
May is EDS Awareness Month!
In honor of EDS Awareness Month (May), Sarah Wells from My Stripy Life and I are sharing details on what you need to do to register for your FREE copy our parenting EDS Kids e-book ‘51 Tips for Parents of Children Newly Diagnosed with Ehlers-Danlos syndrome (EDS)‘ once it’s released!
Cover Photo
What first started out as a joint blog post about parenting and having kids with EDS, turned into a six-month-long project that Sarah and I have been working on off and on, waiting for the right time to finish and release it. As we continued to collaborate on it, we kept finding more and more to add, and even more information and resources that we wanted to make sure were included in our post – which then turned our joint blog post into a full resource e-book.
This e-book is the real; no holds barred advice that we wish we knew, and we hadn’t had to figure out for ourselves, the stuff that the medical books don’t always tell you!
Our parenting kids with EDS handbook/e-book is an excellent resource for parents with newly diagnosed EDS Kids, in fact, all EDS parents! It includes all of the tips and advice it has taken us years to figure out on our own – both moms of three kids with various degrees of Ehlers-Danlos syndrome and its related conditions. This e-book is the honest and practical advice that best friend would give you.
We’ve included details on what you need to do to register for your FREE copy our parenting EDS Kids e-book ‘51 Tips for Parents of Children Newly Diagnosed with Ehlers-Danlos syndrome (EDS)‘ once it’s released!
You can register for your copy in three easy steps:
1) Like our FB pages
2) Sign-up to our newsletters – subscription links are below
EDS Wellness’ Newsletter & Email List – Subscribe!
My Stripy Life’s Newsletter & Email List – Subscribe!
3) Share a post (one post from each of us during the month of May)
Additionally, EDS Wellness, Inc., a wellness non-profit, shares information on integrative and natural approaches to managing Mast Cell Activation Disorders (MCAD), Ehlers-Danlos syndrome (EDS), other hypermobility syndromes, and related conditions.
The new EDS Wellness website will be launched very soon, and we are also holding our second Wellapalooza Retreat in June 2016 – Registration is now live!
We’ve also been working on other exciting projects that will be announced this month!
What is Wellapalooza?
Wellapalooza is the coolest integrative health conferences (& retreats!) ever!
Wellapalooza incorporates integrative therapies and the latest research and information on EDS, MCAD, and related chronic illnesses together in one conference!
Subscribing to the EDS Wellness, Inc. Just 5 Minutes Integrative Wellness Newsletter/Wella News will make sure that you receive updates on all information mentioned in this post, any additional, and relevant updates. Subscription link is below. ***Please note, while this post is shared on my personal yoga journal blog/website, the newsletter/email subscription and content shared here, is different from the EDS Wellness and Wellapalooza email subscriptions and newsletters. There will be some overlaps, but the
***Please note, while this post is shared on my personal yoga journal blog/website, the newsletter/email subscription and content shared here, is different from the EDS Wellness and Wellapalooza email subscriptions and newsletters. There will be some overlaps, but the purposes and content focus for both are different.***
Subscription link for the EDS Wellness, Inc. Just 5 Minutes Integrative Wellness Newsletter/Wella News
Please share any feedback on specific topics that you would like to see covered in our newsletters, including any additional comments when you sign-up. You can also send an email to Kendra@edswellness.org.
Thank you for your interest and support!
We look forward to hearing from you!
Cheers!
- EDS Wellness, Inc. and Wellapalooza
Join us socially!
EDS Wellness Facebook Page: https://www.facebook.com/EDSWellness/
Wellapalooza Facebook Page: https://www.facebook.com/wellapalooza/
EDS Wellness, Inc.
EDS Wellness, Inc. is a non-profit organization promoting health education, integrative healthcare, and wellness strategies for living well with Ehlers-Danlos syndrome (EDS), through the publishing of print and digital media resources and materials, including seminars, webinars, conferences, coaching and patient advocacy.
EDS Wellness, Inc. provides education on various movement, nutrition, and mind-body techniques by collaborating with healthcare practitioners and like-minded organizations, to improve the quality of life and overall well-being of individuals living with EDS and other chronic, often invisible illnesses.
EDS Wellness, Inc. collaborates with other organizations and healthcare practitioners on various projects associated with Ehlers-Danlos syndrome (EDS) and related conditions, to provide information & resources for those living with EDS and the medical professionals who care for them. EDS Wellness focuses on helping patients live well while living with EDS and other chronic health condition(s).
Wellapalooza™ is a registered and protected trademark and trade name of EDS Wellness, Inc.