6 Times Scrubs Mentions Rare and Chronic Illnesses
As it turns out, I am obsessed with Scrubs. The TV show, not the song. When I was at my sickest to date, those TV episodes got me through a…
5 Things My Boyfriend Has Had to Get Used to Since Dating a Spoonie
As much as there is so much to talk about regarding dating while battling a chronic illness, I want to focus for a moment on what my long-term boyfriend has…
5 Tips to Make it Through the Holiday Season with Chronic Illness
I love the holidays. The lights, decorations, family time... even the smells are better! People generally seem to be jollier, even though there are a few obvious stresses that come…
<a href="https://pixabay.com/users/valelopardo/">valelopardo</a> / Pixabay
Holding on to Faith and Hope: Leah’s Story, Part 2
This is part 2 of Leah's story, click here to read part 1 Leah listened as the doctor explained that her body couldn’t continue to be overexposed in addition to…
<a href="https://pixabay.com/users/shixugang/">shixugang</a> / Pixabay
Holding on to Faith and Hope: Leah’s Story, Part 1
As Leah approached her late twenties she was, in her own words, a “tank.” She kept up with her ex-Marine husband’s work outs and ran every day. She was the…
5 Questions I Ask Myself at Thanksgiving with Rare Disease
Thanksgiving is a time of gratitude, family and maybe a little gluttony. It was always my favorite time of the year in high school and college. Now, while I still…
<a href="https://pixabay.com/users/Free-Photos/">Free-Photos</a> / Pixabay
Morgan Share her POTS Story: Part Two
This is part two of Morgan's story. Read the first half here. I was taken off of work and school for three months to monitor my condition. I had to drop…
<a href="https://pixabay.com/users/StockSnap/">StockSnap</a> / Pixabay
Morgan Share her POTS Story: Part One
This is part one of Morgan's journey with POTS. Check out the second half of her story here. Like most stories, mine begins with someone else’s. I was in sixth…
<a href="https://pixabay.com/users/rawpixel/">rawpixel</a> / Pixabay
Stephanie’s Journey
Hello. My name is Stephanie Lewis. I am 48 years old and have been ill over half my life. I have been diagnosed with Asthma, CFS, IBS/C, Interstitial cystitis, dysautonomia,…
Jasmine’s Dysautonomia Story: Turquoise is my Favorite Color!
My name is Jasmine Taylor and I am 12 years old. October is one of my favorite months (July is the other one- it’s my birthday month!)… Let me tell…
Amber Shares Her POTS Journey: Part 2
This is the second part of Amber's story. Check out part one here. June rolled around, and my appointment with the rheumatologist came up. The hour-long car ride there made…
Source: Pixabay
Amber Shares her POTS Journey: Part One
Hello all! My name is Amber Aerni. I am 28 years old, and I would like to tell you the story of my POTS journey. Yes, I refer to my…
My POTS Story: Laura Taylor
Looking back over everything, it all makes sense now. I have been stuck on this never ending roller-coaster for the past 6 years and I have been pushing hard to…
Dysautonomia and Me: Rachel’s Story
I remember being 16 years old and commencing my first drug to help manage my heart rate and endless dizziness. It was strange, because I recall asking my friends if…
A Glimpse into Lauren’s Journey with POTS and IST
My name is Lauren. I’m 24 years old and I’m an ICU nurse from Texas. Last May, I was diagnosed with postural orthostatic tachycardia syndrome (POTS) and inappropriate sinus tachycardia (IST).…
How Changes to Facebook’s Algorithm Might be Affecting Fundraising and Awareness Pages
Facebook has been making changes to how content will be shared on people’s newsfeeds. These are designed to help users connect more with friends and family, and limit the number…
Meet Hannah: a 27-Year-Old with EDS, POTS, MCAS, and Blood Cancer Fundraising for Treatment in the USA
Hannah Evans, a 27-year-old woman from South Wales with several rare diseases, has reached her £37,500 fundraising goal that will support her trip to America to access an experimental and…
Photo courtesy of Lindsay Fogarty
Raising a Son While Managing POTS, EDS, and Gastroparesis: Lindsay’s Story
My name is Lindsay Fogarty. I am a 25-year-old single mother to a wonderful 6, almost 7-year-old son, named Andrew. As I am writing this I am listening to the…
Photo courtesy of Amber Summers
POTS… My Unwanted Blessing
That title. How can blessing and POTS even coexist in the same sentence? Well, my journey started in 2000 when I began noticing strange things happening in my body: intense…
Life With Dysautonomia: Miss Amy’s Story, Part 2
TMI Alert! Pooping, or lack thereof, deserves its own book. Constipation. Hemorrhoids. Ugh! Nothing helped. Over the counter remedies, enemas, plenty of fluids, a diet high in fiber. I tried…
<a href="https://pixabay.com/users/kangbch/">kangbch</a> / Pixabay
Life With Dysautonomia: Miss Amy’s Story, Part 1
Hello there! My name is Amy. My friends call me Miss Amy. I’m 42 years old and I have a 21-year-old son who also shares the same diagnosis as me.…
How Getting Diagnosed With POTS Changed My Life: A Patient Story
The Beginning My story began in February 2011. On January 10th, 2011, my husband and I were involved in an accident in which we slid off the side of a bridge 10 feet face…
POTS and Vasovagal Syncope: A Patient Story
In January-March of 2015, I was the healthiest I’d ever been... or so I thought. I worked out, drank plenty of water, had a great lifestyle and meal plan. In…
Source: Pixabay.com
Maxine’s Dysautonomia Journey: Part 3
To read parts 1 and 2 of Maxine's dysautonomia journey, click here and here. It was a complete scope of my upper gastro track and everything went well with the…
Source: Pixabay.com
Maxine’s Dysautonomia Journey: Part 3
PTEN Hamartoma Tumor Syndrome (PHTS) What is PTEN Hamartoma Tumor Syndrome (PHTS)? PTEN hamartoma tumor syndrome (PHTS) is an umbrella term referring to a spectrum of conditions that are all…
