Experiences with

Transcranial magnetic stimulation (TMS)

Has anyone tried TMS treatment for tinnitus?

Does anyone have experience with this ? FDA has approved TMS to treatmment MDD (Major Depressive Disorder)and the patient is drug resistant or has not found relief with anti depressant medications.

I was just wondering if anyone tried Transcranial Pulse Stimulation( TPS ) for FND symptoms? 3 years ago I tried Transcranial Magnetic Stimulation( TMS ). Actually it was Intermittent Theta Burst Stimulation( ITBS ), new version of TMS. No luck.

So i have been seeking other forms of treatment like transcranial magnetic stimulation. I have been so emotionally unstable Ive almost admitted myself twice this year. I am currently not working because of my condition, I cry daily on and off for most of the day.

Repetitive Transcranial Magnetic Stimulation (rTMS) has been shown to be effective in bipolar depression and has been proved to have neuroplastic effect. Present authors had reported clinical evidence of safe and effective use of a combination treatment protocol.

I'm looking into transcranial magnetic stimulation and wondering if anyone here has tried it and if you find it helps your depression or ADHD symptoms.

This past summer I did a full course of transcranial magnetic stimulation, something like 36 sessions. No benefit. I am now almost finished with a full treatment cycle of Spravato esketamine. No benefit. Hope is hard to find. No drive. Disordered eating. Medications that seem to to nothing.

Has anyone utilized this?

I have already tried TMS Transcranial Magnetic Stimulation with limited success and Spravato nasal inhaler of Ketamine without success. It took at least 6 or 7 treatments for me to notice any improvements. I was only able to get a total of 12 treatments because my practitioner went away.

Then I discovered a new therapy called TMS or Transcranial Magnetic Stimulation. I feel that this treatment, along with an aggressive B12 injection routine (hydro, 1000mcg twice a day) has brought be back from the brink.

I saw a new psychiatrist yesterday because my previous one was not a good match. this new one offered me to consider TMS (transcranial magnetic stimulation) and it is for people who have not responded well to any medications. has anyone tried that and does it work? what's your experience with it.

- Non-invasive brain stimulation techniques - Transcranial magnetic stimulation or transcranial direct current stimulation applied to parietal or premotor regions may help upregulate compensatory activity levels. Combining with rehab tasks may optimize effects.

Has anyone here tried TMS (transcranial magnetic stimulation) and, if so, did it improve your symptoms? Linker below are a few of the articles on TMS for PD:

In this forum, we will explore the potential benefits, experiences, and insights related to Transcranial Magnetic Stimulation (TMS) as an alternative approach to managing depression. Let's delve into this innovative therapy and share our thoughts, questions, and personal experiences.

Yet it’s been a mystery exactly how transcranial magnetic stimulation, as the treatment is known, changes the brain to dissipate depression. Now, research led by Stanford Medicine scientists has found that the treatment works by reversing the direction of abnormal brain signals.

I don't know if TMS helps with PD but it might: Long-term treatment with transcranial pulsed electromagnetic fields improves movement speed and elevates cerebrospinal erythropoietin in PD https://healthunlocked.com/cure-parkinsons/posts/149196804/long-term-treatment-with-transcranial-pulsed-electromagnetic-fields-improves-movement-speed-and-elevates-cerebrospinal-erythropoietin-in-pd

Hi, My psychiatrist has recommended Transcranial magnetic stimulation (TMS). Has anyone done this? Effective or no? Call me old fashioned but weirded out on magnets to the brain. Still open if it’s helpful but would love to hear pros/cons from others?

Has anyone found an implanted spinal cord stimulator helpful for failed back surgery?

If you develop CIPN during chemotherapy, and it becomes permanent, can you subsequently find it has progressed to another site some years after the original diagnosis? I finished 6 cycles of Docetaxel in October 2019. Once the stabbing pains and feeling of being electrocuted had worn off, I was left

for sleeping through the night I take two 25 mg quetiapine and three 36.5/145 rytary. For anxiety I take one .25 mg clonazapam 3x a day. I have been on this regimen for quite a few years now, and it has been very helpful. The quetiapam /rytary helps me fall asleep and get back to sleep if I wake