Supporting FASD diagnosis and treatment in rural areas
Hi! I’m wondering if anyone has thoughts, strategies, ideas for how to support individuals seeking answers about possible FASD when there are no providers in the area (3+ hour radius and a year long waitlist) who can recognize the possible signs, let alone diagnose. I know there is no magic solution, but would love to hear if anyone has lived this or has ever thought “why can’t the [provider, agency, etc] do _________”.
For example, we have very few psychiatric prescribers in our area, and even fewer who work with youth. One agency developed a partnership with a provider in another area who fast-tracked referrals coming from that agency.
No bad ideas!