Experiences with

Arrhythmogenic right ventricular cardiomyopathy (ARVC)

I know nothing about this... Just found it and thought I'd pass it along. ---------------------------------------------------------------- https://youtu.be/oJ1S9R594a4

I don't seem to have much in the way of symptoms. I took motion classes but they said you're fine, come back when you have a problem. I took acupuncture sessions til they said come back when you have a problem. MY problem is the neurologist wants to take my license. I failed a driving test that didn't

Hi , I’ve read up a lot about red light therapy & have held back but now considering buying one. Just interested to know if any of you have bought one, how you have got on with it, re results, plus if so any recommendations. I know I have seen posts in the past where people have mentioned they use one

The effect of light exposure on insomnia and nocturnal movement in Parkinson's disease: an open label, retrospective, longitudinal study 2018 https://sci-hub.ru/10.1016/j.sleep.2018.01.001 Abstract Insomnia, hypersomnia and REM Sleep Behavior Disorder (RSBD) during sleep are major problems for

In the study out of Australia, the new infrared light therapy helmet on patients living with Parkinson's helped improve facial expression, upper limb coordination and movement, lower limb coordination and movement, walking gait, and tremor https://medicalxpress.com/news/2023-04-parkinson-laser-helmet-therapy-motor.amp

Has anyone used a Far Infrared Heat Mat that is filled with crystals? I have MBC with bone mets in spine. A friend let me use her mat and I found it really soothing and felt great afterwards. I would like to buy one myself but wonder if it would be OK for regular use with the bone mets, I don't want

Greetings to you all. I have a question about light therapy. What is the latest research showing? I’m a little overwhelmed by the number of different devices out there, and particularly the different frequencies that are being recommended… 810, 1070, blue light… etc! Can anybody give me some advice

I am a 75 year old male who was diagnosed with PD in November 2022. I am treating the condition with medication and have recently completed a course in BIG therapy. I have also purchased two red light therapy devices. I would be interested in hearing from others who have used red light therapy to treat

This relates to my previous post: https://healthunlocked.com/cure-parkinsons/posts/149309053/added-monaural-beats-and-light-flickers-and-all-my-brainwave-entrainment-is-40-hz-now?responses=149314901 The instructions for this 40 HZ flickering bulb said not to look at it directly but to have it within

My scientist friend, who is working on a vibrotactile coordinated reset prototype for me, drew my attention to an article in New Scientist - which is very interesting https://www.newscientist.com/article/mg25734290-100-restoring-the-brains-mitochondria-could-slow-ageing-and-end-dementia/ Quick take

Studies show positive results. Symbyx Biome’s red/infrared light therapy helmet, improves motor function in Parkinson’s disease, according to data from a small clinical trial. https://parkinsonsnewstoday.com/news/gains-seen-parkinsons-with-symbyxs-red-light-therapy-helmet/

For months now my *** has been dragging around this deep gloomy feeling. While everyone else seems to be Joyfully celebrating their holidays. Part of my gloominess is "SAD" Seasonal affective disorder. I try antidepressants, light therapy, and exorcising ,,, oops exercising. And it helps but the other

Bryan Johnson , a regenerative medicine extremist, uses Laser emitting diodes on his head instead of our standard red light therapy. This peaked my interest. https://www.vice.com/en/article/z34ay8/bryan-johnson-blueprint-aging-biotech https://lightforcemedical.com/improved-cognitive-function-after-transcranial-light-emitting-diode-treatments-in-chronic-traumatic-brain-injury-two-case-reports

I'm not using light therapy, but somebody mentioned it to me again and I found this in depth page that pulls a LOT of light therapy information together in one place: https://www.apdaparkinson.org/article/light-therapy-for-parkinsons-disease/

I live in an area that has at most 20 days of light. After using a light therapy lamp that delivers up to 10,000 lux for a week the severe RLS symptoms are now very mild. I have also found that I no longer need to take medication at night. Hopefully the light therapy continues to work for me. I am

Nothing seems to help with the anastrozole side effect of pain in joints, ligaments, muscles. I have been reading recently about infra-red light therapy (LED phototherapy - has a bunch of names), used on skin but also on athletes for injuries of all sorts. Has anyone tried this? If so, did you get

Here is a partial list of medication, supplements for other therapies used in Parkinsons What do you believe are the most beneficial/essential to treating Parkinsons and/or mitochondrial damage Which way should I go? Most bang for your bucks Carbadopa/Levadopa  L-5-hydroxytryptophan (5-HTP) Actylcholine

therapy with some type of vibration? Looks interesting https://www.neurowrap.com/

hi everyone I hope you’re doing well. I was wondering has anybody ever heard of the so-called red light therapy. someone had passed on this article to me and I have never heard about it is this just another scam to try to take advantage of us? Or has anybody had any experience with this therapy? Happy

Hi all - my main problem is swollen puffy sore fingers that won't flex - I've experienced this since January when all my fingers (except 1 thumb) swelled up and stayed that way for several months. Through the summer things improved a lot, I get outdoors quite a bit and with a bit of management (compression