Health
Related: About this forumAdults with Down syndrome face a health care system that often treats them as kids
It took Samantha Lesmeisters family four months to find a medical professional who could see that she was struggling with something more than her Down syndrome.
The young woman, known as Sammee, had become unusually sad and lethargic after falling in the shower and hitting her head. She lost her limited ability to speak, stopped laughing, and no longer wanted to leave the house.
General-practice doctors and a neurologist said such mental deterioration was typical for a person with Down syndrome entering adulthood, recalled her mother, Marilyn Lesmeister. They said nothing could be done.
The family didnt buy it.
Marilyn researched online and learned the University of Kansas Health System has a special medical clinic for adults with Down syndrome. Most other Down syndrome programs nationwide focus on children, even though many people with the condition now live into middle age and often develop health problems typically associated with seniors. And most of the clinics that focus on adults are in urban areas, making access difficult for many rural patients.
https://www.nbcnews.com/health/health-news/adults-syndrome-face-health-care-system-often-treats-kids-rcna79766
Also true for adults on ASD spectrum with speech disorders. I know, having experienced this personally with oldest son.
Diamond_Dog
(35,204 posts)Warpy
(113,131 posts)because facilities, when available, are generally small clinics with limited diagnostic possibilities.
In addition, the docs might have been older guys educated at a time when people with Down's typically died young and everybody tried to look sympathetic while they said appalling things like "it's better this way."
Good for Sammee's mom in getting her to a city and kudos to Sammee for working hard to get better. Sammee sounds like she's got a great life with the things I've found all adults with Down's want: to be useful and get praise for jobs well done.