This Is MS Multiple Sclerosis Community: Knowledge & Support
Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
CCSVI treatment on the NHS ???
3 posts
• Page 1 of 1
CCSVI treatment on the NHS ???
by Hampshireman » Tue Mar 29, 2011 8:08 am
Does anybody know how long before we may be able to get CCSVI treatment on the NHS? Are any trials being done in the UK to persuade NICE?
-
Hampshireman - Newbie
- Posts: 3
- Joined: Fri Dec 31, 2010 3:00 pm
Advertisement
by Daisy3 » Tue Mar 29, 2011 9:00 am
Doubt it.
I do not know of any trials being done here at all. The Neurology community here are also a tough bunch who think the whole CCSVI thing is a bit of a joke. NICE are a conservative group and right now there is simply not enough information for them to offer this treatment on an already strained NHS.
I do not know of any trials being done here at all. The Neurology community here are also a tough bunch who think the whole CCSVI thing is a bit of a joke. NICE are a conservative group and right now there is simply not enough information for them to offer this treatment on an already strained NHS.
-
Daisy3 - Family Elder
- Posts: 308
- Joined: Tue Feb 09, 2010 3:00 pm
by EJC » Tue Mar 29, 2011 12:27 pm
Our best chance right now is the Edinburgh Health Clinic, they are proceeding and monitoring in as scientific a way as this procedure allows.
They will make all their findings available as soon as they can.
Honestly I think we're in for a long haul but I have a feeling this will not go away.
It's hard to get a trial going whne the reason for not starting a trial is there's never been a trial. That's a belter of a circular argument.
They will make all their findings available as soon as they can.
Honestly I think we're in for a long haul but I have a feeling this will not go away.
It's hard to get a trial going whne the reason for not starting a trial is there's never been a trial. That's a belter of a circular argument.
-
EJC - Family Elder
- Posts: 616
- Joined: Tue Apr 20, 2010 2:00 pm
- Location: Surrey, UK
3 posts
• Page 1 of 1
Return to Chronic Cerebrospinal Venous Insufficiency (CCSVI)
-
- Related topics
- Replies
- Views
- Last post
-
- Atlas/TMJ treatment with Dr M Amir to negate CCSVI treatment
by CindyCB » Sat Dec 17, 2011 5:30 am - 5 Replies
- 3807 Views
- Last post by TheCatsWhiskers
Thu Oct 04, 2012 5:49 am
- Atlas/TMJ treatment with Dr M Amir to negate CCSVI treatment
-
- CCSVI treatment and migraine..any difference after treatment
by Brightspot » Sat Jan 16, 2010 11:53 pm - 2 Replies
- 1783 Views
- Last post by magoo
Sun Jan 17, 2010 10:35 am
- CCSVI treatment and migraine..any difference after treatment
-
- What happens after CCSVI treatment?
by Rosegirl » Wed Mar 10, 2010 1:32 pm - 1 Replies
- 1116 Views
- Last post by esta
Wed Mar 10, 2010 1:42 pm
- What happens after CCSVI treatment?
-
- WHERE IS CCSVI treatment being done?
by Villagemaid » Sun Apr 18, 2010 7:37 am - 3 Replies
- 1162 Views
- Last post by mmcc
Mon Apr 19, 2010 4:57 pm
- WHERE IS CCSVI treatment being done?
Who is online
Users browsing this forum: No registered users
News
Site map
SitemapIndex
RSS Feed
This site does not offer, or claim to offer, medical, legal, or professional advice.
All treatment decisions should always be made with the full knowledge of your physicians.
This is MS does not create, endorse, or republish any content. All postings are the responsibility of the poster. All logos and trademarks in this site are property of their respective owners. All users must respect our rules for intellectual property rights.
This is MS does not create, endorse, or republish any content. All postings are the responsibility of the poster. All logos and trademarks in this site are property of their respective owners. All users must respect our rules for intellectual property rights.
