Health Boards
Fri-08-07-2016, 01:43 AM
Hi there
Hi there, name is Kit and I've been away from this forum for a week or two so I've only just caught up with this thread. WELCOME Sir!
I can see this thread has already made an impact and has attracted the interest of quite a few folks. I would like to add my name to those interested in learning more about how LDN may, or may not, assist me in my personal battle with P.
My history: Had P. (not PsA) for over 40 years - probably longer in reality - but not diagnosed.
Also I'm a cancer survivor (breast) - mastectomy, lymph node removal, chemo and radio. (That was 12 years ago)
I see we have a few things in common.
Found and joined this forum a few months back. Great place! Amazing resource.
My treatments for P over the decades have included topical steroid creams and potions, phototherapy (UVA & UVB), DMF (Fumaderm) - that last has failed twice now over a twelve year period- and now I've started Acitretin. (I'm just 4 weeks into it) I've a couple of journeys recorded on this Forum..... Kit's Fumaderm journey (failed but now completed) and Kit's Acitretin journey (obviously ongoing).
Maybe I've misread one of your posts but I understand you may be too busy to return here until November? Please don't leave it that long. but I do look forward to hearing how LDN has affected your condition.
As a UK politician who recently aspired to become our future Prime Minister recently said:(Paraphrased) "We are tired of hearing from experts - let the British people vote with their feet" and so we did. That politician may have helped his cause at the time but was today thrown onto the political scrapheap.
I agree with Bill.... I am much more interested in learning about your personal experience with LDN and how it affects your PsA than I am reading expert testimonials on a drug that is currently not directly associated, approved or available in many countries to those people suffering from P.
Kit
Hi there, name is Kit and I've been away from this forum for a week or two so I've only just caught up with this thread. WELCOME Sir!
I can see this thread has already made an impact and has attracted the interest of quite a few folks. I would like to add my name to those interested in learning more about how LDN may, or may not, assist me in my personal battle with P.
My history: Had P. (not PsA) for over 40 years - probably longer in reality - but not diagnosed.
Also I'm a cancer survivor (breast) - mastectomy, lymph node removal, chemo and radio. (That was 12 years ago)
I see we have a few things in common.
Found and joined this forum a few months back. Great place! Amazing resource.
My treatments for P over the decades have included topical steroid creams and potions, phototherapy (UVA & UVB), DMF (Fumaderm) - that last has failed twice now over a twelve year period- and now I've started Acitretin. (I'm just 4 weeks into it) I've a couple of journeys recorded on this Forum..... Kit's Fumaderm journey (failed but now completed) and Kit's Acitretin journey (obviously ongoing).
Maybe I've misread one of your posts but I understand you may be too busy to return here until November? Please don't leave it that long. but I do look forward to hearing how LDN has affected your condition.
As a UK politician who recently aspired to become our future Prime Minister recently said:(Paraphrased) "We are tired of hearing from experts - let the British people vote with their feet" and so we did. That politician may have helped his cause at the time but was today thrown onto the political scrapheap.
I agree with Bill.... I am much more interested in learning about your personal experience with LDN and how it affects your PsA than I am reading expert testimonials on a drug that is currently not directly associated, approved or available in many countries to those people suffering from P.
Kit
