Luca⚜️
@tequilucasunset.bsky.social
NOLA➡️Dallas, lgbt, they/them, chronic pain✨ fibromyalgia 10 year anniversary 🎆 music nerd #hassky ☺️ #monsterhunter
if ICE goes to new orleans we’ll be able to use the potholes like the vietcong in nam
November 22, 2025 at 6:25 PM
if ICE goes to new orleans we’ll be able to use the potholes like the vietcong in nam
OH MY GOD. New Lausse the Cat album. I expected new Frank Ocean before new Lausse. Production is soooo smooth. I’m eating between this and Danny.
November 12, 2025 at 7:10 PM
OH MY GOD. New Lausse the Cat album. I expected new Frank Ocean before new Lausse. Production is soooo smooth. I’m eating between this and Danny.
IOP was incredible. Leaving IOP? I’m beyond scared. I’ve learned how to explain how EDS functions, but it sounds like sci-fi. I wish I could keep a group or just one or two people like me.
Nobody ever asks me enough to understand and I feel like my every action is an oddity outside of sitting.
Nobody ever asks me enough to understand and I feel like my every action is an oddity outside of sitting.
November 12, 2025 at 3:38 AM
IOP was incredible. Leaving IOP? I’m beyond scared. I’ve learned how to explain how EDS functions, but it sounds like sci-fi. I wish I could keep a group or just one or two people like me.
Nobody ever asks me enough to understand and I feel like my every action is an oddity outside of sitting.
Nobody ever asks me enough to understand and I feel like my every action is an oddity outside of sitting.
new danny brown album is wild, him finding hyperpop is good for the world
November 9, 2025 at 6:55 PM
new danny brown album is wild, him finding hyperpop is good for the world
Meeting people in Dallas feels so hard compared to when I lived in New Orleans and 50% of my friends were initially just random people grilling in their front yard that I said “smells good” to.
Is everywhere else this antisocial lmao?
Is everywhere else this antisocial lmao?
November 7, 2025 at 5:21 PM
Meeting people in Dallas feels so hard compared to when I lived in New Orleans and 50% of my friends were initially just random people grilling in their front yard that I said “smells good” to.
Is everywhere else this antisocial lmao?
Is everywhere else this antisocial lmao?
I do wish Dallas had more “third places” that aren’t bars. That said, it’s not like my disabled ass can really smoke in public.
November 7, 2025 at 6:27 AM
I do wish Dallas had more “third places” that aren’t bars. That said, it’s not like my disabled ass can really smoke in public.
eyyo first time out in the free world mildly healthy
November 1, 2025 at 2:33 AM
eyyo first time out in the free world mildly healthy
Do I have any Dallas friends near Greenville I like to party
November 1, 2025 at 1:39 AM
Do I have any Dallas friends near Greenville I like to party
I finished my IOP and I’m half-scared that’s the most socializing I’ll get for years.
November 1, 2025 at 1:32 AM
I finished my IOP and I’m half-scared that’s the most socializing I’ll get for years.
> gain back the physical health to leave house after months of undiluted isolation, weeks on end without speaking
> lose singular method of even leaving my house
hell yeah
> lose singular method of even leaving my house
hell yeah
October 19, 2025 at 6:24 AM
> gain back the physical health to leave house after months of undiluted isolation, weeks on end without speaking
> lose singular method of even leaving my house
hell yeah
> lose singular method of even leaving my house
hell yeah
I hate EDS/CRPS cus I still ain’t sure if my high pain today is from the car accident/whiplash or the stress from it.
It’s higher than baseline, but not unusual pain. I’ve always joked I’m gonna blow off chest pain one day before grabbing my chest and falling over tho LMAO.
It’s higher than baseline, but not unusual pain. I’ve always joked I’m gonna blow off chest pain one day before grabbing my chest and falling over tho LMAO.
October 18, 2025 at 3:15 PM
I hate EDS/CRPS cus I still ain’t sure if my high pain today is from the car accident/whiplash or the stress from it.
It’s higher than baseline, but not unusual pain. I’ve always joked I’m gonna blow off chest pain one day before grabbing my chest and falling over tho LMAO.
It’s higher than baseline, but not unusual pain. I’ve always joked I’m gonna blow off chest pain one day before grabbing my chest and falling over tho LMAO.
5 weeks into my IOP for fibro with massive results
Car runs a red light and broadsides me, can’t tell if neck pain is whiplash or stress causing a flareup lmao.
The universe does not want me to get a W.
Car runs a red light and broadsides me, can’t tell if neck pain is whiplash or stress causing a flareup lmao.
The universe does not want me to get a W.
October 17, 2025 at 10:01 PM
5 weeks into my IOP for fibro with massive results
Car runs a red light and broadsides me, can’t tell if neck pain is whiplash or stress causing a flareup lmao.
The universe does not want me to get a W.
Car runs a red light and broadsides me, can’t tell if neck pain is whiplash or stress causing a flareup lmao.
The universe does not want me to get a W.
Okay well I got approved for my 5th week here and probably 6th since my doctor got my MRI results and brain EEG thing he wants to get a bit experimental.
October 7, 2025 at 1:28 PM
Okay well I got approved for my 5th week here and probably 6th since my doctor got my MRI results and brain EEG thing he wants to get a bit experimental.
Week 4 of IOP. Probably getting extended to 6 weeks since we’re still rummaging through treatment options, but excited still as I’ve had some stuff work including my SGB.
October 6, 2025 at 12:23 PM
Week 4 of IOP. Probably getting extended to 6 weeks since we’re still rummaging through treatment options, but excited still as I’ve had some stuff work including my SGB.
The good thing about a fibromyalgia/CRPS/EDS diagnosis is that the million comorbidities it’s tied to makes getting off-label scripts for pain so much easier.
September 30, 2025 at 4:43 PM
The good thing about a fibromyalgia/CRPS/EDS diagnosis is that the million comorbidities it’s tied to makes getting off-label scripts for pain so much easier.
Like I said though I’m getting my stellate ganglion nerve block this week. Idk how it works, but it’s supposed to broadly reduce anxiety and pain.
Efficacy is insanely good, tends towards a 20% reduction in at least one category (I’ll take either), and they can do the other side too.
Efficacy is insanely good, tends towards a 20% reduction in at least one category (I’ll take either), and they can do the other side too.
September 28, 2025 at 3:03 PM
Like I said though I’m getting my stellate ganglion nerve block this week. Idk how it works, but it’s supposed to broadly reduce anxiety and pain.
Efficacy is insanely good, tends towards a 20% reduction in at least one category (I’ll take either), and they can do the other side too.
Efficacy is insanely good, tends towards a 20% reduction in at least one category (I’ll take either), and they can do the other side too.
Fibro is so much more confusing than I thought, which I already thought was beyond confusing.
You’re telling me I need to reset my parasympathetic nervous system and change my CNS’s natural response?
On the flip side I have my stellate block Tuesday which is supposed to reduce anxiety n pain.
You’re telling me I need to reset my parasympathetic nervous system and change my CNS’s natural response?
On the flip side I have my stellate block Tuesday which is supposed to reduce anxiety n pain.
September 28, 2025 at 2:56 PM
Fibro is so much more confusing than I thought, which I already thought was beyond confusing.
You’re telling me I need to reset my parasympathetic nervous system and change my CNS’s natural response?
On the flip side I have my stellate block Tuesday which is supposed to reduce anxiety n pain.
You’re telling me I need to reset my parasympathetic nervous system and change my CNS’s natural response?
On the flip side I have my stellate block Tuesday which is supposed to reduce anxiety n pain.
Is this type of care more common outside the U.S.? Because this is how shit should be done. Psychiatrist working with my doctors lead to rediagnosing me with depression and cPTSD over bipolar, I might not have fibro, so much shit.
So I entered this 1-month out-patient care for fibro/EDS with a whole team of doctors, psychiatrists, and PTs working together and it’s been incredible.
It’s 8-4 every day and fucking exhausting, but getting new methods of treatment 10+ doctors never offered. Feels hopeful. I’m SO tired after tho.
It’s 8-4 every day and fucking exhausting, but getting new methods of treatment 10+ doctors never offered. Feels hopeful. I’m SO tired after tho.
September 18, 2025 at 3:04 PM
Is this type of care more common outside the U.S.? Because this is how shit should be done. Psychiatrist working with my doctors lead to rediagnosing me with depression and cPTSD over bipolar, I might not have fibro, so much shit.
So I entered this 1-month out-patient care for fibro/EDS with a whole team of doctors, psychiatrists, and PTs working together and it’s been incredible.
It’s 8-4 every day and fucking exhausting, but getting new methods of treatment 10+ doctors never offered. Feels hopeful. I’m SO tired after tho.
It’s 8-4 every day and fucking exhausting, but getting new methods of treatment 10+ doctors never offered. Feels hopeful. I’m SO tired after tho.
September 18, 2025 at 1:47 PM
So I entered this 1-month out-patient care for fibro/EDS with a whole team of doctors, psychiatrists, and PTs working together and it’s been incredible.
It’s 8-4 every day and fucking exhausting, but getting new methods of treatment 10+ doctors never offered. Feels hopeful. I’m SO tired after tho.
It’s 8-4 every day and fucking exhausting, but getting new methods of treatment 10+ doctors never offered. Feels hopeful. I’m SO tired after tho.
Like it’s good to push M4A from a class perspective, but that falls short if you’re provided M4A without free and functional transit and local doctors/hospitals.
Which many disadvantaged communities don’t have by design.
I had to fuckin move states to get diagnosed with fibro.
Which many disadvantaged communities don’t have by design.
I had to fuckin move states to get diagnosed with fibro.
I think the best analogy is invisible disabilities. People can’t see my struggles, but ppl in my personal life haven’t experienced it, tho they know it’s real.
Invisible disabilities are barely even talked about within the context of ableism. There are other “invisible” areas in race/gender.
Invisible disabilities are barely even talked about within the context of ableism. There are other “invisible” areas in race/gender.
September 6, 2025 at 7:40 PM
Like it’s good to push M4A from a class perspective, but that falls short if you’re provided M4A without free and functional transit and local doctors/hospitals.
Which many disadvantaged communities don’t have by design.
I had to fuckin move states to get diagnosed with fibro.
Which many disadvantaged communities don’t have by design.
I had to fuckin move states to get diagnosed with fibro.
There’s this white leftist fixation exclusively on class while ignoring how gender, race, etc. is mapped onto it.
That’s normal if you want to foster a white leftist audience, but it’s inherently exclusionary of others.
That’s normal if you want to foster a white leftist audience, but it’s inherently exclusionary of others.
September 6, 2025 at 7:01 PM
There’s this white leftist fixation exclusively on class while ignoring how gender, race, etc. is mapped onto it.
That’s normal if you want to foster a white leftist audience, but it’s inherently exclusionary of others.
That’s normal if you want to foster a white leftist audience, but it’s inherently exclusionary of others.
My endo doesn’t have an opening so I can start estrogen for nearly a year. I hate the medical system here.
September 1, 2025 at 10:07 PM
My endo doesn’t have an opening so I can start estrogen for nearly a year. I hate the medical system here.
I’m tired, I’m moored on my own island, if I weren’t spiteful towards reactionaries I don’t think I’d be pushin forward.
August 27, 2025 at 3:19 AM
I’m tired, I’m moored on my own island, if I weren’t spiteful towards reactionaries I don’t think I’d be pushin forward.
How do you even keep friends at this level of disabled. I’m so isolated.
Every day I wake up and I’m just self-entertaining myself with conversation, and that’s the only back-and-forth for weeks.
Nobody is indebted to be interested in talking to me, but I wish there was ANY outlet.
Every day I wake up and I’m just self-entertaining myself with conversation, and that’s the only back-and-forth for weeks.
Nobody is indebted to be interested in talking to me, but I wish there was ANY outlet.
August 27, 2025 at 3:17 AM
How do you even keep friends at this level of disabled. I’m so isolated.
Every day I wake up and I’m just self-entertaining myself with conversation, and that’s the only back-and-forth for weeks.
Nobody is indebted to be interested in talking to me, but I wish there was ANY outlet.
Every day I wake up and I’m just self-entertaining myself with conversation, and that’s the only back-and-forth for weeks.
Nobody is indebted to be interested in talking to me, but I wish there was ANY outlet.
This has probably been trodden to death, but I REALLY don’t get the hesitance to mask more purely from the utilitarian point of normalizing their usage rather than letting it be painted as a “protest tool”.
I say that as someone w/ immunocomp issues. It’s a net positive.
I say that as someone w/ immunocomp issues. It’s a net positive.
August 26, 2025 at 4:02 PM
This has probably been trodden to death, but I REALLY don’t get the hesitance to mask more purely from the utilitarian point of normalizing their usage rather than letting it be painted as a “protest tool”.
I say that as someone w/ immunocomp issues. It’s a net positive.
I say that as someone w/ immunocomp issues. It’s a net positive.