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Ledderhose (feet)
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 1
11/01/2005 23:04
Stage one

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11/01/2005 23:04
Stage one

not registered

Ledderhose (feet)

Please consider contacting Dr. Lermusiaux in Paris
at Lariboisiere Hospital regarding NA and cortisone
injections for plantar fibromatosis. I am not current with
the treatment; however, previous posts reported some
improvement in foot nodules when treated by NA then
followed by cortisone injections several days later.
I have no personal experience (I do have beginning LD)
but I would avoid surgery and seek an opinion from
Dr. Lermusiaux before deciding on an option. Good luck.

11/02/2005 23:07
Wolfgang Wach

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11/02/2005 23:07
Wolfgang Wach

not registered

surgery for Ledderhose?

Jay is yet another example that surgery can activate Dupuytren or Ledderhose ("and it came back with vengence"). That is one of the reasons why I would generally be reluctant with surgery. While for hands surgery might still provide satisfying results at least for the majority of cases, for Ledderhose surgery seems to be more critical. Feet have to carry weight and it is more difficult and inconvenient to avoid using them in the recovery period after surgery. Also on case of blood flow problems feet are more critical than hands.

Wolfgang

11/02/2005 23:13
ken 
11/02/2005 23:13
ken 
LD

I also would like to hear from those with DIRECT experience of NA treatment for LD. We know that surgery is to be avoided, but it would be good to hear from somebody who has had NA on the feet - successful or otherwise.

11/02/2005 23:57
jim h

not registered

11/02/2005 23:57
jim h

not registered

Lederhose - NA

Hard to see how NA could help Lederhose (I have both). NA weakens a cord allowing it to be snapped - that's all. It doesn't remove any tissue. With LD, there's no cord - no contracting band - just unwanted tissue that needs to be removed.

There's a Lederhose forum on Yahoo where the moderator has been posting about his recent experience with 'cryosurgical' treatment that sounds really promising. Basically the tissue and involved nerves are damaged, in a controlled way, by extreme cold so the condition is no longer painful.

11/07/2005 23:51
Graeme

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11/07/2005 23:51
Graeme

not registered

Lederhose - NA

jim h

I have an appointment with Dr Lermusiaux late December
and he is to perform NA on my foot. I know of others who have had successful NA on their feet - performed by Dr Lermusiaux. I will report on my experience and outcomes.

11/07/2005 23:58
jim h

not registered

11/07/2005 23:58
jim h

not registered

needle aponevrotomy

Thanks Graeme I look forward to hearing about it. Lermusiaux has earned a lot of respect so I'm sure whatever he does will make sense.

10/24/2006 23:07
Mon

not registered

10/24/2006 23:07
Mon

not registered

needle aponevrotomy

Hi

I would be really pleased to hear if anyone knows of a hand surgeon who has trained in Paris and now carrying out the above proceedure in England

Many Thanks

10/25/2006 23:41
Wolfgang

not registered

10/25/2006 23:41
Wolfgang

not registered

NA in the UK

http://www.dupuytren-online.info/needle_aponeurotomy.html lists addresses. Marjorie is most knowledgable about this and posted those addresses also in this forum under the topic "UK NHS acceptance of NA".

NA for feet is typically less successful because feet usually don't develop cords. For the feet (Ledderhose) a variety of other treatments is possibly, see e.g. http://www.dupuytren-online.info/ledderhose_disease.html.

Wolfgang

10/25/2006 23:52
Marjorie

not registered

10/25/2006 23:52
Marjorie

not registered

anybody else have these symptoms?

Hi Mon,
There are no french trained NA practitioners in the UK.
However, there are 3 known practitioners in the UK, there are probably more but they are not yet admitting to it as their colleagues think NA is a load of rubbish.
Mr L C Bainbridge has been doing NA for many years.

email chris@hand-surgery.co.uk

His web page is www.hand-surgery.co.uk

Hope this helps,
Marjorie

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