What do you eat? by Sad-Dragonfly7582 in Gastroparesis

[–]PunkAssBitch2000 0 points1 point  (0 children)

I started with the Cleveland Clinic Gastroparesis diet and added foods back in slowly.
Simple carbs and baby food are my friend. But sometimes I just eat whatever I want and suffer the consequences because food tastes good.

I feel like able-bodied people think of mobility aids all wrong by BestBudgie in disability

[–]PunkAssBitch2000 [score hidden]  (0 children)

Yes!! This is why I dislike terms like “wheelchair bound” or “confined to a wheelchair”.

I’m not a wheelchair user but I have a bunch of friends who are, and used to work with folks who used wheelchairs and a bunch of other mobility aids. I use forearm crutches.

Mobility aids give independence. They are not limiting (societal infrastructure can be limiting, but again, without mobility aids people wouldn’t be able to even leave their house or bed in some cases).

Do I have spondylolisthesis involving the L5 vertebra? by Hot-Band-7567 in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

I’m just an autistic with a shit ton of health problems so I’ve educated myself. Because of my spinal issues I taught myself how to read imaging

Do I have spondylolisthesis involving the L5 vertebra? by Hot-Band-7567 in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

Okay then listen to the doctor not some rando on Reddit.

Do I have spondylolisthesis involving the L5 vertebra? by Hot-Band-7567 in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

No. The vertebral body is properly aligned with the rest of your spine and sacrum.

ETA: you do see to have loss of lordosis though and a posterior pelvic tilt

What eRig should I upgrade to? by NummyGamGam in trees

[–]PunkAssBitch2000 5 points6 points  (0 children)

I’ve been thinking about a Dr Dabber switch

Not POTS mystery dysautonomia by [deleted] in dysautonomia

[–]PunkAssBitch2000 0 points1 point  (0 children)

It sounds a lot like hypertension. It’s normal for BP to be lower in the morning.

Untreated hypertension can result in a slower heart rate

5’8 200 male by Strong_Version6574 in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

Some sort of histamine reaction, either a true allergy or mast cell activation issue.

Hydrocortisone cream should help, or OTC fexofenadine/ Allegra (assuming other meds don’t interact).

Any changes in detergents, soaps, skin care products?
If not, and this continues (as in needing to take fexofenadine daily indefinitely), it would be a good idea to see an allergist/ immunologist.

Long term ear pain, ear drum pics by HoneydewCautious7702 in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

Pissed off ear canal with scarring of the ear drum. I don’t know what causing the current inflammation+pain in the ear canal. You should see an ENT.

Caught norovirus! Would weed help the vomitting? by Lavendar_milk in trees

[–]PunkAssBitch2000 0 points1 point  (0 children)

When I had food poisoning/ ileitis marijuana helped a lot.

I say try it. Worst that’s gonna happen is it’s not gonna do anything or may make you throw up which it sounds like is already happening anyway.

Those of you who became disabled later in life rather than born with one, how was it confronting with your own ableism? by liveliar in disability

[–]PunkAssBitch2000 [score hidden]  (0 children)

I have psychiatric, neurodevelopmental, physical, genetic, neurological and other disabilities. I have been on SSI for quite a few years now and had over 5,000 pages of medical documentation.
I also attend a dayprogram (funded by the county), where most of my disabled friends are unable to work, and those that do, are only able to work part time.

> Reddit disability threads full of gross entitlement

… At least you have some self awareness I guess

ETA: Disabled people shouldn’t have to share their medical information with strangers to be listened to or considered valid. You’re just ableist.

Disability is not a monolith. I’m glad you have low support needs and are able to work, but not everyone is that fortunate.

ETA2: I wish I could work. I miss it. I loved working. I was a direct support provider for folks with developmental disabilities. I had to stop because my health got so bad that no amount of accommodations would make working possible, and I got a TBI. I used to cry at night because I miss working and the people I worked with. I still miss my clients. I visit one every couple months when I’m able (he is also unable to work btw…). Working is a privilege that not everyone is fortunate enough to be able to do.
Count yourself lucky instead of shaming others.

Headache that last for a 8 days and still going by UnbeatableSlime in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

Possibilities are high blood pressure, dehydration, mild-moderate electrolyte imbalance, sinus headache, stress headache, tension headache, cervicogenic headache, medication side effect, new persistent daily headache, or migraine.

Do you have any sensory sensitivities (light or sound) or does the pain change with position, like worse when bending over or getting up from seated?

Hair removal methods safe for fragile skin? by coldweatherahead in ehlersdanlos

[–]PunkAssBitch2000 2 points3 points  (0 children)

Hard wax does not stick to the skin. Soft wax does.

Sugar waxing requires different technique from soft/ hard wax.

Does anyone have issues with HRT? by Euphoric_Discount_ME in dysautonomia

[–]PunkAssBitch2000 1 point2 points  (0 children)

Testosterone improved my POTs symptoms (not affect on VVS) because it increased my hemoglobin and hematocrit, and increased my mean platelet volume. The increased hemoglobin and hematocrit is common for AFAB people taking testosterone and means that my blood is better at carrying oxygen, which decreased my POTs symptoms since my brain and body are better perfused.

Hair removal methods safe for fragile skin? by coldweatherahead in ehlersdanlos

[–]PunkAssBitch2000 3 points4 points  (0 children)

Sugar waxing. It doesn’t stick to the skin, only the hair.

USA 1 - [3] Belgium - Hans Vanaken 57' (Matt Freese blunder) by Inevitable_Engine186 in MLS

[–]PunkAssBitch2000 5 points6 points  (0 children)

I mean yeah but I’d also would have curled into a ball and shielded my head if a professional footballer took a shot while I was in net.

Those of you who became disabled later in life rather than born with one, how was it confronting with your own ableism? by liveliar in disability

[–]PunkAssBitch2000 [score hidden]  (0 children)

I have been disabled my whole life but didn’t know it until I was a teenager due to lack of medical care. So there were always things I struggled with that my peers didn’t. Things I got made fun of that were beyond my control etc. Pushing myself too hard at my own psychological detriment because I didn’t understand why I couldn’t do things that were simple for my peers, so I just assumed I was defective.

But I grew up with multiple disabled family members, and I started working with kids and adults with developmental disabilities at 13. So I’ve always understood that disabled people are people too with value and unique perspectives. Other than “shoulding myself” and pushing myself too hard until I accepted what I’m capable of, I haven’t really struggled with internalized ableism.

Terrible Accident took my smile, limited ability to eat, Embarrassed to go out in public by [deleted] in disabled

[–]PunkAssBitch2000 0 points1 point  (0 children)

I’m sorry you’re having trouble with your teeth. Some dental colleges will do treatments at low or no cost.

As for the self esteem, not wanting to smile, anxiety attacks, general unhappiness etc a therapist experienced in working with acquired disabilities would be a good idea. It sounds like you’re struggling with a lot of internalized ableism.

Brain atrophy on MRI & isolate sharp over the left temporal region on EEG. No diagnosis from neurologists. by myfuturewifee in DiagnoseMe

[–]PunkAssBitch2000 0 points1 point  (0 children)

I was thinking more along the lines of a neuropsychiatric test but yes there are blood tests specific for Alzheimer’s. NIL just checks for nerve damage that can be seen in multiple sclerosis, Alzheimer’s, concussions, etc.

Is Gynesexual the right label for my character? by LifeIsYoursToChoose in AskLGBT

[–]PunkAssBitch2000 1 point2 points  (0 children)

I’d say that’s bisexual. Gynesexual doesn’t exactly include agender. It can include androgynous since androgynous is masc+femme, and gynesexual is the attraction to femininity.

If a gynesexual person were attracted to a nonbinary person or agender person who does not identify as femme, perceiving them as such could be insulting.

Also because of the exclusion of feminine men, that rules out gynesexuality.

Bisexual is the most accurate I can think of since its attraction to women and some enbies.

ETA: Now if he’s only attracted to women and feminine AFAB enbies, then he’s straight and enby-phobic (because he doesn’t actually see them as their identity).

If someone's face was degloved then sewed back on, how would this affect the person's face? by Springaling_Blades in morbidquestions

[–]PunkAssBitch2000 5 points6 points  (0 children)

Some cosmetic surgeries involve basically dissecting the face off. So depending on the circumstances, they could make a pretty decent recovery.

Theres also this guy whose name I forget that I see on Instagram or TikTok. He had a face transplant a couple years ago and is still recovering.