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Want to find doctor in Hawaii who treats DC.
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05/20/2005 23:57
Tolucca

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05/20/2005 23:57
Tolucca

not registered

On Target

After the barrage of personal NA testimonies posted here, it is only the most stanch OS advocates who could possibly remain unaffected by the huge success this French invention obviously has become. Some complain that too much time is spend on this subject. Exactly which other subject should begin to garner this much air time? Yes, Collegenase is a close rummer up. But mostly all we can discuss is the probability of it's availability in our lifetime.

Yes, this Forum has been dominated by discussion about NA. Is there something more worthy of our time? If Yes, what and why?

05/20/2005 23:12
No Name

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05/20/2005 23:12
No Name

not registered

What and Why?

Tolucca,

Your message is exactly the type that generates so much trouble on this site. Clearly, you are suggesting that OS is not a viable option for some people when in fact, OS and NA are the only two practical options available and for some people, OS is the only choice. As we all know, it is not the only choice.

As I discussed in some postings, for DC sufferers like me who a very aggressive form of dups, OS is the best option and I have some good information on this site that has helped with my post-opt care. Hopefully, other OS patients will have similar luck. As to the barrage of NA testimonies - best of luck to them, but the NA folks should be tolerant of other points of view and very often they are not.

05/20/2005 23:21
Toluc

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05/20/2005 23:21
Toluc

not registered

deputytrens of the hand

I suggested nothing about OS. It is a viable option for 100% of DC sufferers, under nearly all circumstances. Ask 95% of CHS and they will all tell you the same thing. What they will NOT tell you is that NA is the OTHER viable option.

Your choice to go with your doctor's recommendation to not try NA in your case must be respected. However, what is at issue here is that the minuscule number of DC sufferers who lave learned that they do indeed have an option to OS are just beginning to balance the scales of the vast majority of others who are continually being told otherwise by the professionals they must trust. LINDA'S post of 5/21 under "Bashers" is a great example of how this lone site is beginning to change that.

All that was implied in my previous post is that of all the great info and sharing of ideas that this site continues to provide, it's completely irreplaceable contribution to the evolving acceptance of NA as a viable option (along side OS) is by far the most significant. Nothing comes remotely close. Yes, perhaps actually stating the perfectly obvious is superfluous.

DISCLAIMER: CHS don't tell their patients about NA because they themselves don't know about it or are misinformed. Naturally, there are a few exceptions. Thanks to this site LINDA'S doctor is now one of them.

05/24/2005 23:06
eileen

not registered

05/24/2005 23:06
eileen

not registered

deputytrens of the hand

there may not be a cure, other then surgery, but stretching the fingers often seems to help, I was told 3 years ago by a doctor in Alexandria, iwould not be able to hold a brush within a few months. There are 2 bumps on my right hand, but I massage the hand and pull the fingers, as often as possible. Another hand doctor did not want to do invasive surgery. Is it hereditary? No alcoholics in my family. I did injure the hand about 4 years ago, by whacking it with a heavy stapler. Would that have caused it?

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