Monday, May 13, 2013

Journey to TMS - Part 3

If you've not read the previous posts on Journey to TMS...please start with the links below.

Part 1 ~ Journey to Transcranial Magentic Stimulation
Part 2 ~ Jourey to TMS ~ An Answer to A Prayer


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I can't promise I will blog/journal the entire process.  However, in the first week or two I will try.  With weekly updates as time goes on.  There are not very many blogs that discuss TMS Treatment/Therapy.

The following was wrote the evening after my first appointment and the day or so after.

Week One....Day One....or so I thought.
5/6/13
Today was the beginning of treatment.
Or so I thought.  It was my hope anyway.  Instead, I sat for almost 2 hours in the TMS chair while the psychiatrist and assistant attempted to find the motor threshold.
No luck.
They were unable to find the spot they needed.
I will return at the end of the week and see a different doctor from the sister-clinic.

My anxiety was high before the appt. today.  It is much higher now. I came home and spent the next two hours puking.  And the last 2 hours I've spent trying to stay present, not give in to the negative self talk and swirling associated with it.

TAKE 2....Week One...Day One...Retake.
5/10/13
Today was the beginning of treatment...repeat.
Dr. W came from another clinic about 1.5-2 hours away.  The psychiatrist that will be overseeing my treatment is local and new(er) to TMS.
Dr. W set up some parameters at the beginning.  Talked to me a little bit about a few options that he/we would have have if he was unable to locate the spot that was needed. It took a great deal of self talk to get me to this appointment.  My toleraence level was markedly less today than when I was there on Monday. After what seemed like hours they found the particular spot they were looking for...or...so they thought and on my way to getting this crap done and over with for the day.

After finding the proper placement they needed to find the proper dose or whatever it is called.I believe it is called MT-Motor Threshold. I can't remember right off hand.

And then they started the first treatment.  I had watched several different videos on what to expect, what  it feels like, and all that other jazz.  When Dr. W described what I may/may not feel he didn't give a very accurate description.  He told me "depending on how well you tolerate it...we may need to tweek the angle a little bit...if it hurts in your eye, teeth, or left side of your face let me know..."

SOB....he was so incredible way off.  I truly had no idea how horrific it would be.  I don't blog this to scare anyone off.  I'm brutally honest.  I wish that I had somewhat of a clue what to expect.  That first set took me off guard. To say it was awful would be an understatement.

Treatments are generally 37-40 minutes long or some damn thing like that.  However, the target dose is higher and requires the system to take a longer break.  Which means treatments will take about an hour and half.

There was much unraveling today.  I received half of the treatment today because of the length of time it took to find the motor threshold.  By the time I was done we were done today.... I was DONE....and I really was MORE than DONE!

It was comforting to have the technician be as understanding as she was.  My gut tells me she will be good to work with on a daily basis. Trusting her will be another story.  The Dr. and Technician from the sister clinic were super nice and sweet.  However, my tolerance for men providers isn't always the best.

It took quite awhile for me to pull myself back together so I could go to work.  I worked the rest of the day.  Stuffed the emotions and feelings associated with this.  The moment I am in my car and alone - the tears turn into sobs.

I'm angry.  VERY angry.
I hate that I have to do this.
I hate that this is my life.
I hate everything about this.


1 comment:

Adriana said...

I just found your blog and I just want to thank you for writing about TMS therapy... I work for a TMS center in Tysons Corner and I find there needs to be more information available. Like you mention on a previous post, there isn't much talk about it (besides all the medical studies) and feedback from patients is always helpful when trying to find the right treatment. I know you hear this enough... but keep being strong. You're a wonderful person and I really hope your next couple of treatment sessions are a bit more positive. Looking forward to your next post!