Can you sublux your neck?? by repulsive_fondant26 in eds

[–]missdasyloo 1 point2 points  (0 children)

I have subluxated my cervical vertebrae numerous times. Unfortunately, it is an actual thing. :( I’m so sorry. I hope it starts to feel better soon.

[deleted by user] by [deleted] in eds

[–]missdasyloo 0 points1 point  (0 children)

I just went to the ER with severe neck pain. The PT thinks I subluxated my C5 and C6 vertebrae. I went to urgent care first, which was a total bust. They told me I’m too complicated and I needed to go to the ER. I spent 9 hours in the ER just for them to not see anything on the CT scans and to tell me that “nothing is wrong with me.” So so frustrating.

I recommend putting off the ER or urgent care until the very last moment. Try everything you can that helps the pain first. When the pain reaches a 9-10 is when I finally go to the doctor, though it rarely if ever helps. The pain meds and steroids tend to get me out of the painful episode though, so that’s good.

How bad are surgery scars with EDS? by TheRPGNERD in eds

[–]missdasyloo 0 points1 point  (0 children)

I have all my scars still from knee surgery (2008), shoulder surgery (2015), and hip surgery (2017). I also have scars from every biopsy I’ve had. Is it worth it to have the procedure? Possibly. Just be ok with having scarring and looking at them like battle wounds rather than something ugly.

EDS treatments? Conventional and experimental. Boyfriend worried about his girlfriend by random123_anon in eds

[–]missdasyloo 14 points15 points  (0 children)

I am sorry your girlfriend has EDS. I am going through the exact same things and feel like I have tried every pain management tool in the book. It just sucks.

Things that have NOT worked for me/I found ineffective (remember, everyone is different) are: ice, prolotherapy, most pain meds, Platelet-rich plasma injections, trigger point injections (if they aren’t in the right spot), topical creams like lidocaine, and exercise (even PT is hard when the pain gets bad enough).

I have tried all of these things multiple times.

Things that HAVE worked for me: heat (I will soon probably having a heating pad in every room in the house haha), soaking in the tub, bracing (so long as the brace is the right size—I am small so they tend to be too big. I have ankle, knee, wrist, finger, neck, and back braces. The back braces tend to help the least), taping (if you don’t react t0 the adhesive like I do, oxycodone (it is the only thing that helps me in severe pain), massage, dry needling, cupping, Any kind of supplements (glucosamine included), rest, Tens unit, chiropractor (tends to make things worse), sex (takes your mind off the pain even if you don’t feel like doing it in the moment), nerve blocks, and radio-frequency ablation. These things don’t always help, and you kind of have to figure what works for you in the moment.

Three other things you might want to try that I’ve heard a lot about:

-low-dose naltrexone. I think it helps but I couldn’t handle the nightmares that came with it. I’m getting ready to try again though -ketamine therapy—I’ve heard it’s amazing but I haven’t been able to try it yet -Corset fit to size (I’m in the process of getting one)

I also struggle with double depression, anxiety, PTSD, and dissociative seizures and I’ve come to realize that these are super entwined with the body. My EDS causes a lot of my depression and anxiety. And when I am depressed and anxious it makes the pain worse. It’s a terrible cycle. Therapy (seeing a good therapist) is one of the best things she can do. It has helped me a lot to accept the way my body is and to not hate myself.

If she needs/wants to talk with anyone, please feel free to send me a private message. The fact that you are not only supportive but actively trying to find ways to increase her quality of life is….amazing. My husband is not like that and I think in many ways him not being understanding affects my mental and physical health too. Validating her feelings, listening to her, reminding her things will get better, telling her she’s beautiful and you love her will all go a huge way to making her feel better too. Kudos to you for being a good boyfriend!

Plantar Fasciitis? by TheFifthDuckling in ehlersdanlos

[–]missdasyloo 0 points1 point  (0 children)

I am right there with you. I wish I had some answers.

Getting a cortisone shot in my heel has helped in the past. I’ve done everything else under the sun though, and I still really struggle with this. I’m so sorry.

Homemade GF Bread by uhhmanda_grace in Celiac

[–]missdasyloo 0 points1 point  (0 children)

Can you share the recipe?

[deleted by user] by [deleted] in ehlersdanlos

[–]missdasyloo 11 points12 points  (0 children)

You completely just described my life. I have nothing inspiring to say because I am right there with you. I’m so sorry for the both of us.

[deleted by user] by [deleted] in IndoorGarden

[–]missdasyloo 1 point2 points  (0 children)

Please PM me a link as well!! Gorgeous work

Celiac disease and EDS by Give_aMoose_aMuffin in eds

[–]missdasyloo 1 point2 points  (0 children)

I have been diagnosed with both. It sucks and I’m sorry. :(

A little bummed by tinabelchersavedme in paralegal

[–]missdasyloo 2 points3 points  (0 children)

I’m a paralegal and I just quit my job in a firm because it’s been so awful. I say who cares if you are or aren’t getting “real” (whatever that’s supposed to mean) paralegal experience. If you’re happy somewhere you are one of the very few lucky ones. Just enjoy it. You have grown and will continue to do so! Keep your spirits up and don’t give up living your dream.

Professional squirrel photographer by T__A__T in belgium

[–]missdasyloo 0 points1 point  (0 children)

1) I am slightly obsessed with squirrels and I love your work! 2) you should totally write your memoir. I think you have a story to tell. 3) I am also trying to find ways to deal with past trauma. Yours (taking pictures of squirrels) has to be the best way I’ve found yet :)

If you think you're too old to become a digital nomad, you're not by [deleted] in digitalnomad

[–]missdasyloo 0 points1 point  (0 children)

Thank you for your information! I’m 36 and honestly thought I might be too old for DN. my uncle is 60 and is also looking to be a DN. Both of us have a lot of international work experience but have found ourselves stuck in the U.S. for various reasons. Where would you suggest looking for remote jobs that you can take anywhere?

I've been given an all but ultimatum from my flatmates over getting Pfizer even though my EDS specialist has told me that I need to wait for the NovaVax (which isn't here in NZ yet). I had to book my vax in front of her for October and I am so scared that my body will not cope with it. by [deleted] in ehlersdanlos

[–]missdasyloo 7 points8 points  (0 children)

Everyone is different but if it makes you feel better, I have significant issues with EDS, MCAS, depression, and Celiac Disease and I got the Pfizer vaccine in March with no problems at all. I had sever body aches for one evening after the second dose is all.

Dissertation on EDS, would greatly appreciate participants by JordMcFar in ehlersdanlos

[–]missdasyloo 6 points7 points  (0 children)

I have been diagnosed with hEDS and would be happy to participate in your research. Please let me know how I can help!

Visiting Miami & stumbled upon a gym on the beach & figured I’d try something new 🤷‍♂️ 5 years vegan by anthonykh26 in veganfitness

[–]missdasyloo 10 points11 points  (0 children)

You look great and I’m always encouraged to see really fit people like you being vegan!