Transcranial Magnetic Stimulation Therapy: What's your experience?

Posted by clutch @clutch, Jun 3, 2020

Just started my Transcranial Magnetic Stimulation Therapy (TMS). Would like to hear from others who have had this experience. Thanks!

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@dfb

I used a low level TMS device at home for two months, I don't recommend it. If I did it again I would definitely seek professional support.

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@dfb, can you talk more about your at-home treatment? I didn't even know that was possible. Why don't you recommend it? Did you have bad side-effects? I know there are some very rare risks and it might be good to have a doctor around. Was it just not effective?

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@sopatient

@dfb, can you talk more about your at-home treatment? I didn't even know that was possible. Why don't you recommend it? Did you have bad side-effects? I know there are some very rare risks and it might be good to have a doctor around. Was it just not effective?

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I believe the device was made by Fischer Wallace. I have discarded it, so I can not be sure. I'm not sure it is on the market anymore. It was a fairly simple affair: two padded electrodes held in place by a headband and attached to a battery-operated controller.

I used it daily for forty-five days; the recommended minimum was thirty days. I did not experience anything, good or bad.

That's it.

I hope you find the peace and good health you deserve.

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@delia74

Reply to @clutch
Thank you for sharing your experience.
I've suffered from major depressive disorder and anxiety almost my entire life, and at 75 find myself resigned. Tried several antidepressants, all which had horrid effects that I just did not want to deal with: night terrors, hallucinations and visual disturbances. For example: not fun seeing huge black spider crawling up the wall, across the ceiling and drop down right in front of my face!); seeing what seemed like millions of tiny, multi-legged black insects crawling all over me and my covers; seeing an opening in the wall above my bed and little people poke their heads out. Night terrors: whooshing sounds by my ears followed by floating "presence" in my bedroom wanting to harm me; feeling my bed move as something/someone pressed down on the mattress. And one medication in particular made my brain feel like it was about to implode, along with deep sensitive of impending death, followed by one of my worst migraine episodes. No way I wanted any of that!
So I asked a medical professional to devise a plan so that I could stop taking the last antidepressant which I was on and was not working, Serzone (the generic for Zoloft). It was hell but over a period of almost 8 months, I was down to just a tincture. Had to have the tincture and be weaned off that because I was having heavy-head feeling and "air sounds" in my ears. Irritability and feeling out of sorts also. I was off that finally but still felt unwell for nearly a year afterwards (ruined my ability to focus and enjoy our younger daughter's wedding, something that I'm upset about to this day and it was nearly twelve years ago). So I take NOTHING. Life is definitely difficult, coupled with all the pain problems that I have, but I just cannot take any more chances with any antidepressants. Uh-uh!
So I was so excited when I learned about the TMS procedure! And my insurance would cover it in full! HOWEVER -- I was not eligible for the procedure because I have a history of brain lesions....

Now that I've read how it has not really helped via the postings here on this site, I'm glad that I did not undergo the treatment. I'll continue dealing with the devil that I know as opposed to what I may have to deal with resulting from any medication. . Presently doing therapy via zoom, and while it does help to have someone to talk to, I can't say that it's helping much.
I take one day at a time.
I wish you days with hope and joy.🌺

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Are MAOIs an option or have you already tried this class of ADs? They’re often turned to in cases of TRD. My success with them has been limited but hope springs eternal. I’m taking Marplan now after not getting any prolonged help from Nardil and Parnate. I had ECT years ago and I now regret it.

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Does TMS cause seizures? My neurologist refused to refer me because she said it would cause seizures.

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A clinic opened near me, but I don't believe it's run by a M.D.

Does that seem right?

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@patj605

Are MAOIs an option or have you already tried this class of ADs? They’re often turned to in cases of TRD. My success with them has been limited but hope springs eternal. I’m taking Marplan now after not getting any prolonged help from Nardil and Parnate. I had ECT years ago and I now regret it.

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All I can say as thank goodness SSRI’s came along. They have side effects but nothing like the previous generation of antidepressants.
Hopefully the next generation will be even more targeted to the areas of the brain that causes depression and anxiety. That appears to be the next hurdle and would eliminate so many side effects.
If anyone has found one without side effects let everyone know.
That will be the equivalent of restoring hair cells inside the ear for people like me with severe hearing loss. It is coming but not quickly enough.

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I had the treatment 2 yrs ago. Five days a week for a total of 36 sessions. Since then, until now, I have had one huge blow after another, going to court w/ my ex, losing my dog- the only thing I had and the one thing I loved more than anything, losing a job, estrangement from my daughter having to move to a place I don't like, to another job I can't stand. So, with all that's happened, I'm still standing. I had to go through all this on my own, with no support or help from anyone. I can say that I've made it through by using my own personal strength and relying only on myself. I can't say how much it helped because of all that's happened. I am considering going back for more. I have doubts about it helping a lot. It's no miracle worker. It's not a permanent fix either. I am in a bad place again with my depression. I think the only thing that would help me is a lobotomy or a lethal injection. So, after all my babbling, if you can commit to the time it would take to do the sessions and have the money to do so, it wouldn't hurt. But don't expect too much.

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I had no seizures or bad side affects from TMS.

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@alicecooper

I had the treatment 2 yrs ago. Five days a week for a total of 36 sessions. Since then, until now, I have had one huge blow after another, going to court w/ my ex, losing my dog- the only thing I had and the one thing I loved more than anything, losing a job, estrangement from my daughter having to move to a place I don't like, to another job I can't stand. So, with all that's happened, I'm still standing. I had to go through all this on my own, with no support or help from anyone. I can say that I've made it through by using my own personal strength and relying only on myself. I can't say how much it helped because of all that's happened. I am considering going back for more. I have doubts about it helping a lot. It's no miracle worker. It's not a permanent fix either. I am in a bad place again with my depression. I think the only thing that would help me is a lobotomy or a lethal injection. So, after all my babbling, if you can commit to the time it would take to do the sessions and have the money to do so, it wouldn't hurt. But don't expect too much.

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I liked your input, so similar to what I would say my response was to the treatment.
You know what I’m responding well to now tho? Like a significant decline in symptoms? Ketamine. I do the infusion therapy. It’s $$$, not covered by insurance. But if your circumstances improve and it’s possible, maybe consider it. Good luck to u. All the best ❤️.

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I completed 36 sessions late last year. Did not do anything for me with the depression or anxiety.

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