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#migraines

1 post1 participant0 posts today

I have to celebrate a small win for my sensory sensitive disabled self.

It’s taken me four years but I believe I have finally won the battle with Concord Hospital over the abusive level of the hold music the call center uses.

It would give me #PEM every time I had to call my doctor. And if I send a message through the portal it takes three days for them to get back to me so that’s not always practical.

They didn’t care when I complained that it hurt because of #MECFS, they didn’t care when I asked them how #autistic people who have more sensory issues than I do even call their doctor, they didn’t care when I told them that everyone on their staff in the clinical locations hates the call center as much as I do, but they did care when I accused them of trying to trigger #migraines so that they can admit me and bill #Medicare $25,000.

But you know what actually did it? I found out there was a civil rights division at Concord Hospital and I complained to them instead of patient relations. When I started talking about the rehabilitation act of 1974 (or 1973 idk) patient relations didn’t care, but the civil rights department did.

And I’m still dying to know who owns that call center because it’s the same call center used by NH #DHHS if you have to call the welfare office. So I suspect it’s someone related to Chris Sununu and they’re locked into some awful contract. The food stamp workers hate the call center too. I’ve been talking to people about this for four years.
I finally won. It’s been a good week for me here in New Hampshire.

Replied in thread

@dustcircle

My undiagnosed vitamin D deficiency caused me to have #migraines for years. If only I had known that taking a simple vitamin would have stopped them! It's amazing what can go wrong with our bodies without us realizing it. (For anyone else with migraines, it took me about three months of taking supplements before the migraines went away completely. Whenever I've left off the vitamins for a short while, they've come back.)

In my case, I'm very lactose-intolerant in an American cheese-loving and milk-loving culture, and I don't like dark green vegetables much, so I can guess why mine happened. I also have #PCOS, which would have added to it.

But I do think our society's tendency towards being indoors on computers or in front of TVs all the time is not helping with everyone's health.

Continued thread

So after I changed jobs I went on They weren’t bad at that time. I paid $50 a month and had a $15 copay- way lower than prev. I could see a specialist who worked magic on my migraines.
Today: UHC plan is way more expensive & they no longer covering everything. My dr has prescribed multiple medications that UHC has denied. The pharmacy works to find some workaround- they get my financials & see if I qualify. I survive no thanks to insurance companies

Some of my friends here know I have When I was w/ Kaiser they didn’t have neurologists to treat my migraines- they tried 3 different blood pressure medications & then it was 🤷🏼‍♀️ we don’t know what your going to do. No denial of coverage just - that’s it. So sad. Take pain relief meds.
Which I did.
And then one day when I was getting my sumatriptan refilled, I overheard the pharmacist yell over the counter, “another refill? My god. She can’t take this much of this medication.”
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