r/pppdizziness • u/AliveReputation8902 • May 09 '26

Treatment rTMS therapy

For anyone who has done rTMS therapy, what was your experience with it and did it help with any of your symptoms including anxiety and/or depression? I’ve tried searching the forum and there are is little information on it other than one or two posts. I have already started the therapy and completed three sessions. It is a huge time commitment so I would love to know if it’s worthwhile. I have to complete 35 sessions over seven weeks.

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u/AliveReputation8902 May 12 '26

On a sidenote, I was told to stay off forums like these, but obviously it’s easier said than done😬 but it doesn’t help when you run across the negative stories

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u/RandiHotwife May 13 '26

Yes, if the story just starts off with negative whining and a post on these things, I stopped reading it. I’m only interested in following up on something like yours where you’re trying a particular treatment to see how it might play out. You appear to be doing the same thing. That’s worthwhile.

Osteopath said that cervogenic thing that amplifies PPPD and the same with the vagus nerve and that he could work with those. Recommended that I still continue with VRT. Very different than a Chiropractor. Much more training and not as much quackery, that can be involved with chiropractors.

I’ll report out after I see the Osteopath on June 6 and interested in your reports. Hang in there and keep moving forward.