On 7 September 2015 people around the world will release digital balloons to raise awareness and money for Duchenne Muscular Dystrophy, a devastating disease. Please join us and start selling balloons or buy balloons!
http://www.duchenneballoon.org/
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Home — Duchenne Balloon | duchenneballoon.org Reviews
https://duchenneballoon.org
On 7 September 2015 people around the world will release digital balloons to raise awareness and money for Duchenne Muscular Dystrophy, a devastating disease. Please join us and start selling balloons or buy balloons!
duchenneballoon.org
Huguette PALM — Duchenne Balloon
http://www.duchenneballoon.org/huguette-palm
Become a balloon promotor. Find a balloon promotor. What happened last year. Euro; 1.410,00 / 282. To help improve care for Alexander, Mattias, Tom, Raphaël, Jonaz and for all children affected by Duchenne muscular dystrophy worldwide! HUGUETTE and MARZENA :-). Nous vendons des ballons afin d'améliorer les soins pour Alexander, Mattias, Tom, Raphaël, Jonaz et pour tous les enfants atteints de la myopathie de Duchenne à travers le monde! Euro; 1.410,00. With a HUGE hug to Alexander! Is organized by UPPMD.
Home — Duchenne Balloon
http://www.duchenneballoon.org/home
Become a balloon promotor. Find a balloon promotor. What happened last year. During the month of September 2016 people around the world released digital balloons to raise awareness and money for Duchenne Muscular Dystrophy. A devastating disease. Our aim is to sell as many balloons as possible. Because the more sold, the more impact we can make. Donate through a balloon. What happened last year. So, how does it work? Prefer to just donate a balloon? Go to Donate a balloon and follow the steps. Around the...
Jordan Davis — Duchenne Balloon
http://www.duchenneballoon.org/jordan-davis
Become a balloon promotor. Find a balloon promotor. What happened last year. Euro; 0,00 / 0. Euro; 0,00. Is organized by UPPMD.
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Memoirs of an Experimenter: September 2015
http://experimenteur.blogspot.com/2015_09_01_archive.html
Memoirs of an Experimenter. Friday, 4 September 2015. World Duchenne Awareness Day. You’re cordially invited to the 2015 World Duchenne Awareness Day event at Cornwall Park on Sunday 6 September. The event will be from 10am onwards. It will be set up near the new café. To show your support for people affected by Duchenne Muscular Dystrophy (DMD), you can:. Come to the event,. Buy a virtual balloon from. Read some real life stories of people with DMD at. Reading this essay on my blog,. Another symptom is ...
World Duchenne Awareness Day
http://www.worldduchenneday.org/aimduchenneballooncampaign
The aim of the Duchenne Balloon. Campaign is raising awareness for Duchenne Muscular Dystrophy around the globe. André Caldas - Conhecer lugares diferentes e experimentar o que a vida nos oferece é o melhor que eu posso viver.-. Gabin Rodrigues de Brito - Quand je serais grand, je serai policier ou dresseur de tigres, ou les deux.-. Maksim Volkov - I love to swim so much even I received a medal and trophy.-. Harry Halpin - I love seeing my grandparents as often as possible.-. ADM – El evento. Duchenne Pa...
Memoirs of an Experimenter: World Duchenne Awareness Day
http://experimenteur.blogspot.com/2015/09/world-duchenne-awareness-day.html
Memoirs of an Experimenter. Friday, 4 September 2015. World Duchenne Awareness Day. You’re cordially invited to the 2015 World Duchenne Awareness Day event at Cornwall Park on Sunday 6 September. The event will be from 10am onwards. It will be set up near the new café. To show your support for people affected by Duchenne Muscular Dystrophy (DMD), you can:. Come to the event,. Buy a virtual balloon from. Read some real life stories of people with DMD at. Reading this essay on my blog,. Another symptom is ...
SDMRC - Educational & Patient Outreach
http://sdmrc.ucsd.edu/education.html
Educational and Patient Outreach. San Diego Muscle Research Center. Center Cores and Technologies. Educational and Patient Outreach. Grants and Funding Opportunities. Directions to the Core Labs. Educational and Patient Outreach. The San Diego Muscle Research Center is primarily aimed at providing San Diego based muscle researchers with administrative, scientific and financial support. However, the SDMRC regularly teams up with patient organizations like CureDuchenne. Or Parent Project Muscular Dystrophy.
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Duchenne Alliance
United to Beat Time. We are an alliance of independent non-profit organizations dedicated to defeating Duchenne muscular dystrophy. The Duchenne Alliance member foundations collaborate to co-identify, co-review, and co-fund the most promising biomedical research. We have established the Duchenne Alliance Research Fund to receive monetary donations and direct these resources to advancing the top biomedical research and clinical trials. United to Advance Therapies. Travel Grant for REVERSE-DBMD Trial.
Duchenne Alliance
United to Beat Time. We are an alliance of independent non-profit organizations dedicated to defeating Duchenne muscular dystrophy. The Duchenne Alliance member foundations collaborate to co-identify, co-review, and co-fund the most promising biomedical research. We have established the Duchenne Alliance Research Fund to receive monetary donations and direct these resources to advancing the top biomedical research and clinical trials. United to Advance Therapies. Travel Grant for REVERSE-DBMD Trial.
Duchenne Analytics - your research hub
Duchenne Analytics represents a collaboration between multiple Duchenne muscular dystrophy-funding organizations to aggregate information relevant to advocacy, drug development and clinical care. This is the only site with a database that combines public and private funding sources for the most complete information about world-wide DMD funding available. What else you can find here: De-identified Duchenne Connect Patient Registry data, attributes of current clinical trials, and real-time feeds fo...
Home — Duchenne Balloon
Find a balloon seller. On 7 September 2015 people around the world will release digital balloons to raise awareness and money for Duchenne Muscular Dystrophy, a devastating disease. Our aim is to sell as many balloons as possible. Because the more sold, the more impact we can make. Your help is much appreciated :-). So, how does it work? Prefer to just buy a balloon? Go to Buy a balloon. And follow the steps. After registration log in and upload a personal photo and add a motivation. Meet our balloon sel...
Duchenne betegséggel élni – Barni és a Duchenne izomdisztrófia
Barni és a Duchenne izomdisztrófia. Május 13, 2014. Meglesz az első DMD-re fejleszett gyógyszer. Már a részeredményekből sejteni lehetett, de ez most már végleges: az Idebenone. A tesztelések III. fázisában elérte az elsődleges végpontot. Bővebben… →. Március 7, 2014. Barnit beválogatták a Tadalafil klinikai kipróbálásába. Bővebben… →. December 6, 2013. Action Duchenne konferencia 2013 – 1. Bővebben… →. Szeptember 17, 2013. Re (részletek a korábbi posztban itt. Bővebben… →. Szeptember 16, 2013. Az intern...
Duchenne Cabinetry - Custom-built contemporary furniture
Plinth and Pedestal Hire. Handcrafted furniture made in Cape Town. Plinth and Pedestal Hire. At Duchenne Cabinetry we manufacture custom-built contemporary furniture. We have a passion for proportions and enjoy the challenge of working with simple, clean lines in a variety of mediums. All our fitted and free-standing furniture is hand crafted with old fashioned durability in mind whilst incorporating the latest style trends and contemporary fittings and fixtures. 4 Penryn Road, Salt River, Cape Town.
Stand For Duchenne Canada - Connecting those affected by Duchenne
Get and give support. Disease & Treatment. How Duchenne is inherited. Diagnosis and genetic testing. Clinical trials and patient registries. News & Events. Get & Give Support. STAND FOR DUCHENNE CANADA IS DEDICATED TO SUPPORTING FAMILIES DIAGNOSED WITH DUCHENNE. FDA grants accelerated approval to first drug for Duchenne muscular dystrophy. To receive information and updates from Stand for Duchenne Canada, sign up here. Sign up for email updates. Pin It on Pinterest. Stand For Duchenne Canada.
Ataluren Ya en Aragón
Ataluren Ya en Aragón. SEGUNDA JORNADA DUCHENNE- CASPE. UNA LUCHA CONTRA EL TIEMPO Y EL SÍNDROME DE DUCHENNE. MANIFESTACIÓN 14 DE NOVIEMBRE CASPE. NOS REAFIRMAMOS en nuestra petición al Gobierno de Aragón. LA VIDA DE NUESTROS HIJOS NO TIENE PRECIO. Para reproducir la foto solicitar permisos. Somos Carmen (mamá de Sergio de 7 años) e Irene (mamá de Carlos y Mario de 9 años). Nuestros hijos padecen una enfermedad neurodegenerativa grave llamada Distrofia Muscular de Duchenne. Podría frenar su enfermedad.
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