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27 Year Old Lesbian Strips Down (Ehlers Danlos Awareness)

1037 ratings | 26523 views
If you don't take care of your body, where will you live? Native : https://www.nativecos.com/ Code "SkinYoureIn" for 10% off! Sara : https://www.instagram.com/sarageurts Talk With Me 1 on 1 : https://www.patreon.com/ArielleScarcella Instagram : http://bit.ly/ArielleInsta Twitter : http://bit.ly/AriTwitter Facebook : http://bit.ly/ArielleFB BUSINESS ONLY : [email protected]
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Text Comments (79)
Eliza Rose (1 month ago)
Thank you so much for sharing this I have eds and it’s amazing to know I’m not alone! Xx
Lainy Isabelle (29 days ago)
+Arielle Scarcella another EDSer here!! This was great! I'm so glad this awareness is getting out there!
Arielle Scarcella (1 month ago)
WOW this is the third comment in the first 10 minutes this video is up that says you also have EDS. I'm so happy I featured Sara and am giving awareness! <3
Her skin doesn't seem like that much of a problem, but the constant joint pain, i could never deal with that.
"If you don't take care of your body, where will you live?" Nowhere, i just won't be alive.
Jess Taylor (3 days ago)
Her skin looks like a loose shirt
styx53ocean (7 days ago)
Sara, YOU ARE BEAUTIFUL!  Don't let anyone tell you otherwise.
Greys Rays (13 days ago)
Everyone take a second to appreciate your health.
gia (15 days ago)
Honestly I think her skin looks so awesome. It looks so different from loose skin after weight loss and wrinkles from age. Beautiful girl with gorgeous hair and skin tone as well. Happy for her that she's been able to love herself and find love❤️
Tierra Nauman (17 days ago)
Do you have a website Airelle? Do you do tours or similar? My campus does this young we call "sex in the dark" and you'd be great to come off we could bring you!
Gillian M (18 days ago)
I just crawled back into bed today after an EDS flare up and was feeling low knowing that what I thought was a good day is now a “bed” day and I came across this video. I am feeling so grateful for people like Sara and Arielle for helping spread awareness and just having such caring hearts to bring a smile to my face when I really needed it. You made a difference in my world today. Mad respect for the both of you!❤️
ading adormeo (19 days ago)
First time I kne2 about thus condition
SF (19 days ago)
Thank you for sharing. Representation is so important
Zayne simard moore (22 days ago)
I have never heard of this disorder, but damn it looks like you really could lose control over having this self consciousness of your skin and body. I at first thought that she was wearing a body and skin suit. That’s sad, but at the same time she’s chose to keep going and to keep living and loving her body.
Gg Gg (22 days ago)
Do window face challenge
djriri (24 days ago)
As a person who also suffers a really rare condition (klippel trenaunay syndrome) I think it’s great her advocating for her condition
bima andreand (25 days ago)
It reminds me of shark skin
tianfang wang (26 days ago)
An easy to fit and use strap-on dildo kit; which REALLY is easy to fit and use! We were pleasantly surprised at how straightforward it was to put on, get comfy and go for it. We had purchased this particular kit on account of the the longer strapping compared to some other kits(I've got a fat arse!) and following advice from other Orgasm Army members. In terms of actually fitting it to yourself, I found that I needed to keep visualising an abseiling-kit! Having never abseiled in my life, to be honest, a diagram on the box would have been of help. Also, I'd advise having a fitting session before you actually want to get down and dirty with it- stopping mid-passion to fathom out where my legs go, adjusting the O-ring etc would have been a right turn off! But in actuality, once I'd got clear in my head how to get it on , it was a cinch to get the positioning correct and comfortable. The straps don't dig in and the pouch is soft and quite sensuous against me. I'd also load in the dildo BEFORE you get lube on your fingers as I found it a bit fiddly to get the O-ring straps buttoned up again- but this probably more to do with my shape and general incompetence than the design itself. In terms of the dildos themselves, we found that the larger one wasn't large enough- but then Mr Mercuria is not exactly new to having things stuffed up his jacksey! I'd second K&J's review with regards to thinking about the width of the dildo and if it is going to be too small. As it is, we're now looking for a broader dildo. Regardless, both he and I enjoyed the sensation very much! In fact, he said it was the hottest thing ever and he is not easy to please! Mr Mercuria said it felt great sliding in and out, no complaints about the texture and moulding quality of the dildo, and the strap-on harness didn't chafe or rub against him. A very erotic and sexy experience for all. The dildo is soft enough not to feel uncomfortable, rigid enough to be easily inserted and straigthforward to clean. Plus purple is my favourite colour! I never got round to using the vibrating bullet on the night (well, that's not exactly true; I forgot to remove the battery seal and although I could reach the button to turn it on, it understandably couldn't work!) but I inadvertently put the whole kit (minus dildo but stupidly including bullet) through the wash. It washed well, dried in no time and amazingly the bullet still works! I've had a play with it on my own and am impressed with it so far. We're looking forward to the next session when we can try it out in-situ! As an introduction to pegging, this has been a great bit of kit. It's not too expensive and is well made. The stitching is robust and the it stands up to being washed on a regular cycle. It's comfortable and easy to adjust. I recommend it as a beginner's kit- try it and you'll be looking for a bigger dildo in no time!https://www.adlutsbuying.com/p-w5880.html
TheFemaleNoob (27 days ago)
Who would even dare to unlike this!!!!!
Elena Lavigne (27 days ago)
I have EDS as well, I never see awareness for it. I have the hyper-mobility type, so chronic pain daily. Thankfully I don’t have any cardiovascular or eye issues, which are common, but my joints are really bad. Physical therapy is a lifelong thing, for sure. Everyone with this disorder, keep going! It’ll be worth it :)
nolan parker (27 days ago)
i have EDS so seeing you doing something to spread awareness and love means a lot, thanks for making me feel a little less alone.
Sarah Marlowe (28 days ago)
🦓🦓🦓🦓🦓🦓🦓🦓🦓🦓
Shintilla08 (28 days ago)
I'm starting to think I have type 3 hypermobility EDS and it's nice to see people who struggle with this syndrome owning it and being awsome
Ashley Bowen (29 days ago)
I have EDS. THANK YOU FOR THE AWARENESS!!!! Fight like a zebra.
Martine Camille Dupont (29 days ago)
Wow nice! Didn't know that she's a lesbian!! I also have eds and am a bisexual (pansexual). Love diversity! Love your colours. Love that everyone has something in common and something so unique and special <3 Love from Denmark
She looks like grandmother willow from Pocahontas!!
bluebyrd (25 days ago)
Beautiful
sylvia wanjiru (29 days ago)
She's such an inspiration to young people
Jude Dimatteo (29 days ago)
Your very pretty
Fawn Lopez (29 days ago)
Hhhgggggggg she’s so pretty
Claire Stockley (1 month ago)
I have eds and gastroparesis, I have a stomach pacer but it does not work so I have lost so much weight I currently sit at around 45kilo, have been as low as 43 and should be 75, it leaves baggy skin and an obvious square where to pacer is inserted. I find it really difficult to accept my body when I look at it and its something I have to work on, I don't like my body but I find the video's and photos that you share beautiful and it helps , its a hard road to accept what this horrible disorder does to our bodies
Cara Sachs (1 month ago)
Wooohoooo!!! Great video (and glad you clarified that it’s NOT a skin disorder, it’s a collagen disorder affecting EVERYTHING)! I’m a lesbian with hEDS, and a survivor of 43 years of severe abuse. I’ve had severe pain my whole life but my abusers did not allow me to have appropriate medical attention. I was finally diagnosed in 2015 at age 46. Sara is exactly right about removing toxic people and energy from your life. I’ve been No Contact with my abusers since Christmas of 2015, and it’s the best thing I ever did. I’m a certified life coach with my own practice. I work specifically with chronically ill folks to help them claim their inner badass and live in a way that lights them up! (I actually spent all day today preparing a presentation I’m giving at the New England Connective Tissue Disorder Symposium next Saturday about exactly this topic - so my apologies for being a bit punchy! 🤪) Beautiful representation and awareness raising Sara! And thank you Arielle for doing this video. People need to know about EDS, because there are THOUSANDS of people struggling with it who have never even heard of it. We need our loved ones and medical providers to learn about it too, so they understand our struggles and that we’re not “faking it”.
Noelle Barnes (1 month ago)
such an awesome message. the world needs more people like her!
fun vlogger (1 month ago)
Wow this is so interesting
Griffin x (1 month ago)
She has a beautiful body! ♥️
It's a great example that she is setting. Having such a condition doesn't mean you should hide away.
Jim W (1 month ago)
This was very inspiring and I had never heard of this condition before. Thank you for sharing her story.
Rockas360 (1 month ago)
Wow, never knew about this syndrome - thanks for educating us Sara. Tbh, I think you're beautiful but most importantly eloquent and well-spoken with a great attitude.
Nordic Tripods (1 month ago)
I have Ehlers Danlos and so does my mom, maternal grandma, and my sister our symptoms are more so the joints (ligaments and tendons specifically) and our cardiovascular system an example of what usually happens in those cases is basically your ankles and knees just falling out from under you at random times, hyper-flexibility, regular dislocations, heart murmurs, and compromised proprioception.. Ehlers Danlos is alot more 'common' per-say in women than in men but that's mostly due to the fact that testosterone tightens everything up and estrogen makes everything more loose, for lack of better terms, so the symptoms are more likely to be present in women and also more severe than they are in men I had never heard of Sara until I watched this video, it was very interesting, thank you for making it
Bexdastar (1 month ago)
Wow this is amazing! She is amazing l! Everyday I keep stumbling one these random videos of amazing people 💖💖💖💖💖💖💖
I’m an 18 year old girl living with mild EDS, thank you so much for some representation. It means the world, thank you
Kim W (1 month ago)
Beauty is in the eye of the beholder, and everything about her is beautiful. Remember this everyone: You don't need anyone except yourself to validate your beauty. Ignore the negative energy in this world.
Naomi Scheenen (1 month ago)
I got eds type 3 so my joints dislocate all the time also my skin is supple and doesnt heal good. Its so nice to see somone who openly support us that we are not alone. So thank you
Christina Vernon (1 month ago)
Thank you for showing this!
Sigrid Heistinger (1 month ago)
i think the folds your skin makes are very aesthetically pleasing...like waterfalls.
SparkzMxzXZ (1 month ago)
she looks fit as FUCK i don't know, she has a great personality and body :D
EDEN ETIENNE (1 month ago)
WOW. BEST WISHES TO A BRAVE SHERO.
Drrck11 (1 month ago)
Very inspirational. Liked.
Danielle Arze (1 month ago)
eds isn’t a skin disorder it’s a connective tissue disorder but even so this was an important video - having hEDS it’s important to bring awareness that these disorders exist
Arielle Scarcella (1 month ago)
Danielle Arze yes she mentions that all in the video. Forgot to add that to the intro title
Charlie X (1 month ago)
Great video. Will help many
Air-Force (1 month ago)
Sara have balls for opening up to a fuck ton of people.💪💪💪💪💪💪💪💪💪💪💪💪💪💪💪✌✌💪💪
Kyrie Wolfi Diantonio (1 month ago)
The code doesnt work.
Freya Blight (1 month ago)
I'm a Zebra too, and I love this!
Claire O’Brien (1 month ago)
She is still beautiful
K Labeck (1 month ago)
Never knew this existed. Thanks for sharing your story~💛K
Angie 978 (1 month ago)
Arielle Can you please fix the sponsor link in the description? Thx!
Svtmme73 (1 month ago)
It looks so beautiful! I’m sorry if this is offensive, but it looks like a beautiful piece of clothing when She moves. I had never heard of this before.
Briana Decembert (1 month ago)
This is so beautiful ☀️
madjoker 2003 (1 month ago)
Can I fuck you
Kaindi Isika (1 month ago)
She's so amazing❤❤radiating positivity😭you go girl❤
Hi i lesbian to and i love u chanell
Randall Roberts (1 month ago)
Sara is amazing
Leland Valentine (1 month ago)
I have EDS hyper mobility type 3! It's so cool to see videos like this on my feed. It's so great to see people spreading awareness. ^_^
Megan Watkins (1 month ago)
I think shes beautiful?
Hailey Allsbrook (1 month ago)
As someone who has hEDS, I'm so happy you made this video. The EDS community does not have nearly enough representation. It's people like you, using your platform to raise awareness, that make such a huge difference. You've allowed a much wider audience to become aware of a highly neglected disorder. These people can now go on to carry this knowledge and understanding with them in the world. #zebrastrong
Mrs Frizzle (1 month ago)
She looks fun to pet. Like I know this is serious but I really wanna pet her skin.
jaclyn camacho (1 month ago)
Thank u for this video
I have this too. ZEBRA STRONG
Kelly Barnes (1 month ago)
thank you. This video honestly made me cry because I have Ehlers dances as well and we don't have nearly enough advocates like Sara to spread awareness for it. I finally found a partner who loves me for who I am and helps me through my hospital trips and keeps me going on the days when the pain is too bad and I just want to die. Its hard for a lot of us with Ehlers Danlos to find the confidence to be ourselves, and being a lesbian didn't help at first but I have found a way to embrace myself and teach myself that I have very right to be just as happy as everyone else. <3
Arielle Scarcella (1 month ago)
Kelly Barnes so happy for you!!!!
Myles White (1 month ago)
This is a beautiful video! I love it! ❤️❤️❤️❤️❤️🙏
Lawren Haggerty (1 month ago)
Connective tissue disorder, not a skin specific disorder. EDS is such a broad spectrum! No two patients have the exact same issues. Sara is such a rare case and is incredibly brave for all of the awareness work she does!
Ulysicca Garza (1 month ago)
Simply beautiful, thank you for sharing.
Darraghsaurisrex (1 month ago)
Seeing this video in my sub feed really sent me through a loop as a fellow EDS having person it's really cool to see it being talked about and having it out there.
TheKnucklebunnie (1 month ago)
I love both you and Sara. Living with EDS sucks. I personally have hEDS and she is one of my favorite advocates.
Algaybroom (1 month ago)
What a horrible disorder! Kudos to you Sara for powering through it.
Angle Buck (1 month ago)
Beautiful
Alisha G-H (1 month ago)
Something about her skin is mesmerizing and kinda beautiful

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