[tempus vernum]

Just an update on exactly what FSM is because after 8 treatments I understand a bit better. I've said elsewhere on the boards it's helping

There are several machines set up and they program them
Specifically. Because I've been hit so many times I get programs
Targeting every area of my brain and "emotional balance." I've not had time to sit through 4 hr ptsd treatment yet.

They Hook two machines up to two gloves w wires, wrap the gloves in moist wet towels. One towel is put on my neck and one on my chest. Some times I tingle, crackle and have recurrence of symptoms during treatments, sometimes i buzz for days afterwards.

I got an hour today and finished 4 hours ago and I'm still tingling.

My insurance is covering my treatments at 90% so far BUT if they stop I will continue. I'm hopeful my treatments will slow down as of January when our deductible resets.

My med needs are dropping rapidly and I'm
Finding that I "feel like myself." I am however very feeble and exhaust quickly.

I saw the doc today w dd2 (her check up not
Mine) and he assured Me fatigue is to be expected after two years of being chronically ill. It's extra important to rest and take my time especially as this causes inflammation to be reduced and flushed away and that alone can be exhausting.

It's helping so much I'm actually considering canceling My appointment w the neuropsych its Sept 11. The neuropsych is going to cost us ALOT of money and time. I'm willing to spend both of those but I'm improving so much and my treatments take hours. I'm attempting to spend 4-8 hrs getting treatments every week and it's exhausting