Experiences with

Diamine oxidase

The other tests he has requested are: LFT RMIN 25-Vitamin D Methylmalonic acid and red cell folate Diamine Oxidase Activity Fasting homocysteine Fasting lipids Fasting glucose Thank you.

I also did a test which showed I have very low diamine oxidase in my gut so have histamine intolerance. My question is regarding my medication. I currently take 100mg sertraline, two blood pressure pills and a statin. Are these not getting into my system either?

And I also have low diamine oxidase which is used to control histamine. I would say my main issue at the movement is extreme fatigue which I am hoping to get to the bottom of soon!

Oxidase 3 times a day Vitamin D 3,000 to 4,000 IU daily This detox (NAC) will get rid of the spike protein to 98% and bring down the inflammation at cell level.

I'm low on ferritin (20) I was told I can't inject because it's low? My b12 was low 232 in 2021 with high mma. Last year when all my neuro symptoms started it was around 390 for b12. I took supplements a few times, it raised to 630 and then got one injection on 6/2024. One month later my b12 was 298

I've been taking a magnesium supplement for years, actually either magnesium glycinate or magnesium L threonate, magnesium oxide is a big no-no, it gives me weird stomach palpatations. But recently I've noticed that my preferred magnesium has been having the same effect, I didn't realise at first that

"L-theanine may help with restless legs syndrome (RLS) because it can increase GABA levels in the brain. GABA is a chemical that can help calm the brain. How it works L-theanine can be taken as a supplement or in tea. It's recommended to take it in the evening before bed. L-theanine can be taken

Hello everyone. I hope as you read this your legs are calm and settled and that your life is good. I've suffered with RLS for about 20 years and as it has progressed my life has gone into the toilet. I presently employ Neupro Rotigotine 2 mg patch to treat it and prior to the patch I took Ropinirole

Why Levodopa and Dopamine Medicines Should Be Avoided in Parkinson’s Disease: A Deeper Ayurvedic Perspective ❌ Krauncha seeds (Mucuna) contain L-Dopa but do not stop neuron degeneration. This can be a herbal claim- not ayurvedic. ❌ It follows the same temporary relief mechanism as synthetic Levodopa

I have had leg pain for a number of years. My movement disorder specialist has insisted that this is not a symptom of Parkinson's. In any case, I had my general practitioner put me on gabapentin to see if that would help with the pain. It actually helped for a short time, but then it stopped working-

I’m 61 and have pretty good health insurance in the United States. I see an internist, a sleep neurologist, and a psychiatrist (the latter necessary because of medication side effects.) Long story short: Klonopin was helpful for many years; they want me off Neupro; Suboxone just kept me spacey and in

When initially diagnosed, we start our medications from dopamine agonists, anticholinergics, and other anti-Parkinson's medicines and then off course the levodopa. The neurologists and movement disorder specialists mere add a new medicine to patient daily regime upon complaints of new symptoms. They

Does anyone have experience of DAWS Is it possible for PWP to experience DAWS stopping Sifrol (pramipexole) 0.75 mg cold turkey Wanting opinions - YES. NO.

Following my appearance on GMB yesterday, reading Twitter/X (I know I shouldn’t) just goes to show how far we still have to go to educate ‘stupid, judgmental, naive’ people (although they probably can’t be). It’s really annoyed me to be honest, I know that’s silly. My son tried trolling some of the

I just wanted to say to every one of you that has sent a message over the past few days a huge ‘THANK YOU’ for your encouragement and kind words. As I am sure you can imagine, it wasn’t easy to ‘go public’ with my story, but reading this forum over the years, and feeling the anguish that so many people

Hello fellow sufferers, I've got a specific question that I'm wondering if anybody else in here has ever had to consider: I am a long time sufferer of rls who has progressed into augmentation using DAs and was able to almost completely get off them replacing them with Gabapentin and low dose opiates

Joined just to share this in hopes that it can offer a deeper look into getting off dopamine agonists and what it entails for people. I've never seen anyone online post a thorough log as to what getting off these meds is like and how they did it, so here is mine. Background Some context, I have been

Has anyone tried velvet beans or velvet bean supplements as they are supposed to boost dopamine levels. If so, what was your experience of them. Many thanks in advance

Anyone dealing with depression ever get tested genetically and find you have FAST COMT Val/Val. This gene allegedly leads to low dopamine and low norepinephrine in the brain. My symptoms have always been low energy, slow cognitive tempo, brain fog, low mood, poor recall memory, poor motivation (

From what we all observe here, most general practitioners and some neurologist are not approaching the treatment of RLS according to what is now the accepted protocol. But who is asking why? For many of us we just want to get better and this question does not matter. But for some who are concerned