Hi everyone hope you can give some advice on getting Sativex when the PCT says NO?!!
Any help is appreciated for and against
Thanks Nonii
Hi everyone hope you can give some advice on getting Sativex when the PCT says NO?!!
Any help is appreciated for and against
Thanks Nonii
Hi It`s very common to be refused sativex on the NHS. A few GPs do prescribe it for their patients.
Dunno if you can get it privately via E med…who arrange LDN for many folk here/
luv Pollx
You could try asking for help from the MS campaigns team. They are always interested to hear of such problems.
Wendy x
Hi Nonii
My GP funded my Sativex from there own budget as my Health authority does not allow it.
I was backed by my Rehab consultant for the original script and was placed on the trial. I should say that my GP and my care team all worked very close together so it was not difficult. For that I will be forever grateful.
However
I have just moved into an adapted property and as a result I have moved GP’s.
I went to the new GP last week and they said they would not prescribe it. In fact the Dr said “my computer has a traffic light system for prescribing drugs. Your sativex traffic light is black” “not good then” “no, it means I am unable to even request it”
So currently I am waiting for a meeting of the practice partners to decide if they will fund it or if I have to do without.
Seeing I was part of the trial I am not to chuffed but as is anything big Pharma, they do charge the most extortionate amounts.
I would get a recommendation from your consultant and have an appointment with the senior practice GP and see what they say.
Good Luck
I had sativex on a private prescription for about 1 1/2 years (cost over £200 a go) until I had an adverse reaction and had to come off it.
Hi , If u can not get it on the NHS talk to your neuro/ms nurse and ask if you can get it private, thats what i did.
Bal