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Fight against Epidermolysis Bullosa Jaclyn's fight

Organized by Jaclyn's Fight
Po24808565 front
Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - front
Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - back
Fight against Epidermolysis Bullosa Jaclyn's fight shirt design - zoomed
Fight against Epidermolysis Bullosa Jaclyn's fight shirt design - zoomed
Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - front
Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - back
Fight against Epidermolysis Bullosa Jaclyn's fight shirt design - zoomed
Fight against Epidermolysis Bullosa Jaclyn's fight shirt design - zoomed
Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - front
Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - back
Fight against Epidermolysis Bullosa Jaclyn's fight shirt design - zoomed
Fight against Epidermolysis Bullosa Jaclyn's fight shirt design - zoomed
Hanes 100% Cotton T-shirt

sweatshirt or t-shirt to raise money for debra

verified-charity
All funds raised will go directly to Dystrophic Epidermolysis Bullosa Research Association of America, Inc.
$290 raised
43 items sold of
50 goal
Thanks to our supporters!
$20
Hanes 100% Cotton T-shirt, Unisex - Black t-shirt
Hanes 100% Cotton T-shirt
Unisex - Black t-shirt
  • Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - small
  • Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - small
  • Fight against Epidermolysis Bullosa Jaclyn's fight Fundraiser - unisex shirt design - small
Organized by Jaclyn's Fight

About this campaign

Raise money and awareness to Epidermolysis Bullosa. As many of you know Jaclyn has been battling this disease since she was born. With the help and information we receive from debra , Jaclyn and I have been informed on medical information and help since she was born, including introduction to clinical trials to lessen her blisters. debra.org is an important organization for all with EB, even her specialists utilize them for the most up to date information on meds and treatments.

I have been living with Epidermolysis Bullosa, junctional, since I was born, I'm 17 now. I have been hospitalized and had many surgeries due to my disease. I have also been helped and was able to participate in a clinical trial last year (which was awesome, hope medication becomes available) all from the information from debra.org

Supporters

Russ DeFranco 4 items + $25
Andrea Hilker 1 item

One of my families dearest friends suffer from this disease. I will wear this hoodie in support of her!

Laurie 2 items

I have DDEB. I know the struggle. We are stronger than our Fragile Skin leads people to believe.

Scott Nowak 2 items
Kelly McCauley 3 items

My mom and uncle both have the recessive form of this disease. And I recently just completed a fundraiser for DebRA good luck!

Kathleen Ryder 1 item + $10

I too have EB (RDEB) and stand shoulder to shoulder for this fight!

Paul Jeffreys 1 item
Mary fisher Cunningham 1 item

Mary fisher Cunningham

Dawn kuznik 4 items

Also have zip ups now

Lanie Mancuso 1 item

Jacklyn kuznik-dodge. Been with her since day one! Love always!!!

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