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About Our Chapter
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The ALS Association Florida Chapter symbolizes the hopes of people everywhere that Amyotrophic Lateral Sclerosis will one day be a disease of the past - relegated to historical status, studied in medical textbooks, conquered by the dedication of thousands who have worked ceaselessly to understand and eradicate this perplexing killer.

Until that day comes, the Chapter relentlessly pursues its mission to help people living with ALS and to leave no stone unturned in search for the cure of the progressive neurodegenerative disease that took the life and name of Baseball Legend Lou Gehrig.

As the only not-for-profit voluntary health agency dedicated solely to the fight against ALS, we direct the largest privately-funded research enterprise engaged to uncover the mystery of a disease that affects as many as 30,000 annually. With more than 5,600 people diagnosed each year - an average of 15 new cases each day - our mission is urgent. The search for answers knows no bounds.

The Association's far-reaching efforts extend to Capitol Hill and some of the world's finest research laboratories. To date The ALS Association has put more than $99 million into ALS research. We've brought the ALS community the historic Medicare waiver of the 24-month waiting period and a 100% increase in funding since our advocacy campaign began.

But nowhere does this battle reach deepest than in our work with ALS patients and their families. We embrace thousands of those stricken with the disease with the world's most comprehensive program of care and services. Our nation-wide network of chapters coordinates services with care and compassion - making a difference in the lives of people with Lou Gehrig's disease. Our hallmark of quality is exemplified in centers and clinics that deliver advanced care and meet The ALS Association's rigorous criteria for certification.

Our accomplishments are made possible by the generosity of others. From the smallest donation to the largest gift, donors touch the ALS community with hope for the future. This terrible disease knows no racial, ethnic or socioeconomic boundaries. It can strike anyone at any time.

Despite the mysterious nature of ALS, breathtaking advances in science, medicine and technology are shaping a future of unparalleled hope for those with ALS. The Chapter is at the forefront in this new world, encouraging young scientists to combine new thinking with these advances to unlock the mysteries of ALS - to push the envelope in therapy and scientific research.

The ALS Association Florida Chapter is waging the war against this killer 24/7. Every 90 minutes, an American dies of ALS. Time isn't on the side of those afflicted. Fighting ALS is a full-time job.

 
The Sherry Murray ALS Medical Futures Scholarship

ScholarshipsThe Sherry Murray ALS Medical Futures Scholarship is for students who have or have had a spouse, parent, or grandparent diagnosed with ALS, also known as Lou Gehrig’s Disease, and who want to pursue a degree in the medical profession as a result of their experience.  Applicants to The Sherry Murray ALS Medical Futures Scholarship must be:

 

• The spouse, child or grandchild of a person who has been diagnosed with ALS. (Families of every tradition will be considered).
• A legal resident of Florida.
• Currently majoring in any medically-related degree or attending any medically-related certification program.
• Any age of student may apply - scholarships are not restricted to graduating high school seniors, high school graduates or current undergraduates.
• Applicants must attend or be accepted to school full-time (as defined by the educational institution) at an accredited twoyear or four-year college or university, or vocational-technical school located in the U.S.

 

All interested students must complete an application and mail it along with a current, complete official transcript of grades (Grade reports are not acceptable. Online official transcripts must display student name, school name, grade and credit hours earned for each course, and term in which each course was taken.), a 500-word essay describing how the student’s experience with ALS has impacted him/her and his/her decision to enter the medical field, and two (2) letters of recommendation. Other requirements are listed on the application.

 

DOWNLOAD APPLICATION

 

Application deadline is July 10, 2015 for fall semester (for August payment of funds). Scholarships awarded based on fund availabilty.

 

For more information, contact Gabby Harrison, Selection Committee Staff Liaison at gharrison@alsafl.org or 1-888-257-1717, ext. 101
 
 
 

 


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The ALS Association Florida Chapter
(888) 257-1717    3242 Parkside Center Circle   Tampa, FL 33619-0907   Fax (813) 637-9010

 
All content and works posted on this website are owned and copyrighted by The ALS Association. © 2015
Lou Gehrig® used with permission of the Rip Van Winkle Foundation / www.LouGehrig.com

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