. 2010 was a busy year – for Duchenne Muscular Dystrophy Research and for Hope for Gus. I’ll talk about DMD research first – it was a year of disappointments and some hope of progress – ‘there’s good news and bad news…’ as the saying goes. Here are some highlights:. In March, PTC Therapeutics and Genzyme Corporation. This was heartbreaking and scary for a bunch of reasons:. 8220;We a...
hopeforgus.com
WiMAX2キャンペーン比較【2015最新版】
まず、キャッシュバックキャンペーンに関しては、5,000 29,990円といった高額キャッシュバックが魅力的です。
hopeforgus.org
Hope For Gus Foundation | Funding Research for Duchenne Muscular Dystrophy
Funding Research for Duchenne Muscular Dystrophy. Our Supporters and Sponsors. What is Duchenne Muscular Dystrophy? Duchenne Muscular Dystrophy, like all muscular dystrophies, causes weakening of the muscles. DMD is a recessive genetic mutation that occurs on the X chromosome. As a result, it almost exclusively affects boys. Unfortunately for the boys who have been diagnosed with DMD, it is the most severe of all the muscular dystrophies:. They die earlier, most boy’s with DMD die in their mid 20’s.
hopeforgus.wordpress.com
Hope for Gus | Searching for a Cure for Duchenne Muscular Dystrophy
Searching for a Cure for Duchenne Muscular Dystrophy. Gus Turned 6 – The Balancing Act (plus a new song! May 12, 2011. It was a mere 5 months ago that I promised to write again soon – seems like only yesterday. But, Duchenne Muscular Dystrophy is a balancing act, and we ended up on one side of the see-saw. We spent the last few months taking care of Gus – we bought a new house – one that’s better for him (not. It was a great birthday! Gus turned 6 yesterday and his disease reminded me that each of those ...
hopeforgusball.com
Hope For Gus -
Hope For Gus Ball - Valentine’s in Vegas - 2/15/14 - 7:30 PM - Manchester. Gus is the 8 yr old son of Steve and Tonya Dreher of Peterborough NH. They founded Hope for Gus when he was diagnosed with this progressive, muscle-wasting disorder at age 4. DMD is currently 100% fatal, but the Drehers hope to change that diagnosis. On February 15, 2014 the Hope for Gus Foundation. Will hold its 3rd Annual Hope for Gus Ball, Valentine’s in Vegas. 7:30pm, at the Radisson Hotel Downtown in Manchester NH. Hope for G...
hopeforgusball.org
Hope For Gus -
Hope For Gus Ball - Valentine’s in Vegas - 2/15/14 - 7:30 PM - Manchester. Gus is the 8 yr old son of Steve and Tonya Dreher of Peterborough NH. They founded Hope for Gus when he was diagnosed with this progressive, muscle-wasting disorder at age 4. DMD is currently 100% fatal, but the Drehers hope to change that diagnosis. On February 15, 2014 the Hope for Gus Foundation. Will hold its 3rd Annual Hope for Gus Ball, Valentine’s in Vegas. 7:30pm, at the Radisson Hotel Downtown in Manchester NH. Hope for G...
hopeforhaas.org
Hope For HAAS
What is the ASC? What is the ASC? HAAS NEEDS YOUR HELP. How your donation will help. What is the ASC? Hawaii Academy of Arts and Science, PO Box 1494, Pahoa HI 96778, Pahoa, Hawaii 96778.
hopeforhagerstown.org
Convoy of Hope - Hagerstown
How You Can Help. Welcome to Convoy of Hope - Hagerstown. About Convoy of Hope:. Hagerstown Convoy of Hope is a huge “carnival-like” event featuring:. 30,000 lbs of groceries. Job and health fair. With prizes and give-aways. Access to dozens of community resources. With inflatable games, entertainment, food and prizes, and lots of other games. And best of all, everything is FREE. To read more about Convoy of Hope International. Will be held on October 3rd, 2014.
hopeforhailey.blogspot.com
Life after HLHS
Living life after losing our first child to Hypoplastic Left Heart Syndrome. Sunday, September 27, 2015. Soalmost 2 years have passed since my last update! We named our precious little girl, Annabelle Faye. She has been the happiest baby we have ever met! It's very rare to hear her cry and she's a great sleeper! She's been absolutely amazing. And Leyna has been the best big sister anyone could ever ask for. She absolutely loves her little sister. Links to this post. Tuesday, November 26, 2013. On the oth...
hopeforhailey.com
HopeForHailey.com
hopeforhailey.tripod.com
HOPE FOR HAILEY
Extreme Make Over Project. Hailey Kent Benefit Fund. This page is set up in honor of a very inspirational girl, Hailey Kent, and her family. Since being diagnosed Hailey has undergone very aggressive chemotherapy and has had several blood transfusions to fight the cancer and help save her life. To learn more about MLL please click the link below. Please View This Special Music Video Tribute for Hailey. Please contact GHKidsEvent@yahoo.com. With any questions, comments or suggestions.
