Experiences with

MST Continus

Since May this year, I started taking 5 mg of MST Continus, which is a prolonged-release morphine sulphate medication, when I go to bed. I have increased this to 10 mg. On the positive side, I am lucky not to suffer at all during the day or evening. It is only when I go to bed.

https://youtu.be/9lb_Js5KMq4?si=0sBd0Bc8XxZA4NqUI watched this and wondered are our problems, fatigue, inflammation etc. to do with toxic build up of homocysteine? I already take B12, of course by injection, B9 l-methylfolate and B6 (though not p5p sort in a larger dose). I take a methyl B complex too

Where do you get mum crystals?What is controlled pursed lip breathing? Thanks

My father was diagnosed with Parkinsons and sudden onset of dementia following a bout of covid 19 2 years ago. He is not very responsive to levodopa after that and after several consults with neurologists have found no other solutions. Tam some tests based on PD panel by Laura Mischley, and gave him

I was recently signposted as this may be my diagnosis by a GP and I'm awaiting a consultant appointment with Rheumatology as appose to a liver specialist despite me questioning this. I have no inflammation markers on my bloods but I do on my antibodies and smooth muscle blood counts which his why it's

My doctors have me on MST Continus, the slow-release morphine which is fine Except that my body does not like it at all. It affects my balance, mood and I have strange dreams even during the day, slightly tinged with fear and paranoia. I’ve read others who’ve experienced the same.

1. Does anybody else feel like they’ve exhausted all anti-depressants, SSRI’s, etc as what once worked now doesn’t? And where do you go from there? 2. I’ve had T and H since 2009, and after about 3 mths I habituated but with the aid of being on Prozac (Fluoxetine), however roll forward 4-5 years later

Hello, The objective of this post is to bring together any information related to Ketone bodies and their benefits / harms, and include all Ketone sources like Ketogenic diet, MCT oil and Fasting. It can be related to any condition like Parkinson's, Alzheimer's or any other Brain or body condition like

Dear all, nearly 2025! All best wishes for the NY. I’m 44 and diagnosed with YOPD 6 months ago. I’m not taking medication yet but do red light therapy, B1, Cinammon, brew my own kefir and eat a lot of fermented products. I also exercise a fair bit and meditate daily. I have a good mainly Mediterranean

I recently posted my latest presentation about Parkinson's and nutrition here https://www.youtube.com/watch?v=W7kT4OonMV0. I call it a ketogenic lifestyle. I combine a ketogenic diet with MCT oil and sufficient exercise. (The presentation is in Dutch. Most here will not be Dutch speaking and can use

There are regular posts and snippets about Ketones and Ketone diets. This is an attempt to provide a more definitive post and reference. I’ve tried to keep it simple and jargon free as much as possible. This attempts to provides information on the following areas. 1. What is a Ketone, how and why

Hi, This is my first post, so please strap in, or skip to where I mention SSRIs (in bold) as I really would like input :) My tinnitus (T) in both ears started after playing a gig where the monitoring on stage was too loud at the end of August. Perhaps as a psychological reaction, I developed hyperacusis

I have my 24 hour ECG on Thursday. I also suffer from sleep apnoea, so I was wondering if it was ok to use my CPAP machine during the test, after reading the restrictions on electronics.

Last night was the best 10 hour sleep I have had since using my cpap machine but still very tired , I felt more comfortable using it specially the full mask not to tight just right hopefully I can continue getting the sleep I need.

Hi I'm never sure which group to post these in because I have overlap autoimmune so if there is a group more suitable to this lost please let me know. I've really been struggling since August last year when I started a flare. I'm currently on the maximum dose of methotextrate and will now be starting

hi all-haven’t been on here for a while dealing with things. Update on hubby: He is currently on 7.5 mg of methadone and .5 Xanax for sleep. He can’t sleep in bed or lying down because he can’t breathe well….mostly due to severe nasal congestion. He is only using saline nose drops now because the

I started a CPAP at the end of October. Boy did that not work out! My sleep study said I was having 9-20 events an hour without it. When I used it my events were often between 25-77!! Why was using one making things worse? Also, the mask was making my face numb all day. Super annoying. the worst

Following on from Flamingheart's earlier post, I'm interested (for my other half, not myself) in hearing others experiences after being diagnosed. To give a very brief background, if that's possible ... After suffering from a single but serious instance of perimyocarditis back in 2017, and with a background

Newly diagnosed Parkinsons, tremor since 2018. neurologist says that sleep apnea machine is very important after my sleep study does anyone have examples of disease progression being slowed or any symptoms being relieved by moving to a sleep apnea machine?

Hello, I will try to be brief but may fail! I am 63 and female. There have been multiple things I have been concerned about for several years now and I [i]may [/i]have got to the bottom of it within the past week or so. I may have PA (or should I call it GA? Only just seen on this forum that there's