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San Diego

CCFA Take Steps San Diego~ De Anza Cove

Last year I went to my first Take Steps for Crohn’s & Colitis event. I was invited by my super cool Gastro and thought it sounded like a fun thing to try.  Why not?

Last years team pic.
Last years team pic.

In fact it was so great that I immediately began looking forward to going again.

The first thing I did was look for the sign in booth.  Before I even got to the table I met a super nice lady who saw my Ask Me shirt and we got to chatting.  She excitedly told me about her Ostomy experience and shared her enthusiasm for upcoming treatments.  How about that for an awesome welcome?!  I love my IBD community.

Anyhoo, I got signed in and went straight for the booths.  I didn’t spend enough time investigating them last year and felt like I missed out.  So off I went.

*Going for big pics so you can see all the goodness as I walk you through a photo tour of the event.*

The first booth was for a pharmaceutical company.

Ferring Pharmaceuticals.  Their motto is 'Medicine on the body's own terms'.  They work to create individualized treatments = less side effects.  My hope is in time this will be available to everyone at an affordable cost.  How cool would that be.
Ferring Pharmaceuticals.

Their motto is ‘Medicine on the body’s own terms’. They work to create individualized treatments with less side effects. My hope is in time this will be available to everyone at an affordable cost. How cool would that be?  That’s their goal as well.  I can’t wait to see it.

The next booth was MotherToBaby.  They offer support for women on IBD controlling medications who are looking towards pregnancy and breast feeding.  There are legitimate concerns about safety for mother and child when taking meds.  MotherToBaby helps answer those important questions.

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Eight years ago when I was breastfeeding this information wasn’t available. Women today have the tools to make educated decisions. I like that.
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MotherToBaby card with more information.

 

Then there was the MPA Event Graphics booth with the bright sign that drew me in.

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MPA Event Graphics creates beautiful signage.  And they had the best team shirts ever!  So if you need a stunning visual and a company that understands IBDers, this is where you want to go first.

 

Next there was Coastal Gastroenterology, a local Gastro clinic with a super joyful group of people.

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Coastal Gastroenterology is a local gastro clinic.  Nice to see so many options out there for people to receive care.

 

There were larger medical groups as well.  UC San Diego has an IBD Center with a focus on patient education and empowerment.

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UC San Diego is a local teaching hospital. They have a large Gastro center where they offer help for every aspect of care.

 

There were some drug reps.

This one is for CIMZIA.  They have a nifty delivery system, after initial dosing it can be done by the IBDer in their own home.  There’s help available for those who cannot inject themselves.  I was most impressed by the pro human side of it.  Trying to really make it as easy and inobtrusive in a persons life as possible, while still providing a high level of care.  The rep was very good.

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This booth was for REMICADE but the gentleman never really pushed or pressed that Remicade is the very best drug. (Some drug companies do that silly stuff ~ can you believe it?!)  He encouraged a conversation to happen between the IBDer and their gastro.  (Which I respect)  What he did highlight was the cost assistance program they offer.  So of course I grabbed a packet to show you, my Sweethearts.  He also stressed the fact that every costly med out there has an affordability program.  The IBDer just needs to know to ask.

Now you know.

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Front side showing three options available.
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Back side giving contact information.

Affordability Rocks!

 

Loved talking to the researchers.  So passionate, intelligent and personable.  Join research or take part in a study if you can.  Researchers and scientists power to understand IBD and find a cure lies in our willingness to participate.  We are the key to helping our own future.

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Interested in participating in research studies? This is a group that does just that.

 

Take Steps CCFA SWAG.  Woo Hoo!  Totally filling this bag with a snack, sunscreen and a towel then heading to my favorite beach.

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Then came time for the fund raising announcements and listening to the stories of some pretty remarkable IBDers.

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This years announcer Mike did a great job.  Can you see me in the front row in my Great Bowel Movement ‘Ask Me’ t-shirt?  I had the best view. 😉

Mikes presentation on stage was positive, informative and kept the ball rolling towards the true purpose of the event.  The fearless announcer was both entertaining and endearing as he highlighted the efforts of those in the community.  A job well done.

 

After the stage presentation it was time for the walk.  This is where I got to visit with all the people. My very favorite part!  Everyone I spoke to was an example of inspiration, strength, courage and love.  I love my IBD community!

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This sweet mother, daughter duo wearing their Crohn’s fighting shirts made by MPA Event Graphics. Such positive, uplifting and hopeful women in love with their family.

More visiting…

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Chatting with the photographer. He was at last years event and is super nice.

 

Before you knew it the event was wrapping up.

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All good things that start must come to and end.

Thank you CCFA for the Take Steps experience.  My family and I look forward to participating next year.

I love Duck Tape

Glow in the dark Batman!
Na Na Na Na Na Na Na Na Na Na Na Na Na Na Na Na (Glow in the dark) BATMAN!

I love Duck Tape. Classify me as a proud addict. I have been known to turn up the music so I could tape in a ‘party atmosphere’. I have included my kiddos to perpetuate the Duck Tape love, and encourage them to tape on their own. I even keep my tape on a stand (repurposed broken floor lamp) that resembles a stripper pole. When I look at it I giggle inwardly at the naughty secret reference and must confess all those bright colors and artistic possibilities make me giddy. I seriously have the warm fuzzies for the projects to come and frequently crave alone time to draw them out for later completion. The anticipation occupies my mind in a day dreamy warm glow. Yes, I love Duck Tape.

Repurposed broken lamp base aka The Stripper Pole.
Repurposed broken lamp base aka The Stripper Pole. (Tee Hee)

But it’s more than tape on a roll. It’s more than creativity. My love of Duck Tape is an outward expression of love for my anatomy just the way it is. My love affair is the gift of acceptance to Crohn’s Disease, Ostomy and myself as a whole human. When I wear my Duck Tape creations I am most frequently in a bikini on the beach. Just me enjoying life in strategically tied triangles of fabric with Duck Tape, sunglasses and a hat as my only accessories.

I earned the right not to hide.  So I don’t.

Feeling like a Crohn's Cutie in my hipster mustachio Ostomy cover.
Ben snuck this pic of me feeling like a Crohn’s Cutie in my super cool mustachio Ostomy.

 
People look, some stare and others inquire. And you know what? All of that is okay. Because I am okay with me.

Beach ready!
Beach ready!

Woo Hoo!  I found a tape that matches.  Totally made my day.

Dog Beach!
Dog Beach!  Check out my Take Steps visor.  Rock’n!

The one time I tried the ‘nude’ look aka no Duck Tape.  Wet nude bag = see through O.o  No thank you.  Lesson learned.

So if you have Crohn’s Disease, Ulcerative Colitis, J-pouch, Ostomy, Urostomy, scars, tubes, tanks, PICC lines, or what have you.  You have earned the right to not hide.  You deserve to live openly in the sun.  And if a little tape helps you along the way, go for it.

Love you my Sweet Bolognas 😀