Graves' Disease Support Group
Graves-Basedow disease is a medical disorder that may manifest several different conditions including hyperthyroidism (over activity of thyroid hormone production), infiltrative exophthalmos (protruberance of one or both eyes and associated problems) and infiltrative dermopathy (a skin condition usually of the lower extremities). This disorder is the most common cause of...
Could you still be having that fluid problem in your throat...?
{{{hugs}}} :-)
Your jump is just about how quickly mine used to move up. Also, some times, after being off of Methimazole I yo-yo'd around a bit (going up and down) until I eventually just got stable and my FT4 wouldn't change very much at all. It never felt very pleasant.
Are your vitamins free of Iodine? How is your diet? If you are worried about going hyper, you can start adding in the goiterogens again (peanuts, broccoli, cauliflower, cabbage, corn, peaches, strawberries, grapes) etc, but with an enlarged thyroid, be cautious and pick one type for the day and have the recommended serving size only (like for peanuts, 1/4 cup is about a serving.)
I'd avoid iodine sources at this time like dairy, deli meats, egg yolks, bakery items and processed foods and seafood, and the sneaky sources like agar, algae, carageenen and irish moss.
I have had good luck eating the following when I was in transition:
Breakfast:
Oatmeal or if I have more time scrambled egg whites with sauteed mushrooms, onion, bell pepper and black pepper
mid morning snack:
Fruit (probably something like an apple or pear or banana if I'm in transition, if I'm slightly hyper I'd have a peach)
Lunch
(Depends on how much time I have) I make homemade tomato based soups with veggies like carrots, potato w/o skins (the skins are often high in iodine), green beans, squash and the like. If I was hyper, I'd add in cabbage.
Mid afternoon snack
Veggies like sugar snap peas, carrots
If I was hyper, I'd add in some nuts like 1/4 cup of peanuts or brazil nuts. I like almonds a lot and they're a good source of calcium. If I wasn't hyper, I'd eat almonds, pecans or walnuts.
Dinner
I like mexican food, and would make chicken or steak tacos with corn tortillas and salsa. Often, I'd just get ground chicken from foster farms with no salt added, and it would be a quick way to make a filling dinner. If I was hyper, I'd make a nice peach salsa with peaches and purple cabbage, cilantro, red bell pepper and green onions. If I'm not hyper, I'd make a tomato based salsa instead of the peach salsa.
If I felt like Italian, I'd use spaghetti squash a lot, instead of semolina pasta and would use no-salt added tomato products to make my own sauce, or would try to pick a sauce at the store with as few ingredients as possible and under 300mg of salt per serving.
I also liked making my own thai food, and would use coconut milk and make curry, etc. If I was hyper, I'd make peanut based sauces, and if I wasn't I'd limit the peanut. I'd usually go heavy on the basil, and would use which ever veggies were around. I get a lot of veggies and fruits I guess.
I hope you feel better, really soon!
Big hugs!!
Hannah
Big hugs!
Hannah
My husband makes for dinner like a stir fry veggies of cabbage, cauliflower, broccoli and onions which helps my thyroid. He tries not to cook these as long as to keep as close to raw state as possible to help with the Free Ts for me. He also uses a special blend of seasonings which doesn't aggravate me.
I tend to eat more veggies than fruits due to my having RA and the sugars if I eat too much of it, will bring on more inflammation.
He's starting to bake more and more wholesome foods with certain modifications to the recipes.
{{{hugs}}} :-)
None of my vitamins have iodine in them... I've avoided iodine at all cost for the last year (since being diagnosed)... I avoid any triggers or possibilities of triggers too...
I just wondered if this is my body fluctuating as my levels try to even out (if I am indeed in true remission). I can't stand it! It's so darn frustrating... I just keep my head up and keep thinking that soon, this will be behind me and hopefully, I will feel better in given time. I keep thinking about the people I have met and come across who have had a TT and years later, they are doing fantastic. I wanna be one of them. :) Of course, they all have the story of trying to find the right dose and I'm okay with that... I just want normalcy at some point! I hate this feeling in my throat.... almost feels kinda scatchy....
MMZ: that pocket of fluid went away on its own (assuming) since when I had the last ultrasound (last Friday), the endocrine surgeon didn't mention it... she mentioned a nodule sitting next to my trachea which is what I feel in my throat. But now my throat feels swollen on the right side as well... :(
{{{hugs}}} :-)
http://www.saintbarnabas.com/hospitals/community_medical/radiology/lowiodine.pdf
It had been really hard to follow at first, but my body seems to do best on it.