This is topic Special note to new member "mb"......others: please welcome mb!! in forum General Support at LymeNet Flash.


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Posted by Lymetoo (Member # 743) on :
 
mb posted this on another thread:

Hi, I have been sick for over 5 months. I feel like I am dying b/c I feel better then worse, it's debiliating and I'm only 31. I have been tested for everything, Lyme titer was negative. WAiting on more specific Lyme tests results. Lived in Southeastern PA for years, moved to TN four years ago. Been bitten by HUNDREDS of ticks b/c I hike all the time, always in woods. Never saw a rash. Nothing else fits my symptoms so clearly and I am soooo sick. Wondering if anyone can tell me some of their feelings/symptoms for LATE PHASE to hear it from a real person rather than lists of symptoms. I am scared and I feel horrible, just HORRIBLE. HELP!!!!

===========================

What you really need to do is get a Western Blot test thru Igenex Labs. If you were tested thru Quest or Lab Corp, I doubt it will come back positive.

It MIGHT, but not too likely as they do not test for all the Lyme-specific bands.

Do you have any of these symptoms??

Lyme Disease Symptoms List
1. Unexplained fevers, sweats, chills, or flushing
2. Unexplained weight change--loss or gain
3. Fatigue, tiredness, poor stamina
4. Unexplained hair loss
5. Swollen glands: list areas____
6. Sore throat
7. Testicular pain/pelvic pain
8. Unexplained menstrual irregularity
9. Unexplained milk production: breast pain
10.Irritable bladder or bladder dysfunction
11.Sexual dysfunction or loss of libido
12.Upset stomach
13.Change in bowel function-constipation, diarrhea
14.Chest pain or rib soreness
15.Shortness of breath, cough
16.Heart palpitations, pulse skips, heart block
17.Any history of a heart murmur or valve prolapse?
18.Joint pain or swelling: list joints_____________
19.Stiffness of the joints, neck, or back
20.Muscle pain or cramps
21.Twitching of the face or other muscles
22.Headache
23.Neck creeks and cracks, neck stiffness, neck pain
24.Tingling, numbness, burning or stabbing sensations, shooting pains
25.Facial paralysis (Bell's Palsy)
26.Eyes/Vision: double, blurry, increased floaters, light sensitivity
27.Ears/Hearing: buzzing, ringing, ear pain, sound sensitivity
28.lncreased motion sickness, vertigo, poor balance
29.Lightheadedness, wooziness
30.Tremor
31.Confusion, difficulty in thinking
32.Diffculty with concentration, reading
33.Forgetfuiness, poor short term memory
34.Disorientation: getting lost, going to wrong places
35.Difficulty with speech or writing
36.Mood swings, irritability, depression
37.Disturbed sleep-too much, too little, early awakening
38.Exaggerated symptoms or worse hangover from alcohol
 
Posted by Robin123 (Member # 9197) on :
 
Mb, I think it'd be helpful to find out if there's a support group in your area you can also connect with.

Like Lymetoo said, you need to be tested properly, and you will need treatment with a good LLMD.

It is all very difficult, and we are here for each other, to try and figure out what's going on and what acould be the next steps to take.

If you were to post more specifically about your symptoms, people could make more comments about what's going on and what they try to do for alleviation.
 
Posted by Lymetoo (Member # 743) on :
 
up
 
Posted by Geneal (Member # 10375) on :
 
Dear Mb,

Welcome!

Sorry to hear you are so ill....I was there before I was dx.

Please get a Western Blot through Igenex and find a Lyme Literate Medical Doctor (LLMD) to treat.

Sorry that you had to find this group, but glad that you did.

Given that you've been bitten hundreds of times, the likelyhood of Lyme must be pretty good.

Hang in there. You've come to a wonderful place, full of people who have or are dealing with

Lyme disease and co-infections. Lymenet has helped saved my life and my sanity as well as given

me the opportunity to have friendships with an incredible group of courageous people.

Hugs,

Geneal
 
Posted by CaliforniaLyme (Member # 7136) on :
 
W E L C O M E !*)*)!*)!*!
 
Posted by hopeful123 (Member # 3244) on :
 
welcome to lymenet. you've come to the right place.
 
Posted by Lymetoo (Member # 743) on :
 
Wonder what happened to mb??
 
Posted by cactus (Member # 7347) on :
 
up for mb
 
Posted by Lymetoo (Member # 743) on :
 
hi mb! [hi]
 
Posted by mb (Member # 11520) on :
 
Hi Ya'll! How sweet of everyone to welcome me. It's so comforting to hear someone who takes me seriously. Just got back from the Rheumatologist. My PCP referred me to him after not knowing what is wrong with me. GUESS WHAT? Dr. Rheumatologist feels that I am suffering from a combination of physical symptoms that are a manifestation of something traumatic or from depression/anxiety. YEP!!! He did test my blood for something called, firbro spondylitis or something like that, can't remember. But, he believes it is most likely from psychological problems. He stressed that he believes my symptoms are real. NO kidding my symptoms are real. Anyway, I am discouraged and so sad. I found a support group here in Nashville and hopefully someone there can give me the name of an LLMD in the area. I guess that is my only hope? Why are the docs so undeducated on this subject? My doc put me on two weeks of Doxycycline while awaiting the Lyme PCR and Wester n Blot tests. Two weeks wouldn't do a darn thing anyway, right????? Help!
 
Posted by mb (Member # 11520) on :
 
Someone mentioned that I should go into more detail on my symptoms. Let me know if any of you feel this way.....The symptoms vary a lot, they come and go day to day, hour to hour...Joint pain in my knees, fingers, hands...muscle numbness, sometimes my arm or leg will just feel numb and incredibly heavy...these HORRIBLE shooting pains that go through my feet, hands, calves, quadriceps...terrible lower backaches that feel like someone is just punching me...dizziness...headaches although they aren't that frequent and aren't too bad...I used to hate taking naps, now I need naps for two to three hours a day, every single day...I never feel rested...sometimes it's hard to just walk...does this sound like anything familiar to any of yall? does it sound like i am missing something fundamental to the symptoms? or do i have a symptom that is completely unrelated? I'd love to hear back..thanks..
mb
 
Posted by mb (Member # 11520) on :
 
Hi lymetoo!
 
Posted by kam (Member # 3410) on :
 
Ah HA! There you are. I have been watching this post to see if you were real or not. HA!

Hope you are able to get to an LLMD soon so you will know one way or the other.

I would suggest an LLMD that is a member of ILADS or recommended by the Lyme Disease Association or people on this site.

I went to a few docs who said they knew about lyme and then were not able to read the test results from Igenex.
 
Posted by Lymetoo (Member # 743) on :
 
HI mb!! Glad you finally found the thread. I don't know of any LLMD's in TN. I can give you the names of drs in nearby states.

YOur symptoms sound like it could be Lyme. Your rheumy sounds pretty CLUELESS!!!

The test that he ran will NOT mean much. Quest or Labcorp is what most drs use. Pretty useless when it comes to Lyme testing.

But MAYBE it will show up positive...who knows?? One can HOPE!!

If it doesn't, begin your search for a dr who is willing to send a test to www.igenex.com

Wild Condor's Links and information:
http://www.wildcondor.com/lymelinks.html

 -
 
Posted by Boomerang (Member # 7979) on :
 
Welcome mb!! We're in TN too. Have been LLMD in MO. I heard recently of a doctor in nashville area who treats for lyme, but we haven't been there yet.
 
Posted by mb (Member # 11520) on :
 
Hi Boomerang,
How far is the drive to the doctor in MO? I'm willing to do almost anything. Where did you hear about the doctor here in Nashville? Help!
Hope you're feeling okay.
MB
 
Posted by Pure Lymie League (Member # 10421) on :
 
Hi Mb,
I'm here in Nashville. Are you going to the meeting Monday night? If you want to talk just PM me.
Sara
 


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