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12-22-2009, 11:25 AM
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Wisest Elder Ever
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I just discovered this website. Others here might already know about it but I just thought I'd post a link to it for those who don't. It's a website by doctors for doctors so we might get some good (and accurate) info here.
http://www.mastersofms.com/index.php
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| "Thanks for this!" says: | barb02 (12-31-2009), Blessings2You (12-22-2009), Debbie D (12-23-2009), DizzyLizzy (12-22-2009), dmplaura (12-23-2009), Friend2U (12-23-2009), gonnamakeit (12-22-2009), Jodylee (12-23-2009), kentucky_wildchild (12-25-2009), MSCherokee (12-26-2009), Riverwild (12-22-2009), SallyC (12-22-2009), Twinkletoes (12-22-2009) |
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12-22-2009, 12:57 PM
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Grand Magnate
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I've had Kathleen nurse-practioner at UMM. She's great.
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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12-22-2009, 12:58 PM
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Grand Magnate
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Kathleen Costello
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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12-22-2009, 01:30 PM
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Wisest Elder Ever
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I saw that she was in Maryland and wondered if you knew her, Kicker!
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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12-22-2009, 05:10 PM
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Grand Magnate
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We talked constipation, an MS favorite. She offered good advice. My male neuro and I never discussed it.
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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12-22-2009, 05:11 PM
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Wisest Elder Ever
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I wish I had a female Neuro. In fact, I may just start looking for one or go to the MS Center in Atlanta. I only go twice a year anyway. I'm supposed to go the Monday after Christmas but may end up having to cancel.
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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12-23-2009, 03:20 PM
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Elder
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Thanks for sharing, Kelly.
I was a bit amused when I read the Q & A section on CIS...it stated in the answer that patients with CIS are in denial and need to get early treatment so as not to have a relapse. It took me years before the neuros were convinced that I indeed had MS...not the other way around  I wonder if I would have been healthier now if the neuros had put me on Copaxone when I first began presenting sxs?
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