by Amber Walker | Feb 13, 2024 | All About MCAS, Hereditary Angioedema, Mindset, Patient Stories, Resources, Treatment Options, Uncategorized
My first book’s account of my story stopped in 2018. Here is my full story, updated through early 2024! If you already read the first part and are looking for what happened after I wrote the first book, if you scroll about halfway down this page it will pick up from...
by Amber Walker | Feb 23, 2018 | Hereditary Angioedema
The goal of this post is to explore potential connections between Mast Cell Activation Syndrome (MCAS), a common (but highly underdiagnosed) condition, and Hereditary Angioedema (HAE), a rarer disease. In order to do that, let’s start with a little background on...
by Amber Walker | Feb 11, 2018 | Hereditary Angioedema
February 28, 2018 is Rare Disease Day. I haven’t found many blogs about HAE that discuss abdominal attacks, so I decided to take a stab at it and share my HAE story. I’ll also share more information about HAE in Part II! My idea of the concept of pain...
