eladnarra

I'm so glad they recommended it for all ages. Get boosted and wear an n95 mask, folks! This surge isn't looking good.

Hm... I'd actually disagree with that conclusion? I think what the author is saying there is that ableism isn't simply a matter of the words being used. A statement that treats disabled people as subhuman isn't okay because it avoids using these words - it's still ableist.

From the beginning of the article (emphasis mine):

Note that only some of the words on this page are actually slurs. Many of the words and phrases on this page are not generally considered slurs, and in fact, may not actually be hurtful, upsetting, retraumatizing, or offensive to many disabled people. They are simply considered ableist (the way that referring to a woman as emotionally fragile is sexist, but not a slur).

Not everyone has the ability to be mindful of how certain language originated in ableism and this reinforces it. But for those of us who can, it's a good idea to try.

Sounds like folks have given a good number of alternatives, but I just wanted to share a resource: "Ableism/Language" by Lydia X. Z. Brown. It goes through a bunch of ableist words and suggests alternatives. :)

I'm so grateful for his work. I struggle to explain how "I'm tired" encompasses so much, often because I'm too tired to explain, hah. But now I can point to this article!

The 21 million includes everyone, not just registered voters. Until 2015, I couldn't vote because I wasn't a citizen. Still had to live with the shitty policies that Floridian politicians passed into law.

Quite a few folks have mentioned Outer Wilds, so I'll add the DLC soundtrack. The titular song (Echoes of the Eye) that plays at the end of the DLC makes me burst into tears every time I hear it. But in a good way, haha.

It's not ideal, but I use Patreon to donate to a few different folks at once (I think it still combines transactions to reduce fees...). Otherwise I usually pay the fee, if the amount I'm donating is small and I'm given the choice.

When I moved in with my partner, I had to let go of a lot food-related shame or sense of obligation. My partner has executive dysfunction stuff, I don't have the energy for cooking - but my parents scoffed at frozen meals and takeout when I was a kid, and my dad got annoyed when something in the fridge went bad

My life got so much easier when I stopped feeling bad about finding easier ways to eat. I'm glad you've found options that work well for you!

Yeah, at least for types associated with low blood volume! I've seen some folks talk about taking a salt tablet and drinking water before they even get out of bed, but somehow I've never really managed to make that part of my morning routine. I do better with salty food and electrolyte drinks (Normalyte).

I've been doing savory oatmeal for breakfast! It's salty for an early boost for POTS, and with quick oats I can just dump things in a bowl and microwave for a couple minutes (low spoons for CFS). Still working on collecting things I can add, like jarred sliced mushrooms and asking my partner to boil lots of eggs to keep on hand in the fridge.

I don't have the energy to cook or make most meals, so I'm usually just helping my partner with ideas. It's exciting to be able to come up with ideas and actually get to execute them.

I don't think I'd put peanut butter by itself in a crepe; the reason peanut butter and jelly sandwiches are so popular is that the jelly/jam helps cut the stickiness of the peanut butter.

But then again, I ate sandwiches that only had peanut butter in them for most of elementary school. Wash it down with some milk, and it's filling and tasty.

I've tried physical therapy several times - and unsurprisingly to anyone who understands PEM, as I gained muscle strength, my endurance got worse and I slowly crashed.

My dream one day is to be able to create my own physical therapy plan. I have some ideas that revolve around some guidelines I've found about aerobic respiration dysfunction, mainly:

• lying down
• do an exercise for no longer than 2 minutes at a time (less is better)
• follow a 1:3 rule for resting between sets (rest for at least 3 times the length of the set)
• keep heart rate very low, and no aerobics
• increase weights, not number of repetitions (to keep time spent exercising at a minimum)

But unfortunately my health isn't there yet. A lot of this is based on this overview of CFS/ME for physical therapists, and this part struck me:

Exercises should be initiated only after the patient can complete all ADLs/IADLs without setbacks due to PEM that result in eliminating ADLs/IADLs or other meaningful routine activities from their agenda.

I don't really consider myself to have trouble with ADLs (Activities of Daily Living), since they're so limited. I can basically shower, dress, and eat on my own, with appropriate aids. (I mean sometimes I skip showering and sometimes I need help putting on compression socks but it's not bad.)

But I hadn't heard of IADLs before.

Instrumental activities of daily living (IADL) are those activities that allow an individual to live independently in a community. Although not necessary for functional living, the ability to perform IADLs can significantly improve the quality of life. The major domains of IADLs include cooking, cleaning, transportation, laundry, and managing finances.

The only one of those I can do regularly is finances, so... Yeah. Not ready for DIY PT...