Favorite Resources Part 2

This month's favorite resource is The New Parkinson's disease Treatment Book by Dr. J. Eric Ahlskog.
Dr. Ahlskog has more than 30 years of experience working with people with PD at the Mayo Clinic. His goal in writing this book is to educate patients so that they can partner with their doctors to get the best treatment. Unfortunately, in today's world, our time with our physicians is limited. By educating yourself, you can make the most of that time by knowing what questions to ask and what treatment options are available. This book will give you the general information, put in terms you can understand, so you and your physician can work out a treatment plan specific to you.

If you just can't wait for next month to learn about other favorite resources, you can see Claire McLean of Rogue PT & Wellness and I discussing all our favorites
here.

Comments

Missing Tom

I recently lost a good friend. Never would I have imagined that I would become such good buddies with a man old enough to be my dad. I met Tom over seven years ago in a Rock Steady Boxing class. I entered class as a shy, teary-eyed, newly diagnosed mess who didn't like to sweat and had never boxed. Tom quickly took me under his wing, introduced me to the movers and shakers in the local Parkinson's community and eventually recognized a potential in me to further help the community. Within a year, with the encouragement of Tom and others, I became a certified Rock Steady coach. Tom and I would go to the same conferences and seek out the newly diagnosed. Ever the salesman, Tom would ask me if I "closed the deal," meaning, did I convince someone to come to an exercise class or attend a support group. Tom knew the benefits of attending these groups and he wanted everyone else to know also. He just wanted everyone to live the best life possible, even while living

Diagnosing with Compassion and Hope

My hackles are raised, my feathers are ruffled, my … I’m not sure I can find the words for how I am feeling. This morning, I read a recently published article called “ Delivering the diagnosis of Parkinson’s disease-setting the stage with hope and compassion.” I am not upset that the article was written. I am glad that the authors have brought this to the attention of others. I am upset that it needed to be written. I just think it is common sense that when someone is given a life-changing diagnosis, it should be given with hope and compassion. The authors note that some say the moment of diagnosis is “almost akin to a traumatic event such as the loss of a loved one.” Of course it is! The person receiving the diagnosis is losing their future self. Everything they thought their life would be from that moment on has now drastically changed! I would count that as traumatic. I was one of these people over seven years ago who walked out of the Movement Disord

Birds of a Feather

The saying, "Birds of a feather flock together," dates back to at least the mid-16th century. In nature, birds are known to stick together in groups with their own feathered kind for protection. There is safety in numbers. Larger flocks are safer from predators. The saying has come to mean that people with similar likes, tend to band together. As a society, we form many different groups based on similar interests or qualities. I find the saying to be relevant also in the Parkinson's community and I am sure it is true for other conditions as well. I am more comfortable hanging out with others who have Parkinson's. They get it. No one else truly understands what it is like to live with Parkinson's except those living with it. Care partners probably come the closest to understanding what it is like, but they also have their own flock. One doesn't truly know what it is like to care daily for someone with Parkinson's unless you have done it. So do

Rock Steady Fighter

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