MS, Community and September 11

By Cathy, Health Guide Tuesday, September 11, 2012
Recently I attended an MS conference sponsored by the pharmaceutical company I represent as a Peer Resource. In attendance were Peer Resources from around the country - people who (like me) dedicate time and effort to reach out to others with MS and who also use the same disease-modifying medication....
9/14/12 3:54pm

How do I do it? By waking up happy every day and feeling grateful for the extraordinary life that I have.

 

It has been said that “success is the best revenge.” I think that happiness is our best revenge, or tool, or weapon to combat the effects of MS. Sure, I have pain every day and it is often tremendous. No, I have not walked for 2 years, but that has not shaken my determination to do so. I have bladder issues, ED, trembling hands and some developing cognitive issues. But none of that prevents me from feeling grateful for my amazing life.

 

My short list includes that I have eyes to see, ear's to hear, arms to hold and hands to touch. I also have a brain to think, a heart to feel, friends and family who care about me and for me to care about as well.

 

I used to be able to do 10,000 things. Now I can only do 9,000 things and that is what I focus on. My glass is not half-full. It is overflowing.

 

These are some of the choices that I make every day. This is how I honor each day and live my best life despite MS.

 

Great question and thank you for asking it.

 

Michael

Cathy, Health Guide
9/15/12 7:51am

Michael,

 

You are an inspiration to all who know you.  Your answer brought tears to my eyes and warmed my heart.  You will do fine in life with these 2 things in your favor - and we will be happier knowing you.

 

Thank you for your wonderful answer.  Happy Days!

Cathy

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By Cathy, Health Guide— Last Modified: 09/15/12, First Published: 09/11/12