Today I had a thyroid ultrasound. The ultrasound office is in the same building as my gyno so I popped by to book an appointment to review my uterine biopsy results.
The receptionist pulled my file to ensure the results were there - and they were and they were signed off by the doctor. She explained that when 'normal' test results come in, they get signed off by the doc and then filed - no specific appointment to discuss is required. So that tells me that the biopsy results were clean and there is nothing for me to worry about.
However, I am not planning on relying solely on that for comfort - I booked an appointment. I want to talk to him about those results. And hopefully report back to him on my other issue now that I have been on the thyroid meds for awhile. And have the opportunity to ask him why the hell he suggested the hormone IUD.
I guess now I'll just be hoping that I don't need to worry about the results of my thyroid ultrasound either....
I saw an oncologist last week (barely since I forgot the appointment and had to race in there almost after hours).... and he said that my last heart scan was good - and also that my mammogram results came back with nothing for me to worry about. So THAT'S good news. Especially since the radiation oncologist had warned me that after my breast reduction, they would probably freak out because everything had changed and call me in for tests etc.
My appointment isn't until November 9 - so I'll probably post to update you guys of the confirmed results then also. I wanted to leave enough time for my cycle to work its way around & have something to report back to the doc on.
Since all my physical ailments are an open book (or blog, I guess), I will report that the first couple of weeks on the thyroid meds had left me with terrible cramping & pooping problems. Excruciating pain daily and requiring an almost full-time hot water bottle for awhile there. But over the last few days that problem seems to have resolved itself. I am REALLY glad about that - because that is the worst pain ever. (that I've experienced).... well, I wasn't really very happy when I got cold in the hospital and started shivering just hours after surgery either - that was also very painful.....
But they say that labour & giving birth is the worst pain - obviously I'm no expert there - however, I'm guessing that severe 'poop cramps' are akin to labour pains. Especially since I had that wonderful experience of using that medication to open my cervix before the biopsy. And the insert on those pills said they were used for inducing labour. And the cramps I had then - and also resulting poop problems again - give me an idea of what labour must feel like. Maybe not full knowledge - but an inkling at least. Which, of course, makes me feel confident that I made the right choice not to have kids. HA HA.
You know, I have been having WAY too many conversations about poop the last couple of weeks. My poor friends. And nevermind my friends....while at chemo last week, I had to report all my issues to the nurse as they always ask if I've been having any problems. And since I walked into chemo with a hot water bottle on my stomach, I had to spill why. And of course, I then had to explain all those other gyno problems to explain the labour-inducing pills and resulting ongoing poop problems and that we're hoping the thyroid meds will solve everything etc. etc. etc. But this discussion was held in the 'pod' - which holds 2 - 3 chairs, which is open to the next pod holding 2 - 3 chairs - and all those chairs had asses in them. So after I gave the rundown, I felt I had to make a comment that the entire chemo room now knows all about my gynecelogical, poop & thyroid issues. What a treat for everyone. Then the lady across from me said 'I could write a BOOK on hypothyroidism'..... as if that was the problem I was most embarrassed about sharing..... ?!?
But then she also went on to say that I should just be thankful that I don't have Graves Disease which makes your eyes bulge out and point in different directions. UMMM - is that a weird thing to say in a chemo room? I think yes. So I said 'like Marty Feldman'? - I don't think she answered me - but of course I couldn't help but look at her eyes thinking she must have said it for a reason. And her eyes WERE a little bulgy - but nothing I would have noticed if she hadn't made the comment - and certainly they weren't pointing in different directions.
So I guess we obviously both had cancer since we were getting chemo, and we both have hypothyroidism since everyone heard everything I said and she could write a book about it (she actually said she was one of the rare cases that almost died and had lost some mental function.... hmmmmmmmmmm LOL) - and so she means thank goodness I don't have Graves Disease as well as the other two like she does.
Just like my own GP explaining hypothyroidism by saying 'put it this way, if I had to pick a disease, this would be the one I would pick'. To which I replied, 'yes, I wish I only had to worry about ONE disease. I would definitely pick that one too!!!!'
But now I can go around saying 'at least I don't have Graves Disease'. That's some comfort anyway.....
Never a dull moment!!!
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