Experiences with

Lutein

Twice a day ingredients: C = 250 mg, E = 90 mg, zinc= 40 mg, copper = 1 mg, Lutein = 5 mg. Except Lutein, all the others are triple digit multiples of recommended daily intake for just 1 dose. One dose Zinc at 364% and copper at 111% and E at 600% scared me.

Hi, I was looking for Macusave tablets on Amazon and found some Lutein etc from a company called Alpha 01, ( or Alpha zero one). They are very much cheaper then the usually brands, so I wonder if anyone knew anything about this company or product? Many thanks

Euthyrox is the only pharmaceutical I am taking currently, however I supplement with magnesium, turmeric, co q 10, red rice yeast , Danacol, stinging nettle extract, lutein, vit D k2mk7, 1 spoon evo. My medical history is , high-ish cholesterol and osteoporosis.

Even bicycle associations advise their members to take B6 because without it they can develop heart issues) Now I don’t take any meds not even metoprolol and below is my list of supplements: (most are just standard amounts) Multivitamin D3 2000 IU K2 200 mcg Beta Carotene Lutein Probiotics Taurine

does any one have an idea about using rutin for parkinson's?

Here’s two: i) Lutein, a carotenoid found in the macula and retina of the human eye and ii) Omega 3 are essential fatty acids DHA and EPA. Every cell in the body has a lipid (fatty) bilayer. These fats are called essential for a reason. We have to get them through food.

Hi following on from my last post I stated I had a levothyroxine increase. My thyroid tsh and T4 had slightly decreased and T3 remained the same before starting increase. In the last few months I started a gluten free diet as I believe it's suppose to help with hashimotos? I can't say I have felt any

Hi I was diagnosed with hyperthyroidism due to 2 ‘hot’ nodules in 2019. I have been on Carbimazole since then. I take 7.5 mg a week. I have been sent back to GP care as I will not agree to RAI Can anyone tell me if it would be beneficial to me to try a gluten free diet to improve my thyroid health

My daughter, a brilliant veterinary surgeon is 49 and 20 yrs ago was diagnosed with PCOS, told she would probably 'develop heart disease and diabetes and she would never have children'. Four years ago, she was diagnosed as being level 1 on the Autistic Spectrum-what used to be called Asperger's, but

Hi Everyone, I was diagnosed with Hashimotos 12 years ago and it has been a challenging journey finding the right combination of medication and self care strategies. Thanks to this forum and all the wonderful people who have shared their stories and advice with me, I now feel pretty good at 88 mcg Tirosint

Hi,I'm hoping to get insights into my latest test results and symptoms I continue to have. I had my thyroid out in 2012 (Graves), I'm located in Australia and currently taking 100mcg of Eltroxin and 16mcg of slow release (compounded) t3 daily. Around 2yrs ago I got quite sick, I had extremely heavy fatigue

hello I am new joiner to this forum. It is only by accident that I came to know about this and I am so much hooked and so valuable info that everyone is sharing and helping each. It is a blessing. Out of my routine blood check, NHS GP did my blood test (14.02.23) and learnt about my thyroid reading

I have tinnitus for years, almost 20 years.At first I thought it was stress related.During the first few years I was able to MANAGE it, by listening to soft music, walking in the countryside, watching tv ,and even flying at 36000 feet was a distraction.I even tried classical concerts and football games

I’m currently trialling gluten free diet (as recommended by my endo) I have done this since November last year. I am just about to do repeat bloods prior to an appointment with him in September. I would like to ask for recommendations for gluten free and lactose free brands for t4 and t3 before my

hi all, I have hashimotos/under active thyroid and have heard the benefits of going gluten free. I have occasional bloating but not many gut issues as such, my symptoms are more brain fog and fatigue. All my thyroid tests are optimal and in range so I’m thinking of trying a gluten free diet. Can anyone

I have been diagnosed with Idiopathic Cerebellum Ataxia for 6 years . My consultant recently arranged for a TG6 test at Sheffield hospital . The result came back as mildly positive ( 4.2 with 4.0 as normal ) As I understand it , a strict gluten free diet should remove antibodies from the body preventing

After watching the video about what can cause Parkinson’s that was posted on this website, I started thinking about inflammation, and inflammation of the body and gut. I found this website from the gluten free society who have found correlation between gluten and rls. My husband who has had RLS for

Good morning!I am 42 years old , and mother of 2. I was diagnosed with Hashimoto thyroiditis, in 2019, between two pregnancies. I've been on Eutirox 75mcg/day since 2020, and fluctuate fron hyper to hypothyroidism since then, weught loss and gain, fatigue... I change my life style, gluten free diet

I was diagnosed with Idiopathic Cerebellar Ataxia in 2018 and had all the usual tests which proved negative . My neurologist in Aberdeen recently managed to arrange a TG6 blood test in Sheffield . The result was 4.2 U/ML , and a result >4 is positive.I have none of the usual symptoms of celiac disease

Hi all. I urge anyone who has not yet been diagnosed with a particular type of ataxia , so idiopathic of unknown cause, which means they do not know what is causing it. To contact Sheffield and see if you can participate in a new study into gluten ataxia. Although a gluten free diet will not cure ataxia