Members of Cure SMA’s Scientific Advisory Board (SAB) have gathered in Chicago, meeting to advance Cure SMA’s research goals. Our SAB is made up of highly respected SMA researchers, including experts in child neuromuscular disorders, SMA biology, SMN splicing, motor neurons, mouse and other animal models, and more. The SAB focuses on identifying the most […]
Cure SMA Scientific Advisory Board Meets in Chicago Read More »
In the last few years, we’ve gotten closer to an approved treatment than we ever have been. Through research funded by Cure SMA, we’ve identified the cause of SMA, and are developing multiple ways to treat SMA. But with this great progress comes even greater needs. That’s why we’ve set a goal of raising $750,000
Great Progress, Greater Need Read More »
The 5th Annual South Florida Chapter Gala of Hope was a fantastic evening to raise funds and awareness of SMA. This year’s event has already raised over $224,000, and money is still being tabulated! In its five-year history, the event has raised an incredible total of over $700,000 for SMA research and family support. The
5th Annual South Florida Gala of Hope Raises Record Total of $224,000 Read More »
This year’s 5th Annual “Hope on the Hill” Congressional Dinner will be held on Tuesday, December 1, bringing together families, government, and industry for an important evening of collaboration. As more SMA drugs reach late stage clinical trials, we remain focused on educating, involving, and engaging all three groups in our community: the patient and
5th Annual Hope on the Hill Congressional Dinner Advances SMA Advocacy Read More »
A recording of last week’s Cure SMA Clinical and Regulatory Webinar is now available online. WATCH Our thanks again to our three panelists—Dr. Tim Franson, Dr. Tim Miller, and Dr. Tom Murray—for their expertise and for their generosity with their time. Our thanks also to everyone from our community who joined in. We received a
Clinical and Regulatory Webinar and Extended Q&A Now Available Read More »
The latest issue of Compass, our research publication, is now available online. This fall 2015 issue covers our 2015 SMA Researcher Meeting. The researcher meeting is held each year as part of our Annual SMA Conference. It is the largest research meeting in the world focused on SMA, where about 300 basic researchers, drug developers,
Fall 2015 Issue of Compass Highlights SMA Researcher Meeting Read More »
Members of Cure SMA’s Medical Advisory Council (MAC) have gathered in Chicago for two days of meetings to set the agenda for the care of SMA individuals and families. Our MAC is chaired by Mary Schroth, MD, a leading pulmonologist, and professor of pediatrics. The MAC is one of the most highly respected bodies of
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We need your help in contacting your Senators to tell them that legislation promoting innovation and research is extremely important to you and that the discovery of the next generation of cures and treatments for disease needs to start now! We are concerned about Congress’ lack of progress on the 21st Century Cures legislation (H.R.
Tell Your Senator to Support Innovations for Healthier Americans Read More »
Cure SMA is pleased to announce the creation of a new chapter in northern New Jersey, serving families and supporters with zip codes starting with 07, 085, 086, 087, and 088. Led by chairpersons Kara Hartnett (family support), Anna Pham (fundraising), and Zainab Jaffar (communications), the chapter is excited to begin helping families throughout their
Cure SMA Welcomes the North Jersey Chapter Read More »
Cure SMA President Kenneth Hobby was a featured panelist at Partnering for Cures, a conference convened by the Milken Institute’s FasterCures initiative. At the event, over 700 research innovators—including senior government officials, patient advocates, scientists, major investors, industry CEOs and philanthropists—gathered to discuss some of the most common barriers to speeding up innovation in medical
