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Slow letters to GPs
Why is it that consultants secretaries take so long to send letters to GPs? I know from experience that it does take a while usually about 3 weeks for the letters to be typed and forwarded to GPs but 5 weeks on and I am still waiting for my GP to get a letter from my Scleroderma specialist, to the extent
Why is it that consultants secretaries take so long to send letters to GPs? I know from experience that it does take a while usually about 3 weeks for the letters to be typed and forwarded to GPs but 5 weeks on and I am still waiting for my GP to get a letter from my Scleroderma specialist, to the extent
PaleIndian2
in
Scleroderma & Raynaud's UK (SRUK)
9 years ago
I created a Petition to make Sativex to be widely Available for Multiple Sclerosis (MS) Suffers- will you sign it?
I need your help, My boyfriend was recently diagnosed with Multiple Sclerosis. The drug Sativex is legal in UK but not available through NHS, So I have created a Petition, can you please share this link with friends and family and on social media, and sign it if you're from UK. https://petition.parliament.uk
I need your help, My boyfriend was recently diagnosed with Multiple Sclerosis. The drug Sativex is legal in UK but not available through NHS, So I have created a Petition, can you please share this link with friends and family and on social media, and sign it if you're from UK. https://petition.parliament.uk
Sativex
in
Behçet's UK
9 years ago
Question?
Has anyone on here suffered with really bad dry mouth no saliva especially at night, I was thinking of trying an artificial saliva spray are they any good? Any answers please would be appreciated thank you our should I book a doctor's appointment?
Has anyone on here suffered with really bad dry mouth no saliva especially at night, I was thinking of trying an artificial saliva spray are they any good? Any answers please would be appreciated thank you our should I book a doctor's appointment?
Silly-mummy
in
Lung Conditions Community Forum
9 years ago
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CBD oil
Hello all, thought I'd let you know about something I've been giving my dad for a while now. Cannabidiol or CBD oil. https://en.m.wikipedia.org/wiki/Cannabidiol The good news is this is completely legal in the UK and you can order it online with no worries. If you've never heard of this medicine Plz
Hello all, thought I'd let you know about something I've been giving my dad for a while now. Cannabidiol or CBD oil. https://en.m.wikipedia.org/wiki/Cannabidiol The good news is this is completely legal in the UK and you can order it online with no worries. If you've never heard of this medicine Plz
Hidden
in
PSP Association
9 years ago
Neuropathy
After three operations on my neck for stenosis I have suffered with intense stinging pain in my hands for the past three years. Tramadol has no effect, I was allergic to morphine patches and I have so far resisted taking anti depressants as I am concerned about side effects. Has anyone any pain relief
After three operations on my neck for stenosis I have suffered with intense stinging pain in my hands for the past three years. Tramadol has no effect, I was allergic to morphine patches and I have so far resisted taking anti depressants as I am concerned about side effects. Has anyone any pain relief
Suzyhayes
in
Pain Concern
9 years ago
Dry Mouth
I was diagnosed with Parkinsons about 8 years ago. I have recently started having a dry mouth resulting from a lack of saliva. This has caused me to have a very sore tongue, amongst other things. As this is a recent problem, I wonder if it is due to an addition to my medication. I have been prescribed
I was diagnosed with Parkinsons about 8 years ago. I have recently started having a dry mouth resulting from a lack of saliva. This has caused me to have a very sore tongue, amongst other things. As this is a recent problem, I wonder if it is due to an addition to my medication. I have been prescribed
Court
in
Cure Parkinson's
9 years ago
Sativex medication
Hi all, I'm really really fed up of no treatment working! I have had 5 laparoscopys with treatment and been on all kinds of medication but nothing takes my pain away! Has anyone been able to try Sativex which is a cannibis based drug?? I'm seriously running out of options :( Xx
Hi all, I'm really really fed up of no treatment working! I have had 5 laparoscopys with treatment and been on all kinds of medication but nothing takes my pain away! Has anyone been able to try Sativex which is a cannibis based drug?? I'm seriously running out of options :( Xx
Tozzy
in
Endometriosis UK
10 years ago
Sativex and Fampyra
Rejected by NICE on the grounds of being too expensive http://www.mssociety.org.uk/ms-news/2014/10/ms-society-responds-new-nice-clinical-guideline-ms-0
Rejected by NICE on the grounds of being too expensive http://www.mssociety.org.uk/ms-news/2014/10/ms-society-responds-new-nice-clinical-guideline-ms-0
Cherie
in
AMN EASIER
10 years ago
SATIVEX petition again!!!!!!
Sorry but I'm not a techy!!!! My son has just helped me and this is the link....... https://you.38degrees.org.uk/petitions/savitex-for-all And yes I know I spelt it wrongly but I did change it eventually but it seems you can still get it in this link. Thanks so much for your time and hits and patience
Sorry but I'm not a techy!!!! My son has just helped me and this is the link....... https://you.38degrees.org.uk/petitions/savitex-for-all And yes I know I spelt it wrongly but I did change it eventually but it seems you can still get it in this link. Thanks so much for your time and hits and patience
billi
in
Behçet's UK
10 years ago
SATIVEX not SAVITEX....sorry
Me again, I was so determined yesterday to set up this campaign and had to do it quickly before I lost my nerve. That's my excuse for getting the bl....y name wrong way round, what a prat. My other excuse is the pain I am in mad the current meds I have to take....lol Sorry, promise I mean well!!! Billi
Me again, I was so determined yesterday to set up this campaign and had to do it quickly before I lost my nerve. That's my excuse for getting the bl....y name wrong way round, what a prat. My other excuse is the pain I am in mad the current meds I have to take....lol Sorry, promise I mean well!!! Billi
billi
in
Behçet's UK
10 years ago
SATIVEX
Hi to everybody and as some of you already know I have started a campaign for all people with long term chronic illness and pain to be able to get this medication. I need you all and your family, friends, workmates neightbours...you get the drift to sign we need at least ONE HUNDRED signatures to comtinue
Hi to everybody and as some of you already know I have started a campaign for all people with long term chronic illness and pain to be able to get this medication. I need you all and your family, friends, workmates neightbours...you get the drift to sign we need at least ONE HUNDRED signatures to comtinue
billi
in
Behçet's UK
10 years ago
Week 3 of sativex
Liam is now on the third week of the new drug ' sativex'. He has to build up his dose slowly but already am seeing noticeable changes in his tone which is great new. Fingers cross that the higher the dose the less tone problems he will have!!! Happy mummy just now xxx
Liam is now on the third week of the new drug ' sativex'. He has to build up his dose slowly but already am seeing noticeable changes in his tone which is great new. Fingers cross that the higher the dose the less tone problems he will have!!! Happy mummy just now xxx
Nickyxjx
in
Headway
10 years ago
Sativex!!!!
My Liam started on a trial of medication yesterday. Sativex is used widely in adults who suffer mainly with MS. It's said to relax muscle, which in turn will lower muscle tone and make patients more comfortable. The drug is not yet available to children hence this only being a trial. Liam suffers real
My Liam started on a trial of medication yesterday. Sativex is used widely in adults who suffer mainly with MS. It's said to relax muscle, which in turn will lower muscle tone and make patients more comfortable. The drug is not yet available to children hence this only being a trial. Liam suffers real
Nickyxjx
in
Headway
10 years ago
Has anybody contemplated using Cannabis Oil to treat their Lung cancer? Seems there's been good results using it.
Here's the background to the use of cannabis oil to treat cancer..... Despite government and UN stance regarding cannabis as an illegal narcotic. It is now an established fact that cannabis is a safe and effective medicine, supported by a very large body of evidence and further supported by patent filed
Here's the background to the use of cannabis oil to treat cancer..... Despite government and UN stance regarding cannabis as an illegal narcotic. It is now an established fact that cannabis is a safe and effective medicine, supported by a very large body of evidence and further supported by patent filed
topgun
in
The Roy Castle Lung Cancer Foundation
10 years ago
what is Sativex?
BarbR
in
Lung Conditions Community Forum
11 years ago
Hemp Seeds or Hemp Seed Oil (Cannabis)
Hi, For the past week or so my legs have been killing me! I'm reluctantly increasing my Amitriptyline and I asked my Neurologist about Sativex and they said there is no way I could have it because it is only approved for MS, I've been reading about Cannabis and Hemp seeds and it looks very promising
Hi, For the past week or so my legs have been killing me! I'm reluctantly increasing my Amitriptyline and I asked my Neurologist about Sativex and they said there is no way I could have it because it is only approved for MS, I've been reading about Cannabis and Hemp seeds and it looks very promising
StevenSims
in
AMN EASIER
11 years ago
Hello everyone I am trying to find someway of trying out sativex as a legal sub. I don't mind even paying. :)
sunnydays2013
in
Fibromyalgia Action UK
11 years ago
Why are people being forced to break the law to gain pain relief when there is a perfectly legal alternative which NHS refuse to prescribe?
Across this country there are people being forced to break the law to gain relief from chronic pain. I am talking of course of the excellent pain relief given from cannabis. For the past 10 years there has been an alternative to the risk of buying or even growing your own cannabis. Sativex has shown
Across this country there are people being forced to break the law to gain relief from chronic pain. I am talking of course of the excellent pain relief given from cannabis. For the past 10 years there has been an alternative to the risk of buying or even growing your own cannabis. Sativex has shown
dori2o
in
Pain Concern
11 years ago
DLA unsuccessfull RANT!! :-(
I applied for DLA in March 2011, I had a 'no' reply in June 2011, it finally went to a tribunal hearing at end of October 2012!!! Which has been unsuccesful and have been informed I'm not emtitled on any level for care or mobility. I have arthritis, lupus, raynauds, fibromyalgia etc to name but a few
I applied for DLA in March 2011, I had a 'no' reply in June 2011, it finally went to a tribunal hearing at end of October 2012!!! Which has been unsuccesful and have been informed I'm not emtitled on any level for care or mobility. I have arthritis, lupus, raynauds, fibromyalgia etc to name but a few
heatherx
in
LUPUS UK
12 years ago
Carpal Tunnel Syndrome
Currently I take hydroxychoroquine, azathioprine, tramadol, diclofenac, lansoperazole, citalopram and co-codamol (30/500) as well as
salivix
and viscotears. None of the pain relief is doing very much at all anymore.
Currently I take hydroxychoroquine, azathioprine, tramadol, diclofenac, lansoperazole, citalopram and co-codamol (30/500) as well as
salivix
and viscotears. None of the pain relief is doing very much at all anymore.
cathbw
in
LUPUS UK
12 years ago
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