Tuesday, March 24, 2015

A Rare Disease Challenge For FPIES

March 18th, 2015

The FPIES Foundation

Chase's FPIES Challenge started out as a way for me to help my friends and family understand what living with FPIES is all about.  Chase is three years old and by now they have all heard about his crazy food allergies and some of them even know the lingo, asking about passes, fails, challenges, and triggers.  A few may even know what FPIES stands for.  But hearing about it and living it are two very different things.

I challenged them to cook just one meal in the month of February, leading up to Rare Disease Day, that would be safe for Chase to eat.  Chase has currently about twenty-five safe foods.  I provided clear instructions and an ingredient list.  I indicated where an ingredient was brand specific or needed to be organic.  I made sure they knew that 'processed in a facility where soy is processed' was a no-go and then I wished them good luck.

Then the questions started coming in.  Can I use pepper?  No.  Can I use spices?  Sea salt only.  Can I use chicken broth?  No.

Then the recipes started coming in.  I was blown away.  My fellow FPIES and food allergy families got it right away.  It warmed my heart that they tried to prepare meals that would be safe for our kids to eat together.  If we could magically erase the miles between us I'm sure we would have!  I was amazed by the culinary skills I never knew some people had and inspired to try some of these creations in my own kitchen.  It brought tears to my eyes when one friend had her 7-year-old daughter help her make a kid-inspired safe meal, complete with a handmade menu.

Then one friend really hit home with me, a friend that I had not seen in 13 years!  She told me her first attempt at apple blueberry muffins was a disaster.  She admitted she was about to just give up and skip the challenge.  Then she thought of us and thought of Chase and realized that's a luxury we do not have.  She tried again and made some amazing looking muffins.

I cannot order pizza, because I had a long day at work or rely on a frozen lasagna, because I did not have time to go grocery shopping.  FPIES is our life, at least for the foreseeable future.  We embrace it, we manage it.  We put on a happy face and positive attitude and thank God everyday for two healthy boys and the progress Chase continues to make.  But at the end of the day it is exhausting both mentally and physically and there is no room for error.

I truly want to thank everyone who took Chase's FPIES Challenge or even those who just followed along.  FPIES can be isolating, but I believe the burden is on those of us living with it to raise awareness.  Truly, we are not alone!

-This Article Was Written By Victoria Warren*
Victoria is a parent volunteer with The FPIES Foundation Volunteer Advisory Board.
And she is a television news reporter for WHDH-TV Channel 7 NBC Boston.

A Meal That Kids With FPIES Can Enjoy

Kid Inspired Safe Meal Complete With A Handmade Menu

Victoria Warren & Her Son Chase And Their Fpies Challenge For February 2015

Saturday, March 7, 2015

FPIES Hat



"I'm a Superhero, God gave me allergies to make life fair."-Mark Linn*
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"I am doing this for my son!"-Victoria Warren*
October 5th, 2014 Food Allergy Walk In Hopkinton, MA

Lets Keep Our Kids Healthy!:)



"My kids are so sweet that they do not need to eat cake all the time."-Kelsey Linn*

Fare Walk Boston 2015

Fare Walk Boston
Coming Soon In October 2015
Date TBD Soon
Will You Be Walking?
Help Raise $ For Food Allergies Research Education
Follow Us On Twitter:  @FareWalkBOS2015

"Let Your Smile Change The World."-Judge Faith Jenkins*

"Americans Suffer A Rare Disease, Including My Son."-Victoria Warren*

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Zazzle Celebrates The Awesome Life Of Kids Special Postage Stamp In 2015!:)

I Care About Someone Rare!:)


 
"There is always hope."-Sarah Linn, age 5*

Living With A Rare Disease

https://www.youtube.com/watch?v=zQIeiQ7S6tQ

I Love Someone That Is Rare To Me!:)



"Jesus loves all of the children in the whole world."-Andrew Linn, age 11*

Raising Hands To Support Rare Disease Day 2015

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BM Brussels Raising Their Hands In Support Of #RareDiseaseDay

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Day-By-Day & Hand-In-Hand

Lets Celebrate Our Tiny Superheroes Everyday!:)

Until Every Child Is Well!:)


"I am running for the Miles For Miracles team in Boston on May 24th, 2015 and I would run for the kids at Boston Children's Hospital any day of the week."-Mark Linn*

Congratulations & Way To Go For The Strides For Safe Kids Fundraising Team!:)

FpiesDay.com

Lets Say Bye To FPIES!:)

Fighting For A Cure For FPIES

I Love Someone With FPIES!:)

Rare Disease Day 2015

American College Of Allergy, Asthma, & Immunology

www.ACAAI.org

Nord Washington Office

Nord Washington Office
1779 Massachusetts Avenue
Suite 500
Washington, DC 20036

(202)-588-5700 (Tel.)

(202)-588-5701 (Fax)

National Organization For Rare Disorders

National Organization For Rare Disorders
55 Kenosia Avenue
Danbury, CT 06810

(203)-744-0100 (Tel.)

(203)-798-2291 (Fax)

Nord Massachusetts Office

Nord Massachusetts Office
1900 Crown Colony Drive
4th Floor
Quincy, MA 02169

(617)-249-7300 (Tel.)

(617)-249-7301 (Fax)

NORD

www.RareDiseases.org

The American Academy Of Allergy, Asthma, & Immunology

www.AAAAI.org

The International Fpies Association

www.Fpies.org

The Fpies Foundation

www.FpiesFoundation.org

Kids With Food Allergies

www.KidsWithFoodAllergies.org

What Is FPIES?

F=Food
P=Protein
I=Induced
E=Enterocolitis
S=Syndrome

With any questions about this website, please contact us at:  fpies@hotmail.com

P.S.  Thank you for taking the time to visit our website & have great day surfing the web.