Radioactive Iodine - should I have it??
Questions in the Thyroid forum are answered by Dr. Mark Lupo. Topics covered include goiter, graves disease, Hashimoto's thyroiditis, hyperthyroid, hypothyroid, thyroid cancers, thyroiditis, and thyroid stimulating hormone (TSH).
Have you been tested for antibodies? some women may develop thyroid disease after giving birth, but it's reversible after a while. This is only a suggestion and I'm not a Dr, but you should make sure you get tested for antibodies and you should be working with an endocrinologist (not your GP) that you feel confortable with. By this I mean, someone that doesn't rush you into doing anything you're not confortable with. But first, make sure your hyper condition is due to antibodies (Graves Disease) and not other condition.
Now, in regards to RAI. I was diagnosed with Graves almost six years ago. The Dr I had wanted me to rush into RAI and I didn't feel quite confortable with it. We're talking about radiation here, and although they say it doesn't affect anything but the Thyroid, I don't think they're sure about it, how can they?. I've always thought that one day (maybe in 50 years or so) they'll come back and say that "it wasn't that safe afterall" or "it has such and such side-effects". I didn't like the fact that my Dr at the time didn't want to discuss any other alternatives. So, I changed Drs, twice, then I found an endo that was willing to sit down with me and discuss my alternatives along with pros/cons and allow me to make an informed decision. These are: meds, RAI, surgery. After a lot of research, I decided to go with meds and it's work out perfectly, with the exception of when I'm under sever stress, then my thyroid usually goes off.
But I know that and usually check my levels when I'm under such situations. Now, in regards to RAI, I found a lot of info about people who had it and deeply regret it. What happens with RAI is by using radiation your thyroid is slowly "burned", this process can take several months and your meds need to be changed and monitored closely as it'll need to change while you're thyroid slowly dies....at the end, yes you end up been hypo, usually very hypo. Maybe someone else can talk about his/her experience with RAI, but this is what I found out and don't regret it. Remember is a type of radiation. If I had to chose I'd go with surgery (you need to find an experienced surgeon for this as your parathyroids are located in your thyroid and if accidentally removed may cause a problem regulating calcium). Again, many people I "met" doing research regret having done RAI. Don't rush into anything, and look for a Dr that's willing to listen and work with you. And don't forget to make sure you get tested for Antibodies before making any decision. Hope this helps and keep us posted!
goodluck with your situation.
I think my doctor may have done that test - she seemed pretty convinced it was Graves although I have no family history. I am seeing her this week and will check and get a referal for a specialist.
Did you try different kinds of pills? I am an Australian and theres apparently only 1 pill (Neomercazole - a carbimazole). How long should it take to make a difference.
And YES when I am stressed I get really sick with all my symptoms and can not sleep even if I am tired - being stressed is such a huge factor - although In think my hyper makes me extra stressed.
It seems like in different parts of the world, there are preferences for different meds. I'm in the states, and the preference here is to start people on PTU (too long to spell out). So I was started on PTU and didn't react very well to it. So my current endo switched me to Tapazole, which happens to be the prefered med in Europe. I have talked with different Drs that have practicing experience here and in Europe and they don't know the reason. Tapazole worked wonders for me and continues to do so. So maybe you can suggest to your Dr to change medications while you wait to see an endocrinologist.
Good luck and hang in there! I know how it feels having been there myself. It's not fun :-)
I have not gained any weight. When I was hyper my physical activey was restricted by my drs because I could of gone into cardic arrest. My metabolism was that messed up plus I had high blood pressure. A lot to handle at 11 years old. I actually gained weight with the PTU (45 lbs). Once I had the RAI my metabolism straightened out and I was able to workout, loose weight. It actually did wonders for me. Now I don't want to leave you with the impression that I haven't had problems but like I said before you always will one way or the other. What my doctors always told me is that hypo is a lot easier to treat than hyper.
Do you think I should try the pills for longer? I have been on them for 3/4 months.
Did you have to stay away from your kids after? Some people have told me I will have to stay away for 2 weeks! ( I have 3 children under 4 & am a stay home Mum)
It's encouraging to hear you're okay now. Did you get sicker and sicker. I feel I am getting progressively worse the longer I have it.
If you need RAI - most people do very well with it, but expect to be hypothyroid and make sure your levels are followed closely after the dose to document when you are getting hypo and start replacement therapy to minimize symptoms.
Good luck.
Dr told me to stay away from my boy for 2 days. I was told to clean the toliet after I was done and do my wash seperatly from everyone elses. I slept on a sheet on the couch, I can't remember he told me to do that or I just did it anyway. I had tests done every month then every 3 months to make sure I wasn't going back