I’m new to this blog and it gives me a lift every morning to tune in and feel a part of my fellow PN traveler community. I’ve had PN three years and I haven’t known anyone else with it to share with about this journey. You look normal, just kind of wobbly, and family/people don’t understand/appreciate the coming and going of the pain and how the ongoing numbness and tingling of 10,000 bees gets old. It’s a lot easier to keep going forward with gratitude for my many blessings knowing there is a community here that really understands.

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