Kick Ass lined hood Cystic Fibrosis cure CF breathe Bella Canva pullover hoodie

This premium kick ass Cystic Fibrosis Cure CF Breathe hoodie has been called the softest hoodie ever made. Sure to put a smile on your face when you put it on. This unisex pullover is a classic and probably one of the most softest hoodies you’ll own. It’s created and spun with plush fabric that is made up of cotton and polyester fibers. Has a slight V neckline for comfort, an ideal hoodie for keeping you warm. It’s got a floral lined hood with a beautiful floral design and Breathe in the front. A large CF design on the back and on top of it it’s yellow. So you’ll look amazing on wear yellow day!! BONUS

This amazing Cystic Fibrosis Hoodie will not only help create awareness, but you will also help CF research as 25% of the proceeds will be donated to CFRI Cystic Fibrosis Research Institute. A bit more on what they do lower down. 

Benefits

• Relaxed fit
• Comes with a front pouch pocket
• Ribbed cuffs and waistband keeps drafts away
• White drawcords
• Unisex style
• Has a hood to keep your head warm with it’s plush poly-cotton blend

Features

• Ribbed cuffs and waistband
• Kangaroo pockets
• Retail fit
• Unisex sizing
• White cord drawstring
• Heather Navy is 60% Airlume combed and ringspun cotton, 40% polyester
• Marble colors are 85% combed ringspun cotton, 15% polyester
• Athletic Heather is 90% combed ringspun cotton, 10% polyester
• 7 oz., 52% Airlume combed and ringspun cotton, 48% polyester fleece

For environmental and human friendly reason, this product is only made when you order it. Typically, this product will be made in about a week, we will send you tracking information as soon as it's in the mail.

25% of the proceeds will be donated to CFRI.

CFRI was incorporated in 1975 by a small group of CF family members whose children were not expected to survive their teen years. These founding members were committed to keeping overhead low so as to raise funds for research. Originally, the founding members were all volunteers, until the first executive director was hired in the early 1980s.

Initially focused on research, CFRI responded to the CF community’s needs and expanded its programs to include educational and support programs. CFRI grew into a million-dollar agency in 2012 and continues in its efforts to fund research and to provide education, advocacy, and psychosocial programs and services to those with CF, as well as their families and caregivers.

Nearly all of CFRI’s original founders have since lost their children to cystic fibrosis, yet they’ve remained active with the organization because of their commitment to finding a cure for this debilitating disease.

www.cfri.org