tag:blogger.com,1999:blog-660534336558900776.post658747179274759943..comments2023-09-24T20:54:29.223+01:00Comments on Ledderhose Disease Blog: Xiapex in the UKGaryManleyhttp://www.blogger.com/profile/03039676015910922554noreply@blogger.comBlogger2125tag:blogger.com,1999:blog-660534336558900776.post-60379590744993996842012-03-21T21:22:57.014+00:002012-03-21T21:22:57.014+00:00Xiapex is being considered for Ledderhose. There...Xiapex is being considered for Ledderhose. There is already some off-label use.<br /><br />The British Dupuytren Society are trying to get data on the off-label use, but no results yet. (Takes time to know how well it works)Judith Proctorhttps://www.blogger.com/profile/09479416091313308184noreply@blogger.comtag:blogger.com,1999:blog-660534336558900776.post-53356495652372871842012-03-21T10:27:57.061+00:002012-03-21T10:27:57.061+00:00Who within the NHS makes the decision that a parti...Who within the NHS makes the decision that a particular treatment will become available? Can we contact other health authorities to lobby for the treatment to be available in other areas and for LD as well as DD? Can we research to find the people we need to lobby? Using your scientific knowledge we can approach them in a calm, informed way and persuade!<br />The Old BagAnonymousnoreply@blogger.com