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peyronie-dupuytren-ledderhose in Washington State
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02/22/2009 20:06
livinglegend47 
02/22/2009 20:06
livinglegend47 
Re: peyronie-dupuytren-ledderhose in Washington State

Upon seeing my GP for a strange "bump" on my right hand, I was told that I had this wierd thing called Dupuytren's, of course, like most of you, I had never heard of this disease and couldn't fathom how I got it. She sent me to a hand doctor in Seattle (I live in central Washington). He took a quick look at my hand, confirmed my GP's diagnosis, told me that it is found in those of a certain geographic area, men in their 7th decade and in alcoholics, (this he said with accusing eyes), and is genetic. He told me that there was nothing that he could do for me until my fingers became contorted and then he could do a very painful surgery with no guarantee that the disease would not return. I left in tears. I am female, just turning 60 at the time of diagnosis, not an alcoholic, and neither of my parents had this disease. I returned to my GP telling her that I did not like that doctor so she sent me to another one in Yakima with pretty much the same results, again I left in tears. Thank God for the internet. I searched until I found Dr. Kline. We called immediately and set up an appointment for the NA. Since my initial visit I have been to see him two times for injections with results that appeared to diminish the nodules and chord. During this process a small "bump" has appeared on my left hand. My disease has been kept in check by Dr. Kline's treatments and I do not have any contracure so he has suggested radiation as my next line of defense. He told us that any facility that does oncology radiation can perform the same treatment as what they are doing in Boise. We contacted the folks at North Star Lodge in Yakima with my request for radiation to inhibit the advancement of my Dupuytren's disease...your what? was their response....and how do you spell that? Since my initial call to the facility Dr. Cleary has researched the protocal and consequently Dr. Cleary will perform the first of my five radiation treatments tomorrow. I guess my point of this writing is to let you know that there is a facility in Washington that will do the radiation therapy and also that it just may be up to us, the ones that suffer from this disease, to educate the doctors that can help us.

































Thy

02/22/2009 20:36
Megan 
02/22/2009 20:36
Megan 
Re: peyronie-dupuytren-ledderhose in Washington State

I'm so glad you found a doctor in Yakima willing to do the radiation for you!

Your experiences with the hand surgeons sound a lot like mine were, unfortunately.

I'm glad you found Dr. Kline, though, and I'm glad Dr. Cleary is open-minded enough to perform the radiation treatment for you!

Megan L, Bellevue WA

03/01/2009 00:35
Shantidog

not registered

03/01/2009 00:35
Shantidog

not registered

Re: peyronie-dupuytren-ledderhose in Washington State

Megan,

Thank-you so much for the info about Dr Klein. I will try calling on a Friday morning. I have called him and left messages and also have emailed, but no one has gotten back to me.Seems like a strange way to run an office.

I had NA done about 4 yrs ago by Dr Eaton, but since I live on the WA/ID border, it makes much more sense to go to Boise. I had almost decided to just have surgery this time, but reading about how long it can take to heal has made me change my mind again.

Thanks again,
Marilyn

03/01/2009 00:38
Shantidog

not registered

03/01/2009 00:38
Shantidog

not registered

Re: peyronie-dupuytren-ledderhose in Washington State

Sorry, Kline, not Klein.

03/01/2009 05:10
fmerk 
03/01/2009 05:10
fmerk 
Re: peyronie-dupuytren-ledderhose in Washington State

If you hadn't already read, Dr. Kline is an ER Dr. practicing ~ 50 miles from Boise. He move his DC clinic to Boise about 1 1/2 years ago. I don't think the office is open or staffed (phone/receptionist) full time. He always has gotten back to me after a few days.

You definitely do not want the full surgery if it can at all be avoided. Not only is the rehab painful and nasty, but the residual scar tissue makes NA more difficult and further surgeries if needed yet worse.

I would also recommend not waiting too long. I did as I was avoiding surgery and didn't want to go all the way to France or Florida and the little finger joint itself became adversely affected and will not fully straighten after the NA.

Fritz

03/15/2009 02:08
Ttownguy 
03/15/2009 02:08
Ttownguy 
Re: peyronie-dupuytren-ledderhose in Washington State

I too have tried without success to get treatment from Dr Kline. Your phone calls will likely not be answered and neither will your emails. If you call first thing in the morning the chance of your call being answered is higher. When I tried to find out if I should go further and seek treatment if no one would answer my calls or mail I was offered an appt. (but without emailing any pics for assessment). I'm going to try other doctors on the west coast listed here on this site. Anyone had any experience with Dr Grabow or Benhaim?

If anyone has had any success with radiation in P Sound area I'd be very interested in finding out how things went and the name of the clinic/doctor.

As for the clinic in Vancouver BC they aren't allowed to treat US citizens that travel for treatment. They can only help you if you are travelling and have some kind of medical emergency or need that must have care before getting back home. They did, however, get back to me in 24hrs. So much for slow Canadian medical stories.

03/15/2009 02:56
Megan 
03/15/2009 02:56
Megan 
Re: peyronie-dupuytren-ledderhose in Washington State

Hello Ttownguy,

When I saw Dr. Kline in November, he mentioned that there is a doctor in the North Seattle area who is doing radiation for Dupuytren's but I didn't get the doctor's name. When you do reach his office, you might be able to get that information.


Megan

Edited 03/15/09 04:58

03/15/2009 17:36
Mike S

not registered

03/15/2009 17:36
Mike S

not registered

Re: peyronie-dupuytren-ledderhose in Washington State

Although I have not personal experience with Dr. Benhaim whi is here in LA, others on this board have, and have reported positive results. Another option if you're open to all west coast locations is Dr. Denkler in SF (Larkspur) with whom I do have personal experience - highly recommended.

05/07/2009 15:59
SeaDog

not registered

05/07/2009 15:59
SeaDog

not registered

Re: peyronie-dupuytren-ledderhose in Washington State

I have also talked with Dr. Kline in Boise, however his practice seems a bit shady and unprofessional to me. He claims to have done over 3,000 NA procedures but refuses to send an email or put anything in writing to verify, and he will not send a copy of his risk disclosure document before doing the procedure. I don't want to put my health at risk with someone who is not totally honest and ethical. And why did he leave Oregon? There are many other good professionals out there.

05/07/2009 17:18
Megan 
05/07/2009 17:18
Megan 
Re: peyronie-dupuytren-ledderhose in Washington State

Hi Seadog,

That's not the impression I have of Dr. Kline and I have seen him twice. I believe he left Oregon because it was a long drive for his patients, many of whom just had NA, to drive to the airport in Boise. His location makes it easier his patients, especially those who are coming from out-of-town.

Megan L (Bellevue, WA)

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