Experiences with

Sativex

I believe this may well be as a result of taking my 'alternative ant-cancer' treatments of drinking ozonated water and drops of 3% Food Grade Hydrogen Peroxide, diet and participation in the phase 1 SATIVEX clinical trial.

There has been one clinical trial (a small one) for people with recurrent GBM using Temozolomide and Sativex (a spray).

This is for those of you who are really struggling with the remedies for RLS. Apologies for not referencing all my research but I’ve been completely wiped out for weeks now. However I wanted to share some insights I’ve had recently and hope it inspires thoughts and research. Adenosine is a chemical

The Brain Tumour Charity has announced that the Aristocrat Phase 2 clinical trial of SATIVEX is now going ahead. Please see the link below for further details.

Anyone else having trouble obtaining these ?

I taper off oxycontin in 10 days after 2 years no problem Etorcoxib- good lord, it's an arthritis med..extreme pain that night Amitryptallin heart pounding. feel weird targiniq- I couldn't wake up.. slept most of the day Gabapentin- while tapering oxycontin. caused suicidal thoughts. scary Sativex

The above drug is a nasel spray that has been approved by the NHS for MS sufferers, dies anyone know if this is ok to take for Ataxia sufferers as helping symtoms a little is better than nothing, have been waiting since March to see my Nureologist and still no word 😡

I came across Sativex and saw that it was approved in the UK for MS and was wondering if any of my fellow AMNers in the UK have tried it before?

The phase II UK trial of Sativex in globlastomas will open in March 2022. TBTC campaign to fund this trial has received an outpouring of public support, which has resulted in over £400,000 raised in just 3 months. More info can be found in the news section of the TBTC website.

Has anyone been prescribed Sativex or nabilone for symptoms of MS without a diagnosis? I take morphine and it no longer seems effective Plus GP wants me off it, I don’t want pain patches again and the above meds are too expensive privately.

Has anyone been prescribed Sativex or nabilone for symptoms of MS without a diagnosis? I take morphine and it no longer seems effective Plus GP wants me off it, I don’t want pain patches again and the above meds are too expensive privately.

Hi All, So for the past two years I've been back at my childhood GP surgery as I've been living with family. It was good in that my GP knew me since I was a child so backed me up against a crappy rheumy and helped me escape to a better rheumatology department. But other than that my GP surgery basically

[u]CAM Therapy[/u] [u]What the AAN Says[/u] [u]Oral cannabis extract (OCH)[/u]Effective for reducing symptoms of spasticity and pain [u]Tetrahydrocannabinol (THC)[/u] Probably effective for reducing symptoms of spasticity and pain [u]Sativex (CBD plus THC) mouth spray[/u]Probably

[u]Benefits for MS[/u] The AAN established that oral cannabis extract (OCE) is effective for reducing symptoms of spasticity and easing pain.1 British researchers looking at Sativex (nabiximol), a drug that combines THC and CBD in the form of a mouth spray that's available only in the United Kingdom

utm_campaign=list_ms&utm_medium=email&utm_source=cn_nl&utm_content=20389786&utm_term= *Oral cannabis extract (OCH)Effective for reducing symptoms of spasticity and pain *Tetrahydrocannabinol (THC)Probably effective for reducing symptoms of spasticity and pain *Sativex (CBD plus THC) mouth sprayProbably

Nabiximols (Sativex) for MS Nabiximols (Sativex) is a cannabis-based medicine that is sprayed into the mouth. It is licensed in the UK for people with MS-related muscle spasticity that has not got better with other treatments.

"Conclusion : This study demonstrates that it is safe to administrate a single dose of Sativex to elderly patients with indolent B-cell lymphoma with regards to adverse events. We show that the cannabis compound quickly reduces lymphoma cell numbers in peripheral blood.

Has any of you heard of or tried sativex?

The recent release of the cannabis extract spray medicine Sativex has been a move in the right direction but it will not deal with the needs of all patients and most doctors are still not willing to prescribe it.

I am looking for alternatives to help relieve pain and regulate the immune system does anyone get low dose naltroxene or sativex through gp, pain doctor or consultant and where and who from ?