Re: PPMS and the neurologist

November 11, 2008

, do you feel the dental work payed off, and are you stable, or getting

worse?...RP

November 12, 2008

Don't ever give up and take one day at a time. Have you ever read 's

website, it's very encouraging how she beat MS. Try it, scorner.com

Stay positive, the same way it took some time for MS to catch up to you, it'll

time some time to get rid of.

Val-

Subject: PPMS and the neurologist

Date: Tuesday, November 11, 2008, 7:50 PM

Well my neuro again told me today he thinks the type of MS I have is

PPMS and that there is no treatment for this type of MS. He wrote a

script for antidepressant and told me to get another MRI in a year.

Gee thanks.

I have only alternatives, which is what I was doing anyway. I always

find it quite depressing to go to the neuro. I only went this time in

prep for filing for SSDI, which I'm still not even sure I'm going to

do because I really want to try to go back to work and frankly I

don't

I am on LDN and BBD or probably would be in worse shape. I have done

colon cleanses, colonics, SCIO testing, various supplments, ion foot

baths, and had all the metal removed in my mouth (which by the way

the dental work was $12K because it included replacement of two

bridges).

I am currently trying to decide what I might want to add--total

fasting for a stretch, juice fasting for a stretch, coffee enemas,

hormone therapy, chelation, Klenner, Cal EAP, candida cleansing,

parasite cleansing have been things I have considered and researched

but not done.

Still feel determined not to live the rest of my life with MS,

especially PPMS. Still in a way can't believe this has happened, even

though it's been 2 years now.

I am 41 and sit in the neuro's office with people in their 60s and up

and have to fight not to say, " why me? "

Thanks for listening.

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