Connie S.'s Profile - Wellsphere

Connie S.

Top HealthBlogger for the Lyme Disease Community

San Francisco, California

Blog: www.lymebytes.blogspot.com/

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Insights From ILADS--Discerning The Symptoms of Four Major Infections

I was fortunate to be able to attend the ILADS (International Lyme and Associated Diseases) conference a few weeks ago. I had never been to an ILADS...

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Lyme Teleseminar--Tonight at 8 PM EST

Join me tonight for a free teleseminar on Lyme disease! I will be speaking about my Lyme disease journey and new book, "Insights Into Lyme...

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Seeing Isn't Believing...Believing Is Seeing

When you have been struggling with chronic illness for years, it can sometimes be a challenge to believe that life will ever bring you anything but...

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Lyme Disease Is Not Your Life

Yes, it may seem like it, because adequately treating the disease requires hours of therapies, research and rest. It sometimes requires every last...

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FREE Sample Chapter from New Lyme Disease Book

Hi Everyone! For anyone who is interested in getting a closer inside look at my current best-selling book on Lyme disease, entitled, "Insights...

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Latest Activity

Connie S. posted Lyme Teleseminar--Tonight at 8 PM EST Nov 17 2009

Connie S. posted Insights From ILADS--Discerning The Symptoms of Four Major Infections Nov 17 2009

Connie S. posted Seeing Isn't Believing...Believing Is Seeing Nov 15 2009

mike wrote on Connie S.'s Whiteboard. Nov 10 2009

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Connie S.'s Whiteboard

Nov 10 2009 by mike

15mg oxy-contin does nothing for my pain.Does anyone have a name of a medicine that actually works so I can tell my dr.??

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Nov 10 2009 by mike

I guess I'm a newly diagnosed lymie:{ This pain is un-freaking-real.Iguess I have had this for approx. 2-4years. I also have hepatitis-c and have hung drywall for 18 years so I'm getting attacked by hurt FROM MANY ANGLES I take oxy-contin 15mg 2x day /no help. anything stronger that works/what is it called?

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Sep 22 2009 by johnnylight

Hey connie tried to answer your blog on Lonely Lyme but it wouldn't let me log in on that page. I agree that we don't get no respect for having this awful Disease, nice to see other out there trying to get their two cents in.

http://lymies.ning.com/

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