About the Author
Bitten by the writing bug at the age of ten, Pen is an avid reader in addition to being a prolific writer. A native Georgian she lived in Hollywood, California for a year and a half (pursuing Film Studies – an interesting distraction) and six weeks in Asheville, NC (attempting to get herself together).
Influenced by the world around her, Pen writes whatever comes into her fuzzy little red head (currently Vidal Sassoon Merlot Vibrant Red). She writes in no specific genre as she has a variety of interests and passions about which to write.
Pen has suffered from Hidradenitis Suppurativa most of her adult life. However, she was not diagnosed with this affliction until 2012 due to the ignorance of the medical profession. She hopes to receive medical treatment soon for Stage 3 HS.
Pen resides in the Atlanta, Georgia area where she spends as much time as possible writing. She is currently awaiting adoption by a new feline/felines.
She may be contacted via the contact form on her website www.pensen.wix.com/neros-fiddle. You may also visit www.penspen.wix.com/hswarrior.
Respectfully,
Pen
From the Author
Dear Reader:
I suffer from an affliction known as Hidradenitis Suppurativa, also known as HS or Acne Inversa. You’ve probably never heard of it. That’s okay. Neither have most doctors.
HS is not contagious. The cause is unknown and there is no cure. Currently, there is no research being conducted into finding a cure.
This malady not only attacks on a physical level, it assaults a person’s emotional and mental states as well. Embarrassment, shame, guilt, depression, isolation, loss of self-worth and self-esteem prevent many people from even discussing their illness.
Conservative estimates state that between 1% and 4% of the world’s population suffers from HS. That doesn’t sound like much, until you crunch the numbers: anywhere from 74,000,000 to 296,000,000 people. To put this into perspective, the population of the United States is 318,000,000.
Theoretically, HS has the power to cripple an entire nation.
I state the estimates are conservative because many people are misdiagnosed due to doctors not understanding or even knowing about Hidradenitis Suppurativa. And there are people too embarrassed or ashamed to discuss this condition with their doctors.
There is no test to determine HS because there is no research. There is no research because there is little awareness of HS among the population and little compassion for HS patients in the medical community.
And it is a vicious cycle.
Despite the debilitation of this illness, many of us HS sufferers do our best to maintain some semblance of a normal life. We go about our daily routine despite the pain, not only from our own determination, but because it is expected of us. For whatever reason, many people refuse to believe how painful and debilitating these lumps are. They don’t understand how we may not appear sick but inside we are exhausted and in pain.
We call ourselves Warriors because we fight daily to have as normal lives as possible.
There is a good chance, dear reader, that you know someone who suffers from HS. And yet you may not even be aware of it.
And be thankful you yourself do not endure it.
Because I wouldn’t wish HS on anyone.
Thank you.
Respectfully,
Pen
www.hsawareness.org
www.hssupport.org
www.penspen.wix.com/hswarrior
Check out these titles and more at
www.penspen.wix.com/neros-fiddle
A little something for Everyone
T-shirts, sweatshirts, tote bags, journals, mugs, teddy bears and so much more! Original art and writing by Pen. Check it out!
www.cafepress.com/ontheqteez
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To learn more about Hidradenitis Suppurativa (a debilitating affliction I and millions of other struggle with daily), visit
www.hsawareness.org
www.hssupport.org
www.penspen.wix.com/hswarrior