CFTC Recipient

Caring for Kara

We share this story of love between Dawn, Kara, her beloved son and the Kirby family in loving memory of Kara.

With a heavy heart, we share with you the story of Dawn and Kara.  In this story roles are reversed. A 2022 CFTC Recipient, Dawn cares for her daughter Kara who was diagnosed with a dementia called Frontotemporal Dementia (FTD) in Feb 2019 when she was only 29 years old. Kara was a mother, natural caregiver and a woman of faith. She was also a nurse who had worked on an Alzheimer’s unit.

After Kara gave birth to her first child, a son, Dawn observered Kara was more “going through the motions” than being a mother. Her daughter was becoming increasingly irrational and displaying misplaced emotions. Kara also began to have auditory hallucinations.

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This is a rare symptom of postpartum depression and so naturally, that is what doctors focused on. FTD was nowhere on their radar. But when Kara’s condition only worsened and nothing was working, her mother, Dawn, refused to give up.

For a year and a half, every day Dawn woke up thinking “today we’re going to figure out what’s wrong and get Kara better…and I’d go to bed every night defeated.” This led them to the Mayo Clinic. Mayo promptly ordered a full workup, including a neuro psych exam and the family finally had an answer.

“The Behavioral FTD (bvFTD) diagnosis came with both devastation and relief,” explained Dawn. The diagnosis was heartbreaking, but her mentality was summed up when she said to the doctor at Mayo Clinic, “we’re already living the nightmare, you just put a name to it.”

Kara moved back home with her parents, her young son with the father. Dawn and Tim devoted their life to caring for Kara. Her dedication for her daughter was clear not in grand gestures but in the everyday attentiveness. “Activities of daily living (ADLs)” is a term caregivers are too familiar with.

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It describes the fundamental skills required to independently care for oneself, (eating, bathing, and mobility). Kara’s ADL’s were declining at a rapid pace. By 2021, only two years into the disease, she was nonverbal, walking slowly, unable to initiate most tasks we take for granted, like getting dressed.

Dawn was by her side, constantly. Similar to how a nurse affectionately discusses her patience’s care, Dawn warmly told me about the discovery of sippy cups to help prevent her 31-year-old daughter from choking. This was their new normal.

Despite it all Dawn focused on loving and find new ways to connect with her daughter. Kara fell asleep every night holding her mother’s hand. Dawn also did a beautiful job of understanding that not every day was going to be perfect and the importance of letting things go. As she said in her interview with For Their Thoughts, “Pick your battles. No one dies from not showering.”

A simple yet real quote from former caregiver, Dawn

When asked how the CFTC Relief Grant will bring relief, Dawn replied, “I want my husband and I to go to my grandsons’ ball games and not have to worry about Kara. We always do things separately so one can stay with Kara. While I do not regret a single moment with my daughter, it would be such a blessing to hire help for a few hours a few times a month to be able to just be grandparents...and spend time with our grandkids.”

Such a simple yet beautiful request. If time with your grandchildren and a few hours of “normalcy” isn’t relief, I don't know what is!! Thank you for sharing your incredible mother/daughter love story. Your dedication to your family and your willingness to share so openly hits the hearts of everyone at For Their Thoughts.

Dementia impacts the entire family. Often it is the family who take on the caregiving responsibilities. They do it without hesitation or second thoughts.
"It's just what you do"
is so often said by care partners and families. But to care for your other half or parent as he or she declines also brings emotional, physical and financial stress. It is 24/7 and can be lonely.

FTTF exists to help these families. We piloted our "Care For the Caregiver's Relief Program" in 2021. The program provides financial relief for the "now" and a customized resource package for continued care. Resources are out there, but the caregiver often is left to figure it out on their own. FTTF aims to point the way and offer a helping hand.

Melissa was the first grant recipient of CFTC Relief Program thanks to proceeds from our Move For Their Thoughts (MoveFTT) challenge to walk a mile a day for 35 days. 

Here is Melissa's story.
Melissa and her family live in a small town in the heart of Kentucky. Several years ago her mother was diagnosed with Alzheimer's. In 2020, Melissa moved in with her full-time and is now her primary caregiver.

The roles have reversed and it is time for the daughter to care for the mother. It's the only way to provide her mother with the care she needs as the disease progressively worsens.

Because of the time and effort involved in caring for her mother, Melissa only leaves the house once every other week to run errands and grocery shop.

The love and commitment Melissa has for family has been exemplified in every conversation with her. In her own words, "Family is everything. I wouldn't have it any other way." 💙

Story Update

We share this story of love between Dawn, Kara, her beloved son and the Kirby family in loving memory of Kara. Kara’s FTD symptoms, including swallowing issues, continued to progress and on Jan 1st, 2023, she took her final breath and is now at peace. From everyone at For Their Thoughts, we extend our prayers for comfort to the family.