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  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Seeking a Doctor » CT-Dr. not in rheumy's list of MDs?

 - UBBFriend: Email this page to someone!    
Author Topic: CT-Dr. not in rheumy's list of MDs?
usyankee
Member
Member # 16173

Icon 1 posted      Profile for usyankee     Send New Private Message       Edit/Delete Post   Reply With Quote 
Well, I went twice to the rheumy, and got nowhere.

Despite my writing twice on the sheet you have to fill out once you arrive at the office that I had ringing in my ears, he was surprised when I mentioned I had ringing in my ears.

Apparently he hadn't read a thing I wrote! Apparently he also did not fax all the MD's I had seen in the past for my previous records.

What a waste of time and money. He wouldn't even give me my previus fibromyalgia pain med (Vicoprofen) even though he rediagnosed me with fibromyalgia. (I also have terrible back pain from multiple accidents when I stand too long at work) including crushing pain in my feet and ankles for some reason and sciatica.

He gave me Mobic which is said to be just as dangerous as Viox. When it didn't work and I stopped it after 6 days, he wanted to double it. I refused. He then started me on Lidane or Lidane or Lidone or something. I didn't get it yet and tool Motrin last night.

I've been taking Colloidal SIlver and started this herbal program called Susans' Herbs 100 day protocol(Samento, Cumanda, Carnivora). Also grapefruit pectin.

I also wrote down something I had said at work when trying to figure out what word to use, and suddenly he decided to send me to a neurologist.

I was trying to say something like maybe the CNA's put your urinal there so it wouldn't get spilt, but my brain just made up words. So it wouldn't get spollen, spillin spilled, spilt.

Since I have been on the colloidal silver, I started with headaches etc, esp. in my frontal lobe (and last night severe headache after the grapefruit) but my brain seems to be getting better. It's pathetic when you can't add all of a sudden, when you had a 98 average at one time in Intermediate Algebra! Or can't spell when you previously were asked and were paid by Simon & Schuster to edit a book!


He is sending me to a neurologist he knows. If he's anything like HIM, I think I'll pass. I asked if he could send me to Dr. K in Orange, and he looked it up in his book and said there is no Dr. K in Orange.

Apparently there may have been a cancellation at his colleage's office because they called me with an appointment very quickly. Neurological Associates it said on the machine.

I called Dr. K's number that was provided to me here, and they took my # down and said they would have the Doc. call me. I am wondering why this Doc. isn't in the Rheumys book?


-donna

Posts: 37 | From Connecticut | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  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.