Living with a disability - What a blessing. Thoughts and lessons learned along the way. Written by Michael B. Gerber
Thursday, November 15, 2012
One of the best weekends ever.
Saturday, November 3, 2012
To me it is a very big deal!
Friday, August 3, 2012
“Staying married is its own reward”
Sunday, October 30, 2011
Jim Morrison taught me how to sing.
Sunday, September 26, 2010
The Medical Report
What happened? We got older. More importantly, our bodies got older too and with aging bodies comes more ailments, diseases….and medical reports.
The truth is that those we care about and those who care about us want to know how we are. It’s more than a morbid curiousity. But rather an “I made it” –“Did you make it too?” type of curiosity. The fact is that we are getting older and to me, that’s the good news.
For many years I have said “If we are lucky enough to live long enough, we will all have something to deal with.” That’s the good news. It means that we have lived long enough to have something. That’s life and I would rather have it than not have it. Some of us are ‘lucky enough to have our health issues earlier…..like me.
God willing you are in your 50’s, 60’s, 70’s or older and are healthy and strong. What a blessing. But chances are that if you have lived that long, you know someone who has had to face serious health issues and chances are that when you ask “How ya doing?”, you really want to know.
Little did I know that way back when I asked my mother-in-law “How ya doing”, the meaning and significance those three little words would take on not that many years later.
Participate. Make a difference. Live a life that matters.
Wednesday, August 4, 2010
Marital Advice From An Expert.....Me!
Ask couples who have been married many years what the secret is and you will get a variety of answers. “Respect”. “Friendship”. “Never go to bed angry”. All good answers, all valid. But I believe that my answer to the question trumps all of those answers.
My advise is different and if you follow it, all those other pieces will fall into place. My advise is to be grateful.
Remember why you fell in love and all the things about your partner that you are grateful for and tell them. By telling them you remind them, and yourself, of what it is you love about them. Gratitude is the key to happiness and to staying in love. Unexpressed gratitude is useless. It must be expressed. Otherwise it is like buying someone a present and never giving it to them. Useless.
The opposite of gratitude is taking things for granted. Whenever things go awry in a relationship, one of the parties always feels taken for granted. Don’t let that happen.
Make expressing gratitude a habit. It has taken some of us a long to learn this, but I can tell you from personal experience that it works. Gail and I just celebrated our 30th anniversary, and I can honestly say that I am more in love with her today, then I was on the day we married and I am more grateful too. Rarely does a day go by without me telling her that I love her and why. And guess what? She does the same with me.
The last several years, and in particular, living with a disability, has taught me more about gratitude than I ever could have learned in a life without incident. But don’t wait for a life changing event to learn these lessons. Remind yourself, and your partner, today why you fell in love and do it all over again.
You, and your partner, will be glad you did.
Happy anniversary, Gail. I love you more today than yesterday.
Participate. Make a difference. Live a life that matters.
Wednesday, June 30, 2010
Rejection has never felt so good.
Is it the good news or the bad news? This past week and for the third time, I was turned down as a participant in a clinical trial. Getting into one of these trials as a volunteer/participant is tougher than I thought it would be. This time, however, being turned down was the good news.
This particular study was to see if exercise could improve the cognitive function of those of us living with MS. You needed to have a minimal level of physical ability and some evidence of loss of cognitive function. The doctor gave me a physical exam and then the Clinical Director administered a test of 60 questions to measure thinking skills and memory processing speed. The good news is that I answered 59 of the 60 questions correctly. A high score.
The bad news was that because of my score, I was not an eligible candidate for the study. Geez……..I may never get into one of these clinical trials.
More than half of the people living with MS will experience some level of cognitive dysfunction. Another fact is that over time, the great majority of us will experience some physical disability. Given a choice (which I am not), I would choose to have the physical disability over the cognitive disability every time. Luckily for me, that is how the course of my MS seems to be going.
Acceptance seems to be one of the best ways to live with a chronic condition….really, to live life under any conditions. By acceptance I don’t mean complacency or resignation. I mean accepting what is true, what cannot be changed and making the most out of whatever abilities I do have.
According to the test, my cognitive function is great. Will it always be that way? I can only hope so and can take steps to maintain the status quo, both mentally and physically. But if it changes, I know exactly what will do. Make the most out of whatever abilities I do have.
Will I ever get into one of these studies? I can only hope not.
Participate. Make a difference. Live a life that matters.
Wednesday, June 23, 2010
Doing the best we can Part Four: "Never Underestimate The Power Of A Smile"
I found what I hope is the perfect ending to this series on doing the best you can. It is a very short video taken from ABC News of a graduation speech given by a very special young man. The video takes less than three minutes to watch and shows us all the power of what can be done when we do the best we can.
Student's Inspirational Graduation Speech
Monday, June 7, 2010
Doing the best we can. Part three: Life and love.
That said, meet Dan and Jennifer. They met several years ago, fell in love, got married and have been happy ever since. A typical love story, except for one thing. They both have multiple sclerosis.
Dan has relapsing-remitting MS and it is not as severe as Jennifer’s (or mine!). He works, he walks and he jogs about three times a week. He also cares for Jennifer.
Jennifer has secondary-progressive MS. She cannot work or walk. But she is a caregiver to Dan, helping in every way that she can.
Dan and Jennifer have something else too. They have a tremendous spirit and attitude that propels them to make a difference in the world. As a result, they are an example to everyone who knows or knows of them.
Having MS does not stop them from participating. In fact, just the opposite is true. They lead and inspire others. They fundraise, advocate and speak. They receive rewards and recognition and are featured in articles and videos. They have even figured out how to dance together. They are alive, in love and living with a chronic illness.
They are not only doing the best they can, they are doing great.
I have never met Dan and Jennifer, but have been a fan for some time now. I am always touched and inspired by the things they do and their extraordinary love for each other. Read Dan and Jennifer's blog and learn more about them. Learn about two people doing their best in life and love and be inspired to do the best you can.
Dan and Jennifer have a prayer that say every night and part of it is as follows:
“Gracious God, help Jennifer and me to accept your will in our illness. As your children we believe that you cause all things to work together for our good, both of body and of spirit. But sometimes in the midst of illness and pain we forget or doubt. Forgive our weak faith. When we become impatient, encourage us by your word. Despite our worries and suffering, help us by our lives to reflect the radiance and confidence of those certain of your promises of help. Restore us to sound health if it be your will, and enable us with new vigor and enthusiasm to serve you zealously for many years to come. O Lord, have mercy. Hear our prayer. Amen.”
I think their prayers are being answered.
Participate. Make a difference. Live a life that matters.
Monday, May 17, 2010
Doing the best we can. Part Two. When is failure a success?
In 2004 she went back and made it to the top. She then decided to be the first person with MS to climb the highest mountain on every continent: Kilimanjaro, Denali,
A climb like this requires much more than physical strength and determination. Many of the obstacles are unknown and unpredictable until the climber gets there and discovers how their body responds. At over 17,000 feet, Wendy’s body could no longer tolerate the lack of oxygen and extreme temperature changes, all compounded and magnified by her MS. She did not make it to the top. She did not realize her goal.
Wendy has set an example for all of us. We all have ‘mountains to climb’. The questions are will we and will we do the best we can?
Participate. Make a difference. Live a life that matters.