June 21: The Longest Day

By Maggie Sanders

June 21 is the day with the most light, and that’s when the Alzheimer’s Association shines light on this sad disease that robs loved ones of memories and personality. But when you’re caring for someone with Alzheimer’s or another dementia, every day can seem to last more than 24 hours.

My mom, Vivian Benson Sanders, is living with one of the severe dementias associated with Alzheimer’s disease. At 15, she was offered a full scholarship to Rice University – located less than two miles from her home – but her father refused his permission for her to attend. Now 94, she still painfully recalls how he stole her future. 

But she doesn’t recognize me, my brothers or our children. Nor does she recall that my father passed six years ago and that our middle brother died two years before. She can’t remember how to walk and struggles with all activities of daily living. This scary smart lady who treasured words like precious jewels is losing her grasp of language, and our conversations are becoming a hodgepodge of unrelated and often unintelligible words and phrases.

When it became obvious four years ago that Mama could no longer live independently, our family decided to move her from Bryan, where my brother Ray had been looking after her, to Waco. At that point, I became her primary caregiver and began juggling work, my own family and other interests with meeting her needs. These have increased over the years, so two years ago I retired from the part-time teaching job I loved to be more available.

Fortunately, my mom is in a good memory care facility, but I still spend a lot of time and energy with her.  She’s among the nearly 400,000 Texas adults over 65 who have Alzheimer’s disease or other forms of dementia. And I am just one of the approximately 1.5 million family members and friends caring for a loved one in the same situation.

The care takes its toll on our bodies, minds and spirits — and drains family finances. In Texas last year, caregivers provided approximately 1.6 billion hours of unpaid care with a total value of $20.5 billion. We deal with stress, lack of sleep and lack of support. We are reminded to take care of ourselves, but that doesn’t always seem possible.

My caregiver’s journey has been eased thanks to the local Alzheimer’s Association chapter. Even before I moved my mom to Waco, I had helped with the annual Walk to End Alzheimer’s, and that helped me tap into some of the resources the group offers. I’ve since attended several support groups and the annual caregivers conference.  I continue to work with the walk committee and try to volunteer with other projects as needed.

Locally, the Waco Chapter of the Alzheimer’s Association provides a range of caregiver support groups where family members can meet others sharing similar situations.

  • Heart of Waco Caregiver Support Group, 6-7 p.m., Second Monday of each month at Heartis Waco Assisted Living and Memory Care. Contact Donna Ginsel at 254-717-4805 or Bobby Don Saylor at 940-595-9355.
  • Hillcrest Senior Health Center, 10-30-11:30 a.m., Second Wednesday of each month at the Hillcrest Senior Health Center. Contact Renee Shepherd at 254-537-3731 or Laura Ellis at 254-202-6500 or Bobby Don Saylor (above).  
  • Early Stage Support Groups. Separate sessions allow Caregivers and Persons with Disease to meet separately for support, information and socialization. Prescreening is required. Contact Christine Schroeder-Moran of the Waco Alzheimer’s Chapter at 254-754-7722.
  • The Gathering Place provides social interaction and support for caregivers and their loved ones. The program meets from 10-11 a.m. the first Tuesday of each month at Austin Avenue Methodist Church.  Contact Sandi Snowden at 713-553-7061, Pam Butler at 254-755-2248 or Bobby Don Saylor (above).
  • The annual Caregivers Conference, always the first Friday in March, is an excellent opportunity to hear about the latest research and to gather tools you can use in your own journey.
  • This year’s Waco Walk to End Alzheimer’s will be Saturday, October 5, at Brazos Park East.

To learn more about these resources or to ask questions, contact the Waco Chapter Alzheimer’s Association at 254-753-7722 or  alz.org/northcentraltexas


Maggie Sanders, left, with her mom, Vivian Benson Sanders




Maggie Sanders is a freelance artist and writer. She retired from McLennan Community College, where she worked in the public information office and taught marketing.

The Act Locally Waco blog publishes posts with a connection to these aspirations for Waco. If you are interested in writing for the Act Locally Waco Blog, please email ashleyt@actlocallywaco.org for more information.

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7 Comments

  1. Beka on June 6, 2019 at 7:08 am

    I see your struggle. <3

  2. Anne Sprain on June 6, 2019 at 7:34 am

    You are a helpful artist.

  3. lisa on June 6, 2019 at 10:04 am

    That was an awesome article Maggie. She is so lucky to have you with her everyday to make sure all of her needs are provided. I know it takes a special person to be a caregiver. Not everyone is cut out to be one. Thanks for all of the info provided also. You are a special person!!!

    • Rhonda Sanders on June 7, 2019 at 1:57 pm

      I’m so thankful you have been there to care for our precious lady!
      I cannot imagine having a better mom in love!
      Thank you for all your hard work!
      🥰

  4. Jenn Warren on June 7, 2019 at 3:54 am

    As always, You Rock Maggie!
    If I can ever help you, PLEASE ask. You gave me the best interview I had the pleasure of writing about your life as a public relations specialist & I drew on your experiences as I did the job at both the Waco Hippodrome & The Art Center of Waco. HUGS.

  5. Sondra on June 9, 2019 at 8:55 am

    Thank you Maggie!!! By sharing your struggles i know you are helping many like you that have trouble expressing their experiences!! It is somewhat like grieving before the real loss… being a caregiver is so difficult.. God bless them all!!!!

  6. Ray Sanders on June 12, 2019 at 11:55 am

    Maggie, you have provided us with very helpful and heartfelt information, especially more important because even with your “almost impossible to do anything about it” situation, but you give of yourself to try to make life better for her and others with this horrific affliction and for the many that are providing loving, caring attention to those who may not even know who they are or how much they give and care. You are a beautiful example for us to try to follow.

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