My daughter was using Dr. Kerr but it sounds like the same situation. I
used to email him with questions/concerns and he would tell me what to
do. When my daughter hit a plateau in November of last year, he is the
one that put me in contact with the Kennedy Krieger Institute for
Children with Spinal Cord injuries. They are the ones that got her out
of the wheelchair. They only do inpatient for children though, they use
outpatient for adults. 
Her PCP is the one that we normally see (although she hasn't been to him
for about 6 months or so. She doesn't tend to need to see a Dr. for any
reason. If I need a new Rx for her Ditropan or her suppositories, I just
call in and they fax it to the pharmacy for me. 
 
Tracey L. Black
Certified Insurance Service Representative
Hockley & O'Donnell Insurance Agency
Phone - 717-334-6741, x 29
Fax - 717-334-3414
 

Thank you for providing information to us. Please beware that no
coverage is bound and no change to your insurance program is confirmed
until verified by a licensed agent during regular business hours. If you
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________________________________

From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] 
Sent: Thursday, May 10, 2007 12:04 PM
To: [EMAIL PROTECTED]; [email protected]
Subject: Re: [TMIC] Another Symptom


Does everyone here on this site have a neurologist?  I have only seen
the neurologist once since I let the hospital, which was in November
2005.  My healthcare is managed by my Physical Medicine and
Rehabilitation doctor(Physiatrist).  Any problems that I have had since
my diagnosis in July 2005, has been handled by my primary care physician
or my physiatrist.
 
My neurologist was key in diagnosing my condition, but once I was
diagnosed and received plasmapheresis, the only thing that would help me
after that was therapy (which I am still trying to get more of).  I
haven't ran into any issues, where my neurologist was needed. 
 
Naomi
C-4 quad since July 2, 2005




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