Put your Boots on with Kimberly Berg
Life can knock everyone down in many strange ways, what matters is how we get back up and rebound from it. Kimberly Berg grew up with a WW2 veteran dad and siblings who deal with Post Polio Syndrome. These were the building blocks for the career she has today as a Clinical Exercise Physiologist who specializes in helping people affected by conditions such as ALS, Parkinson's Disease and other neurological condition through dance, no contact boxing, agility camps and so much more. find out the difference between no contact and shadow boxing, the formation of the PD Rebel Performance Project a dance troop made up entirely of people affected by Parkinson's Disease. To follow along on Kimberly Berg"s journey click the links below and until next time Keep Calm and Roll On
https://www.instagram.com/pd_rebelfitclub
https://www.facebook.com/PDRebelFitClub
https://www.youtube.com/channel/UC66NA1QeeRcTCnc3Usn6p1A
Until next time Keep Calm and Roll on.
Kimberly Berg, MS, CEP,ACSM
Owner Rebel Fit Club
I am a Clinical Exercise Physiologist who specializes in Parkinson's and other neuro or orthopedic condidtions. The Rebel Fit Club is a huge training center for people with neurological conditions special emphasis PD. We use non-contact boxing, agilty bootcamps, yoga, pilates, dance, drumming and brain-games to create neuroplasticity to positively change the brain and slow the progression. The community and love in our center is a lifeline for our "fighters" who say they felt better after their first class and make friends of a life time here. I have headquarters in Tigard, Oregon but also run programs at two other locations. Our full 7 day/wk classes offered virtually are live and offered many times/day reaching people all over the world. We have the support and referals from specializing neurologists because they've seen such great improvements in their patients. I also created a dance company, the PD Rebel Performance Project where all performers have Parkinson's. We perform at conferences and other events internationally including opening night at the World's Parkinson's Congress in 2015. The love my fighters share for each other and the support of my coaches and volunteers is a life line for their quality of life and ablility to stay hopeful.
When asked why I do this, my father lost both legs related to WWII and with his prostheitc legs, was very positive, married 60 years and was a farmer and carpenter. My oldest sister and brother have post-polio syndrome with my brother losing his sight he traveled the world and is living a…
Read More
Listen On
