Speaking at Toastmasters |
It's been seventeen years now since I was diagnosed. In the beginning fatigue, pain, stiffness and spasticity and headaches were the norm. My walking was limited to short walks with very jerky motion. Now, I have great energy and vitality. My walking is almost a regular gait. I have eliminated my headache medicine and another medicine for movement. I would say I feel great 98% of the time. So what's the change? That's what this blog is about.
Over 17 years, I've learned a lot about the disease and about me. My job now is managing me. I embrace the challenge of trying things that are safe, recommended for neurological diseases and especially MS, and fun. I will share what I've learned over time that has worked for me. I will also share my current adventures into some of the new alternative therapies I use for managing myself. Please join me and share your comments, and questions. The destiny begins with drug therapy which is the first big hurdle and decision.
Judy, it is great to see you blogging.
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