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04-02-2019, 02:58 PM
https://www.epilepsyiowa.org/wp-content/uploads/2018/03/Kids_Crew1-1024x538.jpg
Fill out the form to request a Free Epilepsy Foundation Kids Crew Kit. Kids Crew members will receive: A certificate, Kids Crew pin, Lanyard and membership card, and Quarterly newsletter. “The program is free to join and is for kids ages 14 and under of all abilities. If you don’t have epilepsy, we still want you to join. Often, siblings, friends, and relatives of those with epilepsy are the best advocates. We are looking for those who want to learn, spread awareness, and make a difference. And have fun, too!! “
LINK: https://www.epilepsyiowa.org/kids-crew/
GET THIS FREEBIE: https://www.epilepsy.com/node/2093611
Kids Crew members will receive:
- A certificate
- Kids Crew pin
- Lanyard and membership card
- Quarterly newsletter
The program is free to join and is for kids ages 14 and under of all abilities. If you don’t have epilepsy, we still want you to join. Often, siblings, friends, and relatives of those with epilepsy are the best advocates. We are looking for those who want to learn, spread awareness, and make a difference. And have fun, too!!
Fill out the form to request a Free Epilepsy Foundation Kids Crew Kit. Kids Crew members will receive: A certificate, Kids Crew pin, Lanyard and membership card, and Quarterly newsletter. “The program is free to join and is for kids ages 14 and under of all abilities. If you don’t have epilepsy, we still want you to join. Often, siblings, friends, and relatives of those with epilepsy are the best advocates. We are looking for those who want to learn, spread awareness, and make a difference. And have fun, too!! “
LINK: https://www.epilepsyiowa.org/kids-crew/
GET THIS FREEBIE: https://www.epilepsy.com/node/2093611
Kids Crew members will receive:
- A certificate
- Kids Crew pin
- Lanyard and membership card
- Quarterly newsletter
The program is free to join and is for kids ages 14 and under of all abilities. If you don’t have epilepsy, we still want you to join. Often, siblings, friends, and relatives of those with epilepsy are the best advocates. We are looking for those who want to learn, spread awareness, and make a difference. And have fun, too!!