My MS Quest

Here you can introduce yourself and give an account of your medical history, visits to physicians, results of treatments, etc.
Post Reply
beneaththeskin
Posts: 6
Joined: Mon 14 Mar 2016 21:40

My MS Quest

Post by beneaththeskin » Sat 23 Apr 2016 12:35

Hey all!

I was diagnosed with Multiple Sclerosis last year, and have been doing my due diligence in research.
Everything I have done has led me to Borreliosis. I have been diagnosed as such by an LLMD.

Check out some of my personal microscopy work:
https://youtu.be/dH3fGVndMYo
https://youtu.be/aFa6S8fB2Tk

I am working towards getting better. All my personal work has led me here.

Symptomatically, I haven't changed much. But that is better than getting worse.

Does anyone else here have MS?

Have a good day!

V/R,
forum member: beneaththeskin

alfon
Posts: 12
Joined: Mon 27 Apr 2015 1:54

Re: My MS Quest

Post by alfon » Tue 26 Apr 2016 7:53

Where did you get the microscopy work done?

I was given a (it's probably MS diagnosis).

Have you tried the Wahls diet along lyme treatment?

Best wishes

User avatar
ChronicLyme19
Posts: 564
Joined: Mon 11 Aug 2014 17:42
Location: NY, USA

Re: My MS Quest

Post by ChronicLyme19 » Thu 28 Apr 2016 1:40

You guys should read the part about MS in here if you haven't already:

http://www.huffingtonpost.com/dana-pari ... 18660.html

Along the lines of:
How many patients come to you with an MS diagnosis who actually get better with antibiotics?
A lot. I have to differentiate the relapse and remitting folks from the primary progressives. I don’t know that primary progressives have Lyme—they don’t respond the same way—but my relapse and remitting patients respond quite well and the majority have evidence of Lyme if you thoroughly evaluate.
Half of what you are taught is incorrect, but which half? What if there's another half missing?

Post Reply