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A support page for people suffering from Peripheral Neuropathy and their carers. I am hoping with this new group for interested parties to get together online and swap ideas, give inspirational quotes, messages, websites and stories or to just have your say about how tough or great life can be for you! And to support our carers who the Carers Association call “THE UNSUNG HEROES”! So come on lets get together and share some of our amazing strengths of highs and lows. Blessings David
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TIPS I picked up, anyone else have any?
Last week I went to a PN Support group meeting with a good Neurologist as the speaker and got a couple tips I wanted to share with everyone with PN.  Â
Posted - Tue Nov 18, 2008 12:23 am
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Rose Terry
rmterry2003
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I have Peripheral Neuropathy
Hi I'm Rose Terry. I have Peripheral Neuropathy due to 'side-effect' to antibiotic called LEVAQUIN in the QUINOLONE family...poison as far as I'm concerned.
Posted - Sat Jun 28, 2008 11:17 pm
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Rose Terry
rmterry2003
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PN
Hi,Guys another PNer maybe (long story) had symptoms for nearly 5yrs,gone thru 2 Neuro,s who have given up on me.Totally numb from just below boobs been like
Posted - Thu Dec 13, 2007 4:16 am
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rousepatch
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Posted - Sun Nov 4, 2007 6:18 pm
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Rose Terry, Tupperwar...
rmterry2003
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new member
My name is Tammy. I live in Pensacola, FL. I suffer greatly with pn and many other illnesses. I have dysautonomia, gastroperesis, and tachycardia. I just
Posted - Thu Jul 26, 2007 10:28 pm
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tammy961
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Add LifeWithPN to your personalised My Yahoo!7 page   What's This?
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