Medicine box for Techfidera |
Judy Groff, retired Professor, NCSU, shares her journey in redefining herself and adjusting to her new destiny of living with Multiple Sclerosis.
Saturday, October 28, 2017
Embrace Your Destiny: The ABC's of MS Drug Therapy
Tuesday, October 24, 2017
Embrace Your Destiny: Take on Piano Lessons
Starting my lesson with Annett |
My walking has improved to become less spastic and more fluid and strong.
Pain and stiffness in the hips and leg joints is minimal and mostly just after sitting.
I am quicker doing routine activities around the house.
I have learned to handle stress through breathing.
I have energy again.
I believe that all the alternative therapies I do are working together to support my immune system, my neuromuscular system, my digestive system, skeletal system, and mental systems. For example, I have been taking piano lessons for three years. When I started, I discovered that my fingers were as spastic as my legs and arms. I had no idea the spasticity extended into the hands. I should have figured that out because my handwriting had really deteriorated significantly. The regular, daily practice of piano is slowly improving this area of spasticity. I believe the physical therapy work I do has helped looses the shoulders which helps keep the hands soft and pliable. I am grateful that I am able to do piano therapy. My neurologist said it is recommended as a therapy, but he had another patient who didn't have enough strength in her fingers to work the piano keys.
My piano teacher, Annett Hudson, patiently works with me to identify problems and how to correct them. Music is the tool. We work on technique more than anything else now. Each piece I work on requires something a bit different. Some of the specific, fundamental things she reminds me of every week are:
- Keeping my fingers moved up into the black notes
- Relaxing my hands and keeping a dome shape when playing
- Relaxing my arms and using them to help press the finger on the key
The music pieces are fun to work on and challenging. I'm convinced that playing the piano works my brain in a way nothing else does. It's also a great stress reducer. Annett keeps talking about doing a recital next Spring. The jury is still out on that challenge. I've got a long way to go before feeling ready to perform!
Wednesday, October 18, 2017
Embrace Your Destiny: Strength Training with Lacey
Before going to the more complex and stressful topic of drug therapies, I want to tell you how enthused I am about my new strength training regime. My goal is to work with my trainer, Lacey one hour a week. Supplementing that I will go on my own at least once more per week. Some weeks maybe more.
For seniors over 65 on Medicare, the Silver Sneakers program is free. We found a new, beautiful Gold's Gym just across the street from my Hot Yoga Studio. Every time Lacey introduces me to new apparatuses like the big cable machine, she shows me how to work the machine and do the exercise properly. Safety is her mantra, I'm sure. She always asks if I got sore. I answer "no". She starts with small weights. I tell her if we can go up or down.
After four lessons, numerous practice sessions on my own, I can report definite improvement. How you ask? Here is what I know:
For seniors over 65 on Medicare, the Silver Sneakers program is free. We found a new, beautiful Gold's Gym just across the street from my Hot Yoga Studio. Every time Lacey introduces me to new apparatuses like the big cable machine, she shows me how to work the machine and do the exercise properly. Safety is her mantra, I'm sure. She always asks if I got sore. I answer "no". She starts with small weights. I tell her if we can go up or down.
After four lessons, numerous practice sessions on my own, I can report definite improvement. How you ask? Here is what I know:
- I am not getting fatigued standing to cook late in the afternoon.
- I haven't fallen in standing poses at yoga.
- My core balance is helping me get dressed easier.
- My walking is improving. It's not as jerky and the toe tapping is rare.
Since my goal is better walking, more endurance, and improved core strength, I'm happy with these results. Yes, it takes time but I figure this is my work, my job and it's really kinda fun!
We'll do more serious stuff next time.
Tuesday, October 17, 2017
Embrace Your Destiny: Knowledge is Power
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.
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