Neurodivergence

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All things neurodivergent and relating to the broader neurodivergent community (and communities).

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Venting about medication shortages (beehaw.org)

submitted 1 year ago* (last edited 1 year ago) by Kuroneko@beehaw.org to c/neurodivergence@beehaw.org

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Thanks to the DEA’s massive overreach, for the third time in 5 or so months I’ve had to call a pharmacy outside my area to get my Concerta. My regular pharmacy gave me what they had, which I’m grateful for, but that left me short 7 pills. I then had to:

-Find a pharmacy that had the medicine I needed in the proper dose

-Call my doctor to have him send a new prescription over to that pharmacy since you’re not allowed to just show them your current one

-Drive about 15-20 minutes to get there

-Wait in line, give them my driver’s license (which I don’t have to do at my normal pharmacy) and sign a bunch of shit before finally leaving with it.

I’m just tired of this song and dance. Concerta works best for me though and isn’t too expensive with a coupon. I just want the DEA to stop micromanaging ADHD meds. I understand some oversight is needed but they go way overboard. Feel free to vent your frustration here as well.

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[–] shmushroomsh@beehaw.org 3 points 1 year ago

It's now been over three weeks since my son or I have been able to get our medication. I JUST got back on after a years long hiatus because of this exact issue. My life was falling apart, at least internally. I finally bit the bullet and set all the appointments and went to them. It was taxing to say the least. I even started going to counseling, really trying to take care of my mental health. Then boom, no meds and I'm a disorganized mess again. My therapy has been fairly useless because I can't remember anything and I'm not making lists or keeping track of anything like I was on medication. It's been rough.