Graves disease treatment depression
Common Questions and Answers about Graves disease treatment depression
graves-disease
my sister has hd graves disease for about a year she does not take med. right she has not gotten blood work for about four months she just keeps taking med because she has refills she is getting really crazy she thinks people are trying to kill her coul this be from graves disease
This discussion is related to <a href='/posts/show/658154'>TSH Levels at 3.75</a>.
hi i'm a 28 yr old woman and have suffered badly with symptoms from graves disease for 3yrs i've been on propylthiouracil for a year now as i had a severe allergic reaction to carbimazole!
my symptoms include insomnia,severe fatigue,anxiety,bouts of depression,poor concentration,memory loss,bruising easily,dizziness,nausea and graves rage and weakened immune system (sick often). the problem is that i've recently had a blood test that read normal at 5.
s an autoimmune disease that unfortunately always plagues you in one shape or another even after the radiated iodine treatment. Since thyroid disease runs in my family, and I have borderline hyperthyroid tendencies, I always keep an eye on the thyroid board on MedHelp. The folks there are very knowledgeable. You may want to pop in there for some advice as well. Both diseases (FM and Graves symptoms overlap) Make sure you stop back in both places. Take care.
I was diagnosed with graves disease and had the radioactive treatment to destroy it a few years back. I have had a few times where I did not have my meds for a week at a time. Is it normal to feel so tired and cranky? Also I took Zirtec for my allergies and I felt like I was cloudy and just wanted to sleep and tightness in my chest..... I am currently on 137 mcg of Levothyroxine.
I was diagnosed with Graves disease 11 years ago. My endo prescribed Methimazole, which I was allergic to, so he told me he didn't want to prescribe me anything else because sometimes the allergy kills the thyroid. It apparently did, because all of a sudden I was hypo and I had to go on synthroid. Since then, I lost my health insurance and got handled by my PCP instead of the endo (cheaper).
I've been diagnosed with Graves disease over a year ago and the doctor said i had panick attacks and anxiety i didn't want to go to a pshycologist thinking it's all because of my disease and i've been prescriped only with xanax,the problem is that it does work for my anxiety but does nothing for my depression, anger and my parents noticed my mood swings after 6 months of treatment because i was angry or happy or funny and shortly after that i became depressed, and they thought th
I am a 25 y/o female diagnosed with hyperthyroidism at 16 and later with Graves Disease and Goiter. I have been on Tapazol along with Atenelol (for the Tachacardia) off and on for the past 9 years with no results. Every doc I see wants to discuss nothing but RAI or surgery. My husband and I have been trying to conceive for a few years with no success. I finally found out that I was pregnant the beginning of last year and made it to 4 months and suffered a miscarriage for no apparent reason.
Last year I was diagnosed with Graves disease and had a radioactive ablation done in April. Sometime around March of 2009, my eyelids became puffy and my eyes were usually watery. I called my Endocrinologist and asked if this was related to my thyroid and she sugg. I visit my Primary Care Dr. I did and he followed an allergy path. I finally went to an allergist who said that allergies may be playing a role, it was not the primary cause.
In the USA there is a tendency to use more I-131, but in many other countries (and in our office) we often use anti-thyroid meds such as methimazole for Graves and consider surgery for treatment as well. If it is a hot nodule, then would recommend either I-131 or surgery (w/ an expert thyroid surgeon).
my son was a newly diagnosed "graves disease" pt. he was given tatazole tablet 5mg. to be taken after breakfast for one month, what are the side effect of tatazole, the things he have to avoid and if you can give me more/additional information about the disease. thanks!
If your TPO is at the level you say then you have an Autoimmune Disease (Graves) and eventually you will have no choice but permanant treatment as Graves is very hard to treat.
In the meantime....keep doing what your Doctor says BUT research all you can on Graves Disease and Hyperthyroidism as this is something you will need to know eventually.
Dont go for RAI or permanant treatment until you know for sure that yr thyroid is uncontrollable.
My fiance' was diagnosed with Graves Disease late last year. Something we did not expect was him having Aortic Stenosis. Graves Disease causes numerous symptoms so we thought it was the disease causing his heart problems. He just took the treatment for the Graves so it's going to be a month or so before the treatment starts to show some results. He has another test scheduled next week with an Interventional Cardiologist.
Try and relax and just look at it like your on a trip, and turned off on a bumpy road, it will get better. we have all been through the depression symptoms of thyroid disease so you are not alone, we are always here to answer your questions.
Hi, I am a 28 year old woman and was diagnosed with graves disease 3 years ago. I have commented o many forums regarding my problem but would like your advice. I was treated with radio active iodine in 2006 and then became hypothyroid, I now take 150mg of levothyroxine daily. I have never suffered from graves opthalmology as far as i'm aware.
For the last 6 months I have had a chronic daily headache. This started 3 days after purchasing new glasses.
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