My name is Andrea and I was born with Neurofibromatosis type one. I have known as long as I can remember that I have NF. There were times in my life that wanted to run from it or pretend it was not there. Growing up with NF was hard and it continues to be a struggle but I truly believe that I would not be who I am today if life had been any different. Recently I also was told by doctors that I needed to start treatment for MS. I am currently giving myself daily injections to try and stop or slow down the progression of MS. Finding a cure for NF and now MS is a huge part of my life. I will do anything I can to help. When you buy a bracelet from my store you are helping me raise money to help people with NF. All of my proceeds are donated to help find a cure for NF. (I participate in national MS walks, and don't plan on selling bracelets for that at this time. Maybe in the future when I have more time.)
I currently partake in a few different NF groups and I act as an advocate for NF awareness as well as occasionally plan special events for youth and young adults in
♥If you are an NF group and you would like me to add a link on my page or add an event to the calendar please let me know and I will gladly help share the news.
♥Thank you for taking the time to check out my Neurofibromatosis Awareness site and please check back often for updates, events, and NF BRACELETS!