posted
Just thought I would share that my neurologist that I was seeing called to wonder why I havent been back to see him. I had the great pleasure of telling him that I have Lyme Disease not MS. That the neuro and physical symptoms that turned my life upside down were REAL not "in my head" or "stress related". He didnt have much to say after that HA I WIN!!!! It was great telling him off because when I went to him I could hardly say what I wanted to say.
-------------------- "Strength does not come from physical capacity. It comes from an indomitable will" - Gandhi IGeneX results - POSITIVE Bartonella and Babesia (Babesia worst of all) 18+ 23-25 IND 30+ 39 IND 41+ 58+ 83-93++ Posts: 54 | From columbus indiana | Registered: Aug 2010
| IP: Logged |
Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835
posted
Good for you. Sometimes you just gotta let loose. And, on top of it, now you may have planted a seed that will grow. It's so important for us to speak our truth.
Posts: 2238 | From East Coast | Registered: Jul 2010
| IP: Logged |
jackie51
Frequent Contributor (1K+ posts)
Member # 14233
posted
That must have felt good.
Posts: 1374 | From Crazy Town | Registered: Dec 2007
| IP: Logged |
posted
Wow, I never had a neuro that cared if I came back or not..The doc actually called? still in shock..
Now, I've had the MS med company calling me, even after 2 years since I'd been off it, trying to get me back on it..hmmm
Glad you got to speak your mind..there's several "specialists" I'd like to show my + test to, and tell them that yes, I DO have something..and yes, my LLMD did know what he was doing with the Rocephin..Jerks!
-------------------- One day at a time Posts: 409 | From TX | Registered: Mar 2004
| IP: Logged |
dmc
Frequent Contributor (1K+ posts)
Member # 5102
posted
yay!!! the more we go back & show them their errors the more we help others.
great job. I'm happy you had the guts to speak up.
TammyN is right...you planted a seed.
Posts: 2675 | From ct, usa | Registered: Jan 2004
| IP: Logged |
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,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
![[Wink]](wink.gif)
![[Razz]](tongue.gif)
Printer-friendly view of this topic