I will be on Kelly’s Choice Radio Show (click on the link to listen) with Edwina Wilson on today, March 3, from 2-3 p.m. EST discussing Cerebral Palsy Awareness Month, SDR, What CP Looks Like and more! I’m honored to be on the show two years in a row.
Let’s Talk Cerebral Palsy on Love860AMWAEC! Click listen live on http://www.kellyschoiceinc.org to listen to the show.
Nearly 3.5 years after my surgery, I finally found something worthy of some of my fundraising money: a purple (my favorite color) AeroPilates Reformer Plus purchased on eBay!
I’ve heard about the benefits of Pilates, and I’ve wanted to try it. I know it will work my muscles in an entirely different way. Jumping around is fun but I look forward to gentler form of exercise. I know it will work my muscles in an entirely different way. Looks easy? Think again!
Thank you to everyone who donated to my fundraiser. I’m putting the money to good use. This is What CP Looks Like!
A message for everyone who supports my Nicole’s New Legs – SDR Journey FB page:
Thank you for following my journey before and after SDR surgery. I couldn’t have come this far without you. ❤
My SDR article has been re-published on LyfeBulb! I’m grateful for the opportunity to raise awareness for SDR with another audience. SDR Changes Lives!
My first article has been published by The Good Men Project!
Click on the link and comment directly under it (on The Good Men Project’s site, too); this will help a lot.
Please share, tweet, etc. to raise awareness for cerebral palsy and SDR. Thank you! ❤
I wrote to President Obama about my SDR story, Cerebral Palsy Awareness Month and more! This arrived in the mail today. Wow, I never expected to get a response!
I asked POTUS to wear green on National CP Awareness Day, March 25 and to send me a picture so I can post it on my blog — that would be so cool!
I have cerebral palsy. Since seeing is believing, I thought I’d show you how I’m living life FREE of spasticity. Selective dorsal rhizotomy surgery (SDR) changes lives!
There is NO benefit to spasticity! The frustrating part as an adult with CP, is that doctors don’t tell you this information (many of them don’t have a clue) — what they say is hat you won’t get worse, which is not really true. Your CP won’t get worse, but due to spasticity, the effects of it will continue to harm your body over time, often leading to problems in adulthood. I’ve heard stories about so many people with CP who ended up in a wheelchair later in life. I’m not saying this to scare anyone, but rather, to encourage you to learn about how premature aging affects all of us. SDR is the only medical procedure that can permanently reduce and/or eliminate spasticity.
I found out about SDR by accident when I was 39 and, if I hadn’t stumbled across the information, I would still be struggling to do (or in some cases, not even be able to do) things others take for granted. And because I had SDR, I rest assured knowing that I’m free of spasticity,Yes, I still have CP, but thanks to the surgery, the wear and tear on my body — with respect to spasticity only — will not continue. This is why I am so passionate about sharing the information. I want more adults and children to get new legs like me, and be FREE of spasticity and so much more!