Blog · Complex Regional Pain Syndrome · CRPS · Fashion · I Am A Voter · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Truth To Power · Vote

WHY I VOTED

#IAMAVOTER! It has taken me 26 years to realize that my voice does matters, that my vote does matters! I was one of those people who never fully understood the way government works or how it applies to me. It took me being diagnosed with CRPS a very rare, very painful chronic diagnosis that I… Continue reading WHY I VOTED

Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · legacy · Life · Personal · Photography · Platform · Reflex Sympathetic Dystrophy · RSD · Truth To Power

CRPS Is An Everyday Thing!

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!

Blog · Guest Post · Invisible Illness · Life · Platform

Diamond Headache Clinic

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

Blog · Clothing Line · Complex Regional Pain Syndrome · CRPS · Fashion · honor · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Truth To Power

A Letter To The World 

Dear World, My name is Margaret Twitty and I am a 26 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 

Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Truth To Power

Birthday Donations

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

Blog · Complex Regional Pain Syndrome · CRPS · honor · Invisible Illness · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD · Sports · Truth To Power

Pain Makes Us Who We Are 

Let your pain empower you,Not all of us are destined to break. And if you find yourself broken, Allow for each broken piece To faithfully make sense I would never put public speaking on my "special skills" list, but over these past years I have been called to do just that more than a number of times. That… Continue reading Pain Makes Us Who We Are 

Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD

Chronic Pain: A Burden Often Shared

Chronic Pain: A Burden Often SharedBy JANE E. BRODYChronic pain is a family problem. When people experience unrelenting pain, everyone they live with and love is likely to suffer. The frustration, anxiety, stress and depression that often go with chronic pain can also afflict family members and friends who feel helpless to provide relief.Healthy family… Continue reading Chronic Pain: A Burden Often Shared

Blog · Complex Regional Pain Syndrome · CRPS · Invisible Illness · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD

5 Do’s and Don’ts When It Comes to People with CRPS

So often we find ourselves in situations where people are trying their best to help us when in reality they very well may be hurting us. I can see how being a loved one of someone with CRPS can be challenging in more ways than one. You may find yourself not knowing what we want… Continue reading 5 Do’s and Don’ts When It Comes to People with CRPS

Blog · Complex Regional Pain Syndrome · CRPS · CRPS Trial Treatment · GoFundMe · honor · Invisible Illness · Italy · legacy · Life · Personal · Photography · photoshoot · Platform · Reflex Sympathetic Dystrophy · RSD · Travel

My New Normal 

Dear World, My name is Margaret Twitty, I'm 25 year old and I've been diagnosed 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 My New Normal