To on Lymes

[Guest guest]

, Hi, funny you should say that my friend just did an interview on Lymes

and she thinks I have it. Heres the link to her interview, she almost was Olymic

material, (not quite), and got hit with Lymes.

http://thestory.org/archive/search_media?review_state=published & start.query:reco\

rd:list:date=2010-06-24%2023%3A59%3A59 & start.range:record=max & end.query:record:l\

ist:date=2010-06-24%2000%3A00%3A00 & end.range:record=min & month:int=6 & year:int=201\

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Her name is Downer she is first pic at top of page. Scroll to bottom of

page and see the arrow to start the interview to listen. Keep listening, at

first it sounds short but it continues even when it sounds like raidio MC is

stopping.

She has told me the places that " really " know how to test as some test and it

comes up negative when you have it, because of insufficient testing or knowledge

of how to test.

She and her boyfriend saw me walking like someone who was 80 at this fund raiser

I was volunteering at and they empathetically walked over and grilled me for 35

mins on my symptoms and looked at each other and said they thought I had Lymes.

I used to be a strong athlete too, but that is over.l I had a bite too with a

bulls eye, and it went into synovial (sp?) sack in shoulder and bad pain and

loss of mobility somewhat in shoulder for a year. It spread to left shoulder and

then finally went away.

I'm so tired. It's been a an ordeal of more yrs than I'm comfortable to admit. I

must get tested for Lymes after your post. It's just so many drs and you get

very tired.

Take care and ty.

Love,

Jean

Recently I feel like though Corvalen M is helping with Fybromyalgia and CFS a

lot, but I feel there is sometimes no cushion in joints every so often and it's

a bit scary. Like connective tissue disease or something. I have the marker but

don't have connective tissue problem as far as I know but feel as if I do.

Ty, hearing this twice, I will get tested, as Corvalen M is helping a lot but

some tiredness last few days and just a bit more fybro pain than I want.

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>

> You may have lyme. I started VCO for the same reason and I have CFS...which i

discovered is a symptom of Lyme. It causes all the symptoms you have mentioned.

There is a lyme group. If you live in the USA,get tested. On the

group it will tell you where the tests cans be done.

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> Lyme effects thyroid,hypothalimus and causes many problems including MS.

>

> Do some research via the or just google. .

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