Come along with me. Thanks to Myasthenia Gravis I do not walk. Heard of it? Not I until my ophthalmologist diagnosed me with it. After researching it, I found what I needed – remission is possible! I am going to live my days of IVIG treatments on my Road to Remission right here before the world, be they good days or bad, bright or sunny. The Myasthenic. The Ragdoll. Me. *MY* Myasthenia. Please join me.
"Just for you, Sleeping Beauty," said Ana light heartedly as she brought me a large plate of salad after bringing me the *regular* for lunch today.
Ana has always been very special to me ever since she began working in Food Service. I think the first thing I ever asked her was the pronunciation of her name, and she liked it that I pronounced it correctly. I continued showing an interest in her, and she just opened like a flower. So appropriate. That smile of hers is just like a flower. Little flower. Petite flower blowing, tilting in the wind. Now then when she brings my food tray, and I am sleeping, she will sing, "Wake up Sleeping Beauty," as she sets my tray down, and will make sure I waken before leaving my room. Quite a personal service rendered!
As she left my room after breakfast this morning she said in her cute little El Salvadorian dialect that she would bring me a salad to augment the skimpy meal that was coming for lunch. My mind pictured a bowl of salad.
Lunch time came.
She brought my regular lunch plate in, then left the room.
In a moment she returned, surely a dance step to her feet as she bounced in on her toes. In her hand was a dinner plate, one of those big smiles on her face, one just like the you see in the picture above, which was taken when she came back to pick up trays at lunch.
The plate was overflowing with a yummy, 'licious looking salad, a salad filled with just the right things for a diabetic to eat! It took a split second for me to realize that was *the salad* she said she was going to make for me! Oh, my goodness!! Did she ever!!
Thanks, Ana.
Kindness begets kindness.
Toodles Striving for a world without Myasthenia Gravis
From growing up in the 40s and 50s on the banks of the Mississippi River in Helena-West Helena, Arkansas, I traveled the world in the 60s and 70s, courtesy of husband Jim’s Air Force career, then we retired back home in Arkansas. . . Blytheville, AFB. I have had a full life with three children, four grandchildren, four great-grandchildren with a fifth one due in August. Stick around. The road might get rocky at times, but then, that is LIFE, and Life Goes On, One Day at a time, One Step at a Time.
Myasthenia Gravis Foundation of Arkansas Mission Statement
MISSION STATEMENT
Of Myasthenia Gravis Foundation of America, Arkansas Chapter is the conquest of Myasthenia Gravis through programs of research, education, information, and patient servises to improve the lives of all people affected by Myasthenia Gravis.
"We will not concede until Myasthenia Gravis is only a memory".
Followers
Ashton Sears, a helper he will be.
Their shirts say "Brothers for Life"
It's 4 the Kids (Shown Julian Avery)
Kennedy Garcia - Downs syndrome and a leukemia survivor! Yay Kennedy, you GO girl!
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