I know it's been a long time but since little Madeleine I've obviously had other things to talk about.
There have been some ups and downs over the last 8 months. I saw Dr. Tamagna on Thursday and here is the low down.
First a little education: The thyroid works off what is called a negative feed back loop. The pituitary gland in your brain does many things, one of which is produce a hormone called Thyroid Stimulating Hormone (TSH) and it does just that...stimulates your thyroid to produce two hormones T3 & T4. When more thyroid hormones are needed your pituitary produces more TSH and when you need less, it produces less. This system in my body is derailed because my immune system produces antibodies called Thyroid Stimulating Antibodies (TSA) which themselves stimulate my thyroid to make way too much T3 & T4. When you have Graves your body realizes this and stops producing TSH.
Usually, when you've been taking anti-thyroid medications for a few months the normal system starts working again and your pituitary starts producing TSH and is back to normal by 6 months. Here we are 14 months since beginning treatment and while the medication has finally gotten my T3 & T4 levels in the normal range - my TSH is at a big fat ZERO. This means the disease is still raging and shows no signs of stopping. Over the last couple of months my gland has actually gotten a little bit bigger and my right eye is measuring bigger, too. Despite my relative high dose of PTU. The Thyroid Eye Disease (TED) is a whole other animal for another day.
What does this mean? It means this all just plain sucks. We have switched to the other anti-thyroid medication called Methimazole, just as a shot in the dark to see if my body responds differently. Normally, PTU is considered safer for pregnancy and nursing but some recent studies show that Methimazole may be better for nursing and there is some question about long-term PTU use causing liver damage.
For the future she thinks I should have my thyroid surgically removed and I will just take thyroid replacement hormones for the rest of my life. Especially if I plan on having any more children. Not a decision I am ready to make as of yet, but we'll see. I left her office feeling a little down, in some weird way my always healthy body has let me down. I guess I just thought this would be treated, I would go into remission and it would fade into the background. But that is not the plan, apparently, so I will just roll with it for now. :)
10 comments:
Hang in there. Chronic health problems are scary and definitely have their ups and downs, but you guys will figure it out and find a new normal for your body!
What can I say except that I sure love you and Heather is right. It will work out, it's just a pain getting there!
I am so sorry....that does not sound like fun, but I'm glad they are trying everything they can!
That's a bummer. But being a member of the "neck smile" club with Pam and I isn't too bad.
So sorry to hear this news. I hope the new meds work out for you and you're able to manage it easily. What a bummer!
I'm sorry to hear that. I'm hoping the new meds work for ya. That way you don't have to think of surgery for a long time.
Okay, when we get catching up on the phone and I'm talking too much, you need to tell me to shut up and fill me in on what's happening with you. I love you and hope this new medication helps!
I am so sorry to hear that, I'm glad they are trying different things rather that just doing the surgery. Hopefully this will work, our prayers are with you good luck.
Lih-beh!!!! Oh my goodness, I'm so sorry to hear about what you're going through. But thanks for being willing to keep us all informed!! I will definitely keep you in my prayers. And I have to tell you how beautiful your daughters are. Little Madeleine is darling!! They are both getting so big! Good luck with everything. Love ya!
I feel your pain! I am not a huge fan of the thyroid! Even with half of mine out..it still sucks!! (Sorry for the angry outburst) Hope all works out:)
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