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Her Story
Jaycee was born on January 20, 2022. She lived a quiet life and was very easy to care for. Around 9 months old, it became clear that she wasn't reaching her milestones.
Rigorous testing followed, including an MRI, genetic testing, (including the most advanced genome sequencing available).
Her Diagnoses
At this point, no one is quite sure what the root of Jaycee's unique situation is. She has many sub-diagnosis:
- Severe Hypotonia (low muscle tone)
- Global Development Delay
- Focal Epilepsy
- Hip Migration
- Functional Scoliosis
- Strabismus
- Pituitary Microadenomas
- and more keep getting added to the list
Her brain scan, DNA sequencing and all other tests tried have revealed nothing conclusive. The medical community is stumped!
She is undergoing further testing to see if they can pinpoint the source of Jaycee's unique condition.
Her Treatment
The Abrams family has a long road ahead. In the first 2.5 years post diagnosis they have had regular visits with specialists, occupational and physiotherapists, and equipment techs. Over 50 different specialists and therapists have been involved, and the team keeps growing.
In search of meaningful progress, Jaycee’s family found Dynamic Movement Intervention (DMI) — a therapy designed to stimulate brain-muscle connection. At Stable Connections in Winnipeg, Jaycee’s progress has been tangible:
- Pain relief from previously unexplained hip issues
- Improved sleep
- Core strength and self-bracing
- More vocalizations — a critical step toward communication
- Safer eating
- Improved vision
- Increased cognitive awareness and social engagement
Every week and every repetition counts — her brain is most receptive before the age of 6, and the window for major developmental gains is getting smaller.
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