Top 69 alternative sites to harrisonsfund.com
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en.care-nmd.eu
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zackhegerfoundation.org
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actionduchenne.org
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progena.ch
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vision-dmd.info
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genetherapy-muscular.com
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duchenne.com
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onlywatch.com
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cureduchenne.org
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parentprojectmd.org
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duchenneandyou.eu
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takeonduchenne.eu
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joiningjack.org
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worldduchenneday.org
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consortium.ai
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alexswish.co.uk
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catabasis.com
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littleherculesfoundation.org
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mda.org
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Michael's Cause – Fighting Duchenne Muscular Dystrophy
Fighting Duchenne Muscular Dystrophy
Jett Foundation | Home
Empowering families. Fighting Duchenne muscular dystrophy.
Author: Aug 5
CARE-NMD: Improving care for Duchenne muscular dystrophy
Improving care for Duchenne muscular dystrophy
News - Zack Heger Foundation
The Zack Heger Foundation is an organization dedicated to raising money for finding a cure for Duchenne Muscular Dystrophy. We are part of the The Duchenne Alliance
Duchenne UK - Bringing an end to Duchenne muscular dystrophy
Duchenne UK is the leading UK charity for Duchenne muscular dystrophy. We're going further and faster than ever before to find effective treatments for DMD.
Annual Sam's Night to End Duchenne - Benefiting PPMD
Sam's Night is an opportunity to help raise funds to benefit the research programs of Parent Project Muscular Dystrophy, and to fight to end Duchenne.
Home - Action Duchenne
Formed in 2001 Action Duchenne was the first national charity dedicated to supporting those living with Duchenne muscular dystrophy (‘DMD’). Our work to date has seen over £10m invested in ground-breaking research, educational programmes and campaigns.
Homepage - Emflaza (deflazacort)
PRESERVE WHAT MATTERS TO YOUR CHILD AFFECTED BY DUCHENNE MUSCULAR DYSTROPHY
Home | STC4Duchenne
STC is running the marathon in april for Duchenne Muscular Dystrophy
Home - Progena
Progena is a Swiss Duchenne Foundation for patients with Duchenne muscular dystrophy, their families, doctors, therapists.
Home • Solid Biosciences
Life science company focused on solving Duchenne muscular dystrophy
VISION-DMD – Designed to ensure a timely & cost-effective **** development for Duchenne muscular dystrophy
Designed to ensure a timely & cost-effective **** development for Duchenne muscular dystrophy
Jesse's Journey | Duchenne Muscular Dystrophy | Canada
Duchenne Muscular Dystrophy (DMD) is a progressive genetic muscular system disease that affects 1 in every 5,000 boys.
Home Page 1 - Pietro's Fight
Help Pietro fight Duchenne Muscular Dystrophy (DMD). Join us in learning more about this disease that affects 300,000 children worldwide and donate to help fund the fight for a cure. This is our mission of love and our fight for a cure!
The Romito Foundation -
The Romito Foundation - Striving to improve the quality of life of those living with Duchenne Muscular Dystrophy
2nd Gene Therapy for Muscular Disorders Summit | April 2022 | Home
The 2nd Gene Therapy for Muscular Disorders Summit will focus on overcoming the challenges of developing genetic therapies targeting muscular disorders, including Duchenne Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, Pompe Disease and X-Linked Myotubular Myopathy.
Sarepta Therapeutics – Duchenne.com
Visit Duchenne.com to learn about Duchenne Muscular Dystrophy (DMD) symptoms, testing, genetics, and resources.
Only Watch - the official website
Only Watch is a biennial charity auction of luxury timepieces made by the finest watchmakers for research into Duchenne Muscular Dystrophy. Only Watch is an event organised by Association Monégasque contre les Myopathies.
Finding a cure for Duchenne | Caring for Duchenne | CureDuchenne
CureDuchenne is the global leader in research, patient care and innovation for improving & extending the lives of children with Duchenne muscular dystrophy.
Other sites like harrisonsfund com
Parent Project Muscular Dystrophy (PPMD) | Fighting to End Duchenne
Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
Welcome to Duchenne and You - Duchenne and You
This website provides educational resources to support healthcare professionals recognise the early signs and symptoms of Duchenne Muscular Dystrophy.
Welcome to Take on Duchenne - Take on Duchenne
This website provides educational resources to support healthcare professionals recognise the early signs and symptoms of Duchenne Muscular Dystrophy.
Joining Jack - Join Jacks' fight against Duchenne Muscular Dystrophy
Jack has Duchenne Muscular Dystrophy, DMD. There is no cure at the moment. We're raising money to fund research to find effective treatments
What is Duchenne? • World Duchenne Awareness Day
On September 7, we raise global awareness for Duchenne and Becker Muscular Dystrophy, two rare muscle wasting conditions. Join us! 🎈
Author: Worldduchenne
Consortium.AI
Consortium.AI - the joined force to apply the latest advances in AI to discovery of novel small molecules for the Duchenne Muscular Dystrophy (DMD) and other rare orphan diseases.
Alex's Wish | fundraising charity for Duchenne Muscular Dystrophy
Alex’s Wish is a charity set up to eradicate Duchenne Muscular Dystrophy, an aggressive form of Muscular Dystrophy that affects 1 in every 3,500 boys born and results in total paralysis. Established by Emma and Andy Hallam (parents to Alex) in late 2012, Alex's Wish helps raise vital funds to help bring about new treatments and ultimately a cure for this devastating condition.
Catabasis
Our mission is to bring hope and life-changing therapies to patients and their families affected by rare diseases, and our primary focus is Duchenne muscular dystrophy.
Little Hercules Foundation » Little Hercules Foundation
Little Hercules Foundation was founded by three moms, two of which have sons living with Duchenne muscular dystrophy. We are working to raise money to fund groundbreaking research that will save this current generation of boys.
¿Qué es Duchenne?
¿Qué es Duchenne?. Duchenne y tú es un espacio dedicado a las personas que conviven con la distrofia muscular de Duchenne.
Author: Admin
Facioscapulohumeral Muscular Dystrophy Info - Treatment - FSHD Society
Get Involved in the fight to cure FSHD muscular dystrophy. Newly or recently diagnosed? Please contact us to - Volunteer - Join - Donate.
Duchenne Muscular Dystrophy Foundation (Duchenne SpierDystrofie Stichting) - Home
WE are so glad that you visit this site of DUCHENNE MUSCULAR DYSTROPHY. This is a registered Humanitarian FOUNDATION located in the country of SURINAME SOUTH AMERICA. WE are here to help you and your loved ones to have HOPE as you face the challenges in
Muscular Dystrophy | Neuromuscular Condition | Spinal Muscular Atrophy
Muscular Dystrophy NSW - Helping our muscular dystrophy community build strength and reach potential. Contact us today to find out more.
Muscular Dystrophy Association
MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research.
Indian Association of Muscular Dystrophy Solan | Symptoms | IAMD
Muscular dystrophy is a progressive neuromuscular genetic disorder. Know more about its initial symptoms & what indian association of muscular dystrophy does to provide relief.
Dystrophy Annihilation Research Trust – Aspiring to achieve Total Annihilation of Muscular Dystrophy
Aspiring to achieve Total Annihilation of Muscular Dystrophy
Spinraza Muscular Dystrophy
Spinraza Muscular Dystrophy,SMA Clinical Trials,Spinal Muscular Atrophy Therapy,Spinal Muscular Atrophy Treatment
Save Our Sons Duchenne Foundation: SOS
– sosdf
Save Our Sons is the peak body for Duchenne muscular dystrophy in Australia. We have focused our energy and fundraising efforts toward finding a cure. Open Monday To Friday. Donate Online. Founded In 2008. Highlights: Founded In 2008, Donation Option Available.
TimothyGriff.in
A certified inhabitant of The Universe living with FSH muscular dystrophy.
Author: Timothy Griffin Timmargh
Muscular Dystrophy | Laughing At My Nightmare, Inc. | United States
Laughing At My Nightmare is a 501(c)3 nonprofit dedicated to providing equipment to those living with muscular dystrophy and teaching students that all people deserve kindess and respect, regardless of their differences.
What else harrisonsfund.com alternative websites
The Kezi Silverstone Trust || Raising funds and awareness for children's charities
The Kezi Silverstone Trust raises funds and awareness for children's charities and in particular, charities that fight to prevent the abuse and neglect of children.
Muscular Dystrophy Australia Muscular Dystrophy Assoc
Muscular Dystrophy Australia (MDA) the one stop shop for information and support for people living with neuromuscular diseases.
Author: Boris M Struk
Timothy Griffin (Timmargh)
A playing card collecting, science fiction absorbing, certified inhabitant of The Universe living with muscular dystrophy.
Mayopathys Home - Muscular Dystrophy Ayurvedic Treatment Home in Tamilnadu
Mayoapthys Home - Muscular Dystrophy Ayurvedic Treatment Home To provide 100% cure and to make the people come to us for Muscular Dystrophyt reatment, Paralysis or Cerebral palsy
Author: Mayopathys Home - Muscular Dystrophy Ayurvedic Treatment Home
Oesophageal Cancer Fund - National charity for Oesophageal Cancer
We are the national charity for Oesophageal Cancer in Ireland; bringing the good fight to a bad cancer.
The Travels of Justin's Famous Sports Chickens
Muscular Dystrophy Association a 10 year tradition of Hans getting rubber chickens signed by sports heroes for Justin.
Enrique Brandan home web page. Enrique Brandan Laboratory
Enrique Brandan web page. Brandan Laboratory is concentrated to study skeletal muscular dystrophies. Process of fibrosis and function of proteoglycans.
The Speak Foundation - Limb Girdle Muscular Dystrophy
Established in 2008, The Speak Foundation is the first patient led organization to help those living with Limb Girdle Muscular Dystrophy and other forms of NMD.
Author: The Speak Foundation
Fight for the Future Education Fund
Fight for the Future is dedicated to protecting and expanding the Internet’s transformative power in our lives by creating civic campaigns that are engaging for millions of people.
About Charity Funding - nditrust.ca
Charity organizations are very important, and in Canada, there are several of them that can be found through each of the provinces in Canada. These organizations are not for profit. Which means they have very little funding to work with. This website is dedicated to bringing more attention to these organizations. Although for charities being...Read More
Fight Cancer Foundation | Give Hope. Save Lives.
Fight Cancer Foundation is a national charity dedicated to providing care, treatment and support for cancer patients and families, and funding cancer research.
Asian American Advocacy Fund
The Asian American Advocacy Fund is a 501(c)4 nonprofit dedicated to building a progressive Asian American base in Georgia and fighting for all communities of color.
Academy of Applied Epigenetics
In Memory of Joshua Dubcak - Muscular Dystrophy - Why Jerry Lewis was fired - Dr. Joel Wallach - Marvin Ropp - Youngevity - Colloidal Minerals - Selenium - Donations
Stem Cell Therapy Hospital & Centre In Delhi India - StemCellCareIndia
StemCellCareIndia is a Stem Cell Therapy Centre in Delhi, India; provides treatment of muscular dystrophy, multiple sclerosis, spinal cord, Stem Cell Therapy
Home | Crann Centre Ireland
Our services are focused on, but not limited to, people who have Spina Bifida, Hydrocephalus, Muscular Dystrophy, Cerebral Palsy, Childhood ****, Spinal Cord Injuries, and their families.
Fight for Sight - Stopping sight loss through pioneering research
Fight for Sight is the leading UK charity dedicated to stopping sight loss through pioneering research. We want to create a future everyone can see.
Aged Care Service, Massage Therapy, Muscular Dystrophies Therapy Sydney
Mega Therapy providing aged care service, massage therapy, relaxation massage, and Muscular Dystrophies Therapy Sydney. Contact us today to avoid problems with your health tomorrow.
Stem Cell Therapy India: Diabetes, Kidney Failure, CP - Dr. Sagar Jawale
Call: +91-9370000380 - Dr. Sagar Jawale for Stem Cell Therapy in India - Risk-Free and Effective Treatment | Contact Us for Muscular Dystrophy and Kidney Failure Therapy/Treatment India to avoid muscular, kidney, diabetes and various other serious problems
Author: Stem Cell Therapy India Diabetes; Kidney Failure; CP - Dr. Sagar Jawale
Sugar Free September | Go Sugar Free for MD!
Join us for Sugar Free September and give SWEET opportunities to kids living with the devastating impacts of Muscular Dystrophy. You will improve your health and wellbeing, just in time for summer. It's a win-win!
Home - Kay Yow Cancer Fund
Kay Yow Cancer Fund is a non-profit organization dedicated to supporting innovative ways of fighting ALL cancers affecting women and providing support through giving strength, courage, and hope.
Other websites similar as harrisonsfund.com
Polskie Towarzystwo Chorób Nerwowo-Mięśniowych | Polskie Towarzystwo Chorób Nerwowo-Mięśniowych
choroby nerwowo-mięśniowe, dystrofie, rdzeniowy zanik mięśni, miastenia, miopatie, polineuropatie, stwardnienie zanikowe boczne, Duchenne’a, Becera , ALS, DMD, LGMD, SMA, spinal muscular atrophy, Muscular dystrophy, limb-girdle dystropny, dystrofia obręczowo - kończynowa, FSD, twarzowo - łopatkowa
CP- Innovation - Compassion - Purpose, Green Bay, WI
Serving persons of all abilities including those with cerebral palsy, als, muscular dystrophy, multiple sclerosis, autism, and other special needs. Leaders in caring, personalized and progressive solutions for a fully inclusive community.
Home - RAF Central Fund
Welcome to the RAF Central Fund. We are a charity dedicated to safeguarding the health and wellbeing of serving personnel through the funding of sport and physical activities. Find out more about our charitable funding and our RAF Sports Lottery.
Author: WO Justin 'Max' Wall
Home - LGMD Awareness Foundation
ABOUT US LGMD Awareness Foundation, Inc. is a 501(c)(3) non-profit advocacy organization dedicated to globally raising awareness of the rare neuromuscular conditions known as limb-girdle muscular dystrophy (LGMD). In collaboration with other LGMD foundations, our focus is to provide curated educational information and resources for the LGMD community and public. By increasing
Author: Dooley
Home
ABOUT US LGMD Awareness Foundation, Inc. is a 501(c)(3) non-profit advocacy organization dedicated to globally raising awareness of the rare neuromuscular conditions known as limb-girdle muscular dystrophy (LGMD). In collaboration with other LGMD foundations, our focus is to provide curated educational information and resources for the LGMD community and public. By increasing
Author: Dooley
Our Shooting Star
The Jacob Issac Rappoport Foundation fighting spinal muscular atrophy in memory of our shooting star.
Ploughshares Fund
Join us in our fight to keep the world safe from nuclear threats.
House Challenge
Lizzy Chakkalakal,Global Housing Charity Fighting Poverty
One Israel Fund: Four-Star Charity Dedicated to Israel's Security
One Israel Fund is dedicated to supporting the welfare and safety of the men, women, and children of Judea, Samaria, the Jordan Valley, and the reemerging communities of Gaza evacuees. These nearly half million residents are the vanguard of Israel’s security and sovereignty as a Jewish State. Recognized as a 4-Star charity by Charity
Author: Shana Laufer
George Harrison Fund for UNICEF |
