Experiences with

Dronabinol / Cannabidiol

Mum passed last Tuesday aged 85, very peacefully and without pain in her bed at home. Her death certificate shows cause of death as cortico basal syndrome. She had been living with us since April 2023, symptoms of CBD having begun in 2019, with a left hand that would not behave, and a confirmed diagnosis

Hi, I have pain and on gabapentin, co codamol, I have neuralgia and not RLS and I have spoken about this in this forum. The issue I want to talk about is the use of cannabis for pain relief. My doctor will not prescribe opiates and I understand this. I found a company c in the UK. I have had an appointment

Hi, I have pain and on gabapentin, co codamol, I have neuralgia and I have spoken about this. The issue I want to talk about is the use of cannabis for pain relief. My doctor will not prescribe opiates and I understand this. I found a company c in the UK. I have had an appointment with a doctor from

Hi, I have pain and on gabapentin, co codamol, I have neuralgia and I have spoken about this. The issue I want to talk about is the use of cannabis for pain relief. My doctor will not prescribe opiates and I understand this. I found a company c in the UK. I have had an appointment with a doctor from

Hi just read an article in telegraph about medical cannabis use and parents who are growing their own and have had good results. Just wondering what has been peoples experience? Have refractory epilepsy and at the end for med options.

Do you have experience or knowledge of using CBD products.It is new to me but many here talk about it .Is it good for pain killing or sleeping..? If you have tried what is your opinion?Thanks.

Hi guys! Been a while. I'll keep it short. 41yo male. PAF diagnose in oct'23. Cryoablation in march'24. No afib since dec'23, but I developed a health/cardiac anxiety since and struggle with it for more then a year now. Some weeks everything is alright and some not. Lately it's getting more frequent

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

My husband has recently been diagnosed with CBD, He was struggling with certain things ie, buttons zips, holding things in his left hand. Our GP referred him to the memory clinic, but they discharged him as they felt it was a neurological problem. We went back to the GP where they did some basic tests

Hello everyone, I think my fatigue problems started when I had Steven' Johnson's syndrome in 1995. I just kept pushing through. In 2019 my asthma became severe, shielded for 14 months of the pandemic. Got covid within a couple of months of coming out of shielding. Had covid multiple times since then.

Hello everyone, I think my fatigue problems started when I had Steven' Johnson's syndrome in 1995. I just kept pushing through. In 2019 my asthma became severe, shielded for 14 months of the pandemic. Got covid within a couple of months of coming out of shielding. Had covid multiple times since then.

curious if any of you have tried using the tincture to help treat symptoms and help with inflammation and autoimmune? I diagnosed 7/23. Several flares back to slow reduction from 10 mg. I exercise 4-5 times a week at my crossfit gym so know I push my body but so far so good. I have tailored my workouts

Today is 6 years dx. Crappy timing. Quite a journey. I finally feel hope. I’ve been on the carnivore diet for the last 5 months. I’ve been feeling better and better until about 3 weeks ago. I was so disappointed because it had basically cured my non motor symptoms. I was way down. But what I realized

✋ MOST IMPORTANT PROTECT the SUPPLY I was going to wait until I had full results , I have decided that it is unfair of me to do so due to the time frame it can take for research and results . The Facebook page will direct you to the WIKI page which will answer ALL questions you have and were a list

I was thinking about you all today so decided to send you a Christmas wish. I know that for some of you you are still in the middle of the PSP/CBD chapter of your lives and that for others, like myself, are now on their own with only memories. Which ever situation you find yourself Christmas is not easy

O.K. as you are aware I talked my doctor into prescribing Gabapentin instead of Ropinirole. One obstacles out of the way. However I'm not sure that how she wants me to take them is correct. Also I have no Idea as to when they will arrive. She also has prescribed potassium tablets for my low registry

Hello, My 87 year old Mother in law was dx 4 years ago with PD, She is now started experiencing severe shuffling symptoms in the afternoon when trying to walk. She takes Sinemet, but doc switched her to Ritari to see if it helped...it did not. shes back on sinemet ANy suggested other meds that may

I previously had targeted radiation to my skull. They made a tight fitting mask and put my head in it and clamped this to the table. I have confinement claustrophobia and this was just plain torture. For the last of t treatments I took ativan. now I am going to have radiation to cervical vertebra

My spouse was initially diagnosed as having Parkinson's Syndrome. In February a different Neurologist suspected that it might rather be CBD and this has just been confirmed. I am currently the sole carer and hoping to find advice, etc from others on this site who are further along the line in order

I have been taking Alendronic acid for a year and want to start taking CBD gummies for something else. My GP said there’s very little info about any possible contra-indications and the CBD manufacturer says to ask your GP! Has anyone done this?