FLOWER IN A SIDEWALK

Cultivating Resilience & Joy On The Other Side of Heartbreak

Tuesday, August 28, 2012

Setting The Table

Tonight I am setting the table for four instead of three as I have been this summer.  Tony is home tonight after spending the summer in Chicago and I could not be more happy to have my boys under my roof again.

This will be our future.  A week here and couple of weeks there.  The long summer months of time on our hands is in the past, but the visits during breaks and at the end of internships will be  just as precious.

Welcome home Tony.

Friday, August 24, 2012

The DNC is Coming...

...to Charlotte and today I picked up my tickets (after volunteering to register voters) to attend Obama's acceptance speech on 9/6 at the BofA stadium.  Whether you like him or not what a great opportunity to see our democracy in action.  I am also able as an employee of the Blumenthal Arts Center to work such great venues such as the International Forums, where by the way Madeline Albright will be in attendance hopefully wearing  one of her great pins, and the Domestic Forums.  I will usher the Echo Foundation with the keynote speaker being General Wesley Clark.

Charlotte will be alive with delegates, protesters, the curious, the interns and volunteers.  What a wonderful opportunity that has been laid at our feet .

Wednesday, August 22, 2012

Education Series for the FAC

Once again I stood in front of nurses, interns, and support staff of LCH recounting our story of Joe and sharing how this impacted our family.  Yet again my voice quivered and broke sharing our history.  I so want to be able to stand strong during that part.  I guess that will take time.

But even with my shaky start an incredible dialogue emerged.  Where and when is the right time to approach families who have had their world rocked to the bottom of their souls.  Should we have Palliative Care be involved at the start for rare cancers.  When do we bring up insurance coverage and the right time to introduce Medicaid or SSI as a supplement to your insurance.   When is the right time to say this will take a toll on your family and your finances.  When do you say to a family in a devastating spiral you need to look out for yourselves, your other children and we are here to offer help.

I do not know all the answers to these questions but I am feeling better that they are being asked.  And that is what Levine Children's Hospital is all about. Treating not only the patient but the family as well and I am proud to be a part of the Family Advisory Council at LCH.

Sunday, August 19, 2012

The Thank You's

Every year after Joedance I send  personal notes thanking everyone who donated their time and money to raise awareness for rare and complex cancers.  And every year I write with blurred vision of tears in my eyes.  I get the zip codes wrong, the 9's look like 8's, I write and rewrite the cards till I think they are right for those who have sent money, those who gave their time and talent to make Joedance a success.  These cards are sent to so many people that knew Joe's journey and to those who have just learned of our heartbreak.  I as write these notes the tension that filled my shoulders preceding Joedance starts to lessen, replacing it with your love and willingness to gather every year for Joedance to remember a son and a brother.


Thursday, August 16, 2012

I am back

After a small break I am back.  My last post was just before the Joedance Film Festival and I have to be honest with you preparing for this event floods me with memories of Joe and it takes a toll on me.  I am a mess before and a mess after.   So I  left the blogging world to get through this tough time.  And after all of  my distress Joedance was a success thanks to all of you that volunteered your time, your love and your support.  It starts with Julie and Arkon doing the flyer.  Matt and Steven rocked the Joedance Glass Table.  Bert Woodward put the word out to the newspapers, Mollie did the popcorn, Dave and Deb came back from their beach trip to be here to set up the film and John Schwert was on hand to introduce his film.  And you all came to remember Joe and raise money for The Rare and Complex Cancers Fund.

Thank you.

Sunday, July 29, 2012

Press Release

There it was, above the fold (very important in the newspaper world), the press release about the Joedance Film Festival.  Left hand side under "Briefly" in the City News section.  I nearly dropped my coffee cup on the floor, but I found my composure to only set it down with a loud crack on the kitchen counter.

What were the odds of a small neighborhood fundraiser being published in the Charlotte Observer?  Well, if you have Bert Woodward on your side the odds are good.  He has worked tirelessly, as have Julie Marr, Friends of Fourth Ward, our friends and neighbors to make this film festival a success and grow it to another level.  And then came the partnership with the Carolinas Health Care Foundation and just recently the Charlotte Film Society.  Which, by the way, gave a wonderful plug for Joedance at their event last night at Theater Charlotte.

When we started three years ago with the idea to raise money for poorly funded research for rare cancers, such as Osteosacroma which claimed Joe's life, never did we think the support would have grown this much. I thank you, our family thanks you and all the kids that are afflicted with rare cancers thank you.

Monday, July 23, 2012

Carol's Birthday

Carol Zadel's birthday was today and it gave us an opportunity to call her and Bob, who is Mike's older cousin.  Bob and Bill Zadel always are a source of good laughs of remembering the wonderful times of growing up in a close knit neighborhood.  Where grandparents were across the street, cousins were around the corner and every child went to school together.  We have ditched the neighborhood of relatives for neighbors who don't know our past.  We are disconnected having our relatives living on either coasts and the Midwest.  And with the dissolution of our families being our neighbors for some reason that yearly visit makes us uneasy, makes us want to prove we are successful, makes want to hide our pain or struggles, makes us put on a face of perhaps a hint of perfection.

My Mom and Dad moved to Charlotte seven years ago, my niece Sarah was already living here and I was relieved to be able to show my pain and suffering every day to them without the pretense of a visit here or there.  They saw and witnessed our incredible sorrow as Joe died.  I am forever grateful they were around the corner and down the street.