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.
Posted by Tammy N. (Member # 26835) on :
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.
Posted by jackie51 (Member # 14233) on :
That must have felt good.
Posted by twicebitten (Member # 5412) on :
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!
Posted by dmc (Member # 5102) on :
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.
Posted by Lymetoo (Member # 743) on :
Now send him a letter... so it's documented and you let off even more steam!!
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