The Reluctant Spoonie is currently producing a series of eBooks to help those who have been newly diagnosed with a long-term illness. The first book in this series The Reluctant Spoonie’s Guide to Living with POTS is now available as an instant PDF download. The next book in this series will be The Reluctant Spoonie’s Guide to Living with Chronic Fatigue is due to be published in early 2021.
We are currently seeking contributors for our Guide to Living with Chronic Fatigue. Please see below for more details.
The Reluctant Spoonie’s Guide to Living with…
POTS- out now
Our Guide to Living with POTS covers a range of topics from fashion, studying with POTS and planning for the future with POTS. It also includes three stories from real people who live with POTS in addition to a Q+A with someone who uses a service dog for POTS. A must-read for anyone who has been recently diagnosed with POTS or want to improve their life with POTS.
“As a person living with dysautonomia, it is refreshing to read a book that covers so many areas of life that are affected by the condition, but are rarely spoken of.”– CLAIRE, THROUGHTHEFIBROFOG.COM
Sophia, personal story @complicatedpatient
Dottie, personal story @dotwithpots
Elizabeth and Henry, assistance dog Q+A @hero.dog.henry
Sophie, mobility aid feature @thesophieproject_
Lindsay, dating with POTS feature @chronically.sunny
Get it as an instant PDF download here
Chronic Fatigue – Due Spring 2021
We are currently looking for contributors for our next book The Reluctant Spoonie’s Guide to Living with Chronic Fatigue. It will be written in the same style as the Guide to Living with POTS with personal stories from real people who live with chronic fatigue in addition to sections on specific topics such as working from home and socialising.
Your experience is more important than your diagnosis. Anyone who experiences chronic fatigue as part of their chronic illness is welcome to contribute.
We are currently accepting the following submissions:
- 1,000-word personal essays about living with chronic fatigue. e.g. your diagnosis story, a day in your life or how you manage your chronic fatigue at school or work.
- 300-word testimonials about working, attending school or pacing and resting with chronic fatigue.
- An interview with someone who has a carer/ home help (someone that you pay or is provided for you) for household tasks. Interview questions will be emailed to you and you can complete them at your own pace.
If you are interested in sharing your chronic fatigue journey with us then please email firstname.lastname@example.org for more details. You can submit your story as a word doc., in the body of the email or as an audio file for transcription.
Submission Deadline: 18th December 2020
Please follow our Instagram for further opportunities to contribute to this book. Details will be released throughout the year.
Why chronic fatigue and not M.E/CFS?
We have chosen to focus on the symptom of Chronic Fatigue as opposed to M.E/CFS as it can sometimes be difficult for people to get an official diagnosis of M.E/CFS and we didn’t want to exclude people who had a vital story to share. Additionally, as many conditions have the symptom of chronic fatigue, we believe that we can learn for each other’s experiences. For example, how a person with fibro manages their fatigue may be of benefit to someone with M.E and vice-versa.
I have Long-COVID, can I contribute?
People with long-COVID are welcome to contribute. However, as you have been experiencing symptoms for less that a year, you may not be in the best position to offer advice to others as you may well still be figuring things out for yourself.
Can my contribution be anonymous?
Absolutely! We value privacy here at The Reluctant Spoonie and understand that people may wish to raise awareness without their boss or future employer being able to search for it.
Do you pay for contributions?
Unfortunately, we do not have the capacity to pay people for their contributions at this time. You will receive an advance copy of the eBook along with a thank-you card and a small gift for your time and effort. The main goal of these books is to raise awareness of living with a chronic illness and to help those who have been newly diagnosed feel less alone. All profits from sales go towards our web hosting fees and book production costs (cover art + proofreading).