My window is open and I can  hear the birds singing as a warm breeze   brushes against my face. I watch  a squirrel sprint up a freshly budded   mesquite tree in search of  nourishment. My amaryllis plant, sitting  by  my window, has burst into a bold and colorful blossom with soft swirls of white and pink, as though in  some sort of unspoken  celebration.  Spring has arrived once more.
It's  been  10 years now  (14 years ill) that I have watched the seasons come  and  go beyond  my  bedroom window. Ten springs have turned into  summer, and ten autumns  have slowly given way to winter.  Ten years of  passing seasons that could have been  filled with work, children, travel and adventure have slipped away from   me, never to  be retrieved.  Ten birthdays of each and every one of my friends and   family members  have passed by without my presence.  There have been   many hundreds of  unexplored weekends, thousands of missed opportunities   and adventures,  and millions of small everyday moments, never experienced, forever  lost.
As I  watch the various   budding leaves and  cactus flowers bloom into another season, I wonder   how to measure so  much loss of time. A full decade has gone by as I lay   on the sidelines  -- forced to spend each day in this tired and lonely room, quiet and  immobile. While time escapes me, the magnitude of that   time does not.
What  would my life had been had I not   gotten sick? What would the lives of  17 million others afflicted with   this disease have been?
Today  is International  ME/CFS  Awareness Day. For the millions who are sick,  for the millions  who have  lost years of their lives, and for the  millions more who will  later  become afflicted, please take a moment  from your day to reflect  and  remember.  If you know someone with  ME/CFS, take the time to  write them a  quick note and let them know you  care, and you have not  forgotten them.   Take time to learn more about  this devastating  disease and help spread  the word to increase  awareness.  Take the  precious time and the  blessing of good health that  so many ME/CFS  patients have lost, and  savor it. Savor it not just for  yourself, but  for them. For all of those  who have lost so much, and  who so  desperately want their lives back.
  
 

You're always in my thoughts, Laurel! *hugs*
ReplyDeleteLovely,
ReplyDeletewell written. I couldn't agree more.
Beautifully written!
ReplyDeleteFrom our beds to God's ear!
ReplyDeleteSo true...
ReplyDeleteIt's amazing how fast the sick years mount up. Reading this, I really felt the length of those ten years. It's not like ten years in a normal life.
ReplyDeleteThanks for posting all the right words today.
Really Lovely written
ReplyDeletemy dearest laurel, nothing but tears for this.
ReplyDeletesending all my love xx
Thank you for posting these words, you have conveyed what I have been to scared to admit. ... I really needed someone else to say it. xoxo
ReplyDeleteLaurel this was an emotive and brave post. I so relate. I feel like I am still whilst life is slipping away and around me. (8 years now housebound/bedbound, 15 yrs ill)
ReplyDeleteI know how much effort it must have taken to write, and I just wanted to say thank you to you for spending that energy and taking that time.
((((Laurel))))
Hi Laurel, Glad your post is back up! I did my post with a link here and included one of your paragraphs. Your post is so touching.
ReplyDeleteFondly, Lori
Dearest Laurel, A beautiful post. Yes, those years - and moments - lost are hard to measure. I am happy you have those white and pink swirls of softness in your window. This is indeed a small 'celebration' of the way you deal with severe ME with such dignity. Wishing you better days. NASIM
ReplyDeleteOnce again, a beautiful and thoughtful post. Sending hugs and prayers your way.
ReplyDeleteI only discovered your blog a short while ago - this post made me tear up... I'm not totally bed bound or house bound (just mostly) - but I can really relate to that feeling of lost years...
ReplyDeleteThank you, everyone. It's always so nice to read your lovely comments full of kindness and support.
ReplyDeleteThey are all well-deserved.
ReplyDeleteThanks, Jay. :)
ReplyDeleteI started to say that I was so sad for you, Laurel, but I'm not sure that's the right way to put it. I know you know this is just your life, but I'm sure that does not make it any easier for you to not be an active participant.
ReplyDeleteI have just discovered your website after seeing your video and I have added you to my blog roll on my own blog. If you have the energy sometime and are interested, I write about my own chronic illnesses, fibromyalgia and bipolar disorder at www.lifeonthedomesticfront.blogspot.com.
Very beautifully written and eloquently said. I hope that the researchers are doing all they can to figure out why you are sick and how to fix it. I have fibromyalgia and I cannot even begin to compare this illness with what I have.
I'm glad that you are able to connect with others who share your illness online and maybe get people who don't have it to take notice and remember you are out there.
So, I am thinking of you!
Chelle