graves disease symptoms children

7 of those children had Graves disease. 66 children had a positive ANA; 4 with Graves disease. Unfortunately the study does not list an ANA pattern for these 4 children. 20 of 93 children (21%) had another autoimmune disease. 3 of the 7 children (43%) with Graves disease had another autoimmune disease. "The ANA pattern was homogeneous in 61/66 (92.4%), coarse/fine speckled in 4/66 (6%), and nucleolar in 2/66 (3%).

I really thought I was losing my mind, I have had this for about 4 yrs and just now was diagnosed with Graves disease. My Dr put me on Methimazole and after 3 weeks had a severe reaction and was covered head to toe with a horrible insanely itchy rash. Mr Endo told me I have a couple options radio active iodine or somthing else which he did not tell me what. My question is how has the radio active iodine worked for others?

My mother was diagnosed in her early 40s with graves disease and her thyroid was removed, around the same time she was diagnosed with stage 3-4 colon cancer. I'm aware there are connections between autoimmune diseases and thyroid and intestinal diseases/conditions. As I'm getting older I'm noticing I'm following in the same physiological footsteps my mother did before she was diagnosed.

I am 27 years old ... have had thyroid problems since pregnant with my daughter almost two years ago! they were watching my thyroid levels prior to that pregnancy though. They say that I have hypothyroidism (thyroid don't work) buut I also have antibodies for graves disease ... although my thyroid jumps from hypo to hyper frequantly ... my question is will I ALWAYS have the antibodies for Graves disease? Makes it possible to get graves disease and most importantly ... is it heretitery?

s 24) testing her would probably not alter her treatment. Her father was just diagnosed with Graves. So now, she is hypo after RAI, her dad has Graves and I have Hashi's. The doctor was very concerned then about my grandson who is almost 5 and said we need to keep an eye on him. He has been diagnosed already with ADHD and is on meds for it (i hate that). My question is - do children have thyroid problems that young or is it usually later in life?

I was diagnosed in April 2011 with Hashimoto's (the dx came after several different rounds of bloodwork, a thyroid ultrasound and the nuclear uptake scan.) I was prescribed synthroid and was told "we'd have to wait and see" how my symptoms responded to the meds. I would go for labwork every 6-8 weeks and each time, either I had to increase or decrease my synthroid dosage.

My daughter was diagnosed with Graves on June 4th. She is 6. Luckily, I'm a teacher and have been able to stay at home with her the past couple of months to get this under control. I feel like our lives have been turned upside down. We started out with a sore throat and a diagnosis from an ENT of Thyroiditis......We ended up seeing a pediatric endocrinologist in an emergency visit because of her heart rate. We've been on methimazole since.

I am very concerned for her and have talked to a friend who is an MD and they said without a doubt it is Graves disease. This MD has not met her, though says she needs to see a doctor asap! She also mentioned to me that she should not be caring for young children as the episodes I described to her demonstrated her emotional state. My question is...can someone tell (as this doctor has) without a doubt with a list of physical symptoms that she does indeed have graves?

s disease, then still not feeling well, and finally diagnosed with graves disease and vitamin D deficiency. Then came Graves eye disease, not severe and under control. So yes have levels checked, I had only TSH checked in Feb of last year, and it came back in normal range, when i had my physical my tsh was 0.00 so they tested T3 and T4 and they were not normal. Good luck, it is a slow process, and i get depressed about it often, it is not a disease with an easy cure, it is a long battle.

why after almost two years do I still have graves symptoms.

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.

i feel like my legs are going to collapse, i feel sick all the time, im just looking for a doctor that will listen to me because my symptoms are getting worse. what i understand about graves disease is that it is an autoimmune disease and that there is no cure, but the endocrinologist is taking it so lighly because my readings are fine, what am i to do??

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.

Through this process, several people have recently come out of the wood work and ask if she might have Graves disease. If she does, would an increase in TSH have shown up on the standard blood test taken a year ago? What questions should I ask her neurologist and endocrinologist?

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.

Hello. I'm 36 and I am almost 9 weeks pregnant. I have Graves' disease and had radiation treatment back in 2009. I hadn't been taking my thyroxine constantly for a few months as I was super stressed and now that I am pregnant haven't missed a dose. My thyroid levels are still very high and I'm worried that this will affect my baby's brain development/IQ levels. Has anyone else had similar experiences? I'm scared and worried.

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>.

Graves is an autoimmune disease and unfortunately for life. Controlling whether they raise or suppress is key to beating the symptoms of the disease. If you are on Levo now - your labs must be abnormal and now lean towards hypoT levels. You would feel like cr@p right now with the swinging patterns you have been on. "Once Graves.... always Graves" is the saying here. But I am positive your endo or ???

Hello! I was diagnosed several years ago with graves disease and had my thyroid removed due to a large nodule that formed. After the surgery, my ANA started becoming positive (not sure of any tiers) and now my RNP is elevated at 2.5. I have no symptoms except fatigue and brain fog, but I also have a toddler...so that's pretty common :). My rheumatologist said that everything is fine, but I am worried that this will turn into something later on.

My husband was diagnosed with graves disease this last week .He sees the endocrinologist Monday is there anybody that can help me understand this and are the partiular questions he needs to be asking the doctor .

During the chemo symptoms appeared of hyperthyroid (I had it in my twenties)Bloodtest was negative. Symptoms stayed and was just diagnosed with hyperthyroid still being tested for Graves. My labresults: TSH: <0.03 Ref: 0.30-5.60 T4 Free: 59.5 Ref: 7.2-21.0 Free T3 25.7 Ref: 2.9-6.0 At the same time as my labtest a MRI was made.

) I think it unlikely that the Graves Disease will attack your body in another place once your thyroid is gone. My aunt had the Radioactive Iodine a few years ago and now has to take thyroxin every day because now she has no thyroid gland to make it. I guess my advice would be not to rush into it (which I guess you're not). Either way, the chances are both of us will have to take medication for the foreseeable future, perhaps forever.

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.

Graves disease symptoms children

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