ALS Texas

Forever Grateful: A Farewell from Julia Dyer

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Julia Dyer has served patients at the ALS Association of Texas for the past 12 years. As she moves on to pursue new opportunities, we wanted to take this time to thank Julia for her service to people with ALS and their caregivers. She wrote this farewell letter to the ALS community that beautifully describes the impact of her time with ALS Texas. Thank you, Julia.

The ALS community is unlike any other. I’m sure many people say that about an organization or group of people they completely admire and love, but really.  Over the past 11 and a half years, I have learned some pretty valuable life lessons from people who were also learning as they went along. Not to mention, most would probably agree they had just received the worst news of their life. I witnessed families come together and rally harder than I’ve ever seen and show unwavering amounts of support and love.

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ALS Texas: 2015 by the Numbers

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At ALS Texas, we’re dedicated to serving people with ALS in any way we can. That includes running clinics, hosting support groups, providing grants, loaning equipment, funding research, educating people about ALS, and much more.

It’s only through the support of people like you that we’re able to do all this, and we want to thank you for helping make the past year a success. By almost any measure, 2015 was a banner year, with ALS Texas providing more services to more people—about 13% more, compared to 2014. Here’s a look at the numbers that help show what we were able to accomplish:

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What Would You Do with an Extra Day of Life?

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Today is February 29, or what’s more famously known as Leap Year Day. It’s basically our human attempt to even things out by piecing together scraps of time from the past into one additional day every four years. An extra 24 hours, how great is that! It’s even better than gaining an extra hour of sleep every November when Daylight Saving Time ends.

If you’ve never been impressed by the concept of Leap Year Day, perhaps now is the time to start viewing it as a bonus to be spent on doing something special. Some people write themselves letters (or have their children write letters to themselves) and read them in four years to see what’s changed. Others set aside the day to do a special project they have been putting off. Some of us plan to make a $29 donation to our favorite charity. Regardless of the act, the idea of doing something unique in honor of this extra day has merit.

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Calling All Texas Advocates for the 2016 National ALS Advocacy Day & Public Policy Conference

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National ALS Advocacy Day 2016
In 2015, The ALS Association of Texas took its largest contingency of advocates ever to Washington, DC to lobby congressional leaders to make ALS research and services to people living with ALS a priority. If you’ve never before participated in this important and powerful event, we are pleased to announce that registration for the 2016 National ALS Advocacy Day & Public Policy Conference is officially open!

Held this year from Sunday, May 8 through Tuesday, May 10, in Washington, DC, National Advocacy Day is a great opportunity to share your story with Washington, DC legislators as well as other advocates. Registration is open to everyone, so don’t let this opportunity to have your voice heard pass you by.

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ALS BrainStorm Stem Cell Clinical Trials Update

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JAMA Neurology has published a paper titled, “Safety and Clinical Effects of Mesenchymal Stem Cells Secreting Neurotrophic Factor Transplantation in Patients With Amyotrophic Lateral Sclerosis – Results of Phase1/2 and 2a Clinical Trials.” This study comes out of a collaboration of researchers from BrainStorm Cell Therapeutics and the Hadassah-Hebrew University Medical Center both located in Israel.

The researchers set out to understand the safety and clinical effects of treatment with mesenchymal stem cells induced to secrete neurotrophic factors (MSC-NTF) in patients with ALS. Stem cells used in this study are adult mesenchymal stem cells derived from bone marrow samples given by participants in the trial. The bone marrow cells are turned into stem cells that secrete the NTFs. NTFs are a type of nutrient for cells and were previously shown to have protective effects in animal models of neurodegenerative disease.

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ALS Association Awards $1.3M to 9 New ALS Research Projects

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We are excited to announce funding for  nine new ALS research projects! The ALS Association awarded more than $1.3M to projects across the country, furthering investigation into the cause, treatments and cure for ALS.  Projects include research on the C9orf72 gene, which has been identified as the most common cause of familial ALS.  The research awards include ALS Association-Initiated Grants, Investigator-Initiated Biomarker Grants, and the Milton Safenowitz Postdoctoral Fellowships.

To learn more about these research grants and initiatives, visit alsa.org.

New ALS Film Tells Story of Dallas’ “Luckiest Man”

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A new documentary tells the true story of how ALS has changed one Texan’s life—for the better.

John Paine, known as a devoted father and hardworking businessman, was diagnosed with ALS 15 years ago. Though the disease has weakened him physically, in other ways he believes ALS has made him stronger. “The Luckiest Man” explores his journey and tells the inspiring story of how he has chosen to live life to its fullest.

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Why We Walk

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The Walk to Defeat ALS is an annual fundraiser with one goal in mind: help create a world without ALS. Since its inception 15 years ago, the Walk to Defeat ALS has raised over $215 million to help fund research and provide services and support to people affected by ALS.

But the walk isn’t only about raising money. It’s about showing support to family and friends. It’s a chance to come together as a community, standing up for a common cause. It’s a way to show how much you care.

We walk for many reasons; here are just a few examples.

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Why We Need the ALS Ice Bucket Challenge

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Trece Porrata - Why We Need the ALS Ice Bucket ChallengeGuest post by Trece Porrata, a patient with ALS

My husband was challenged to do the Ice Bucket Challenge last year when we were visiting friends in Port Aransas with our kids. As he was filling the bucket with ice, he jokingly asked me, “Wait, what am I doing this for?” I replied, “ALS, silly!” realizing that I didn’t actually know what it was.

Quickly, I went into the house to do some research about ALS. I ended up on the ALS Association of Texas website, reading through ALS symptoms. As I went down the list — muscle weakness, fine motor control issues — I noticed that I had been experiencing some of those same symptoms lately. But I didn’t think much of it at the time — after all, ALS is a man’s disease, right? And we had an Ice Bucket Challenge to complete. I went back outside to tell my husband what ALS was, and moments later I was laughing at his reaction to the freezing water, handing them towels and forgetting all about my symptoms.

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ALS: Worth Fighting

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Ernie Worth, Patient with ALSGuest post by Ernie Worth, a patient with ALS

My name is Ernie Worth. I am a 38-year-old husband, a father of three, and an ALS patient.

For months leading up to my diagnosis last fall, I had been experiencing speech difficulties. For me, this was very strange, as I have always enjoyed giving presentations, public speaking, and the like. It started out subtly, and gradually got worse as time went by. I was also rapidly losing weight, and since I have always been very physically fit and health-conscious, the physical change was quite obvious and disturbing.

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