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Funny thing -Marie is that neither of them used Dr Hiatt so how much could they really know about him.

----- Original Message -----

From: perlesetlacet@...

Sent: Monday, May 13, 2002 10:22 PM

Subject: Re: My Story

:'s correct. I too heard mixed reviews about Dr. Hiatt. Ang and Nik who used to post her told me he did awful work. I personally can't say if this info is correct as I don't know the man. I know I remember seeing good post about him too. Check it out for yourself. Best wishes.-Marie

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I agree totally I think he got on the recommended list for a reason at some point I guess someone used him that was happy, while I know Patty is happy I also know that if she could of I think she would have used Feng, I think that if you cannot travel and are sick then probably any PS that will remove them en bloc seems like an option for some women.

Take care

Hugs

----- Original Message -----

From: perlesetlacet@...

Sent: Tuesday, May 14, 2002 11:25 AM

Subject: Re: My Story

Hi :Nik went to him for a consult. and Ang (used to live in AZ--her sister still does) says she has a friend who had surgery by him and she saw the results and it looked very bad. She told me not to go to him under any circumstance (remember I was in AZ in Feb.I tend not to believe Nik b/c she thinks every PS is bad news except for Demas, but with Ang, I don't know.I'm just reporting what was said to me. I think if a patient is interested in him--they should see Dr. Hiatt and judge for herself. After all, outcomes of surgery results are subjective.-Marie

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  • 1 year later...

I have the same story, herniated discs, sciatica....bla bla took 6 years to diagnose. Never MRI'd brain and upper thorasic till my RR became permanent. Oh well , HERE"S TO LDN! Kiki

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11 years ago I was mri'd and dx with a herniated disk, after having

total numbness from my waist down. The neuro didnt offer any

treatment so I guess I just 'left it alone', hoping it would go away.

Well, being RRMS, of course it went away, so I felt I was ok again.

The numbness came back a few years later, plus some walking

difficulties and a few other 'weird' symptoms. My doctor suggested

another mri, and that was when I was dx with MS. The neuro (who is no

longer in practice) offered any of the ABC's, but saip I could try a

better diet and some exercise. Fortunately, for me, my MS has never

really been anything more serious than numbness and walking issues. I

can remember only one bad excaberation around christmas about 3-4

years ago. It felt like a terrible flu, with spinning, dizziness,

nausea, the whole bit. As a matter of fact, the flu season was

probably the trigger. That was the bout that took me from RRMS to a

more permanent type of MS. I have not went into remission since. Just

this last year I learned of LDN from the Goodshape forum. Having lost

my med. ins., I knew I needed to do something. You always hope that

you'll go back into remission, but you know eventually that what you

have is permanent. I crush and measure my own 4-5 mg doses, and have

done so for about 4-5 months. I run my own small business in Phoenix,

and for the most part, have been doing pretty good. I'm hoping that

LDN will keep it that way (until theres a cure, that is) I just wish

I wouldve known about LDN 11 years ago!

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