LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » General Support » how annoying

 - UBBFriend: Email this page to someone!    
Author Topic: how annoying
ToriT
Junior Member
Member # 6954

Icon 1 posted      Profile for ToriT     Send New Private Message       Edit/Delete Post   Reply With Quote 
Check out this link. http://www.quackwatch.org/01QuackeryRelatedTopics/lyme.html

I am not diagnosised yet with anything... still trying to find out what is wrong with me.
After reading the above link I was angered because (many reasons) but I have had such a awful time with doctors. Why do they think people with unexplained illness go online to research?

My life has spiraled downward and the doctors don't seem to think it is such a big deal. I tell them my symptoms and they shrug - don't say much. I feel like I am talking to someone in a check out line when I am suppose to be talking with the "expert".

I have been accused of a drinking problem because of my hand tremor by one doctor.

One doctor ignored my compliants of chest pains and shortness of breath... He asked what meds i was on so I told him synthroid and he felt my thyroid and was generally surprised that it was in fact a goiter. As if I was lying about this stuff.

I felt that I had no choice but to turn to the interenet to research my symptoms and other peoples experiences to help myself because they sure as hell were not jumping up and down to aid me in my recovery.

I find I am most like CFS and Lymies in my symptoms. Mine come and go.. never know when the fatigue and neuro problems will hit me.

Thanks - just wanted to vent.... after reading and researching online I least know what questions to ask the "experts".


Posts: 8 | From Pittsburgh, PA, USA | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 6 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think VERY little of Quackwatch.......and don't care what they think. Bunch of quacks!

Welcome to Lymenet, Tori! I hope you will find an LLMD and get some treatment soon so you can get well!

Tincup's Links for new members
http://flash.lymenet.org/ubb/Forum1/HTML/009342.html

Dr. Joseph J. Burrascano's Guidelines http://www.ilads.org/burrascano_1102.htm

Rose's 15 Facts for Newcomers http://flash.lymenet.org/ubb/Forum1/HTML/011977.html

Camp A and Camp B http://flash.lymenet.org/ubb/Forum1/HTML/021395.html

Abbreviations for Lyme-speak
http://flash.lymenet.org/ubb/Forum1/HTML/020494.html

Making the most of your LLMD visit
http://flash.lymenet.org/ubb/Forum1/HTML/020605.html

Success Stories http://flash.lymenet.org/ubb/Forum1/HTML/022173.html

Western Blot explanation: http://flash.lymenet.org/ubb/Forum1/HTML/022767.html

More info: http://www.ilads.org/

Lyme Wars http://www.wildernetwork.org/Lyme_Wars.html


Most people are over in Medical, so if you'd like to introduce yourself and tell us your symptoms, we'll see if we can help you!

------------------
oops!
Lymetutu


Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 6 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lyme Symptoms

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


Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
TheCrimeOfLyme
Frequent Contributor (1K+ posts)
Member # 4019

Icon 1 posted      Profile for TheCrimeOfLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
ToniT:

I actually live very close to you, in a suburb of Pittsburgh- about 20 minutes.

If you need help finding a doctor, or just want to chat give me a call.

My number is listed in the forum titled "Seeking a Doctor" under my username.

I'll be out from right about now to 10 am this morning.

Jodie


Posts: 3169 | From Greensburg, Pennsylvania | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
ToriT
Junior Member
Member # 6954

Icon 1 posted      Profile for ToriT     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Jodie, Lyme Too and lymetutu,

Creative names! Thank you for replying.

I have read and read and read about not only Lyme's diesease but all thyriod and parathyroid related problems, Chronic fatigue, early althimers ( won't try to spell that correctly), all neuro problems... Thus far I match the symptom list of Lyme the most, specifically the neuro Lyme.

I have just come off a long and bad spell of extreme fatigue and extreme mental confusion. It has gotten better over the last week but I kind of feel myself slipping in out somewhat good to bad.

Perhaps I will write a post in medical, as suggested. I want to know about the off and on again symptoms.

I am interested in reading the link above about Camp A and Camp B. I have read the opposing views but I like the sounds of that title. Sounds more specific then others.

Jodi, I avoid the phone like the plague! lol I seem to only answer for my immediate family or few close friends. On bad days I only answer for my mother. If I feel strong in spirit then I will reach out to you. Thank you for the offer . Makes me feel good.

I have found some local doctors who are LLMD - both are MD's. But they are 30 to 60 minutes away. I have appointment with one and the other has not returned my calls.

In addition, I have appointments with neuro, cleav clinic, and digestive people. I must keep these appointments because my dad is going with me. Mind you I am 37 years old but I can not longer see a doctor and communicate clearly. He is going to be my strength and words.

Thank you all,

ToriT


Posts: 8 | From Pittsburgh, PA, USA | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
bg
Junior Member
Member # 46416

Icon 1 posted      Profile for bg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Welcome Tori to this 24/7 educational, support group board! The best info & experiences are here.

Please print off Tincup's or Treepatrols newbie links. Check them off as you read as there are months of reading there.

Betty G., Iowa


Posts: 1 | From US | Registered: Aug 2015  |  IP: Logged | Report this post to a Moderator
ToriT
Junior Member
Member # 6954

Icon 1 posted      Profile for ToriT     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hey - thank you,

I have read many of the links listed above and ran across this one http://www.mentalhealthandillness.com/tnaold.html
Some links I may have not explored yet.

The link I posted was really helpful for me.

I am coming off a period of "good days" and feel my self slipping as I try to read and write. This sucks.

The above link describes what I feel and go through. When this all started for me (over the last three years), I have been told that i am acholic (due to hand tremors), told I was bi-polar (happy when well vrs. slowed down when ill), and that I had post tramtic stress disorder... just like the article in above link describes.

Hate this.

ToriT


Posts: 8 | From Pittsburgh, PA, USA | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.