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Chic polymer clay earrings | Designed to spread awareness about Ehlers-Danlos Syndrome | % of sales donated to The EDS Society | Hypoallergenic, Nickel-free | Handmade in Nashville by Hayley

Diagnosis of EDS or HSD often takes 10+ years from the onset of symptoms. Some spend a lifetime looking for answers. 🦓♥️...
06/09/2021

Diagnosis of EDS or HSD often takes 10+ years from the onset of symptoms. Some spend a lifetime looking for answers. 🦓♥️


Has physical therapy, Pilates or any other form of movement saved you??? 💪🏼 Last year, after becoming quite chronically ...
06/07/2021

Has physical therapy, Pilates or any other form of movement saved you??? 💪🏼

Last year, after becoming quite chronically ill, I became the least active I’ve ever been in my life. My body had a whole lot of muscle atrophy and because of that many issues started to arise. One of them was extreme tailbone pain. It almost seemed like overnight I couldn’t sit or even lay down comfortably anymore. Then I started having (what I thought were) frequent UTIs. There was constant burning and pain all the time, even during my bridal festivities and wedding, which made that season of life much more challenging to enjoy.

I’ve had great physical therapists, but have also had some that made my pain worse so I didn’t know what to do. After searching and trying out several places, I met Erin. Her therapy and treatment has changed my life. 🙏 She’s a pelvic floor specialist who also specializes in Pilates and physical therapy. We found that through losing all that muscle, my pelvic floor had become so weak causing all the other issues.

It’s been a full year of treatment and I’m finally turning a corner. I still take what I call my ”grandma butt seat” everywhere with me to sit on which is a lifesaver, but hopefully one day I won’t need it after becoming strong enough!

If you are frustrated feeling like everything you do hurts or sets you back further, be patient with yourself. Just the other day I thought I could handle 3 pound weights but it messed up my shoulders pretty bad. Now I know instead of quitting I just need to alter my workout routine for the millionth time. 😜

It can be challenging to find the right therapists or providers who understand Ehlers-Danlos or chronic illness, but they are out there. And I’ve found that if they are open and willing to learn and have the patience to work with me, we can discover the best solutions for therapy together.

Also, if you’re in the Nashville area and need a therapist check out at Root Physical Therapy. She’s an amazing listener, attentive, highly adaptable and very knowledgeable. If you scroll all the way across you’ll see “Ze Jarrett” earrings that were named after Erin! ♥️🙌🏼

“Hope is passion for what is possible.” 🙏-Søren Kierkegaard
06/02/2021

“Hope is passion for what is possible.” 🙏

-Søren Kierkegaard



Restocking Ze Paprika Moonbeams ✨🌙
06/02/2021

Restocking Ze Paprika Moonbeams ✨🌙

We are having a 24 hour 50% off sale for these two types of striped earrings!!! Celebrate your stripes by snagging a pai...
06/01/2021

We are having a 24 hour 50% off sale for these two types of striped earrings!!! Celebrate your stripes by snagging a pair or two!! 🙌🏼🦓

*Valid while supplies last.
*Sale goes from 5/31-6/1.



Ze Striped Heart Studs are here to celebrate the last day of EDS Awareness Month!! 🖤🤍🖤Only 8 pairs available! Wear your ...
06/01/2021

Ze Striped Heart Studs are here to celebrate the last day of EDS Awareness Month!! 🖤🤍🖤

Only 8 pairs available! Wear your stripes proudly 🦓



Ze Sahara Blaze 🦓🧡Up in Etsy today!! Go get yours to show off your stripes!! ...
06/01/2021

Ze Sahara Blaze 🦓🧡

Up in Etsy today!! Go get yours to show off your stripes!!



⭐️ Ze EDS Star of the DayMEET ZEBRA WARRIOR MACY ✨“One of the biggest challenges of finally getting diagnosed with EDS i...
06/01/2021

⭐️ Ze EDS Star of the Day

MEET ZEBRA WARRIOR MACY ✨

“One of the biggest challenges of finally getting diagnosed with EDS is the misunderstanding and lack of belief of it's existence from the majority of my family and friends. It has been a more challenging time trying to figure out how to learn and manage everything that I go through while having this along side of the feeling of people almost trying to not understand it because they don't "see" it or never knew I had these issues growing up, so how can it be real. I encourage people reading this to hold space for those in your life who go through struggles that you know nothing about. Stay open to what they are opening up to you about because chances are, it's already difficult to express, to invalid their experiences just makes it that much more painful."



Ze EDS Star of the Day ⭐️MEET ZEBRA WARRIOR MIQUETTE 💪🏼“When I was a child our GP told me that I have rubber joints as I...
06/01/2021

Ze EDS Star of the Day ⭐️

MEET ZEBRA WARRIOR MIQUETTE 💪🏼

“When I was a child our GP told me that I have rubber joints as I sprained my ankles more than I ate probably. I used to enjoy the attention with the "party tricks" I could do - bending my fingers and hands and contorting into weird positions. But unbeknown to me all these things left irreparable damage as I didn't know I had EDS then.
It is cool, though that I can scratch my whole back.”



⭐️ Ze EDS Star of the DayMEET ZEBRA WARRIOR BRIANNA 🤍"I was diagnosed with Hypermobile Ehlers-Danlos Syndrome, Behcets D...
06/01/2021

⭐️ Ze EDS Star of the Day

MEET ZEBRA WARRIOR BRIANNA 🤍

"I was diagnosed with Hypermobile Ehlers-Danlos Syndrome, Behcets Disease, POTS, and MCAS in December of 2019 after nearly ten years of searching for answers to my worsening health. After being dismissed by countless doctors, I was fortunate to wind up in the hands of a rheumatologist who was not only knowledgeable, but more importantly, believed me. Since being diagnosed, I've become an advocate for zebras of all kinds and made it a priority to educate others. Coming to terms with my own limitations is still difficult at times, but I am so grateful for the body that keeps fighting despite challenging odds."



Ze EDS Star of the day ⭐️ MEET ZEBRA WARRIOR CARA 🙌🏼“I was diagnosed at age 16 after I had injured my shoulder and my do...
06/01/2021

Ze EDS Star of the day ⭐️

MEET ZEBRA WARRIOR CARA 🙌🏼

“I was diagnosed at age 16 after I had injured my shoulder and my doctor wanted to do surgery. He decided before surgery to have me find out if I had EDS because my left shoulder was just as lose as my now injured right shoulder. Getting this diagnosis shed so much light on my life and all the issues I’ve had my entire life. I also found out that it could be related to a blood disorder I was diagnosed with at age 14, they are positive on this though. Now I just try to do the best I can and not over do anything because I don’t want to hurt myself. But then again walking on flat ground has caused many injuries for me.”



⭐️ Ze EDS Star of the Day... MEET ZEBRA WARRIOR RACHEL 👏🏼“For me, living with EDS feels like constantly wondering what’s...
05/26/2021

⭐️ Ze EDS Star of the Day...

MEET ZEBRA WARRIOR RACHEL 👏🏼

“For me, living with EDS feels like constantly wondering what’s next. My symptoms and the severity of them are always fluctuating. Getting a diagnosis and having a name to attach to my symptoms was definitely a relief, but knowing what causes them doesn’t make them easier to live with. But I’m really thankful for the community of people I’ve found in the online chronic illness community. I’ve never even met most of them, but they’re all such empathetic, kind, and truly caring people!”



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