Services and Locations
SERVICES
We offer a packet of information from a variety of organizations, foundations and bloggers who are positive about the future of CF and the warriors who fight it everyday! Currently the packets include 12 informative brochures from:
Blooming Rose Foundation
-Foundation brochure
-Faith, Hope and Belief
Boomer Esiason Foundation
-Team Boomer, “It’s all about exercise!”
-Be Prepared to Breathe Easy
-Living. Breathing. Succeeding.
-Foundation Brochure
CysticLife
-Life after the diagnosis (a parent’s guide)
CFRI
-CF Website Guide
-Cystic Fibrosis in the Classroom (or daycare!)
-Growing Stronger Everyday
RunSickBoyRun
- Blog Flier
Usana Health Sciences
- Take Charge of your Nutrition
LOCATIONS
We are currently offering in-person services within the state of our home office in Bozeman, MT.
-Including all cities in Montana
I would like to emphasize that our services are available ANYWHERE nationwide. If you have a child with a new diagnosis with CF we want to help support you anyway that we can.
We are so excited to announce that our list of “consultants” is growing rapidly all across the US. (all services through consultants, unless desired by consultant, will be via email or phone). Packages for families will be sent by mail.
Please go directly to our document section, download and complete the BRF Packet Request Form. Once you have filled out the form, please email it directly to me at kat@bloomingrosefoundation.org.
Our goal is to be able to render our services immediately following a diagnosis, however (this is our sad disclaimer) if our little girl is going through a rough patch, or we are low on funding, we will not be able to offer in-person visits. If this is the case we will make an initial phone call, send a basket with everything we would like to have brought in person and then we will follow-up weekly, as desired by families. However, we hope to always be able to offer our services in-person!
An additional thought- if you are an outgoing, positive individual with CF or who has a loved one in your immediate family with CF and would like to help us to extend our services outside of our current radius, please contact me. We love the idea of networking across the nation and not allowing any families with a new diagnosis to feel alone on this journey. kat@bloomingrosefoundation.org
