It’s harder than you’d think to take photos where both Bruno the #bassethound and I look ok.
I took this picture of myself at the end of a day I spent in bed, scared and crying, feeling alone and hopeless and completely desperate.
This is the face of my mental illness. This is the face of my sadness when it is at its most inexplicable and its most pronounced.
I am not ashamed of it.
Open Letter To D&D/WOTC--Please co-sign and re-share -
Please RE-TUMBL and co-sign (my permission is granted to put this on blogs, forums etc
(I’m sick in bed, so Zak wrote the following):
This is a notice that any and all individuals that endorsed, contributed to-, or passed on (via tweet, Google+, blog, Tumblr etc) Tom Hatfield’s Fail Forward…
I’m pulling together a list of papers cited in the online EDNF 2014 presentations. First up: Dr. Claire Francomano’s literature overview, video here.
Links are under the cut, but I only have full access to a few of them. If you’re on a campus, you probably have access to more - if you can send me anything I don’t have, I’d appreciate it! I’ll keep the list updated, but for the articles behind a paywall, try 1) your local library or 2) your doctors/hospital/hospital wi-fi (hey, you may get lucky).
I’m also happy to put my biochem studies to good use if anyone has questions.
Stabilizing #silverringsplints with some @georgiavaridakis bling thrown in to brighten my day #ehlersdanlos
More testing ordered, few answers received & I got caught in the #hospitalglam act. Could be worse, for sure. (at Cedars-Sinai Medical Center)
EJ: You’re obviously a very bright and beautiful woman, but dealing with such a debilitating illness still has to demand an enormous amount from you. How do you cope? What advice would you give to other young women to cope if they were disabled by EDS, fibromyalgia, ME, etc.?
Mandy Morbid: This is also a subject I feel like I have an awful lot to say about. To simplify, for now, I’ll make a list:
Let yourself grieve at times. It’s normal given what you are going through. It’s the appropriate and healthy emotional response at times. You can’t be positive and determined all the time nonstop. The same goes for anger. You will need to vent.
At the same time, try to be mindful of the people you love and who love you – your caretakers. It’s hard on them too, so learning how to express your grief and accept theirs as well can be useful. You can go to therapy to help with this. I did. I did a year of one on one cognitive behavior therapy during the somewhat traumatic aftermath of my first surgery for my endometriosis.
Find a support group of other people you feel like you can relate to, peers, whether it’s a group you meet in person when you are able or a Facebook group, or email, it helps. My support group is mostly on Instagram’s direct (private) photo sharing app and also Twitter, apps like Kik and via text messages. I was very open about my situation and over time I made friends with other young people all over the world with EDS who are generally as severely affected as I am. We now have a close group of friends who try to keep in touch daily. We learn from each other, share resources and info about doctors and treatments, vent and offer emotional support. I am also lucky enough to have a few friends in real life who also have the same syndrome. One girl I was friends with before either of us were diagnosed!
Take advantage of your hospital or city’s social services. Don’t be afraid to ask for help when you need it. They will try to help you obtain equipment or teach you adaptations you need. The same goes for fundraising. Your quality of life has value regardless of how it feels to live with these illnesses and disabilities sometimes.
Find hobbies you can still participate in as your physical abilities change. I can’t play video games as much as I’d like but I will watch Twitch or play tabletop RPGs. I can’t read as much as I used to be able to but I can still listen to audio books or ask my friends to read aloud to me. I may not be able to go hiking with my friends but we can still go to the park or an accessible beach. I may not be able to go out as often as I’d like but I make sure my friends know I am always, always up for movie night at my place or whatever… at my place.
You are going to have to explain to your friends and family – educate, educate, educate. Some will feel overwhelmed. Some will ask you how you are doing and when you are honest with them they will be angry and upset. But they will learn why you can’t do certain things anymore or why you have to cancel plans last minute, and then you won’t have to talk about it much anymore. There will be some who will never learn and you might have to let them go. There will be some who can’t cope and will never try to make plans with you again. But you will value the ones who stick with you even more.
It’s OK to ask for help or tell someone you can’t do something. This is a hard one. Keep working on it. I still am. It’s likewise OK to say no when someone is asking too much of you.
If you’re in a romantic relationship you are going to have to be very understanding of your partner’s needs, as s/he will need to be of yours. Sex and intimacy might change. You might have to adopt new practices and arrangements. I am always the one who instigates sex. My boyfriend isn’t psychic and he cannot always tell without me saying so explicitly if I am well enough or not. You might have different issues to address but it’s going to come up. And keep in mind there are things like special pillows and positional supports you can buy, wedges, chairs, swings that can help get around physical limitations. So educate yourself! The internet is great for people with disabilities. Don’t give up. Your quality of life is worth fighting for.
You are going to have to learn to find a balance (trial and error, and research and planning ahead) between accommodating your disability/illness and maintaining the lifestyle you value. Whether it’s your education, your career, your relationships, at bit of all of those things, you will have to compromise, and you will have to prioritize. It isn’t easy. I have had to give up both performing and university. For now.
Remember you are not alone. I know it is isolating – but we develop strengths others do not, we have resources and insight and compassion others don’t.
Find ways to keep occupied and calm during the worst times of severe pain and illness, those times you cannot do anything else. I have my little quiet lap dog, a white noise machine, visualization techniques, chocolate if I am able to eat, soothing and pretty lighting, oils to help me breathe (peppermint and eucalyptus), certain books or music I only listen to when I need to retreat, sleep masks and headphones and binaural beats to help with sensory over stimulation. There are all sorts of things. Certain stuffed animals, a room painted in certain colors. Someone you can call just to hear their voice – these little things have helped me in the long run preserve my energy, my sanity, through the worst times.
As much as everyone says “fight fight fight,” you might need to take breaks from doctors appointments, tests, hospital errands, etc. I need two week breaks every few months at least. No doctors, no lab tests, no going anywhere near the hospital (unless there’s an emergency).
Read more: http://www.everyjoe.com/2014/07/10/girls/mandy-morbid-nude-model-interview-photos/#ixzz376uKNRNs —
Mandy Morbid Interview: Photos of Model with Ehlers-Danlos Syndrome
Read the whole interview for lots of information on Ehlers Danlos. Mandy’s a great advocate.
#Shoulder #brace #selfie for that #glamorous #ehlersdanlos #lifestyle
You’re not unreliable - your health is. — shout out to all my chronically ill people who get shit for being late, for cancelling, because their health prevents them, and feel like jerks because of it. It’s not your fault. (via runningonspoons)
(Source: sickfacemcgee, via myinvisibleillnessdiary)
Also: Stop coming up to my wife when she uses her handicapped parking placard and telling her that “she doesn’t look handicapped”.
(Source: abilitiesunitedorg, via tinytruant)