Candace D. @DiaryofaSickGrl
Wife. Mother. Dog mom. Chronic illness advocate. 🥄♥️ #hEDS, #MCAS, #POTS, #foodallergies, #cornallergy, etc. Arizona, USA Joined February 2021-
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I cannot stress enough how important it is to avoid getting COVID, a virus that causes Long Covid, autoimmune conditions, mental health conditions, heart attacks, strokes, diabetes etc etc etc when there is less and less support for those who are ill. Don't think it won't be you.
Why has the public accepted that people will die and become disabled by Covid? They know it’s happening, they know it could happen to them, but they go along with it. Why?
Some people will never like you, but that is not a challenge. Just let them not like you.
😐😐
Please don’t assume that EDS / HSD patients aren’t trying hard enough with their exercises. You won’t see the same pace of change as a non EDS patient. There are many reasons people may struggle with exercise. Listen to their whole story before making assumptions.
Unmasked people in a cancer hospital are a certain kind of selfish.
It has taught me to enjoy the little things and cherish memories. But it has also taught me how terrible people can be.
It has taught me to enjoy the little things and cherish memories. But it has also taught me how terrible people can be.
Is it ever possible to get the perfect temperature in the shower or do I just have to play HOT COLD HOT COLD HOT COLD for eternity?
Hello, I unfortunately can’t “positive thinking” my way out of faulty collagen. Sincerely, I have ehlers-danlos syndrome
Just a reminder that while you can be checked for elevated tryptase when suspecting MCAS it doesn’t completely rule it out if you don’t have it. I very much have MCAS and do not have elevated tryptase. Most of us don’t.
Just a reminder that while you can be checked for elevated tryptase when suspecting MCAS it doesn’t completely rule it out if you don’t have it. I very much have MCAS and do not have elevated tryptase. Most of us don’t.
It’s ok if you are open & honest about the reality of your chronic illness/disability. And it’s ok if you don’t feel like talking about it too. It’s difficult to navigate & we have to do what works best for us individually. What we can’t do is decide what works for someone else
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@DiaryofaSickGrl According to my Oura ring: (And it 100% matches my experience)
collagen machine brok.. @chronicallybeee
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2K Followers 3K Following I love photography bc it allows me to show people how beautiful they truly are. EDS, autoimmune, poet, birder & bookworm. ❤️ Loved by DW. Bi 👑🌈 She/Her BLMhally @birdbrainmd3
3K Followers 2K Following 24 ✡︎ absolutely hate chiropractors. she/her Chicago«-»Memphis@DiaryofaSickGrl Yes, very much so. It’s epigenetics, the things that switch the genes on and off, culmanitive damage, and the effects of stress on the body. ‘The body keeps score’ is meant to be a really good book.
I cannot stress enough how important it is to avoid getting COVID, a virus that causes Long Covid, autoimmune conditions, mental health conditions, heart attacks, strokes, diabetes etc etc etc when there is less and less support for those who are ill. Don't think it won't be you.
“It’s too easy to get disability benefits”… said by people who have never had to apply, appeal, go to tribunal, and have lost loved ones due to the inhumane process.
Do you think the more times a virus is reactivated in our body, like EBV, the more susceptible we become to autoimmunity illness?
@DiaryofaSickGrl ‘What other people think of you is none of your concern’ is the best life advice. You can’t live for other people, and you can’t please everyone- so please yourself. If they aren’t paying your bills or giving you orgasms…no thanks!
@DiaryofaSickGrl I was just thinking about this and then I see it, so true girl. 🩵
“You should care about disabled people because you might become disabled” “You should care about women because they might be your mum/wife/daughter” No, you should care about these people because they are people, they deserve to be cared about and their rights to be protected.
Why has the public accepted that people will die and become disabled by Covid? They know it’s happening, they know it could happen to them, but they go along with it. Why?
@DiaryofaSickGrl Just read a great book by Polly Atkin - 'Some of us fall' which describes the awfulness of EDS
It's frightfully common how ignorant people can be, and yet we were *completely* in the dark about our own daughter having migraines for far too freaking long. And I am totally leaving aside the dismissal of long covid. Ignorance is bliss 😭😤😡🤯 Thx @DiaryofaSickGrl
My coworker dead ass looked at me in the face today and said, "You know, even outside of your *dismissive hand wave* covid stuff, it's been a bizarre sick season. Last week 2 kids were out of my son's class for migraines, MIGRAINES! Since when do kids get migraines?" 🫠
It is supremely inappropriate that medical professionals are not masking in clinic. It makes me unbelievably angry.
How many people did you kill or disable today? Me: zero.
My coworker dead ass looked at me in the face today and said, "You know, even outside of your *dismissive hand wave* covid stuff, it's been a bizarre sick season. Last week 2 kids were out of my son's class for migraines, MIGRAINES! Since when do kids get migraines?" 🫠
I've met my goal! So these hoodies will be made for sure! The guaranteed pre-order period ends April 30th. So get yours soon!
🌸 IV Hoodies Pre-order 🌸 They have forearm zippers for IVs, etc. Chest zippers for Ports, etc. They can be worn by anyone! 100% cotton. Oversized fit. Thick. Puff printed details (strawberries, flowers and stars). What do you think of them? Please share!! Details below!
Please don’t assume that EDS / HSD patients aren’t trying hard enough with their exercises. You won’t see the same pace of change as a non EDS patient. There are many reasons people may struggle with exercise. Listen to their whole story before making assumptions.
@FrostingSloth @DiaryofaSickGrl And how does it affect it? In my case I have a prolapsed uterus and bladder, all that because of low quality collagen. 😶
@DiaryofaSickGrl Man, I wish I could positive think my way into getting my brain to produce the feel good chemical - or my heart into pumping right - or my veins into working. Source: Panic Disorder, POTS, Venous Insufficiency
Same but only that last part
It has taught me to enjoy the little things and cherish memories. But it has also taught me how terrible people can be.