28-Year-Old Model with Rare Ehlers-Danlos Skin Condition Is Bedridden from Health Complications

28-Year-Old Model with Rare Ehlers-Danlos Skin Condition Is Bedridden from Health Complications

Sara Geurts became a body positive inspiration for women after sharing her experience with Ehlers-Danlos syndrome, a rare condition that causes baggy skin. But now the model is in need of help, after months of health complications from her condition.

The 28-year-old has type 1 and type 12 Ehlers-Danlos syndrome, which affects the collagen and connective tissue in the skin. In Geurts’ case, she has chronic fatigue syndrome as a result of the condition, and was recently diagnosed with cranial cervical instability, which is causing problems with her neck. The added complications left her bedridden in the last few months.

“This past winter was by far the roughest. I think in two months I went to 10 urgent care visits. I was sick to the point where I’ve been in bed for the past four weeks, haven’t left this apartment for six,” she told Barcroft TV. “It’s been a lot, not only physically, but emotionally, and it has a lot of people concerned, and a lot of people really wanting to know what’s going on, especially family and close friends.”

Geurts’ main job is at a YMCA in her hometown of Minneapolis, and she’s had to go on extended medical leave without pay due to her health. A recent MRI revealed that a “slipping disk” in her neck may leave her unable to support her head, requiring surgery.

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EMOTIONAL HONESTY POST • • This is me. This is me vulnerable and emotional, raw, no makeup and completely a wreck. This is me at this exact moment...After a 5 hour Ehlers Danlos specialist appointment there was lots of information, questions, answers and more questions... Dr. Dorff's expertise and knowledge with Ehlers Danlos was very enlightening, helpful and overall caring... which was a very refreshing approach in this field... That being said, as is with all appointments there's not always just 'good news' and this is definitely usually the case for us zebras.. After the evaluation the specialist did find the high possibility of gastroparesis as well as possible mast cell disease or another underlying disease/disorder...We have scheduled the tests and are staying positive for the results... With all thats been done and everything I've learned today im almost in a state of shock...My emotions are all over.. idk what to think.. im scared, anxious and a even a little angry, all wrapped up in onee.. I'm so used to being the strong one, unbreakable... but today, today was a lot and an emotional toll I can honestly say wasn't prepared for.. I don't know what I'd do without my amazing partner @brianaberglund by my side... I prolly would have cried the whole time.. thank you bby I love you soo muchh 💕💕 I wanted to share these photos in hopes to help other struggling with their EDS, other disorders, or just life all around.. sometimes you just gotta let it all out... be vulnerable...even though its easier said than done.. This appointment did aid to my vision of why we do what we do ik raising awareness and assuring all are educated with EDS... It's been a long day and please continue to send all good vibes our way. We lovee you all so much and thank you for all your neverending love and constant support 😘❤😘 it means more than you know • • • P.S GoFundMe LINK IN BIO 💕💕💕 • • • • • • • • • • • #ehlersdanlos #sick #love #honest #cry #real #raw #loveislove #girlfriend #loveher #girlswholikegirls #iloveyou #perfect #loveyourbody #loveyourself #selflove #goodvibes #blessed #inspire #embrace #happy #thisisme #model #ilovemybody #beyou #beautiful #positive #bodylove

A post shared by Sara Geurts (@sarageurts) on Apr 23, 2019 at 1:30pm PDT

She’s also having stomach problems, which caused her to lose 18 lbs. in the last few months. After a five-hour appointment with an Ehlers-Danlos specialist, Geurts learned that she may have other health issues.

“After the evaluation the specialist did find the high possibility of gastroparesis as well as possible mast cell disease or another underlying disease/disorder,” she wrote on Instagram.

Sharon Berglund, the mother of Geurts’ partner Briana, set up a GoFundMe page to help them manage her medical costs, as the Ehlers-Danlos specialists do not take insurance.

Geurts said she is struggling to stay positive, but she’s determined.

“I’m trying to re-spark the flame of my vision and inspirations and not fall into a complete negative state but find these recent events to be taking their toll…BUT I will not give up,” she wrote on Instagram. “I will try my hardest to remain positive and strive today and every day to do as much as I can when I can, and to be patient, vulnerable and love my body.”

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"She distanced herself to save herself." • • My recent sickness and journey with Ehlers Danlos Syndrome has been really hard on me, emotionally and physically...After a very painful MRI last week we are now worried about slipping disk in my neck not being able to support my head weight as well as numerous upcoming appointments with specialist for my Gastroparesis, MALS & POTS. I also have now found I will not be able to return to my regular job even after we are able to complete these tests..which for someone who has worked since 14 has been hard to grasp.. I apologize for my absence and hope you are able to understand it's a day by day process for me and your support and love means so much... I'm trying to respark the flame of my vision and inspirations and not fall into a complete negative state but find these recents events to be taking there toll... BUT I will not give up. I will try my hardest to remain positive and strive today and everyday to do as much as I can when I can, and to be patient, vulnerable and love my body in the times and events I can't... this is something I am really working on and is all so new to me.. I am hopeful during this time I will remain positive and there will have been some good... answers provided for long awaited questions...this too shall pass..and thank you all again for your neverending uplifting love and support.. yall keep me going & special shoutout and love to mama @sberglund3 whose been there through all of this... and dealing with my emotional self..love you so much and I will keep everyone as updated as possible. Love you all. 💕💋 • • Photographer 📸 - @brianaberglund MUA - @lunaglow.makeup • • • • • • • • • • • #womancrushwednesday #wcw #f21xme #photoshoot #nofilter #influencer #asian #love #ehlersdanlossyndrome #effyourbeautystandards #inmyskiniwin #loveyourbody #loveyourlines #bodylove #bodypositive #selflove #beyou #doyou #bebeautiful #blessed #inspire #embrace #beauty #sorrynotsorry #perfectlyimperfect #model #inspire #model #real #goodvibesonly #perfectlyimperfect #thisisme #beautiful

A post shared by Sara Geurts (@sarageurts) on May 15, 2019 at 10:07am PDT

Geurts told PEOPLE in 2017 that she initially wanted to share her story — which she continues to do on Instagram — to help others with the condition.

“I hope that it raises awareness for Ehlers-Danlos,” she said. “Even if it inspires just one person who thinks they might have it to look up the symptoms or talk to their doctor about it, that alone is the whole reason I’m doing it. That, and to ease the journey to self-love for every individual out there who thinks they need to hide their imperfections because society tells them to. Our imperfections are our perfections and they’re worth celebrating.”