Contact

ALS Worldwide welcomes any questions or comments you might have.  We provide free, personalized and confidential support services to anyone in the ALS community—whether you are a patient or a loved one, friend, health care professional or caregiver of someone diagnosed.

Get help now! Fill out the Online Profile Form or if you would prefer to talk with someone by email or phone first, please contact Sarah Byer, Director of Outreach and Counseling at [email protected] or 1-608-630-0407.

For all other inquiries, please use the email form to the right and we will respond promptly to your request.Thank you.

ALS Worldwide
5808 Dawley Drive
Fitchburg, WI 53711‑7209

ALS Worldwide

Research + Trials

Virginia Commonwealth University's Laboratory

About Research + Trials

Research is at the heart of our mission. ALS Worldwide funds, facilitates and shares groundbreaking research that helps patients, families and others understand the disease’s causes, determine how to best slow its progression, and seek ways to cure ALS/MND. As challenging as it is, significant research is being devoted to symptom reduction, slowing disease progression and achieving greater stabilization while searching for a cure.

There are now as many as 100 genetic permutations known to affect ALS/MND and related diseases. Researchers, clinicians, scientists and neurologists remain totally committed.  In the past five years, research efforts have grown tenfold.  Being clear about what hasn’t succeeded is as important as identifying effective relief.  Breakthrough therapies, current human trials and future directions all offer hope. 

About Astrocytes

February 19, 2015

Introduction to MicroNeurotrophins

February 06, 2015

Why Scientists Believe MicroNeurotrophins Are So Promising

February 05, 2015

The ALS MicroNeurotrophin Research Consortium

February 05, 2015

How to Avoid Fraudulent Stem Cell Practitioners

January 28, 2015

How do I contribute to bring MicroNeurotrophins to a Phase 1 Clinical Safety Trial?

February 10, 2015