July 2010
I hope everyone is enjoying a safe and happy summer. This summer take advantage of your local museums and libraries to perhaps learn something new and to avoid those peak UV hours between 10am and 2pm. If you are in the Boston area join in some bowling fun at King’s in Back Bay and Dedham. Get you coupon for some free bowling here. We can’t spend our entire summer indoors though, so make sure you follow the SunWise sun safety guidlines:
- Cover up
- Use sunscreen appropriately
- Seek shade
- Limit your time in the sun
- Don’t forget those hats and sunglasses too!
Have a great summer!
May 2010
As May is Melanoma Awareness Month, I have asked one of my friends to share her story on this blog. My wish would be that not one more person ever has to be told they have Melanoma. Remember as you are reading this, that skin cancer is almost always preventable and treatable if diagnosed early. Please get your skin checked and protect your children from harmful UV rays between the hours of 10 am and 4 pm. Here is my fellow baseball-wife friend, Alison Mahay’s story.…
My cousin Landa was 35 years old when she lost her battle with Melanoma.
Landa was petite, beautiful and very much into fashion. She was married to Chris for eleven years and together were raising three wonderful children – Isabella 11, Sofia 7 and Christopher 2. Landa had it all. Chris was an incredible loving husband. They both loved to cook and entertain family and friends and enjoyed traveling as well. Their children were their greatest accomplishment. Landa always had a mole above her lip since I can remember. After Isabella was born her mom told her she didn’t like the way it looked so she went to her dermatologist and sure enough it turned out to be Melanoma. She immediately had the mole removed and some cosmetic surgery followed. She had follow-up visits and the doctor seemed to think he had gotten all the cancer. Little did we all know that this insidious disease stayed and was lurking in her body.
Eight years later in August 2008, Landa was not feeling well so a visit to her doctor was truly a shock when he told her she must see a surgeon. Her Melanoma had spread to her liver, her kidney’s and her brain. From that day on she lived in pain each and every day. Her parents moved into her home to help and so she began her journey. She encountered endless treatments. She went back and forth to New York City. And she was in constant pain while never once saying “God, why me?”
Her concern was for her children. She was a fighter all the way. Her belief in God got her through each and every day. Physically, our Landa changed. Unrecognizable in her last months of life, her heart and soul remained as beautiful and passionate as she always was. She lived her last year, like she lived the rest of her life for her children. As an early elementary education teacher, Landa loved children, and put her heart and soul into Isabella, Sophia and Christopher. She would go to every birthday party, and soccer game in her wheel chair with a smile on her face and cheer them on until her final moments. She wanted to be there for everything she could and never second guessed doing it!
She was also surrounded by the most remarkable family in the entire world! My Aunt Kathy, her mother moved in with her and took constant care of her, as her husband Chris never missed a doctors appointment and fought just as hard as Landa did to the bitter end. Landa did really have us all find blessings in each other.
I am not sure what lesson we are to be taught by Landa’s passing. Why a beautiful, intelligent 35 year old mother of three, and loving wife was taken in the prime of her life still shakes me to the core.
I always thought, in a strange way, skin cancer was just an easy cure, a nothing disease that was easily cured. The most ignorant way a person could ever think! This vicious disease hit our family so hard; it is something that we will never get over, but something that has made us embrace one another even more than we already have! We have always been close, but it’s beyond that now! We are all dedicated to finding a cure for this beastly disease and praying that another family won’t have to suffer the loss of a loved one like our Landa.
Melanoma is the beast that attacks with a vengeance. We need to stop it!
Feb 2010
Spring Training has always been my favorite time of year.
It meant in just a short time we would be packing away
the hats, gloves and winter sweaters. In no time our
shorts and flip flops would be replaced in our closets.
If you live in a place like Boston or Maryland (where I grew up)
you were sick of winter after Christmas and ready to feel the warmth
of a summer day. When I was younger it meant visions of summer vacation
and as an adult it reminds me of the beginning of a new baseball season.
We can still have those feelings and be safe at the same time.
Lets start from the beginning by remembering to apply sunblock
to our children and ourselves. Remember our skin is our biggest
living organ on our body. It protects everything in our body.
Lets keep our skin safe and get a healthy jump on spring which
is right around the corner.
Shonda
Jan 2010
I know it has been a long time since I have written on this blog.
I did something I never thought I would do. I wrote a book!
As of yesterday it is complete and ready to go to print.
The book is called “The Best Kind of Different” My family’s
journey through Aspergers. Like SHADE this was a very
healing process for me. My third child has Aspergers.
The release date is March 23rd and you can pre-order it at Amazon.com .
I do hope that during these much colder months
that you take this oppurtunity to really look at your
body for changes in your skin. This is the best time
to do so. Our bodies have not been exposed to the sun
too much when it is 20 degrees outside like here in New England.
Wishing everyone a Healthy, Happy 2010.
Stay Shaded,
Shonda
Oct 2009
Hello Everyone,
I spoke at the Glenna Kohl Fund For Hope’s First Annual Angel’s Masquerade Ball on Saturday, October 17th. This is in memory of my dear friend who recently lost her battle with melanoma.
15 years ago I stood before the FDA waiting for my turn to give my
testimony on a clinical drug trial for ALS.
One by one I heard families plead to have the drug.
They explained what could happen in a human life over the course of
three months, because that was the average increase in life expectancy
of a person taking this clinical drug.
One person in particular who was in her mid thirties explained what
three more months would have meant to her husband:
celebrating their 12th wedding anniversary
watching their son turn 9
seeing their daughter’s first dance recital
and watching their third child start kindergarten
This moment will be etched in my memory forever. How much time three
months really means.
As I stood there shaking and crying, I searched to find the words that
could even come close to the message that this person was giving.
As I walked to the podium carrying my one year old son, I shook and cried
so hard that my husband had to find the words to say to the four stone
faced adults, who sat on the board and with a yay or a nay, approved or
denied a request.
Many of you probably don’t know how I came to know Glenna. When Red Sox
nation was so excited about our coming to the Boston one person reached
out to me to say “Welcome, I love what you are doing, I too am a melanoma
survivor.”
The email friendship began. Over the next three years we kept in touch
on our health, our families, and of course our Red Sox.
I remember the first time I ever met Glenna. It was with her brother and
during a rain delay on what ended up being a very long game.
Glenna was always positive, smiling and never seemed to complain.
She touched my heart for so many reasons.
She was graceful and confident even though you knew her days and months
had to be filled with needing a break.
We would check in with each other time to time and once or twice a year
I would invite her to the game so we could catch up.
I was fortunate to meet mom and dad also.
I introduced her to Kelli Pedroia at one of these games.
Just as I thought Glenna had a way of making you feel good being around
her.
Kelli would always check in to see how Glenna was doing. Of course
Glenna’s version was always positive and filled with humor.
As Glenna rooted for the Red Sox, the Red Sox rooted for Glenna.
Even though Glenna was sick she worked hard to spread the word about
melanoma and how it could be prevented. She shared her story only to
make a difference.
She was a good person with a heart of gold.
When Glenna passed it broke all of our hearts.
She was too young and spent too long fighting.
I was shocked when I saw a picture of Glenna with long beautiful blonde
hair.
She was a very beautiful girl.
You see, I had never seen Glenna not sick or with hair.
The confidence that she showed and love of life was all that I could
see.
I would be lying though, if I said I saw her without hair, because Glenna
always wore a Red Sox hat!
If you are wondering why I started telling the story of standing before
the FDA here it is:
I can not tell you anything that you don’t already know about Glenna.
What I can tell you is what I learned after the FDA hearing, that like
ALS or melanoma, not one voice will change the world. It was the stories
that were told that day; the stories that will be told of Glenna for
years to come.
Glenna in her darkest days still looked to help others. That is what
she wanted. Tonight is a perfect example of carrying her legacy on. Her
passing will bring life to others.
I love the saying:
What we do for ourselves dies with us. What we do for others lives on!
Glenna’s name will live on through each of us in the stories that we
share about her courage and love of life. Thank you to each and every one
of you out there tonight for being here.
Thank you to the Kohl family for sharing her with everyone. We are all
better people for knowing her.
Please let us all have a good time tonight and celebrate Glenna’s life.
Shonda Schilling