To mark the halfway point of November, CRPS awareness month, I began a short series of posts to help dispel some of the confusion that clouds any discussion of this rare disease. These posts are focusing on five specific questions that tend to occur in Read More …
Yesterday I began a short series of daily posts, to mark the middle of CRPS awareness month. There is a great deal of confusion about this rare disease, so I thought it would be helpful to dispel some of it. Confusion exists about what it’s Read More …
November is the annual awareness month for Complex Regional Pain Syndrome, or CRPS. We’re halfway through the month, so I thought this would be a good opportunity to dispel some of the confusion surrounding this rare disease. There is confusion about this medical condition on Read More …
This wraps up the sixth annual awareness day for Complex Regional Pain Syndrome (CRPS), the disease with which I’ve been struggling since 2016. It causes a multitude of symptoms, including a variety of different and distinct types of pain. From the pain of ankylosis, similar Read More …
Today’s the 6th annual Color the World Orange Day, to raise awareness for a rare and usually invisible disease. This disease is called Complex Regional Pain Syndrome (CRPS). This year, due to the efforts of a number of volunteers around the globe, More than 120 Read More …
Some days it feels as though there’s an invisible timer running between my hand and my brain. Then, whenever my rare disease decides that I’ve done too much – or it gets too cold or hot, or for no reason – the timer goes off Read More …
