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» LymeNet Flash » Questions and Discussion » General Support » New here...Hello!

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Author Topic: New here...Hello!
ourplanet
Junior Member
Member # 10933

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I am a regular poster on a Fibromyalgia

messageboard, but our Lyme messageboard is quite

"inactive" so I came here to introduce myself. I

am 30 years old, live in South Jersey in one of

the most tick infested areas. I have been bitten

more times than I have fingers, toes and honestly

I gave up going to the doctor each time and docs

in our area often will not appoint unless you have

a huge bull's eye to accompany the bite....so I

have been diagnosed for fibromyalgia for 7 years

and probable MS 5 years ago.


The last time docs tested me for Lyme was 5 years

ago and I had positve bands, but was 1 short of a

CDC diagnosis so it was deemed negative for Lyme.

So I moved on.....yet I continue to get sicker

and continue to search for answers and I am now

aware that a LLMD would test using different

tests and criteria, and I indeed have a positive

medical history for Lyme. I continue to get sicker

despite the many meds I take and I really want

this investigated by a doc who is truly literate

in Lyme.


Now....I am rambling. I hope this board becomes a

source of support for me. I will be happy to

support all of you in your journey to better

health and thus increse happiness and calm.


Thank you and hello to all. [hi]

[ 07. January 2007, 07:53 PM: Message edited by: ourplanet ]

Posts: 4 | From Mays Landing, NJ | Registered: Jan 2007  |  IP: Logged | Report this post to a Moderator
cara
Member
Member # 10940

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Hi,

I know how bad it is there. I took my daughter to Jersey shore to a great doc there. Spent 5 weeks there. The people were so great there. One of the places they even believe in Lyme.

Cara

--------------------
God so loved the world he didn't send a committee

Posts: 12 | From Green Bay | Registered: Jan 2007  |  IP: Logged | Report this post to a Moderator
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200

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Hi, Ourplanet. Welcome.

So glad you found us!

It's sad to hear you were one band short of a "positive" test.. Doctors are supposed to diagnose you clinically and as usual, they are much more invested in DISPROVING lyme than in helping you.

You really need to be seen and tested by an LLMD (lyme literate medical doctor). With all your tick bites, there's no telling what co-infections you have. Regular ducks (non lyme literate docs) are normally clueless about even the existence of coinfections, much less how to treat them.

Find a doctor (post in the 'seeking doctor' forum), read everything you can from the Newbie Links, then keep coming for questions and support. You're hopefully on your way to better health!

Michelle

Posts: 3193 | From Northern California | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
tdtid
Frequent Contributor (1K+ posts)
Member # 10276

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Ourplanet,

I am so very glad you found us. I too use to be a regular on a fibro board and did the back and forth between lupus and M.S. for five years.

It was two months ago that I tested positive and see a LLMD. You talk about your test not having enough bands to be CDC positive, but that would make me tell you to please, please seek out a LLMD in your area.

It is a known fact that lyme tests aren't very reliable so it needs a clinical diagnosis, much like they are doing with fibro or chronic fatigue.

Getting a specialist will atleast help you know if you have it or else rule it out. But with that said, many researchers are saying that most fibro IS lyme. So please get tested by someone reputable.

To get a LLMD near you, please post a note over on the section of finding a doctor and someone will give you a list of the doctors in your area.

Just finding this place was a major breakthrough for you. I wish I had had the insight to find it when I was told I had fibro. Good luck and please stick around.

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
ourplanet
Junior Member
Member # 10933

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Thank you all for your warm welcomes and great

suggestions. I have a lot of work to do it seems.

But...it gives me something to work toward if I can

get a doctor to genuinely hear my concerns and help

me seek the answers I need. I hope I may also help

some of you who are more knowledgable than myself

also. You will be seeing more me. I wish you all

the Energy to keep on..keeping on. [Smile]

[ 07. January 2007, 07:54 PM: Message edited by: ourplanet ]

Posts: 4 | From Mays Landing, NJ | Registered: Jan 2007  |  IP: Logged | Report this post to a Moderator
tdtid
Frequent Contributor (1K+ posts)
Member # 10276

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Ourplanet,

I do believe one of the hardest parts of this is the overwhelming feeling of all we have to do when we just don't feel well.

I do know what a relief it was to see my LLMD and be told that he DID understand what I was going through, that I had tested positive and he was going to start treating me.

The whole process is very hard to fathom but getting treatment is better than taking all the band aid drugs for all the mis diagnosis's most of us get along the way.

This is not to say that you personally have lyme or co-infections, but you have said enough that if I were you, I would seek a lyme specialist and atleast know one way or the other.

Most of us have found our lyme doctors to have a quality that most of the other specialists lack. COMPASSION. So the visit isn't nearly as hard as I was expecting. I had told my story to so many specialists, I didn't want to go through that again, but wow....what a life changer.

Please keep us posted on how things go for you. We really do care.

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Cassie
LymeNet Contributor
Member # 2106

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Hi Ourplanet,
Welcome to the best place in our planet [Big Grin]

Sounds familar, I too was diagnosed with fibromyalgia. Was bitten in 1988, became very ill in 1996, seen a fibro specialist who sent me down to Long Island, dz lyme in 2001.

Pleased to meet you
Your new friend Cassie
[kiss]

--------------------
 -

Posts: 564 | From Toronto Ontario Canada | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
AZURE WISH
Frequent Contributor (1K+ posts)
Member # 804

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[hi] Welcome

Many of us went mis/undiagnosed for a long period of time...

unfortuantely it is quite common.

South Jersey is crazy with lyme... I have known quite a few people who have/had it.

Please find a llmd.If you post in the seeking a dr section someone will pm you a lyme literate dr's info.

so make sure you private message is enabled.

Best wishes [Smile]

--------------------
multiple chemical sensitvity group:
http://www.lymefriends.com/group/multiplechemicalsensitivities

Group for artists. All media welcome:
http://www.lymefriends.com/group/creativecorner


http://groups.yahoo.com/group/Lyme_Artist

Posts: 3860 | From nj,usa | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
CaliforniaLyme
Frequent Contributor (5K+ posts)
Member # 7136

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W E L C O M E ! ! !

I had fibromyalgia once. It sucked!!!
It is 100% gone through IV Rocephin.
I have zero pain on a daily basis now with the one exception of once a month I get a pre-period flare in my left knee for a few minutes total!
Hope you get better- this is a good Lyme board.
Sincerely,
Sarah
in CA

--------------------
There is no wealth but life.
-John Ruskin

All truth goes through 3 stages: first it is ridiculed: then it is violently opposed: finally it is accepted as self evident. - Schopenhauer

Posts: 5639 | From Aptos CA USA | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
catalysT
LymeNet Contributor
Member # 10786

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Welcome ourplanet!!! I sincerely hope you can sort your health problems out really soon! If you think I can be of any help, ask away.

--------------------
"You know, the worst, meanest, nastiest, ticks in the world are politicks," - Steve Nostrum

Posts: 242 | From South NJ | Registered: Dec 2006  |  IP: Logged | Report this post to a Moderator
hopeful123
Frequent Contributor (1K+ posts)
Member # 3244

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welcome!!! this is the place to get the information, support and courage to fight the lyme battle and win.

i think it's outrageous that they were that ignorant about a diagnosis, but i can't say that i'm at all surprised/

don't worry, you get what you need to move on!! [hi]

--------------------
some days you're the bug, some days you're the windshield  -

Posts: 1160 | From NY | Registered: Oct 2002  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

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Yep, I had "fibromyalgia" too. I was dxd in 1980. "It" is now gone! I took abx for four years and knocked out Lyme and babesia. Kicked butt! [Razz]

Your number one job is to find an LLMD. I have a list of names if you need help.

Glad to have you among us!! [hi]

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
   

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