Our New Normal

Feb 08, 2021

If you’ve read the story of Libbi turning 60, you’ll know that our childhood was normal. Our lives have been normal. Honestly. We were likely raised much like everyone of you. We lived in a small community, we walked to the movies on Saturday afternoon, went to church on Sunday, we bickered over who got the one bathroom before school.

We never considered ourselves abnormal—— especially not because Libbi had a developmental disability. That WAS our normal and we knew nothing else and never thought to question it. She was a precious little girl with long black hair, adorable clothes, a sassy personality and always a great big smile.


Fast forward 40 years. Our parents were gone. Libbi lived independently in a pretty house in a safe neighborhood just as Mom had told her she could do. She enjoyed her life, her neighbors, her puppies, and our sisters days out. Then she became confused while dressing. Then she began to fall. Then she’d forget to eat.


A new normal.

Libbi seemed to breathe a sigh of relief when I tucked her in the first night in our home and so did I. The move had been Jerry’s idea and his words were very plain...I think it’s time we moved Libbi in with us. I’m quick to say, that moving in with family isn’t an answer for everyone, but it was right for us. We were empty nesters whose kids, and grandchildren live in the northeast. We had three extra bedrooms and a small guest house. I’m no longer working and had plenty of time to devote to Libbi.


I didn’t consider myself a caregiver —- that came later. Libbi’s easy to have around and we fell into her routine of breakfast at 9:00, lunch at 12:30, tea at 3:00 and a little glass of wine at 5:00. It’s important to note that wine at 4:55 won’t happen, although laying out the cheese tray and getting the glasses ready is fine. Despite all her confusion she still stuck to her regimented schedule. After supper, she always says “what do you think about a little something sweet?”


And so, three years ago we all fell into our new normal. A Little Something Sweet, indeed.


Alzheimer's creeps in slowly then rapidly grabs hold of entire families. She went from setting the table every night and tossing a salad to being “a little muddled”. Her sleep patterns took a crazy turn and her days and nights were confused . Her food likes and dislikes changed frequently. She grew slower, and more determined. Changes occurred quickly and in slow motion at the same time. Companions became caregivers and caregivers became Home Health providers. She continues to smile. While often Alzheimer’s disease brings on belligerence and anger, Libbi smiles....when she pets the puppy, when she sees the new baby, when she enjoys a bowl of fresh fruit, when she sits by the fire.


Our new normal is sometimes silly, sometimes sad. It is reciting nursery rhymes, it’s listening to Alexa playing oldies. It’s looking at photo albums. It’s sitting outside on a sunny day. And, sometimes, Libbi still smiles. That is her gift to me.

05 Jun, 2024
Nancy Kristen Miller – March 8, 1965 – November 29, 2019 At times, God sends angels in a different form. Ours was called Nancy. She came into this world weighing less than 2 pounds and we were told that she had Down’s Syndrome. At the time, Down’s Syndrome babies weren’t expected to live past their teenage years, if that long. Not only did Nancy survive being premature and spending her first month in the hospital, she also blessed our lives for 54 years. She was loveable and she was loved by all. Nancy had an infectious giggle. She thought things were funny that other people might not, like if someone fell, stumped their toes, sneezed, or had the hiccups, she would break out in giggles that would have the person in pain giggling through the pain. She also loved country music and not only knew every word to every country song, but knew every country artist, where they were from, who they were married to, how many children they had, and the names of each of those children. She spent hours in her room listening to her music, singing along, and because she had more rhythm than anyone I know, she danced to each song. We were often the audience for the performances that she planned to take on the road. She always considered herself a star and in a way she was. She was our shining star! There was also a bit of a mischievous side to Nancy. For instance, we would sit for hours sorting out her hundreds of CDs and putting them in CD cases so that they wouldn’t get scratched. A few hours would pass and when we would go back into her room, every single CD would be out of the case and scattered around her room. This too she found to be very funny. She found great joy in having us look for a particular CD for hours. When we would give up on the search, she would pull the CD from the place where she had hidden it and giggle. Nancy enjoyed the TV series, Dallas. After its final season, she continued to watch it on CDs. Thank goodness we could buy each season on CD. As one season wore out, we would have to replace it. She loved the whole Ewing family, especially J.R. It was very upsetting to her that anyone would have the audacity to kill J.R. Until the next season came out, we were all questioned about who killed J.R... Needless to say, she was one happy girl when J.R. survived.  Where some may consider having a child with special needs a sentence, our family considered Nancy a Blessing. She brought boundless love and joy to our lives, and we miss her every single day!
16 Mar, 2021
Shreveport - Elizabeth "Libbi" Anne Thomas was born on November 4, 1960, and returned to Heaven on Thursday, March 11, 2021. A Memorial Service was held at First Baptist Church in Shreveport at 2:00 p.m. on Saturday, March 13, 2021. Officiating the service was Dr. Jeff Raines. The family requested that social distancing protocols be observed.
03 Mar, 2021
Though I made many requests for one, my parents refused to get me a baby sister like I wanted. What I wouldn’t realize until much later was that I always had one. My aunt Libbi and I grew up together. Though she was born sixty (!!) years ago with Down Syndrome, she was always the sister I never had. We vacationed together, played together and of course, sometimes fought...as sisters do. While we never looked at Libbi as having a disability, she certainly had some limitations but always seemed to have a dream life in spite of them. Worldwide travel, famous friends, the daily glass of wine at exactly 5:01pm as soon as her “stories” were over-the list goes on and on. In the past few years, however, those limitations have grown more severe with her diagnosis of Alzheimer’s disease.
17 Feb, 2021
Emery Catherine This is how a young friend described her little Emi-Cate and that made me smile. It was also a reminder of an encounter I had with a young man who was shopping with his parents during the holiday season. Even with his mask on I recognized his gait, his small round stature, and his eyes. Oh, those eyes sparkled with a splash of mischief and a twinkle of love.
11 Feb, 2021
Libbi was admitted into Hospice recently. Home Health was no longer meeting her needs. She remains alert, happy, has a good appetite and a hearty laugh which brings us all joy, but she is very frail. When she’s frustrated she’s quick to threaten me “you just wait til Patti gets home”. Early last week we were snuggled down watching our Hallmark Channel and she randomly said, “ I’m not your Mother, you know!”
09 Feb, 2021
Photo by Aaron Burden
04 Nov, 2020
As we celebrate Libbi this year, we realize what a true celebration we will have in watching my sister Libbi turn 60. We’ll celebrate her life, our family and all the people whose paths have intersected with hers and made Libbi Thomas who she is. My family has celebrated every milestone in Libbi’s life in a big way. There is a thought, ever tucked away since her birth, that her length of her time here is uncertain. We celebrated 40 big. We celebrated 50 big. And now 60! It is beautifully uncharted territory.
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