Talk:Tolosa–Hunt syndrome
![]() | This article is rated C-class on Wikipedia's content assessment scale. It is of interest to the following WikiProjects: | |||||||||||||
|
![]() | Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about Tolosa–Hunt syndrome.
|
Major revamp
editIn about an hours time I should have finished converting this from a stub to a start class article. I've resourced the article, noting references appropriately, and expanded significantly into sections (signs and symptoms, diagnosis, treatment, prognosis, epidemiology). Any issues please contact me on my talk page. CycloneNimrod (talk) 21:01, 21 January 2008 (UTC)
Comment moved from end of article
editmy husband is 54 and has had THS for 7 years. firstly infrequent attacks now permanent loss of normal eye vision and frequent headaches pain and weekness,leathargy andmuscle pain without respite. no cures found from your lists. just a depressing life to look forward to. —Preceding unsigned comment added by Antifamilymang (talk • contribs) 02:51, 13 January 2010 (UTC)
I am a patient with THS
editI am a 39 year old female and have had Tolosa-Hunt syndrome for 11 years. I have been on infliximab and a low dose of methotrexate for the past 6 years. Immediately after starting infliximab treatments, my symptoms were gone. I have been in remission of THS since beginning the treatment. Steroid treatment as noted in this article did not work for me. Melaniesue72 (talk) 16:48, 28 October 2011 (UTC)