ALS Texas

Another Winning Hand in the Fight Against ALS

by Leave a Comment

On Saturday, January 20, more than 250 people attended the 14th Annual All in for ALS Poker Tournament. The event raised over $185,000 for the fight against ALS and to help fulfill our mission of finding treatments and a cure while serving, advocating for, and empowering people affected by ALS to live their lives to the fullest.

All in for ALS began in 2004 in honor of Stu Nichols. Stu and his son Andrew had a mission to visit every ballpark in the U.S. throughout Andrew’s childhood. Amidst their journey, Stu was diagnosed with ALS. After his diagnosis, he was still committed to visiting the remaining ballparks, but he also wanted to find a way to fund research for a cure for ALS. Andrew had been playing online poker at the time and was interested in playing in the World Series of Poker tournament. They decided to start a poker event that would benefit people living with ALS.

[Read more…]

Houston Marathon Participants Run for a Reason: To Fight ALS

by 4 Comments

On Sunday, January 14, 35 runners participated in the Chevron Houston Marathon Run for a Reason Program in support of the ALS Association of Texas. The Run for a Reason program “connects the philanthropic community to passionate race participants willing to fundraise and raise awareness for meaningful causes,” according to the Marathon website. This is the eighth year that the ALS Association of Texas has been chosen as an official Charity of Choice.

[Read more…]

Your Support Makes a Real Impact

by Leave a Comment

Our vision at ALS Texas is simple: to create a world without ALS. Everything we do – the services we provide, clinics we support, research we fund, and laws and policies we advocate for – is done to help search for effective treatments and find a cure for ALS.

None of this is possible without your support. Would you support our mission by giving a tax-deductible, year-end donation today?

Donate Now

ALS Texas Mission Impact from ALS Association of Texas on Vimeo.

[Read more…]

ALS Texas: 2017 By the Numbers

by Leave a Comment

At ALS Texas, we’re committed to providing quality services to people with ALS. From multidisciplinary clinics to support groups, financial assistance, loaning medical equipment free of charge, and research investment, we’re dedicated to helping patients live their lives to the fullest.

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. View the graphic below to see the impact of your donations in 2017.

[Read more…]

Letter from the Executive Director: Year in Review

by 1 Comment

Executive Director Tanner Hockensmith and his family

Texas is big, really big. Our friends at Texas Humor stated that “if you drive long enough through Texas, you still might not get all the way through it.” As Texans, we pride ourselves on the sheer size of our great state.

However, its sprawling cities, growing suburbs, and vast rural areas pose a real challenge when we think about access. At ALS Texas, we believe that everyone living with ALS deserves to have access to top-notch clinical care, programs and resources that increase quality of life, clinical research studies, and an ALS community advocating for change.

[Read more…]

Support Plays Important Role in Living with ALS

by Leave a Comment

By Ben Stephens

Ben and his family

Like most people with ALS, I’d noticed some changes long before the diagnosis came. In August 2013, I began having difficulty buttoning my shirt. After seeing three different neurologists, receiving an incorrect diagnosis of multifocal motor neuropathy, and a series of tests like a spinal tap and MRI, I finally received a diagnosis of ALS in December 2014.

ALS has forced a lot of changes on my life. As an estate planning and probate attorney, I have a number of clients who rely on me. After my diagnosis, I hired an associate, which allows me to continue to work while living with the realities of ALS. I quit driving about two years ago, and I’ve learned to work remotely. I had to sell my house because of the stairs, and my family and I moved to a duplex. ALS has affected almost every area of my life.

[Read more…]

A Letter from the Board President: Multidisciplinary Clinic Access Expands in Texas

by 1 Comment

When my father was diagnosed with ALS in November 2011, he and my mother began attending an ALS multidisciplinary clinic. He had been sick for three to four years and had seen doctor after doctor trying to get a diagnosis.  When he started attending clinic, the ease of a one-stop place for patients to see all the disciplines necessary to treat ALS gave my parents both relief and empowerment.

Aside from the relief of constant travel to numerous doctor’s appointments, multidisciplinary clinics help provide a better quality of life for a patient and caregiver.  From bonding with another patient or caregiver in the lobby over a shared experience to the ability to learn about new developments in treatments and research, the benefits are endless.

[Read more…]

Vote for ALS Texas to Win $25,000 from the Chevron Houston Marathon!

by Leave a Comment

Here’s a quick and easy way you can make a big difference and help ALS patients throughout the state of Texas!

Join the 2018 Chevron Houston Marathon Run for a Reason Charity Challenge! From Dec. 20 – 31, 2017 at 11:59 p.m. CT, you can vote for the ALS Association of Texas or make a donation. Three prizes will be awarded in the amount of $25,000 each in the following categories:

  • Charity Organization Who Receives the Greatest Number of Contest Votes During the Voting Period. Click here to vote now.
  • Most Money Raised by a Single Charity Organization During the Voting Period. Click here to donate.
  • Highest Number of Donations Made by Individual Donors During the Voting Period. Click here to donate.

Vote Now

Donate Now

[Read more…]

Austin Family Grateful for Outstanding Support on Their ALS Journey

by 1 Comment

By Jackie Barry

Jackie Barry lives with her husband Tom in Austin, Texas. She was diagnosed with ALS in 2016 and has been involved with the ALS Association since then. Read her story below.

In early 2015, I began having a speech problem, like a lisp, which seemed to get a little worse when I was stressed or tired. We were in the midst of getting home repairs done, so I thought it would just go away if I ignored it.

In August that year, I saw the doctor about it, and he suspected it could be a stroke or a brain tumor, among other things. I had an MRI, MRA and a carotid sonogram done, which all came back normal. Shortly after that, I was referred to a neurologist, who sent me for a swallow test, after which he believed it was a neuromuscular problem. He then referred me to Dr. Carlayne Jackson at UT Health in San Antonio. Dr. Jackson diagnosed me with ALS in February 2016.

[Read more…]

San Antonio Family Learns to Live with ALS

by 1 Comment

By Guillermo Garcia

Guillermo and his family

My name is Guillermo Garcia. I am from San Antonio, Texas, and I was diagnosed with ALS in November 2015. It was ironic, because in August of 2014 we saw the Ice Bucket Challenge explode. Prior to that, we didn’t really have any knowledge of ALS and didn’t personally know anyone who had it. A group of us got involved in the challenge with my daughter’s softball team, and we started challenging everyone to do it. But we still didn’t really have a good idea of what it was.

In October of that year, my wife asked if I’d noticed that I had some twitching going on. I hadn’t until she pointed it out. We waited about a month to see if it would go away, but it didn’t. It just so happened that at the time, I was also having some issues with what we thought was carpal tunnel. I told my doctor about the twitching and was referred to a neurologist for some tests. I was diagnosed with ALS in November 2015, a year after initially noticing symptoms.

[Read more…]