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A.L.S. Family Charitable Foundation
| Last updated on September 28, 2011 |
The A.L.S. Family Charitable Foundation was started in hopes of creating a brighter future for those living with A.L.S. in New England and is dedicated to the loving memory of Clifford Jordan, Jr. and Edward Sciaba, Sr. and honors all the courageous individuals and families touched by A.L.S. The A.L.S. Family Charitable Foundation, Inc. is a federally recognized 501(c)(3) non-profit organization dedicated to raising funds for cutting edge research to cure A.L.S. in the future and providing patient services for those suffering from Amyotrophic Lateral Sclerosis today.
Description:
This disease, maybe more than others, has a tremendous effect on families both physically and emotionally. The inevitable decline of patients takes a toll on the family who can only watch helplessly as their loved ones slowly become incapacitated. As small tasks become insurmountable and individuals remain fully aware of their loss of independence, the dedication of caretakers becomes increasingly more important.
The needs of A.L.S. patient’s and their families run the gamut from financial and emotional support to extensive medical and therapeutic treatment and ultimately advocacy. The A.L.S. Family Charitable Foundation works to raise money for in-house patient programs that ensure patient’s needs are met, as well as funds crucial medical research to one day cure this terrible disease.
Until there is a cure, there is the A.L.S. Family Charitable Foundation.
History:
The A.L.S. Family Charitable Foundation was started in 2001 in hopes of creating a brighter future for those living with A.L.S. in New England and honors all of the courageous individuals and families touched by this disease.
Over 30,000 people are living with A.L.S. today, a disease that causes a progressive degeneration of motor neurons in the body affecting voluntary muscle control. Those affected eventually lose their livelihood, their independence and ultimately their lives.
We help those living with the disease today celebrate their time left with their loved ones, offering strength, hope and joy through our Patient Programs. We help future generations through financial support of cutting edge research to one day find a cure.
Until there is a cure…there is the A.L.S. Family Charitable Foundation.
Contact people:
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Mary Ann Singersen, President, (508) 759-9696, (email)
Ernie Bliudnikas, Administrative Assistant, (508) 759-9696, (email) |
Main office number: (508) 759-9696Office fax number: (508) 759-9606
Address:
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P.O. Box 229 Buzzards Bay, MA 02532
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Web Site: http://www.alsfamily.org
Miscellaneous Information
| Does this agency require a CORI (Criminal Record Offender Information) check of its volunteers? |
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No
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| Last updated on September 28, 2011 |
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