Graves disease quality life occupational disability

Common Questions and Answers about Graves disease quality life occupational disability

graves-disease

Avatar m tn 17 yrs of living with and trying to be a productive person in society, after aortic valve replacement, my quality of life is such that I can no longer consider myself employable. With attendance issues being the foremost reason for this conclusion, Is it too far out of the question for me to be eligible for disability. I have applied in the past, and have always been denied.
470168 tn?1237471245 I have a query regarding provision of Occupational Therapy in the USA. I want to compare it with provision in the UK. In the UK provision is divided between Health and Education. Education do not have any Occupational Therapist Department as they say "it is not essential to learning". As any mother with an autistic child with sensory differences knows sensory stuff has a huge impact and does make it hard for them to access learning in a school environment.
Avatar f tn Conventional treatment options for Graves' disease include: * Anti-thyroid medication: In the US: - Methimazole [brand name Tapazole] - Propylthiouracil [PTU] Approximately 30% with Graves' disease will have a remission after prolonged treatment with anti-thyroid drugs.
Avatar m tn Selenium helps with thyroid inflammation so this may help with your throat symptoms. Also, in 2011 a study demonstrated that selenium supplementation (200 mcg per day) can slow the progression of eye disease and improve quality of life in patients with Graves' disease with mild ocular involvement (Graves' ophthalmopathy). In supplement form, the most bioavailable form of selenium is L selenomethionine.
Avatar f tn I have Graves Disease and had RAI in June 2008 and it was BEFORE RAI that my TSH was suppressed.Prior to RAI, I could never get my TSH past the 0.10 mark. My antibodies were over 4000. Since RAI my antibodies have been under the reference range meaning I am in remission at present and have been for some time.. Since RAI I started on a T4 med when my TSH rose to just over 6.0. I was actually surprised to see my TSH go over 0.10 as it had been that for many years. It hasnt gone under the 2.
15915009 tn?1488868338 m hoping to get off of them soon, but is it possible to have a relapse later in life after I have not been taken them, if Graves Disease will be with me for the rest of my life and if I need to get my blood checked every so often?
Avatar m tn My mom and grandma both have thyroid disorders! I just want to get back to a quality of life! I am a mess worrying about all of this and not feeling well besides! Thanks and Please Reply........
Avatar n tn I am so sorry your daughter has these challenges..I am not certain if we are expert in the matters of celebral palsy , take a look back to the forums page you will see a list on the right of expert/Doctor forums , click on the pediatric one .
Avatar m tn thanks for all the help.iam gonna try to apply for some health insuarance through the state.i dont have an appointment until july,but i can wait that long.so when i make an appointment i ask to do the free t3/t4/Hashimoto's disease and graves disease testing?
Avatar f tn Graves Disease is never cured BUT it is managed better without a thyroid or after RAI. You still have the antibodies but no thyroid for it to attack. As for meds, you swap one lot for another. You go from anti-thyroid meds to a T4 medication so basically you are on meds for life. The thyroid regulates every organ in your body and if no thyroid, meds have to do the job. Hyperthyroidism is a lot easier to manage without a thyroid.
Avatar f tn I was diagnosed with Graves disease 8 months ago, making my thyroid very overactive. I didn't respond well to the medication as it was affecting my White blood cells and a full thyroidectomy was decided upon after taking Lugol's iodine for a week to bring it under control. The huperthyroidism had left me with rapid heart beat, palpitations, severe anxiety, muscle loss, weakness, non-existent periods, the list is endless.
Avatar n tn 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 ???
Avatar n tn I have had steroids for my eyes and and tapazole nothing has worked. I have toxic nodoles along with Graves disease. I have changed my diet and tried different things what do you suggest. I'm not sleeping, I have gained most of my weight back with increased heart beat. What can I do.
Avatar n tn Hyperthyroidism lists fatigue as a symptom. This can be due to insomnia and difficulty sleeping, a rapid pulse, and/or higher blood pressure. Conventional treatment options for Graves' disease include: * Anti-thyroid medication: In the US: - Methimazole [brand name Tapazole] - Propylthiouracil [PTU] Approximately 30% with Graves' disease will have a remission after prolonged treatment with anti-thyroid drugs.
Avatar f tn Six months of selenium supplements had a beneficial effect on thyroid eye disease and were associated with improvement in the quality of life of participants. These positive effects persisted at 12 months. There were no side-effects. Selenium acts as an antioxidant and also has effects on thyroid autoimmunity, though the exact mechanism of its action in patients with thyroid eye disease is unknown. Reference Marcocci et al. Selenium and the Course of Mild Graves' Orbitopathy.
Avatar f tn I am a 43 year old female. I was diagnosed in February (2008) with GravesDisease. I was started on methimazole (10mg 3x/day). In March I was switched to PTU (50mg 2x/day) when I developed a rash from the methimazole, and after blood work (Free T3 1.6, Free T4 0.38, TSH 4.05). In April I went back for blood work (Free T3 1.69, Free T4 0.29, TSH 42.3) and my dose was lowered to 25 mg once/day. In May my labs indicated that I am still hypo from too much PTU (Free T3 2.06, Free T4 0.
Avatar f tn I also have Graves disease and from my understanding you are never "cured", but, once your thyroid is either dead or you have it removed you should no longer be suffering from the symptoms. Except the protruding eyes, that is the only symptom that they can't reverse. That you are going to have to live with for the rest of your life. That's why it's so important to get treated before that happens. I would say that your tiredness is from being perimenopausal.
2102364 tn?1334181277 Prognosis also depends on the duration and severity of the disease before treatment. Swedish research of 2005 reports a lower quality of life for 14 to 21 years after treatment of Graves' disease, with lower mood and lower vitality, regardless of the choice of treatment.
Avatar f tn The most common forms of autoimmune thyroid disease are Hashimoto’s thyroiditis and Gravesdisease. Hashimoto’s thyroiditis (also known as chronic thyroiditis) may lead to hypothyroidism, while Graves’ disease is usually associated with hyperthyroidism.
Avatar f tn 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.