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 

Clothing Line · Complex Regional Pain Syndrome · CRPS · Fashion · honor · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD

She’s Fit To Lead Article 

"We’re big believers in Margaret Twitty’s favorite saying,"Know The Person Not The Disability.” But sometimes, learning more about a disability is an important way to understand what others around us are going through. With that in mind, we asked Margaret Twitty, founder of the 2/17 clothing line and Complex Regional Pain Syndrome sufferer to share… Continue reading She’s Fit To Lead Article 

Blog · Complex Regional Pain Syndrome · CRPS · honor · legacy · Life · Personal · Platform · Reflex Sympathetic Dystrophy · RSD

Move Forward PT 

“I am 24 and performed gymnastics practically my whole life. I was recently diagnosed with Complex Regional Pain Syndrome (CRPS), a rare neurological disorder. It began after I had suffered trauma to my right foot when a horse stepped on it. A few months later I had surgery on the same foot to correct a… Continue reading Move Forward PT 

Blog · Clothing Line · Complex Regional Pain Syndrome · CRPS · Fashion · honor · legacy · Life · Personal · Reflex Sympathetic Dystrophy · RSD

She’s Fit To Lead Article (Coming Soon)

Once again I'm honored to be able to share my story of being diagnosed with CRPS you and with the world. This time I was asked by @shesfittolead to do an interview with them and I couldn't be more excited! She's Fit to Lead is dedicated to Girls and Women everywhere. This past year I've… Continue reading She’s Fit To Lead Article (Coming Soon)

Blog · Clothing Line · Complex Regional Pain Syndrome · CRPS · Fashion · legacy · Life · Personal · Reflex Sympathetic Dystrophy · RSD

Sharing My Story 

Hi my name is Margaret Twitty and I live in Connecticut. For 18 years I was an Athlete more specifically I was a Gymnast for 18 years.  But that all changed on February 17, 2015 when I was diagnosed with CRPS. CRPS is a rare illness/diagnosis called 'Complex Regional Pain Syndrome' (CRPS).   CRPS is… Continue reading Sharing My Story