Prickly Hug Card

This super cute, and super prickly card was designed by Jess and features two hugging cacti. Designed to bring cheer and support to our warriors who are going through an especially prickly, difficult time along their journey!

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Meet the artist

Jess

My name is Jess, I’m 32 and I create greeting cards and other little works of art I’m inspired to. In 2016 I developed a rare migraine condition called New Daily Persistent Headaches (NDPH) which is a headache/migraine that starts out of the blue one day and never goes away. Art is my escape and has been a game changer for me. Whether you’re a fellow artist, a fellow chronically ill warrior like me, a sponsor, or simply a beautiful fan of art and life, I hope you’ll say hi.

Meet the Warriors who signed your card

Maria

Terra is a ME CFS warrior and advocate. She lives in New Zealand with her partner, pet bunnies and rat. You can find her on IG here.

Arriana

Over the past 6 years, Arianna Anthony has been diagnosed with Lyme Disease, Sjögren’s Syndrome, Gastroparesis and Ehlers-Danlos Syndrome (EDS).

Jess

Jess Albert was 27 when she developed a rare migraine condition called New Daily Persistent Headaches (NDPH). It took 4 years and 4 neurologists to get her diagnosis.

Sadie

Sadie Veselka was diagnosed at age 4 with MCTD including Juvenile Arthritis, Scleroderma, Dermatomyocitis and Raynaud’s. She loves spreading hope and cheer!

Fuschia

Fuschia Kempen was diagnosed at age 5 with Gastroparesis, POTS, Panhypopituitarism, and Raynaud’s. She knows the isolation that illness can bring. Follow her on IG here.