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» LymeNet Flash » Questions and Discussion » General Support » Lymies without joint symptoms

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Author Topic: Lymies without joint symptoms
Piercethedrk
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anyone here with lyme and no joint symptoms?
Posts: 68 | From COATESVILLE, PA! | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
suki444
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Me!

I have no sore joints except a sore/stiff lower back but I have European strain Borrelia - perhaps B. garinni. My symptoms are predominantly neurological and started with chronic fatigue.

BW
Emma


Posts: 37 | From Whitehead, Northern Ireland | Registered: Feb 2009  |  IP: Logged | Report this post to a Moderator
lymewarrior03
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Me. The only joint symptoms I have are:
sore wrist which comes and goes, base of my neck, at the bump, and upper leg joints...
like they were kicked hard and I've sustained a constant deep ache.

First symptoms: head stuff, foggy/dizzy like feeling, achey eyes, base of neck/shoulder aches and pains, mild ear ringing

At year 5: intense fatigue, upper leg joint stuff, wrists, constant piercing ear ringing, many food sensitivities

At year 9: all above continues, along with mild muscle and nerve twitches.


Posts: 661 | From NY | Registered: May 2003  |  IP: Logged | Report this post to a Moderator
lla2
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I"ve never had joint problems ...only neuro stuff...I"ve had lyme, bartonella and babesia for over 16 years!

finally better...but never had any joint stuff or pain other than headache pain..

I consider myself very lucky

lisa


Posts: 4713 | From saunderstown, ri Usa | Registered: Apr 2002  |  IP: Logged | Report this post to a Moderator
minoucat
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I have had very few joint issues. When they've occurred, they've been limited in duration -- usually 3-4 months -- and in location (hands and feet, and only once in my elbow).

Mine's been mostly neuro, with major headaches, weakness, and fatigue; sweats on and off; aching muscles and gastro stuff, and a very stiff neck.

Always made me feel insecure in my dx. I was very happy when I finally got at least 1 band (41) on my WB.

Just editing to say that I'm now being treated for babs to, and have also had this for 16 years. Dunno about the bartonella. I hardly ever test positive for anything, it's all been evidence based tx for me.

[This message has been edited by minoucat (edited 13 May 2004).]


Posts: 2331 | From WA | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
lla2
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minocat you just described all the symtpoms of babesia and /or bartonella...have you been treated for either?
duh, editing here..didn't read your post right...good for babs..don't be surprised if it turns out to be bart...both sysmtoms overlap a lot I find..if the babs treatemnt doesnt' help, think bartonella...and treat that!~ i got similiar symtoms with both! and had to treat both!

classic....

Lisa

[This message has been edited by lla2 (edited 14 May 2004).]


Posts: 4713 | From saunderstown, ri Usa | Registered: Apr 2002  |  IP: Logged | Report this post to a Moderator
Sue vG
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My symptoms are mainly fatigue, brain fog, neuro and myalgic. I have pain AROUND some joints - the tendons, I think, of my knees and occasionally my hips, but no in-joint pain....so far. Knocking on wood.
Posts: 1307 | From TX | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
   

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