He states in the comments that he didn't use the steroid or antibiotic creams prescribed to him, and instead put tea tree oil on it.
It’s normal if your goal is to transition into Edward James Olmos.
Why are they always fathttps://www.reddit.com/r/phallo/s/3MC0y9tQEo
Two Weeks Post-Op: Pump and Testicular Implants
Two weeks post-op and I’m feeling amazing! The pain is basically completely gone, and there have been no complications so far. I’m absolutely loving how everything is looking—it feels incredible to see things coming together so well. Grateful for this journey and excited for what’s ahead!
Found additional horrors in a different subreddit:
https://www.reddit.com/r/TransMascNSFW/s/HBzy6JQ4BL
Another fatty asked a more diplomatic version of that:Why are they always fat
If this comes off offensive, I apologize in advance, but how was the Kaiser team when it came to being a bigger individual? I'm currently in the ~260-290 lb and I am trying to find surgeons that will work with bigger BMI. I am hoping for ALT but want to know all of my options to make the most informed decisions going forward. If you'd rather answer over DMs, my box is open as well. Thanks in advance!
Doubt x2, this woman is not merely fat but well into obesity. I'm guessing the "extremely small"/eating disorder bit means she surrounded herself with even fatter friends, tried like one crash diet, gave up when it was hard, and diagnosed herself as "anorexic" & "unhealthy" (for not embracing her fatness), so now she has a free pass to be obese forever.Hey! Definitely not offensive you are all good! When I began phallo I was extremely small due to an ED. I began recovery after I had the phallus created. After that point they didn’t really care about my weight as long as I was in good health but during the first two stages (meta and phallus creation) I had to be between a specific BMI and they are pretty strict.
And this guy wants to get his cock cut off. Imagine how fast the hole's going to rotHe states in the comments that he didn't use the steroid or antibiotic creams prescribed to him, and instead put tea tree oil on it.
You'd think they could have taken skin from a fat roll instead of destroying her arm. And why are the fake balls always tiny?https://www.reddit.com/r/phallo/s/3MC0y9tQEo
Two Weeks Post-Op: Pump and Testicular Implants
Two weeks post-op and I’m feeling amazing! The pain is basically completely gone, and there have been no complications so far. I’m absolutely loving how everything is looking—it feels incredible to see things coming together so well. Grateful for this journey and excited for what’s ahead!
Found additional horrors in a different subreddit:
https://www.reddit.com/r/TransMascNSFW/s/HBzy6JQ4BL
Of all the media in this thread, this has to be the absolute most horrifying.
If I go to hell for laughing at that, I put the blame on you
I have a lot of questions about this. Billboard Chris is a sus and faggy character, and he is not responding to questions about where he got this, even from other prominent anti-troon/detroons figures- Laura "funk god" Becker asked him and he hasn't replied to her, for one.
What The Actual FUCK Is This??
Update: finally got a lead via X. archive Will dump evidence and links here and we can sort it all out as we go.
DISABLED GIRL WITH DOUBLE MASTECTOMY FOUND.
The female's name in the viral video of a disabled girl who received a double mastectomy is "Micah Leroy". She is found on an Instagram account with the username **disabled_trans_boy**.
This is one of the many videos found on the Instagram account, showing a young person with autism, and "Micah".
In the bio is a link to a GoFundMe account out of Shakopee, MN. However, the GoFundMe seems to be seeking money for another child requesting money for "rent, food, and monthly bills".
The GoFundMe seeks funds for "Raine Brick".
The description states - "I'm a disabled and chronically ill person with unsupportive and harmful parents; this money will go to my life expenses until my Social Security pay is set up".
Who is behind the camera? Who is typing the Instagram video and photo descriptions? Who is making the doctor appointments?
Who is running a GoFundMe for a child and encouraging the child to distance themselves from “unsupportive parents”?
(From Performing Institute of Minnesota Arts High School 7255 Flying Cloud Drive Eden Prairie, MN 55344)Random Recognition
Random recognition celebrates the achievements and community efforts of you and your peers. Today we recognize a Junior Instrumental and Vocal major – Raine Brick. Raine has what it takes to be a great friend. He will drop anything and offer to help you. He is what we mean when we say, “PiM is a community of creatives…” From drawing, clothing design and creation, to makeup for shows, to songwriting, instrumental and vocal performance, Raine crosses many artistic boundaries and always leaves a solid trail blazed behind him for others to follow. Thanks Raine—for being who you are!
Experienced problem solver, cyclist, and snowboarder with the belief that everyone should have a seat at the table.
I've done a lot of things and a little of a lot of things. I've worked in retail management with a focus on outdoors sports and electronics. I've guided my child with cerebral palsy through childhood and watched them wrap up high school and head off to the U of Mn. I've volunteered leading 150 people through the streets and paths of Minneapolis on their bikes. I've learned how systems work, from the ones that provide health care, to the ones that get the coolest things into your hands. Along the way I learned how to talk to anyone at their level and include everyone in every way they're able. Now, I'm headed into the tech sector to see how I can contribute as a full stack developer.
Another:This is our daughter, Mara. She’s a thriving 14-year-old with Cerebral Palsy and epilepsy. She gets around by driving a power wheelchair with her head, and has a computerized speech device that she can operate with her eyes. She loves doing anything adventurous and accessible. Some of her favorite activities have included adaptive downhill skiing, indoor skydiving, power soccer and riding her adaptive tandem bicycle with us. She’s always had an independent streak that we’ve tried our hardest to nurture and also teach her to use that to self-advocate for her needs. She has expressed a goal of advocating for others in the disability community as well when she grows up. So far we’ve been really pleased to be able to give her a wonderful variety of opportunities and everything she needs to achieve her goals in terms of medical care and equipment, her education, environmental modifications, day-to-day care, and adventures.
This fall, she is in the process of getting a service dog and is going to participate in the Youth In Government Conference in January. But despite all the good, it's been a tough year—especially this past summer and fall. In July, Mara had a deep brain stimulator implanted. This is a device that basically is a pacemaker to her motor center through wires into the frontal lobes of her brain. Her goal was to reduce extra unwanted movements and hopefully gain some additional motor function. Unfortunately, she suffered rare complications during the surgery, including additional swelling and a small stroke in the left side of her brain. While she has recovered many of the physical skills that were affected by these complications, she still has a lot of work ahead of her and the challenges from it continue to require a great deal of energy and resources. She has been aggressively working with both physical and occupational therapists to try and regain the baseline motor skills on the right side of her body. In late September, she spent an additional week in the hospital with non-epileptic episodes that appear to be result of this summer’s stress.
As she came home from that hospitalization at the end of September, we embarked on a house remodel with the goal of giving Mara additional independence at home. This project has been in the planning stages for nearly five years, so it’s exciting to have it finally underway. Some features include adding an automatic opener and new front door, redoing the accessible main bathroom to fix design issues in the shower and add a overhead track system to help with transfers. (We do currently have a rented hoyer lift to assist us, but we’re the only two that can transfer her safely and quickly at the moment). Within 48 hours of the project start, we ran into multiple major issues. The bathroom subfloor had rot from the design issues we were already fixing, there were crossbeams that precluded the overhead track lift in the bathroom, and, most importantly, the contractors found asbestos-type insulation in the eaves of the house. After three weeks of additional planning, we are finally moving forward with the project with some significant cost increases.
So here’s where we are. The good: A large proportion of Mara’s costs are covered. We are fortunate to have good health insurance as well as Medical Assistance for her, a great county- and community-based waiver program to work with, and no fewer than three top pediatric hospitals within 90 minutes of our house. The county is covering the original project scope and should soon be letting us know what they can do about the updates. While making a major impact on everyone’s time and energy, Mara’s stroke recovery is progressing really well. The Deep Brain Stimulator is also helping quiet her extra movements quite a bit. The not so good: Resources are getting tight and some big bills are coming up. We will need to pay for parts of the remodel out of pocket. We hope to put in a fence to increase Mara’s ability to care for her new dog herself. We want to continue being able to keep one of us at home so she has access to help 24x7 when needed. We have other bills that aren’t getting paid while we focus all of our energy on getting Mara the intense level of care she needs. We hate asking for help. We quite frankly suck at it. Along the way, people have offered, suggested, and given it freely even when we haven’t even been able to clearly ask for it. Thank you. It has meant everything to us. This time we’re asking loud and clear. Please help if you can. Even sharing the link for this, or reaching out with other ideas, is useful right now. We will get through this, and appreciate everyone’s consideration of this, and your continued support, in whatever form you are able to offer. Thank You Kathie and Paul
For those of you who don’t know, let me introduce you to my friends Paul and Kathie. They have two daughters, Luci and Mara. Mara, the older daughter, lives with Cerebral Palsy. Mara has limited motor skills, and relies on a power wheelchair to get around; her bicycling experiences have been limited to riding in a trailer.
Hase, a German bicycle manufacturer, makes a tandem designed with a recumbent on the front and a “normal” bike on the back.
The first time I saw a Hase Pino tandem was several years ago, (maybe 5, I don’t really remember) but I do remember I was biking on the Cedar Lake Trail, right by Louisiana Ave. I met a couple by the stop sign, and two things went through my head. The first was, “Wow! That solves sweaty back syndrome!” (One ongoing tandem joke is many tandem Stokers/Co-pilots loose interest after a while, because all they have to look at is the Captain’s sweaty back). My second thought, and likely the more important one, “This was the perfect bike for Mara.” I mentioned the bike to Paul, it was old news to him, and he proceeded to tell me all about it… in great detail…
Fast Forward
Two things happened earlier this month:
First, Mara actually got to demo one of these fancy tandems for the first time. As you can see from the pictures, the day was a hit and got lots of smiles. The tandem has enough adjustments that both Paul and Kathie should be able to ride it with Mara.
Second, Paul has found a used Hase Pino tandem for sale-we just need to help make it happen.
My goal is to raise $3000 for the purchase of this tandem. $1700 gets us the used Hase Pino (a new one would be $5500). An additional $1300 will be needed to make necessary adaptations for Mara-pedals, a 5-point harness, etc.
My favorite part will be when Mara shouts “He’s not pedaling back there!” (It’s the old tandem joke, that the person in the back isn’t pedaling, usually it’s, “She’s not pedaling back there!”)
Thank you for your generosity.
Looking back over the social history, it's really apparent that mom and dad decided trooning their severely disabled daughter out was going to make their life easier in a couple ways:It’s bad enough when it’s done to someone mentally healthy, but what kind of demon does this to a physically and mentally disabled woman? Evil exists and we need to recognise that it does.
TBH people with CP arent retarded its a motor thing so that makes more sense