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The ALS Association
Vision Express

 

 
 
  01. Letter from the President
  02. Feature Story
  03. Advocacy & Public Policy
  04. Research Updates
  05. How You Can Help

 

 
 
 

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Spotlight

assistive-technologyAssistive Technology
for Caregivers

Celebrate those who provide assistance to people living with ALS.
Read more.


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October 21
How Caregivers Can Benefit
from Assistive Technology
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November 25
Insights into Motor Neuron
Disease from Drosophila
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Letter from the President

November is National Family Caregivers Month

November is National Family Caregivers Month. Nationwide, more than 65 million individuals are family caregivers to those with physical, developmental or emotional needs. This month, The ALS Association thanks the many dedicated caregivers who provide crucial support to loved ones living with the devastating effects of Lou Gehrig's Disease.

Caregivers encounter many challenges in dealing with ALS, some of which include the new experience of providing assistance to those developing physical limitations affecting mobility, swallowing, speaking and breathing. An ALS diagnosis impacts every aspect of caregivers’ lives as they adjust their efforts to meet ongoing work, family, personal and financial obligations, which change as this disease progresses.

To support caregivers, we offer helpful resources on our website. Additionally, there will soon be an ALS Association hosted webinar on November 18 for caregivers on how they can benefit from assistive technology.

We will also offer individuals the opportunity to thank a caregiver through an online e-card. People can create customized messages to send via email to the caregiver in their lives who has chosen to fill this vital role. For each e-card sent, Permobil, the world’s leading manufacturer of power wheelchairs, will donate $10 with a $25,000 maximum donation.

So please join us this month in celebrating those who are dedicated to caring for people living with this disease.

Sincerely,

9-28-10 Match Email 2 Signature

Jane H. Gilbert
President & CEO

 

FEATURE STORY

ALS Association Chapters Highlight Partnerships
With Major and Minor League Baseball Teams

ALS Association chapters continued their partnerships with Major and Minor League Baseball teams around the U.S. to spread ALS awareness to the game’s tens of millions of fans, including awareness of the National ALS Registry and the connection between ALS and military service. These were major themes of the more than 30 events that chapters held with professional baseball teams this season. Some chapters saw their names on stadium Jumbotrons, while others spread the word by participating in game day television and radio broadcasts..

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Fall Issue of Vision Magazine is Now Available

Vision Magazine

>> View Publication

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  • New ALS Clinical Trials
  • Certified Center Cost Study 
  • Message from Jane H. Gilbert
  • Tales of Hope, Strength, and Grace
  • Certified Center Program
  • VA Benefits for Surviving Spouses
  • Veteran Reveals his ALS Story
  • A Gift for Ginnie and Marian
  • Campaign Exceeds $50,000 Goal
  • Company Culture of Support
  • Extention of IRA Charitiable Rollover
  • Lasting Legacy of Marital Devotion
  • Community of Hope
  • Walk to Defeat ALS Growth

 

Advocacy & Public Policy

Honoring Military Veterans with ALS

Veterans Day is Monday, November 11, and The ALS Association once again is launching a letter-to-the-editor campaign to raise awareness of our cause and the impact ALS has on our military heroes.

VeteranWe encourage everyone to participate. Simply go to the Advocacy Action Center of our website, personalize the sample letter that is available and send it to your local papers directly from the website. It takes just a few minutes to send the letter, but it can raise awareness of ALS across the country and build support for our cause.

Wall of Honor:
In addition to the letter-to-the-editor, please visit the Wall of Honor, which can be found on our website. See the faces of veterans with ALS and read their stories of courage. If you know a veteran with ALS or a veteran who has been lost to ALS, help tell their story by sharing it on the Wall. And don’t forget to tell others and help us spread the word about this disease and its impact on our military heroes.

New National ALS Registry Website Unveiled

Each person battling ALS is a hero. Family, friends, and all those who observe the way ALS patients fight this disease witness their courage, resolve, and dignity. You can help by telling your loved one about the National ALS Registry. Check out our brand new website dedicated to the National ALS Registry at http://registry.alsa.org. Learn from people with ALS themselves about why they enrolled in the National ALS Registry.

The National ALS Registry may be the single largest ALS research project ever created. It is designed to identify ALS cases from throughout the United States. The Registry is collecting critical information about the disease that may improve care for people with ALS and help us learn what causes the disease, how it can be treated and even prevented.

Learn more about the National ALS Registry today, and find out how this research can help, including by informing people living with ALS about new and ongoing clinical trials. Visit http://registry.alsa.org for more info.

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Research updates

Antisense for the Most Common ALS Gene
Appears Safe in Initial Study

In work supported by The ALS Association and published in the Proceedings of the American Academy of Science, researchers showed that reducing the production of an ALS-causing gene mutation in mice is safe over the long term. This provides support for moving this therapy forward in people with ALS, whose disease is caused by mutations in this gene, called C9orf72. 

“These results are very encouraging for the field, as we develop new approaches to ALS therapy based on specific gene defects,” said Lucie Bruijn, Ph.D., Chief Scientist for The Association. Read full story.

Studies Highlight Findings Involving the C9orf72 Gene Mutation

Three studies supported by The ALS Association expand the understanding of the effects of the C9orf72 gene mutation, the most common genetic cause of ALS.

“These studies provide important new insights into this gene,” said Lucie Bruijn, Ph.D., Chief Scientist for The Association. “By learning more about the all consequences of the mutation, we can look for multiple therapies to address them.” Read full story.

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How You Can Help

IRA Charitable Rollover Extended for 2013

There is now an additional way to make a tax-efficient gift to The ALS Association: an Individual Retirement Account (IRA) Charitable Rollover. Extended as part of the American Taxpayer Relief Act of 2012 (section 208), the IRA Charitable Rollover allows individuals age 70½ and older to make direct transfers totaling up to $100,000 per year to 501(c)(3) charities, such as The ALS Association, without counting the transfers as income for federal income tax purposes.

How you or a family member can make an IRA Rollover Gift to The ALS Association:

  • Contact the custodian of your IRA and request that a gift be made from your IRA before December 31, 2013

  • Distributions must be made from a traditional Individual Retirement Account or Roth IRA

  • Distributions must be made payable directly from the IRA custodian to The ALS Association You are not required to count the amount of the gift as income for federal income tax purposes. 

Thank you for considering the IRA Charitable Rollover as part of your giving to The ALS Association. Please feel free to contact us if you have any questions.

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Vision Express is a companion to The ALS Association's national publication, Vision Magazine.

The ALS Association
1275 K Street NW - Suite 250 - Washington, DC 20005
Phone (202) 407-8580     www.alsa.org
 

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