“We are not meant to be boxed in. To be labeled. To be defined by the outside world so that it may feel more comfortable when it looks at us. So that it feels like it has us figured out. We are multifaceted. We are MANY things.” Sophia Bush What are the MANY things that… Continue reading I AM MANY
Having CRPS you have no idea what the day will bring! CRPS is an EVERYDAY thing! It’s been a long day! I’ve been in and out of one urgent care clinic to be sent to another for a full work up. I left the house at 9:30ish this morning and didn’t get back home until… Continue reading CRPS Is An Everyday Thing!
A few weeks ago I was contacted by Diamond Headache Clinic, the oldest and largest headache center in Chicago, Illinois. They asked me to help raise awareness about invisible illnesses by sharing their Slideshow. This incredible Clinic created a presentation about the different types of migraine headaches and symptoms in children. Children between the ages of… Continue reading Diamond Headache Clinic
Some are teachers, some are musicians, and some legacies are in themselves dynasties. But my family’s legacy has a number of things. For instance.. Girls have ALWAYS been born first on my dad’s side of the family, my ancestors come from slavery, my dad, my brother, and I can’t read music but we know how… Continue reading Every family has a legacy, and this is mine
Education is the key to success in life, and teachers make a lasting impact in the lives of their students. ~ Solomon Ortiz Over the years I've had remarkable and inspiring teachings.. rather it was from my countless years of schooling or from people I've met in between nevertheless I've looked up to and admire… Continue reading For My Teachers
The stories we want to hear the least are the ones we need to hear the most. To my fellow Sister Survivors and Army Of Women. I’m so proud of every one you! You showed no fear and looked evil in the eye for the very last time! As a former USA Gymnastics gymnast, who… Continue reading Dear Sister Survivors
Dear World, My name is Margaret Twitty and I am a 27 year old suffering with Complex Regional Pain Syndrome/ Reflex Sympathetic Dystrophy also called (CRPS/RSD). You may know me personally or you may not, but who I am is not really important, only the fact that I live in chronic pain. Having chronic pain… Continue reading A Letter To The World
Taking a moment to reflect and appreciate each up and down that I've faced in my life, and how thankful I am that even survived to celebrate another birthday, when a dear friend of mine didn't. So many things, places and people I’ve met who have touched and changed my life both personally and professionally…I… Continue reading Hello 26!
Raising Money For a Cause I Care About: On February 17, 2015 I was diagnosed with CRPS/RSD a rare and non-curable illness that has changed my life in so many ways. I have decided that instead of making my birthday all about me I want to make it all about finding a cure for this… Continue reading Birthday Donations
The hardest part of saying goodbye is having to do it again every single day. Every day we face the same truth. But life is fleeting. That our time here is short. And to honor the fallen, we must live our own lives well. As I’m writing this tears are falling from my eyes because… Continue reading 1 Year Without You