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Author Topic: Dr lue diagnosed mondors disease  (Read 9394 times)

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emasculated

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Re: Dr lue diagnosed mondors disease
« Reply #50 on: February 02, 2014, 12:16:47 PM »

Mentos: Make a picture of the erect situation and send it to Lue perhaps? Also even though in general ultrasounds are more reliable than MRI's. Sometimes an MRI can detect scarring an ultrasound misses.
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"Without health life is not life; it is only a state of languor and suffering - an image of death."

NeoV

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Re: Dr lue diagnosed mondors disease
« Reply #51 on: February 02, 2014, 07:03:28 PM »

That is similar to my condition,

Oddly enough I've nearly fixed all my symptoms by pushing down on my erect penis from the base. I stretch out whatever it is holding my penis up carefully. I've done this for half a year and it has changed my penis completely. Whatever it is it's constricting and stretching has helped me.

Of course you could damage yourself doing that, but honestly it's the one thing that has rid me of my peyronies, I would put VED at #2. 

I'll message you about it soon. That certainly is troubling.

Mentos

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Re: Dr lue diagnosed mondors disease
« Reply #52 on: February 03, 2014, 12:45:06 PM »

Walked straight into lue office and told them I need to see him. REDIAGNOSED WITH PEYRONIES :(.

We increased my Pentox prescription and cialis.

He advised against VED or TRACTION at this point as well as verapamill. Stating that if the Pentox will do the trick why waste money etc on shots and that the other manual therapies may do more damage. ...
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damian

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Re: Dr lue diagnosed mondors disease
« Reply #53 on: February 03, 2014, 01:27:36 PM »

He obviously told you what you wanted to hear. Did he ultrasound again?
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Mentos

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Re: Dr lue diagnosed mondors disease
« Reply #54 on: February 03, 2014, 01:47:51 PM »

He obviously told you what you wanted to hear. Did he ultrasound again?


That's the stupidest thing I have heard on this forum. No I did not want to hear that. I just wanted him to feel the hardness instead of ultrasound and tell me what is up.
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damian

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Re: Dr lue diagnosed mondors disease
« Reply #55 on: February 03, 2014, 05:00:56 PM »

There is the knowledge border of our doctors. He probably isn't sure what you have, but you have symptoms similar of peyronie's (curvature etc), so he decided to treat you like you have peyronie's. It's simplier, than saying that he doesn't has a clue as a doctor.
I'm not saying that he's wrong (how can I), but I'm unsure about plaque that doesn't show up with ultrasound.

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Mentos

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Re: Dr lue diagnosed mondors disease
« Reply #56 on: February 03, 2014, 05:17:42 PM »


As mentioned before he say a little bit of plaque... but the hard line that goes from base to top did not show. just a little portion i geuss.?

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damian

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Re: Dr lue diagnosed mondors disease
« Reply #57 on: February 03, 2014, 06:10:41 PM »

I mentioned before. I have TWO lines like you describe. And I'm pretty sure that they are HF related, because they seem to go away at times. Especially when HF is better.
Plaque doesn't come and go.

And yes, I have scar tissue too (injury), so I know what it's like to have both.
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james1947

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Re: Dr lue diagnosed mondors disease
« Reply #58 on: February 03, 2014, 06:59:04 PM »

My hard line is not going nowhere if my "HF" is better. Just can't feel it same as when the penis is hard.

James
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Age 71, Peyronies from Jan 2009 following penis fracture during sex. Severe Erectile Dysfunction.
Lost 2" length and a lot of girth. Late start, still VED, Cialis & Pentox helped. Prostate surgery 2014.
Got amazing support on the forum
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