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» LymeNet Flash » Questions and Discussion » General Support » once MS now Lyme pls help

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Author Topic: once MS now Lyme pls help
trishee
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S.L.A.M. has met a family who was given a diagnosis of MS now to find out it may be Lyme.

While so many of us have had this very diagnosis and have been treated to find a better quality of life, this family is confused and would like to hear from those who have been thru the same.



If you were once dx with MS and are now undergoing Lyme treatment please contact me if you are willing to talk to this family who desperately needs direction. contact [email protected]



Thanks,

Trish

Posts: 142 | From Sturbridge, MA | Registered: Jul 2006  |  IP: Logged | Report this post to a Moderator
dmc
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17 yrs MS found a LLMD and found out yea its Lyme.

Sent you a PM that you can forward to them.

Posts: 2675 | From ct, usa | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
tickled1
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Was up in the air as to whether it was Lyme or MS for me. I had 10 oligoclonal bands on spinal tap as well as many other markers and 2 brain lesions on MRI.

Luckily my neurologist is "Lyme friendly" and wanted to wait to see how I responded to antibiotics before throwing an MS diagnosis at me. I have responded to antibiotics so I guess it's obvious it's Lyme (and many co-infections) with me.

I'm not cured (yet) but the antibiotics definitely have brought me a long way and the neuro symptoms are much improved.

Please forward this this to them. Thank you

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Keebler
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What or who is S.L.A.M. ?
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
ping
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quote:
Originally posted by Keebler:
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What or who is S.L.A.M. ?
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My question too... Why don't you suggest the family, or one member of it post on this site? That way, the info is a matter of record for others just like them...

--------------------
ping
"We are more than containers for Lyme"

Posts: 1302 | From Back in TX again | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
Keebler
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Also, I see there is an email. Most people will not email to a blind email as then that person has the sender's email address and most like to know who that person is before sending.

MS misdiagnosis is frequent. There are many past threads if you'd want to search and collect the best selections and send to your friends that way.

Here's the link to search archives for past threads:

http://flash.lymenet.org/scripts/ultimatebb.cgi/ubb/search/search_forum/3

Search in the subject line for both "MS" and "multiple sclerosis"

A Google cross- search will also bring up links. An alternate search term for lyme is borreliosis and neuroborreliosis.

Good luck for your friends, whomever S.L.A.M. may be.
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karenl
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Some people say MS can be chlamydia pneumonia or both.
Please post your question there as well cpnhelp.com

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LymeXtu
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This is a website from a woman in Minnesota diagnosed with MS and the story of her recovery with Lyme disease treatment.

Be sure to watch part 1 and part 2.

www.michelleonlyme.org

Posts: 448 | From minnesota | Registered: Feb 2010  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
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http://www.angelfire.com/biz/romarkaraoke/whento.htm

When to Suspect Lyme

by 
John D. Bleiweiss, M.D.
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

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