Jules of Nature

ē„ę„ / Permanent Vacation
let's talk about Bridgerton tea, my ask is open
PUT YOUR BEARD IN MY MOUTH
Alisa U Zemlji Chuda
wallacepolsom
trying on a metaphor

romaā

shark vs the universe

@theartofmadeline
hello vonnie
2025 on Tumblr: Trends That Defined the Year
Stranger Things
will byers stan first human second
Cosimo Galluzzi

titsay
I'd rather be in outer space šø

if i look back, i am lost

Kaledo Art
Misplaced Lens Cap

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@wizardxcore

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Hi!! This document is divided up into 3 categories - Can Ship Supplies, Local Help / Deliveries, and General & Other. Within these categories, entries are organized alphabetically by state and country. If you are adding an entry, please put it under the applicable group/s and location! If ...
People talk about how hard long distance relationships are but nobody talks about the struggle of long distance friendships. I would give my left leg right now to just be able to sit in our pjs and watch movies or to just be able to give a big fuckingĀ hug.Ā
i see posts all the time that say āshoutout to trans kids who are closeted and misgendered constantlyā but letās give a shoutout to those who already came out of the closet and are STILL misgendered.
I know it hurts to find the courage to come out only to be denied. one day you will find people who will respect you for who you are. you deserve better.
I found some pics from Dr. Devin OāBrien-Coonās phalloplasty surgeries on transbucket, and they are some of the best phalloplasty results I think Iāve ever seen!!! Holy shit.
And there are pics from someone who had surgery with him whoās nonbinary and had RFF phalloplasty with a scrotoplasty but no vaginectomy, no urethral lengthening, nerve hookup but no āclitoralā (their term) burial into their dick. Thatās really interesting - Iāve never seen those options together before, only heard about them. Thatās not what I want, but itās really interesting to see ā especially seeing someone specifically nonbinary whoās had phalloplasty, I havenāt seen that before.
Anyway, the more I look at these different phalloplasty photos, and other phalloplasty pics of OāBrien-Coonās ā and some other phalloplasty pics ā and think about it, and what I see in my head when I think about the body I need, I have a feeling Iām gonna end up going for phalloplasty ā but who the fuck knows.
I definitely am gonna see about setting up a consultation with OāBrien-Coon sometime this year.
Iām also listening to this interview (the longer one to download) with OāBrien-Coon with the nonbinary patient mentioned above about their experience with getting a phalloplasty with him. Here it is: https://www.hopkinsmedicine.org/news/articles/gender-affirming-treatment
^ thatās my transition blog

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i found out that a surgeon in Baltimore at Johns Hopkins who does trans surgeries does metoidioplasties, not just phalloplasties!! i re-found this blog https://gaytranswerewolf.tumblr.com/tagged/bottom-surgery with a tag full of stuff about his meta and he went to Devin OāBrien-Coon in Bmore this fall!! so important for me to know!!
i still havenāt gotten around to calling surgeons because i donāt have the money for surgeries, i still donāt feel sure enough about what surgery exactly i want, iām not in the shape i want to be in exactly, and iāve had other things in my life that took priority.
i moved back to my dadās last week though for a few different reasons, and he lives out in the middle of nowhere in a small rural town where i partly grew up. iām stealth here (have been since i think not long after i started T in 2004), and being stealth specifically in such a small, rural area makes me even more conscious of my body dysphoria, more anxious, etc. than i already was basically every fucking day. iāve packed while sleeping for days since i got here, which i donāt usually do.
i havenāt looked into Devin OāBrien-Coon again yet, and havenāt looked more into others, but i have a list of them on here somewhere. i only remember McGinn, OāBrien-Coon, and Schecter.
^ thatās my transition blog
it is such complete bullshit because of FOSTA/SESTA (anti-sex workers law) that tumblr is banning porn & i guess other nudity on Dec 17!!! fuck that. this ban is gonna cut into a lot of sex workersā livelihoods! they deserve to make a living just like everyone else does, and tumblr seems to be part of a good way to do that. i have a feeling that a lot of people are gonna ditch tumblr because of this. iām personally not going to delete my blogs or anything because i wanna keep them for zines (like i wanna keep this one) and other stuff, but iām in solidarity with people who are. anyway brb deleting all the cool / sexy pics i reblogged on here :C
just a reminder
my current blog is stimmycore. follow if you want. iām on tumblr a lot less than i used to be cuz it eventually got overwhelming / i got out of the habit, but iām still on some.
READ!! THIS IS MY LAST CHANCE!!!! (This is all I have!!)
My health is actually failing. Iām not being dramatic when I say I could die If I donāt get the medical help I need.
I suffer from chronic illnesses (a rare version of MTHFR HOMOZYGOUS, HIT, DEEP VEIN THROMBOSIS, AUTOIMMUNE DISEASE + more) and I am disabled and trans. I am jobless due to my illnesses and I am currently without any necessary resources to survive, be healthy, stable, or safe..
I have a rare blood clotting disease that causes me to be at the HIGHEST RISK possible to have a heart attack, aneurysm, or stroke. This disease has also resulted in multiple major surgeries, and countless other major procedures that have left me with debilitating chronic pain and other disabilities (limited use of my dominate arm, and even tasks like sweeping leave my arms in immense pain). I have two stints in my chest keeping my main vein open to my right arm so the blood can flow to it. And it still has trouble flowing back which causes swelling and excruciating pain in my arm. The main vein in my chest has been patched and dissected from a vein from my thigh because the veins in my right arm and chest are so damaged they werenāt able to save much. I had to get a rib removed because it was pinching my vein and causing clotting during which damaged a lot of muscles in my chest and shoulder causing even more chronic pain. They also wired my chest shut.
So I NEED to have access to good health care. Iām chronically ill with horrible and scary diseases. Iāve already almost died three times, and have been on my death bed twice.. Iām in and out of hospitals constantly, they donāt have the resources to help. I NEED HELP. I NEED TO LEAVE AND MOVE IN ORDER TO SURVIVE!!! Please fucking help me!! Boost my links, donate whatever! Iām grateful for anything !!
I DONāT WANT TO DIE Iāve been fighting for my life since I was 16. Iām taking my health seriously and using the little bit of energy that I have to get shit done.
Iām honestly only asking for the bare minimum of what I need to move, and for rentā¦
Iām trying to move to Colorado to escape (my abuser and stalker that I have a really traumatic history with. Violence and including assaults) Iām stuck in my hometown right now in northern MN. Where Iām at right now IS NOT safe for me and I NEED to leave..
My friend in Colorado has a place that I can move into ASAP, I just need first and last months rent. I have to move this month or she has to find a different roommate because of her own financial situation, so this is my ONE and only lucky chance!! I NEED to move to Colorado for access to better health care (to keep me alive), and for my own safety.. This is VITAL for my health (mentally and physically).
PLEASE DONATE OR BOOST MY LINKS!!!
NOW IS THE TIME TO SHOW YOUR SUPPORT AND BE AN ALLY !! ALSO PLEASE READ AND SHARE MY STORY/LINKS!! REPOST, & REBLOG!! Copy and paste my links & story & share on ALL your social mediaās (twitter, Facebook, tumblr and Instagram!!!!) it helps me so much !
USING PayPal/Venmo IS A DIRECT WAY TO HELP ME!!
https://www.paypal.me/YvesOrage
https://www.paypal.me/YvesOrage
https://venmo.com/code?user_id=2272988271476736476
If you donate, message me so I can thank you personally !!! Thank you ā„ļø
Please help this person get the safety they deserve.
Please help this human get the help he needs.Ā
I STILL NEED HELP!! I only have days left!!!
Signal boost!
Please help Yves! If you canāt donate, please reblog. This is literally life or death.
IM RUNNING OUT OF TIME AND IM SO STRESSED! PLEASE, PLEASE, donate ANYTHING, and BOOST!!
This is ALL I HAVE AND IM LITERALLY JUST TRYING TO SURVIVE!!!
signal boost
everyone who encounters this
STOP SCROLLING
reblog
I only have like 36 hours left!!!!!!!please help me !!! Please !!
I only have one day left !!!! Please help me!!!
I NEED TO SURVIVE. I NEED TO MOVE. I NEED TO BE SAFE
//Instead of donating to my ko-fi (which a lot of you have been doing and Iām so grateful and can actually get the medication I need this month, so Iām good), please please donate to Yves. Living with chronic disease in an unsafe environment is terrifying. Thereās a way out for him.
please help him. he deserves to live. everyone deserves to live and heās got the roughest end of things. if anyone wants to donate, ill do a drawing or tarot/pendulum reading for you. please help him.
PLEASE HELP ME !! I NEED YOUR HELP!
IM AO STRESSED PLEASE, ANYTHING AND EVERYTHING COUNTS!! ā„ļø
He has LESS THAN 24 HOURS LEFT AS OF TODAY 12/11 SO PLEASE SIGNAL BOOST AND DONATE WHATEVER YOU CAN!!!
If you see this, stop, and re blog. If you have even a few dollars you can spare, please help him!
I ONLY HAVE HOURS LEFT!!!! Please help me!!!
Anything and EVERYTHING COUNTS!!!!
STOP SCROLLING
Please boost this or donate or both!
Please reblog & signal boost this, and donate if you can!!
Fighting Lyme disease and co-infections as Queerly as I can. I figure if my pile of pills is organized by gay colors š Iāll get healthier faster. Sound logic, right? In effort to update you all, I saw a Lyme literate doctor earlier this week and got diagnosed with several infections, including Borrellia, Babesia, Bartonella, and intestinal parasites. As well as heavy metal and pesticide toxicity. Iāve been having troubles with short term memory and often feeling lost in the day. I continue having seizures almost every day, pain everywhere and so much fatigue. I feel like Iāve aged so many decades In just a year. But itās no wonder with all these infections and toxins. Thatās why Iāve gotten so sick. Yikes. So Iāve got a long road of healing to go, probably a couple years, and itās frightening how much itās going to take. Time and energy and money. I need to drop out of school but I canāt support myself or house myself. I hate needing so much but having very little ability to meet my needs. Itās so many complications stacked up, y'all. I could really use all the help I can get. šš«š
So, my good friend Jo is really, really sick with late stage Lyme Disease, hasnāt been able to get much better with treatments so far, and doesnāt have the money to keep up with their medical stuff. Their health has declined rapidly even just over the past year, and itās really scary. They super need money, but if you canāt donate, please please please share this and copy/paste my status so people will know. Thanks so much <3
https://www.gofundme.com/jolymemedicalexpenses

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Hello there, Friends! My name is Jordyn Wagner and I am writing on behalf of Jo (formerly Joy McCracken). Jo and I are the same age and we grew up together in the Yakima Valley. As adults, we have both been diagnosed with chronic, late-stage Lyme Disease. For me, my battle with Lyme started w...
So, my good friend Jo is really, really sick with late stage Lyme Disease, hasnāt been able to get much better with treatments so far, and doesnāt have the money to keep up with their medical stuff. Their health has declined rapidly even just over the past year, and itās really scary. They super need money, but if you canāt donate, please please please reblog & signal boost this!! Thanks <3
Also idk yet whatās up with how the info on the fundraiser is written (havenāt heard back from Jo about that yet), but Joās name is Jo, they use they/them pronouns, theyāre nonbinary. Donāt misgender my friend, k thanks.
https://www.gofundme.com/jolymemedicalexpenses
boooooooost pleeeeeeease <3
i get new email notifications of new followers and stuff on here every now and then, so reminder that i switched a while ago to a new blog: stimmycore
Yves seriously needs help right now so if y'all can go to his bio on his profile & go to the link & share that and donate if possible, thatād help him. Heās a chronically ill trans guy & lost his job because heās ill, he canāt afford his rent now & could be homeless next week, he canāt afford the meds he needs to survive with a rare blood clotting disorder, heās got doctors appointments he needs to get to, etc. You can donate here: http://www.paypal.me/YvesOrage
Repost from @maaiingan using @RepostRegramApp - I still need your help!! Please boost and repost wherever you can!! my donation link is in my bio and Iād appreciate everyone who boosts my link and story, Iām doing the best that I can right now, but itās not enough at the moment.. I love every.single.one.of.you. Who have donated or boosted my story. I still have a long way to go and I need as much help as I can get! (Medical bills and surviving funds are a lot) Thank you from the bottom of my heart ā„ļø Mii-gwetch ā„ļømessage me if you donate so I can thank you personally, I love you, and again THANK YOU for helping me in my time of need
i guess some people are still following me here? this is a suuuuuper old blog that i really donāt come on anymore. my current one is stimmycore
^me
Today I was actually able to crouch and lean to plant a bunch of seeds in the gardens with my dad's new neighbor/tenant :) We planted beets, carrots, radishes I think, turnips, replanted some peas. :) I wasn't here last spring because of school (and doctors appointments) but wasn't able to do that much last summer. I've been in a really, really awful pain flare-up for almost a week now, enough that I went back to my pain meds I'd been on before my first dose of ketamine a week ago, but I'm starting to feel better finally. Still not sure how much I'll actually be able to do overall because it's really, really inaccessible here, but I got a barrel and hanging planters so I can have smaller spaces that are higher up, and I've got a camping chair, so we'll see.

Anya is live and ready to show you everything. Watch her strip, dance, and perform exclusive shows just for you. Interact in real-time and make your fantasies come true.
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Yesterday was my last dose of T gel, and I donāt think it was even close to my weaned dose (around 0.4g). Anyway, Iām off T again. Not entirely sure how I feel about it at this time, but itās too fucking expensive for my very limited budget, itās not like Iām in puberty mode anymore so itās just maintenance, T did what I wanted it to do a long time ago, etc. Maybe Iāll change my mind later on, but for now, I think Iām good, I dunno.
Although ideally I want to let my body just chill and readjust, Iām thinking about getting an IUD or something else like that since Trump is gonna be prez (ugh) and I donāt wanna get knocked up or anything, and Iām worried about a lack of access to something like Depo shots, etc. Weāll see.
^also, 5 days ago (Nov 17), i stopped testosterone again
(cn: ableism)
Had an appointment with a physical medicine & rehab (PM&R) doc (a resident) at an inconveniently-located hospital in the city yesterday. Yesterday was my first day using my crutches in the city also. And I was so incredibly anxious from the election result of fucking Voldemort (trump) that not only did my Lamictal tremor feel worse, but pretty much my entire body was just shaking with anxiety. I couldnāt take more valerian root (herb that can calm anxiety) than my usual one capsule per morning because Iād also already taken Neurontin, and they both can make me drowsy.Ā I took my medium-small backpack with my planner and a notebook and so on in it, and it was awkward getting that off and on, and trying to lean my forearm crutches against walls or across chairs in ways so that they wouldnāt fall over.Ā
Some of the first things that happened at the outpatient PM&R unit was, when I still had my crutches on and the receptionist tried to give me too many things at once to carry back to my chair (which was only a few feet away, but still, cāmon) and the pen started rolling off the clipboard and I couldnāt grab all the papers and my ID and insurance card at once, an older woman came over and told me to sit down and sheād hand me the clipboard and pen, and took it away, without me asking for someone elseās help. I mean, it was ultimately nice of her, but she should have thought to ask if I needed help ā I could have (and was going to) just put a bunch of the stuff down and slide the pen under the clip so it wouldnāt fall. I just put my crutches against the wall, put my backpack down, and the woman handed me the stuff. I filled out all the patient intake forms as easily as I usually do, if not more easily, since Iām used to this, and gave the clipboard and forms back to the receptionist. She looked and me and smiled and said in a babying voice,Ā āGood job!ā as if Iād performed some monumental task. UGH. Iām not a fucking child, asshat.
I was not very impressed with the PM&R doc. Actually, there were two, both residents, which means theyāre still new to being doctors. Iāll call them Resident #1 (my new doctor) and Resident #2 (his coworker). At least Resident #2 was pretty funny and easier and to engage with because he seemed warmer personality-wise. I had to take Resident #1 down a notch and put him in his place in relation to me toward the end of my appointment and it felt really, really good to allow myself that confrontation and for me to come out on top. Still exhausting though.
[cut for length⦠very long] TL;DR at the end!
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so basically iāve been diagnosed with Cerebral Palsy (CP) by the PM&R docs, and my primary doctor basically as well. my neurologist is assuming CP as well, but wants to take a look at my brain MRI that i just had done last week, just in case.
this is the first time in my life that iāve ever had any real diagnosis regarding my brain injury and its effect on my legs and left arm.
itās incredibly validating, especially since i stumbled upon PVL (periventricular leukomalacia) back in the springtime just googling my type of brain injury + chronic pain + premature birth, or something like that, and knew that everything fit, and that it tends to lead to CP.
really fucking validating and relieving that thatās what it is and (assuming my MRI confirms PVL as opposed to some other thing) that itās nothing progressive.
also unofficially-for-now diagnosed with fibromyalgia as one part of my chronic pain. the other part with my legs and left arm now we know is CP. i also have degenerative disc disease in my neck and lower back, but it doesnāt really extend too much beyond those areas according to EMG tests at my neurologistās office. gonna get tested for different stuff next month to try to cross some potential things out. so far my neurologist and pain doctor think itās all central. finally getting somewhere.