I’m in Uk and have a Savitex question for you
So I’ve asked my GP in writing for some Savitex-he said that this is hospital prescribed only, so I wrote to my neurologist, who said it wasn’t available to prescribe at her hospital - (the northern neurological centre of excellence)
I’m perturbed.I thought this had been approved for MS patients in the UK?
I have had Savitex paste, made by a guru type person at great expense... it was the first bit of relief I had had for years... but I can’t afford to keep buying it privately from someone who essentially is a drug dealer..
And wtf should I, when this is purported to be available and other patients can get much stronger, much more expensive toxic drugs ....( and they are encouraged..! )
SAVITEX is very much cheaper and has the power to alleviate the ball ache of MS, calm everything down and gives you a brilliant nights sleep...(unlike the will they/won’t they work toxic ‘treatments’ that offer no relief and come with a suitcase of issues)
So I ask you, in the UK (and around the world)
1. What country are you from?
2. Is Savitex allegedly available on prescription in your country?
3. Have you ever tried to get a prescription?
4. What happened?
I realise that this is mainly applicable to Uk residents, but I just wondered if it was available anywhere else in the world, or had anyone else tried it?
I’m going to write a group letter with regards to this (NICE/parliament etc as you do) - so please let me know your thoughts and observations.
I’m not on faceplant, twirker, insta or any of that - hence why I am asking here.
There’s what ? Over 300 local authorities in the Uk , so any of them making it available to pwMS?
All observations gratefully received. Thank you x