Please give Ryan Walker and his family from South Africa a holiday gift of hope that reflects the true spirit of the season at igg.me/at/newALSmedication. Like hundreds of thousands of ALS/MND patients and their loved ones around the world, they desperately need your help to make a miracle happen. Help bring MicroNeurotrophins, a promising ALS/MND medication, to patients in record time—just 12 months from now. This grassroots fundraising campaign is led by ALS Worldwide, a nonprofit organization based in United States that was co-founded by Stephen and Barbara Byer in 2008 to honor the memory of their son Ben, who died from ALS/MND that year at the age of 37. In 2013, Stephen and Barbaras daughter, Sarah Byer, and her husband Barry Wein, who lost his beloved grandfather to ALS/MND, joined the nonprofit organization to contribute their extensive professional expertise and personal experience. We understand the urgency to find a cure as soon as possible. ALS Worldwide is not affiliated with the ALS Association (ALSA) that received more than $100 million though the Ice Bucket Challenge. It’s just our organization, a promising ALS/MND medication, a group of dedicated scientists, and you. There is no fancy website, no motivational wristband and no rock concert—just the opportunity for all of us to do something truly wonderful, historic and miraculous together. Please give whatever amount you can afford, no matter the size. 100% of all donations are tax-deductible (in US) and all funds go directly to the efforts of the ALS MicroNeurotrophin Research Consortium. Thank you for your support. Don’t wait for miracles to happen. Make your own miracle by giving today. Thank you and Happy Holidays. #Crowdfunding4ALS #Crowdfunding4MND
Posted on: Thu, 11 Dec 2014 16:00:09 +0000
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