[Anonymous]

#1166088

Yo Yo is right on the money. Doctors gave me little mind exersizes to help cope.

[Anonymous]

#1057477

As you start to feel better on anti-thyroid meds, is this a two steps
forward, one step back situation? I mean, do you have periods of feeling
well (or just better in varying degrees), punctuated by occasional slips
back to symptoms (but never as far back)? That seems to be what is
happening with me. The periods of feeling better get longer and the
bad days come less frequently or severely. I’m wondering if this
is just the way of it…and eventually will there be a continuous stretch
of feeling better that knows no relapse?

Even though the periods of okay (and a better type of OK each time) are
longer, it seems that the slight relapse are more aggravating because
they are so disheartening when in direct contrast to the wellness. This
probably doesn’t make much sense…so, could anyone share their experience
with how they felt with treatment on PTU, such as did you just FEEL better in
10 – 14 weeks, or did you yo-yo? Thanks. Glynis

[Anonymous]

#1166089

I was on different dosages of PTU for about a year before I opted for
RAI–I had already spent one miserable year before I was diagnosed-they
thought it was post-partum stuff–my girlfriend actually diagnosed
it NOT the doctor!!! I also had had two babies in 13 months,
was 38 years old, and worked full
time as an academic counselor at a university–talk about stress.
The PTU year was a
roller-coaster of emotions with lots of back-slides-I finally quit my
job, decided on RAI–I just couldn’t take the uncertainty of each new
problem with Graves-even after RAI it took about a year to get the
synthroid levels right BUT I did feel better, gained weight, my hair
grew back (curlier even!!) and I was much less depressed. I would
never try to convince anyone of any course of action but I can just
give you a little bit of my experience. Hope it helps. Denny

[Anonymous]

#1166090

Dear Glynis and all,

I have the same Q about what to expect with PTU. I have been on PTU for 3 weeks, at which time the endo halfed the dosage, and now another about 3 weeks at the lowered dose, and there has been an almost immediate improvement, heart rate down to about 84 the first step, and down to 74-80 now. My energy has been consistently good, and I find myself waiting for the other shoe to drop so to speak. Maybe it won’t. Maybe this is it, and this is right. I still sometimes have a little thigh muscle weakness, but now it comes after cleaning the attic all day, instead of after squating to get a carrot out of the fridge! I continue to meditate 2 times a day as first recommended by Dr Stoll, and thank you for the Bible verses. I also am continuing all the other treatments. Anyone with PTU answers…do you take it just until your symptoms subside and your blood work is normal, or do you take it for a set amount of months? Will I get to a point where my heart is too slow and I am too cold? Dumb question, sorry. Not getting enough sleep tonite. Happy New Year to all, especially Glynis, Pam, Kathleen, Trish, Donna(s), DianeN, Jake, Bruce, Denny, Jessica, Linda, and everyone who has taught me this past several months and all who I’ve forgotton to mention, and all who have put up with my too long posts. Karen B

[Anonymous]

#1166091

Hi Karen,

Your doctor sounds a whole lot more intelligent than mine. I was barely
hyper, IMO, which of course doesn’t count for anything. After 3 weeks of
Tapazole (not PTU) I felt better. Then, I started feeling worse and
worse. I called doctor who said Tapazole doesn’t cause such problems
like nearly wrecking car and becoming very suicidal. My blood work after
taking it indicates T3 and T4 levels are fine, although TSH is suppressed.
The insanity leaves within one to two days of not taking medicine. Also,
Tapazole now is like a diet pill. I eat almost nothing after taking it.
The good doc said that Tapazole still doesn’t cause any of these problems
and it’s something in my environment. Why do I feel normal when I stop
for a day or two if it’s not Tapazole?

Note, my pulse wasn’t real fast when I went on Tapazole–only in the 80’s.
Since taking it, it dips down in the 60’s when I’m not smoking. Back when
I was hyper a couple of years ago, I had a high pulse of 120+bpm, constant
heat and hunger.

I don’t like how the doctor calls me a liar and says I’m wrong when I know
better, but I can’t afford to throw away a bunch of money trying to find
the right doctor.

Linda

[Author]

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