Graves disease

Do your reading and come up with some good succinct questions for the doctor. Please keep us posted with your decision and situation.

It's been so long, I don't remember really how long it was when I noticed things improving - although I do remember it was 2 years until I needed thyroid medication.

As I posted earlier, I did gain 15-20 lbs. during the hyperthyroidism. Well, the hyperthyroidism can be gradual over many years but I think the weight gain was probably over a period of 2 years. I do recall though, after the RA iodine treatment, I did not gain any more and I lost it.

But bodies are different. I only had 20 lbs to lose. I do understand your fear, as I would have it too.

You have an autoimmune disease, so be on the lookout for other things, like pernicious anemia, which I developed about 16 years later. But you probably know this already.

No I didn't know that already. Thanks for letting me know.

Yeah, ok I know, like you need another thing to consider...

They can fix this too though! Easy. I need it mainlined. Monthly B-12 injections. Some people can take pills.

But to the present. As I said, please keep us posted. I am interested in how this turns out for you. This must be so frustrating for you.

Quote:

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Originally Posted by DDH

I picked it up this morning, and after reading through all the information, reluctantly took it. I am a terrible pill taker, have a hard time swallowing them, and remembering to take them. But I'd rather try this route than have surgery or do the RI treatment. I may change my mind later. I've decided I'm going to do some research and write out my list of questions for the next time I go see her. (the doctor)and sat down for a bit before I left.

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Donna, I can't make any suggestions on the swallowing part, but I too struggle with remembering to take meds on schedule. I have a new helper, though. Well, it's not really new, but it's fairly recently that I've realized it was here to take advantage of.

It's my cell phone - the alarm feature! I'm doing a uch better job of remembering since I set y phone to "holler at me" every day!

Karen in Boise

Donna, I can certainly understand your anticipated frustration with dialing in medication dosages. It seems to be a hallmark of endocrine disorders and one that I've been round and round with regarding insulin dosages. But it's always worth it in the end when I do get things nailed down and feel better.

Do you have a good endo who's being supportive in all of this? I seem to recall from your earlier posts that you weren't thrilled with her.....maybe it's time for a new one?

Hang in there!! *hugs*

Thanks girls. I'm actually doing a good job remembering to take my meds this time.
I have lots of research to do still and I need to get more organized about it, and start taking notes. So far I have just been reading.
As far as my doctor, she is a Endo doctor that I am just now seeing, hadn't seen her before. The one I was frustrated with was GP doctor, he always seemed to blow me off thinking I was fine. I have been telling him for a year, that my heart rate was so high and I was worried something was wrong with my heart, then I talked to him about my ankles swelling so bad and he gave me a water pill, but did nothing to see why this started happening to me, then I complained about the heat, and thought I was menaupausal but he said as long as I was having regular periods I was not yet going through menapause. So, I kept walking away with no answers. Problem is I'm on an HMO and I have to have him refer me before I can see anyone else. I have often said I need to change from him, I've seen him since I was 19 or 20 and I think he has gotten complacent with me. I dont' know, but I guess he didn't think about my graves disease coming back anymore than me, since I am sooo heavy and weight loss is a normal sign. Problem is, he did nothing to try to find out why I was so miserable. I never even said anything to him about my moods. LOL

Okay, now I have a question, I can't see the doctor again until after I have been on this medicine for a couple weeks and then she is going to check my levels again. Anyway, she told me not to get my heart rate up, but I can't do anything without getting my heart rate up.
Can anyone tell me why they wouldn't want you to exercise and get your heart rate up to an areobic level just because of this. I would think exercise would be fine, and that since I have had this going on for a year now, and nothing has happened and my heart is still fine, that I would still be good to exercise.
I rode this morning, but only went 11 miles and kept an eye on my HR monitor and tried very hard to go slow and not push, but still at my highest point it got to 170 when climbing some hills, is that bad? Most of the time it was in the 140 and 150's.
I dont' know, I just can't see how they expect you to sit and do nothing.
I need to get all my questions together about this stuff before I go in again. I have an appt for labs, and then I guess they will call me to see her again, like they did the last time after labs.

Sorry this was so long. I've searched everywhere trying to find some information about exercising with this and cannot find anything except for people to say not to do much.

Thanks for all the support girls.

DDH - the experience I draw from with a thyroid issue was my darling fur-baby who was hyperhtyroid in his last few years. I hope you don't mind. Anyway, his poor heart really took the brunt of it. With his thyroid cranking, his heart worked overtime and became thickened (cardio myopathy) and, well, I don't remember all the things wrong with it, but the heart specialist vet told us after the ultrasound that those three problems can't all exist in one heart. He truly was on borrowed time that last couple of years.... From what they told me, I gathered that the extra work his heart was doing, just becuase his thryoid was making it run faster, overdeveloped the muscle. The muscle tissue gets so thick that the heart eventually doesn't do it's job properly as it sort of gets in the way of itself and also loses it's elasticity.

Based on the little I know about it, I'm thinking your endo doc is concerned that the more your heart works at that higher HR, the more potential there is for thickening. While the treatments should get your thyroid back to normal, it's possible that the damage it's doing to your heart in the meantime might not be reversible. Your body is precious - every part of it. Sometimes, as hard as it seems, you need to do just the opposite of what you think you need to do, to give it a chance to heal.

Sending you butterflies of patience, calm, healing and hope. You'll get through this.

Hugs,
~T~

ps - if you are interested in an alternative, natural method of testing and balancing your systems, that can work in conjunction with your medical treatment, let me know, and I'll tell you my own story and find someone in your area you can see.

Hugs and butterflies from over here too, DDH. If it's any comfort, I cling to a line from a folklore lecture I have on an old LP. Supposedly this is something some really old Mormon elder said when asked how he'd managed to live so long:

"The secret of a looong life ... is to get yourself an incurable disease ...
and take care of it!"

So take care, DDH. Take it easy these two weeks, then ask the endo doc about the HR issue when you go back for your next check-up on the meds.