Jump to content

Search the Community

Showing results for tags 'TMS'.

  • Search By Tags

    Type tags separated by commas.
  • Search By Author

Content Type


Forums

  • Research - Actively Recruiting
    • Research Advertisements
  • Main Forums
    • PREPARATION FOR LIVESTREAMS
    • MAIN AND GENERAL FORUM
    • Introductions
    • Symptoms: Descriptions, Discussion, Debate
    • Medications & Other Treatments
  • Active and Future Research
    • Research Articles, Publications and Studies
  • Community Area
    • Community Open Space
    • Forum Information, Questions and Suggestions

Categories

There are no results to display.

There are no results to display.

Product Groups

There are no results to display.


Find results in...

Find results that contain...


Date Created

  • Start

    End


Last Updated

  • Start

    End


Filter by number of...

Joined

  • Start

    End


Group


AIM


MSN


Website URL


ICQ


Yahoo


Jabber


Skype


Location


Interests


Administration Role

Found 1 result

  1. So, I met with my psychiatrist today, full session because of recent and persistent suicidal thoughts/ideation/planning (not relevant to this discussion). He bumped my visits up from once monthly half-session visits to once weekly full session visits for the reason mentioned above. Anyways, because my depression is treatment resistant, or rather untreatable with medication (aside from bupropion, but he wants to hold off on that until I see a neurologist), he recommended that I either try ECT or transcranial magnetic stimulation (TMS) considering that both are highly effective at treating extreme depression for short periods of time (~6 months or so). He recommended TMS over ECT though because of the risks associated with ECT and subsequently referred me to a local psychiatrist specializing in treating depression, PTSD, and anxiety disorders with TMS. Has anyone had experience with TMS? If so, did it have any effect on HPPD, positive or negative? I know for depression they target the limbic system and frontal cortex. I mainly just worried about it making HPPD worse, however unlikely that may be.
×
×
  • Create New...

Important Information

By using this site, you agree to our Terms of Use.