Megathread The Pooner Zoo - A thread for collecting wild Pooners and posting OC Pooners, and anything Pooner related

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I, too, tried my hand at searching but went for “trans + stroke”. Didn’t find the poor girl but found these VERY manly dudes. You can tell how totally male they are from their short, concise writing that starts with CW: trauma, abuse, trans discrimination, disability discrimination, stroke.

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CW: trauma, abuse, trans discrimination, disability discrimination, stroke

Hi! I'm Bri. :)

My partner and I are in our early 40s. We've both dealt with illness/disability, poverty and trauma for the vast majority of our lives, both developing C-PTSD as a result.

I was homeless as a teenager because my parents couldn't handle my queerness; we later ended up homeless together briefly, as queer, disabled adults. Neither of us has ever had a chance to know what it's like to be secure in our housing, so that we can heal and find peace and productivity in other ways.

When I met AJ, they had a job in social work and were making decent money, but they were living with their mother, who took over half of their paycheck for the privilege of having a roof overhead and being abused in a myriad of ways. Eventually, shortly before they began their medical transition, they were fired from their job because they'd gotten too butch and made people too uncomfortable. After a period of struggling to find another job, they ended up working at a gay men's dating website. They began medically transitioning while there, and they were fired for asking a manager for help when coworkers kept asking inappropriate questions about their genitals at work.

We've lived repeatedly in apartments that have made us sick, with landlords who would do nothing meaningful about mold, bedbugs, and other pest infestations. We've had housemates who didn't believe we were disabled, declared us lazy, and harrassed us the entire time we had to live with them. A housemate once screamed at me, causing a panic attack and cornering me under a table, blocking the room's exit because I fell behind on rent.

Over the past decade, we'd begun to find our way and slowly pull ourselves out of extreme poverty. I started a small business making jewelry. Over 10 years, I made and sold thousands of pieces, constantly increasing my skill and working with more precious materials. I had to work way too many hours and usually brought in less than minimum wage, but it was work that I could do on my own terms, with chronic pain and multiple chronic illnesses. AJ found a corporate WFH job, which they excelled at for 7 years, getting glowing reviews, raises, and more responsibility right up until they had multiple strokes and nearly died 3 years ago.

As you might expect, everything changed overnight. We spent 5 weeks living at Tacoma General; except for the few days I stayed home with a stomach bug, I only went home for a couple of hours a day to shower, cook for us, and do laundry. Then AJ spent 5 weeks at Good Samaritan rehab in Puyallup, where I was only able to spend a few hours every other night and had a couple of sleepovers so that the nurses could train me to take care of AJ when they came home. I continued to cook and bring all of their food, do all of their laundry, and pack up our entire apartment by myself in preparation for their homecoming.

Thankfully, there was a ground level apartment available in the building where we already lived, so I moved everything from our 3rd floor apartment down to the new ground level space. A couple of neighbors helped me with a few heavier items, but I moved everything else. A friend in the building charged us far too little to help with cleaning the old apartment.

I had to quickly move everything from our cluttered 400 square foot apartment, which housed both of us and a small business, into a 250 square foot studio. Three years later, I'm still working on giving away items that we haven't used in this apartment.

I've been AJ's full-time caregiver for over 2 1/2 years now. I'm so grateful that I'm able to do this, both physically and legally. It's hard, but it's the best job I've ever had, my supervisor is extremely flexible and understanding (hehe), and I wouldn't ever wish AJ the indignity of having a stranger come into their home to help with things like bathing and toileting. I sincerely hope that I am able to keep doing this as long as AJ needs the assistance.

The single most heartbreaking thing for me about our current living situation is that AJ doesn't have enough space to use their wheelchair. The chair makes it so much easier for AJ to get around than their walker. The space is also so tiny that their entire world most weeks is their half of an adjustable split king bed, the bathroom, and the 10' walk in between the bed and toilet.

We're both high risk for covid complications, and that was terrifying when we were dealing with deadlier strains. We self isolated for nearly 2 1/2 years and are finally starting to slowly, carefully reintegrate ourselves into the world... But our world has always revolved around our home because we're so chronically ill and disabled. We've never gotten out that much.

I just want us to have a safe, comfortable, accessible nest. And I want AJ's world to grow a few sizes, even when we're not well enough to get out much.

How do I expect to do this? Well, dear reader, I'm hoping that some of you will be willing to help me gather funds toward a down payment that will be sizable enough to give me actually affordable mortgage payments, despite living in Tacoma. I'd also be very open to a donation or discounted sale of land in a spot that would be both accessible and in a part of the city that would be safe for visibly LGBTQIA+ folks, with an emphasis on the T+. We'd be thrilled to connect with a contractor willing and able to give us a discount on a build or repairs, etc. If you have helpful skills and would be willing to help, please get in touch!

I love AJ so much, and they have been abandoned and traumatized so many times in the 4 decades they've been on this planet. In addition to having a home that is wheelchair accessible, I want to try to help their traumatized brain run out of excuses to be perpetually anxious that we will end up on the street again, so that they can finally learn what it's like to relax. Not that I'm much better at it, but I'm great at dissociating via books and that can get pretty close sometimes. ;)

Anyway, loosely, that's the plan, or the hope. I know that I can get first time homebuyer's assistance, but there isn't much funding available per household in Tacoma, and today's interest rates are pretty steep when the suitable houses on the market are generally in the ~$400K range. I'm hoping to be able to gather many small bits of help and use them to manifest a home.

I've already opened a brand new savings account, and any donations received will be deposited straight into that account for costs related to buying a home. I will be happy to periodically show statements, receipts, etc. If we fail to find a solution for buying a home, funds may be used to help us afford to rent a truly accessible home, but we really don't want that to happen. If we are able to find our home and there are funds left over, they will be used to help pay for the extensive oral surgery we've both needed for years but couldn't afford. After that, anything remaining would be donated to help with short- and/or long-term housing solutions for disabled and/or unhoused folks. We really don't expect to have excess funds at all, but wanted to be clear about our intentions upfront, just in case we're blessed beyond our wildest hopes.

If you've read this far, thank you so much. If you're willing and able to make a donation or offer other help, I'd be so incredibly grateful. We're spiritual folks, dedicated to the goddess Brighid, and we also highly value prayer, Reiki, and other good mojo. Please feel free to also send these helpful energies our way, or on our behalf, and know that we appreciate it deeply.

With love, hope, and gratitude,
Bri
TLDR? Well, how about “We've had housemates who didn't believe we were disabled, declared us lazy, and harrassed us the entire time we had to live with them. A housemate once screamed at me, causing a panic attack and cornering me under a table, blocking the room's exit because I fell behind on rent.”

Best of luck, fellas!
 
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I'm being sarcastic, but it wouldn't be unsurprising if someone were fundraising for her, in which case it'd be matching up the campaign and the dates. But it also wouldn't be unsurprising if nobody were fundraising for her, and she's being quietly turned and tube-fed in a nursing home somewhere, a body in a bed for the next couple-four decades.
When she was first mentioned here on KF I actually did do an extensive search for fundraisers and found nothing.
 
Realistically, though with something like this, I cannot imagine what sort of quality of life she would have. I mean, it probably would have been better if she died from the stroke. At the very least, I think that she would probably look into assisted suicide.
When someone's that impaired, often they don't have to be that proactive. The Diving Bell and the Butterfly's author died of pneumonia two days after his book was published; she could just wait on the "old man's friend." I hope she is able to communicate enough to get an advance directive/POLST written, and that the people around her have time to listen, and that they care about her wishes.

Best of luck, fellas!
At least they're sticking together, even if I don't hold out much hope for a $7,000 house.

These two could have saved so much time, money and side effects by just being boring ol' lesbians together. All gender got them was unconvincing facial hair and a stroke for the one with a real job.
 
When someone's that impaired, often they don't have to be that proactive. The Diving Bell and the Butterfly's author died of pneumonia two days after his book was published; she could just wait on the "old man's friend." I hope she is able to communicate enough to get an advance directive/POLST written, and that the people around her have time to listen, and that they care about her wishes.

 
found these VERY manly dudes.
Bruh you gotta archive links and then just right click google the names, this pair is a known set of grifters and looks like a treasure trove of content.

Bri Crofton, "Blessed Baubles":


Hello! My name is Bri Crofton. I’m also known as Bri the Bearded Spoonie Babe.

I am a bearded genderqueer woman with PCOS and multiple disabling diagnoses. I live in the beautiful Pacific Northwest with my non-binary trans spouse, AJ Spellman. I am on a mission to normalize women’s facial hair, and to spread love and awareness, both in general and as they pertain to chronic illness, the LGBTQIAP+ community, and intersectional feminism.

We are Reiki practitioners and eclectic witches devoted to the Celtic goddess Brighid. Together, we tend her sacred flame and do our best to stand up for love and justice in the ways that we are able.

I’m a contributor to Fembot Magazine; read my first submission, Becoming a Bearded Woman, to learn more about my perspective and goals.

You may also wish to read my work on HuffPost.

I first intended to use Medium as a place for my prose, but essays that don’t fit elsewhere will pop up here from time to time as well. I plan to update this introduction regularly as I have articles published elsewhere.

If you’d like to see what else I’m up to, feel free to follow me on Instagram. Check out my jewelry, prayer beads and items created from my graphic designs in my shop.

If you’d like to support my writing and activism, you may be interested in becoming a patron. You can also send a one-time tip via PayPal.

I look forward to posting more here.

Wishing you many bright blessings,
Bri


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Hello! I'm Bri, the person behind Baubles & Blessings. I started B&B from the most humble of beginnings in 2010. It's taken a long time and a lot of hard work, but after many years of honing my design and beading skills, becoming attuned and beginning to practice Reiki, and doing a whole lot of networking, B&B has become what it is today — a fully legitimate small business providing a humble income for one disabled person.

I am the full-time caregiver for my partner, who had multiple strokes several years ago. Even with better wages than caregivers in most states and my partner's SSDI check, the additional income from my jewelry is what enables us to actually afford to live in a safe, clean, mostly accessible apartment after spending nearly a decade in a crumbling building full of mold that made us very sick.

I served one year as a member of the Tacoma Human Rights Commission before having to resign due to my health.

I am unapologetically queer and nonbinary. My only pronouns are they/them. I'm an eclectic pagan witch, child and flamekeeper of the Celtic goddess Brighid. Coming from the perspective of a queer, trans person dedicated to a goddess who's all about justice, and who has been homeless and continues to know a degree of housing insecurity... To say that fairness, justice and compassion are a big deal to me is an understatement. My little family does our best to regularly support people and animals battling adversity, and we're always open to hearing about organizations that would benefit from the modest financial contributions that we're able to make.

For the foreseeable future, I'm donating 5% of gross sales to getting clean water to folks in West Virginia coal camps. Learn more here.

You can keep up with my newest work by following me on Facebook or signing up for my mailing list.

You are also welcome to follow me on my Facebook page, Bri the Bearded Spoonie Babe, as I work to celebrate self love, normalize facial hair for non-men, and encourage body positivity, while sharing sporadically about my life as a human who is queer, trans, neurodivergent, and disabled. I no longer post here regularly, but I do post about these same issues from time to time on the B&B page, and I'll probably use it as a backup if there's ever an issue with the B&B page.

Thank you SO much for your support! Your purchases and word of mouth seriously mean so much to me.

Much love and brightest blessings to you all!

xo
Bri

AJ Spellman:

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They have been together for at least 15 years, moved to Tacoma from Boston:


Bri Crofton and AJ Spellman created the Skewed & Screwed Revue in response to AJ’s having been discriminated against by his former employer, four months into transitioning from female to male. As a result of that discrimination and a consequent year-long battle for unemployment, coupled with Bri’s inability to work a traditional job because of disabilities (with an ongoing SSI battle), they have found themselves in a position where they had run out of money and options.

Bri and AJ decided to start organizing fund-raising shows to acquire the money necessary to avoid on-the-streets homelessness back in June. As of this writing (12.16.10), there have been six Skewed & Screwed Revue shows, featuring burlesque dancers, live music, a magician, sideshow performers, spoken word artists, stand-up comics and other performance artists. These shows will continue for the foreseeable future, though new ideas are constantly being brainstormed and put into action in regards to format and promotion.

Once their need has passed, Bri and AJ intend to continue organizing benefit shows in order to help other GLBT/Queer people in similar situations (with an emphasis on the T, simply because they know firsthand how few resources exist specifically for transgender individuals and their families). To be clear, the name and intent of the Skewed & Screwed Revue is meant only to reflect upon the cause and not the gender, orientation or political leanings of any performers or anyone else working to help the cause.

Currently, at least 20% of the door from each Skewed & Screwed Revue will be donated to a nonprofit group in New England that is doing the sort of work that Bri and AJ aspire to be doing.

Previous GFM:

Hello, friends new and old! As most of you are aware, AJ developed a rare condition called PRES —posterior reversible encephalopathy syndrome — back in May, which led to bilateral strokes. They were intubated and sedated in the ICU for several days while a brain bleed slowed down. They were sent to rehab too early, just a week after nearly dying, and only lasted a few days before landing back in the ER and being readmitted to stabilize their blood pressure. In total, AJ spent five weeks at Tacoma General. They were then transferred to inpatient rehab at Good Samaritan hospital, where they stayed for another five weeks and learned how feed and dress themself, use a wheelchair, and start walking again withassistance.

AJ has been home since the first week of August. I lived at the hospital with them the entire time they were at TG, minus a few days that I had a stomach bug of some sort. My small business has been on hold while I have been a caregiver, single-handedly moved us into a new apartment which is smaller andmore expensive but is also more accessible, and have taken on the entirety of the chores which we shared before the strokes. Our only income has been AJ's short term disability checks, which don't even cover our new rent.

At first, AJ's caseworker at DSHS made a typo which led us to believe they were only approved to receive 14 hours of care per month. It seemed like a lot of hoops to jump through to become a paid caregiver, only to be paid for 14 hours per month. We finally learned, just within the past few months,that AJ is actually approved for 114 hours of care per month.

So I started looking into how I could start getting paid for some of the caregiving I've been providing every day for months. (Pay is not retroactive, but will help us so much moving forward.) I hit another wall when I called SEIU 775 and was told that the benefits of free training along with paid training hours only applies if you take their own in-person course. Because of my own disabilities preventing me from being able to attend early morning classes five days a week for two weeks straight plus needing to be at homefor AJ, I need to take a class which is offered online, with just two days of in-person skill labs. It took alot of digging for me to learn that this was even possible.

The home care aide (HCA) certification course I'll be taking is offered through Cornerstone HealthcareTraining Company. The cost is $553 for training, plus $222 for the testing and exam fees. If I were getting paid for the training hours, I'd make $1,125. So the total goal for this fundraiser is those three amounts added together, plus $100 to account for fees.

Meeting the above goal of $2,000 will take care of my training, licensing and exam fees, and will also cover our living expenses until I start getting paychecks, which can take up to a month after the 5 hour orientation is completed. This will enable me to focus on my training and caregiving duties, without constantly stressing about how we are going to buy groceries or make up the gap in rent.

I've been waiting three weeks, since submitting my background check application, to start this fundraiser and be on my way to signing up for my courses. I finally heard back this morning, and my contracting appointment is December 5th, so here we are.

We need one last rally, one big ol' push, and then we'll finally have some stability and breathing room. Once I've finished my classes and exam, I will be focusing any free time I have on getting my business back up and running again in our tiny new space. This has been an incredibly overwhelming task, but I believe that it will be possible — and that I will actually have the energy to joyfully create — once my currently superhumanly high levels of stress and resulting depression have eased.

AJ and I know how blessed we are to have been surrounded by so much love and received so much assistance since their strokes just over six months ago. We owe our current safety and warmth to each of you who has helped in any way. We truly hate having to ask again, but there is simply no other way forus to find stability right now.

Please help us out from between this rock and hard place in any way you are able. Even a $5 donationhelps!

If you'd like to send a donation via a fee-free method, I can accept funds via PayPal friends and family, Zelle or Facebook Messenger. Gift cards for Lyft or Amazon are also incredibly helpful. All of the above can be sent to [email redacted]. Any donations of funds from any source (other than gift cards, which help SO much but can't be used to pay course fees or bills) will be included on this page; I will manually add other contributions daily so you can all see exactly where we are in relation to our goal every step ofthe way.

Please note that I do not use or plan to sign up for any additional online payment methods not mentioned above.
Cards of encouragement for AJ are absolutely welcome and cherished. AJ was so heartened by the many wonderful cards they received in rehab, but they have received just one card since coming home.In addition to cards for AJ, I can also accept checks made out to Bri Crofton at the address below.(Please don't send surprise large packages, as I don't get to the post office often and it can be difficult to schlep packages around while running errands.)

AJ Spellman & Bri Crofton
PO Box 7690
Tacoma, WA 98417

Please know that we are also incredibly grateful for prayers, Reiki, candles, signal boosts of this fundraiser and Facebook posts about it, as well as general good mojo. We appreciate your love and well wishes so much, and we truly believe that they help!

Much love and bright blessings to you all, friends.


Important update 12/7:
There are only three HCA training programs in Washington which are DSHS-approved and mostly online, which is why it's so difficult to find them among the dozens of classes offered in person. I did some more digging and finally found the newest one, Washington Care Academy.

Not only does WCA off er the two day in-person skills lab right in Tacoma, but the course is over $200 less expensive than the one I'd planned to take from Cornerstone. Tonight, I registered for the class. I'llbegin the orientation this weekend.

Unfortunately, I found out at Thursday's contracting appointment and mini orientation that it could take up to two weeks longer to start receiving a paycheck than we'd initially expected. AJ's long term disability checks, our only reliable income in the meantime, are $781 per month. Our rent alone is $950. Because of these factors, I'm going to keep the total goal the same even though I found a less expensive course. We'll definitely need more groceries before my pay starts coming in.


December 30th, 2019
by Bri Crofton,
Organizer
Oh my goodness, y'all. Thanks to a few very generous folks, we're suddenly very close to our goal. Thiswill cover most of our needs until I get paid. Anything that may come in over goal will help with my$1,000 credit card debt, so that we won't have to worry about interest and my paycheck can actually goto current needs rather than scrambling to catch up. Thank you all so much for your support. This hasbeen such a hard year, but it would have been impossibly diffi cult without the love and assistance we'vereceived from our extended family and kind strangers.

This is mostly just a gratitude post, but if you want to help us get that last little bit to goal, help with thecredit card debt or transportation funds, here are some ways to do that.

PayPal friends and family, Zelle, Lyft and Amazon gift cards in any amount can all be sent to [emailredacted], with zero fees. (We have most of our groceries delivered through Shipt, but order somestaple food and supplies from Amazon.) I can also accept donations through Messenger. Any funds sentelsewhere will be added to this page as offl ine donations.

Blog started by someone around 12 years ago about their scamming. At the time they had moved from MA to TN- they later moved on to WA:


June 24, 2012

Purpose

The purpose of this blog is to allow people who are assisting, are considering assisting, or have assisted Bri Crofton and her partner to get a clearer picture of who they are and what they do. There are numerous people who have helped these two, and the stories I’m going to present here are meant to inform. I don’t necessarily mean to encourage people not to help them. That’s a choice you need to make for yourself, and if you feel inclined, by all means do so. I just think you should hear the whole story, rather than the one sided view presented by Bri Crofton and her partner. It’s their life, and they can only tell the stories from their perspective.
Who are Bri and her partner?
They are a couple currently living in Chattanooga, TN. They are originally from the Boston area. You may have seen them selling jewelry outside of the Davis Square train station with their pet rats. Various online presences include Bri’s blog, http://bribroken.wordpress.com , the LiveJournal account Miss_Jett, and an Artfire store here: http://www.artfire.com/ext/shop/studio/Brigyn . There’s also an association with the username “duelingscorpios” . You can find Bri’s Facebook here: https://www.facebook.com/bri.broken . Bri also has an account on Reddit, DisabledArtist. BriBroken is a frequent nickname online.
They have been teetering on the edge of homelessness for a couple years now. To hear them tell it, it’s a really sad story. I’ll give a brief rundown here, and you can read the long version on their blog.
After losing their housing in Boston, a friend took them in. It took less than a month for that friend to decide it wasn’t working out and kicked them out. This scenario happened three times, with different people. After the second shot, They ended up homeless, sleeping in Davis Square. After a post on Davis Square’s community blog on LiveJournal, they were taken in by another kind soul, this time up in Salem. They were told they’d have a month of housing to get on their feet. This, too, did not work out, and they were kicked out after two weeks. To hear them tell it, it was totally unfair and they were doing everything they could. To hear the person who took them in tell it, they sat around all day, did very little, always had an excuse for why they were unable to do anything, yet were easily able to do fun things, and they were really stinky all the time.
After this, rather than end up back on the streets, Bri and her partner checked into a rooming house in Salem, at a cost of around $250 per week. They were unable to pay their rent on their own, and instead their various friends, acquaintances and internet strangers ended up giving the money to them after many MANY desperate, pleading, last minute posts on Bri’s blog. During this time, a friend purchased a Santa Suit for Partner to attempt to dress up and entertain, or get a job during the holidays. This was purchased well in advance of Christmas, yet they couldn’t even be bothered to get on the train and go to the city to pick it up. By the time they got around to it, the season was essentially over.
Bri earns a small amount of money selling bead jewelry on Etsy. Well. She used to. Her shop was closed down by Etsy for failing to actually ship the items she sold. Her excuse was that she didn’t have the money to send them and that she couldn’t walk to the post office to do so. I’ll note that the post office was 2 blocks from their home and that all Etsy transactions included shipping charges. I’ll also note that the USPS will pick up packages. She still couldn’t get things mailed out and her shop was shut down by Etsy for stealing from customers.
At some point during their time in Salem, it appears as though Partner was offered a work from home job, and that in order to start working, he had to send in notarized paperwork. It took them nearly three months to send this in, and the excuse was that no notary would work with his’s ID. Partner is transgendered, and passes for male, while his ID stated he was female. I personally called the 10 nearest notaries to them and asked them if this was a problem. All 10 said it was not, and all 10 said they had never seen either of them. These two didn’t even try.
Recently, they were offered the opportunity to live and work on a farm outside of Chattanooga, TN. This, predictably, went the same way as the other housing situations they were given. Bri and Partner didn’t hold up the end of their bargain and were asked to leave after about 2 weeks. They’re now in another hotel in Chattanooga, and are again begging for money to pay their rent.
They have both applied for disability. Both cases have been denied. This is because they aren’t actually disabled to the point where they cannot work. I don’t doubt that they THINK they are… they certainly have pain, IBS and whatnot. However I’ve witnessed these two bounce around happily when something they WANT to do comes up. If it’s work, they’re too tired, too hurt, too disabled. If it’s fun, they’re ready and raring to go.
Bri is a social parasite. She infects the community that takes them in and nearly destroys it. Once no one is willing to step up for them anymore, she moves on. An example is the trans community in Boston. After all the lies, deceit and just plain bullshit, they were forced to move on. Now they’re infecting the pagan community. Watch out.
I’ll tell you more detailed stories in this blog. This was just a very basic overview.

Fundraiser for weed, 2016:

Hello! My name is Bri Crofton. I'm 35 years old and I've been a chronic pain patient for 15 years now, having finally received diagnoses of fibromyalgia and arthritis in the past year, along with a slew of related health issues. After five years of struggling to get back on our feet after a difficult job loss and increased illness, my partner and I moved to Washington state in November of 2014.

I'd previously been on narcotic pain medication for a number of years. When I stopped taking them, I realized that there were a number of negative side effects I'd been experiencing, which vanished fairly suddenly... So I wouldn't be interested in being on narcotics on a daily basis now, even if there were doctors willing to prescribe them with the current war on narcotics.

In my new home, I started seeking relief by going to a clinic where I saw a naturopath who recommended herbal medicine. For the next year, I was able to do a relatively decent job of keeping this pain medicine around, but when my business slowed down significantly this year, I began to struggle.

I spoke with my PCP about other methods of pain relief. I started taking small doses of gabapentin (generic Neurontin) and duloxetine (Cymbalta). They seemed to help for a while, then petered out. After the duloxetine dose had been increased for some time, I started noticing lots of weird, random symptoms like extra nerve pain, painful and embarrassingly excessive flatulence, increased headaches, a chronic sore throat and much more. I was shocked to discover that it is common for Cymbalta to cause all of the odd side effects I was experiencing. I slowly tapered off and have been completely off of duloxetine for several months, but I'm still experiencing side effects, which I have since discovered is not uncommon.

My dose of gabapentin was increased, and I was switched from one muscle relaxer to another. This is all that my PCP would do for the increased pain post-duloxetine. It soon became clear that the gabapentin was actually causing increased nerve pain, so I've now tapered off of that as well.

Not only does my herbal regimen bring me significant pain relief, but it has also lowered my blood pressure to the point that I no longer need to take lisinopril, which I'd been taking for years. When I can afford to take it consistently, I don't need to take my prescribed clonazepam (Klonopin) for anxiety or sleep, either.

As of July 1st, the cost of my natural medicine regimen has more than doubled suddenly, and it costs me up to $20 per day to get enough meaningful relief that I am able to run my small business, run errands for my small family when my partner (who is also disabled and works from home) is too unwell to join me, and to focus on learning, developing new skills and finding ways to forge more stability for ourselves in the future.

Our ultimate plan is to save up to reinstate my partner's license and get a car so we can move to a small town near the Oregon coast within the next few years. I need to have the ability to keep working toward this goal, which is why I am here, asking for your help. Once we make it to Oregon and have the space to do so, we'll be able to grow our own plants and make our own medicine from them.

In the meantime, every penny donated will help to make dreams come true for one disabled couple who already moved cross-country to make a better life for themselves. Because of the increased cost of my medicine, I now need help raising funds for rent and monthly bills.

The goal for this campaign reflects the funds needed to cover the rest of those expenses for the remainder of 2016, plus the cost of PayPal and Fundrazr fees.

With your help, we can thrive, grow, and continue to climb the ladder of self-sufficiency despite our physical limitations.

Whether you are able to help by making a contribution, spreading the word to those who may be able to do so, or just wishing us well on our journey, I appreciate you caring enough to read this far!

My partner and I are currently studying Reiki, with the intention of helping ourselves and others to heal. We're about to get our Level II attunements and we will be at the point where we are ready to send distance Reiki out this autumn. Unless you let me know that you'd prefer we didn't include you, we'll be sending Reiki to everyone who has contributed on a near-daily basis once we are able. (We may need to occasionally take a night off due to illness or pain.) We already practice self Reiki nightly, so we're not promising something we don't know we can keep up with. We'll just be expanding upon our current practice. If you have any specific intentions you'd like included for you, please just let us know.

Feel free to join the Facebook group connected to this fundraiser for updates.

Much love and many blessings, friends!
<3 Bri

PS: If you'd like to check out the jewelry that I make along with the metaphysical items recently added to my shop, you may do so here. If you'd like to check out our Amazon wishlist, we try to keep it up to date with OTC medicines and supplements of which we are currently in need.


Pooner number 1's name is Bridget Crofton. Still working on finding "AJ"s original moniker. They have scrubbed themselves off of people finders, which 9 out of 10 multi-millionaire rock and movie stars have not bothered to do- this is something hackers/cybersecurity elites, antifa, and KiwiFarmers do. And scammers. The top percentile of scammers.

Love the "long distance Reiki." Also impressive how much money every one of her fundraisers actually has made. As of 12 years back she was already into 5 figures:

Bri by the numbers. $18,646 and 6 houses.

$18,646. That’s about how much money Bri has received by begging, scamming and grifting over the course of the last couple years. That’s $18,646 worth of “if we could just do this one thing, everything will work out!”
Let’s start with the ChipIn Fundraisers. They’re here: http://duelingscorpios.chipin.com/september-needs , http://duelingscorpios.chipin.com/transitions , http://duelingscorpios.chipin.com/sos-calling-all-spiritworker-friends , http://duelingscorpios.chipin.com/rent , http://duelingscorpios.chipin.com/rent-fundraiser , http://duelingscorpios.chipin.com/help-us-break-this-cycle-of-skirting-homelessness, and http://duelingscorpios.chipin.com/rent-and-special-show
That’s $2,237. According to people who were there, her “Skewed & Screwed Review” “benefit” shows netted about $2500 between them. I’ll even be conservative, and say $2000, to be generous.
That’s $4,237.
She never, not once, paid rent in Salem with earned money. She paid some rent with jewelry that was purchased. Not much. And many of these jewelry items were never shipped. Bri herself admits this. She admits that she spent the money paid for shipping on other things. And pretty much all of those purchases were by people she linked her shop to and were buying something to help. AJ was not employed in Salem. Bri was not employed. Every dime of that money came from other people. So let’s do some math.
They spent about 30 weeks living in Salem. The rent was $240 per week. That’s $7,200.
That’s $11,437 dollars we’re up to.
Her phone bills. They’ve been on for most, but not all the time. They’re about $50 per month. Over 2 years, let’s just say she’s kept it on 3/4 of the time, though I’m 95% sure it’s been a bit more than that. $50 times 18 months is $900.
We’re at $12,337.
First month’s rent at both the JP and Brighton apartments were paid for by other people. And not her Skewed & Screwed Review. I don’t know what the rent was, but the bare bottom for 1 bedroom in a multi-roommate house in Boston is $500 per month, and that really is the bare minimum.
We’re up to $13,337.
She received about $150 worth of pizza (for lactose intolerant AJ, who can’t even eat canned vegetables because he hurts so much from the trace lactose) and other food and “necessities” on Reddit.
$13,487.
The Amazon Wishlist. Look at it yourself: http://www.amazon.com/registry/wish...er=all&sort=priority&layout=standard&x=14&y=9 . That’s just the stuff that has been purchased, by the way. Added up, the total, including an oh so necessary smartphone, tablet, and mobile wi-fi hotspot, and it’s $559.11.
We’re now up to $14,046
What about all those times they asked for donations for food in Salem, because their $400 in food stamps per month just didn’t go far enough? In the course of their time in Salem, they received $2,600 from people for food, various things like hygeine products, things she just “had to buy” and other “necessities”. This is my math that I saved from past posts of her based on what she was asking for and later said she received.
We’re up to $16,646 . And we haven’t even left Massachusetts for Tennessee yet.
Bri began the begging pretty much right away in TN, receiving about $200 for miscellaneous crap she “needed” at the farm, including transportation to her hotel in town.
$16,846.
Rent is around $150 per week in Chattanooga. They’ve been there 2 days shy of 13 weeks. That’s $1950 But AJ has a job now, right? So they don’t need to beg, scam or grift money from people anymore, right?
Wrong. The Lokean community rallied around these two, as well as her normal group of whoever it is that gives her money. From emails and comments on this blog, the Lokean community has given them just shy of $1800 since they left the farm. This includes a kind soul, whose comments you can find a few posts down from this one, who gave her three weeks rent, three weeks ago. What’s that about AJ’s job?
We’re up to $18,646.
And that’s a minimum. She has begged for food, henna hair dye, bills and other random stuff she wants at least 2 dozen times that I haven’t counted here because I can’t verify how much she received. She hasn’t worked in 2 and a half years, and even then it was a part time job. She received donations for rent while she lived in the Brighton and JP homes. I just don’t know how much.
That’s $18,646 dollars worth of begging, outright lying about being starving, outright lying about being sick, and, most of all, $18,646 dollars worth of “one more chances” to get their shit together.
And speaking of homes, Bri has been kicked out of at least 6 of them in a few years. Kicked out. Not left on her own. She was kicked out of the JP and Brighton houses for not paying rent. She was kicked out of a house in Somerville for being extremely gross. She tried to move in with her friend in NH (remember, she brought her bed up there.). She was kicked out of steelbluelily’s housing in exchange for very light work around the house situation. And she was kicked out of the farm in Signal Mountain, TN.
The numbers don’t lie. Bri does.
EDIT: believe the deadname of "AJ" is Lea M Spellman. Bri has a previous aka of Bridget M Dellamano.


One innovation both male and female students said they don’t like is the college’s new escort policy. Women and men live in separate halls, but they can only visit opposite-sex areas with an escort. Students also need an escort to visit friends’ rooms in other dorms. “If you ask me, it’s pretty retarded,” said Lea Spellman, a 21-year-old junior.
 
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One and the story it's based on is fucking horrifying.
If that was my friend or even worse my kid and the doctors wouldn't do the right thing I'd smuggle my gun into the hospital and give them peace and I'd tell the Judge do what you want because my conscience is clean.
That's no way to live.
It's the only thing worse I can think of than what they put that Japanese guy through when he got irradiated.
At least he died after a few months.
Being locked in your own head would be hell.
 
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You said that like a rapist but I get it.
Maybe you are one. haha
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The part I always found funny/baffling about pooners is the average height of a woman in the US is 5'3.5" and I know for a fact that are actual men that height who are seriously depressed and borderline suicidal because of their height. Pooners actively choose to be turbo manlets.
Pooner height cope: 'I know a cis man who's 4'3" dood!' :smug:
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When someone's that impaired, often they don't have to be that proactive. The Diving Bell and the Butterfly's author died of pneumonia two days after his book was published; she could just wait on the "old man's friend." I hope she is able to communicate enough to get an advance directive/POLST written, and that the people around her have time to listen, and that they care about her wishes.
This made me think of an article from last fall. This woman has been living with locked-in syndrome for nearly 20 years. She's definitely an outlier, but it is a possibility.

 
A young pooner got an unwanted dose of facts and truth… She reacted in the most manliest of ways: Blocking, crying and then posting an essay on Reddit:

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This is awesome, frankly. So much truth in one message. It's great that someone told her the truth for once.

Can't wait for her posting about having no help anymore despite being "disabled" and how this is the fault of transphobia and capitalism. Also her new gofundme.

Edit to add - dude, post a link!
 
This made me think of an article from last fall. This woman has been living with locked-in syndrome for nearly 20 years. She's definitely an outlier, but it is a possibility.
Definitely, and like this article said, with PT and long effort she was able to regain facial expressions and some head movement. "Facial expressions" sounds like a silly, small achievement, until you realize what it's like to not be able to make them.

Facial expressions would mean the world for someone with no visitors who lives in a profitably-staffed nursing home. Nobody's got time for the communication board when you have 14 other people to get up with the full lift. Smile or wince would increase her quality of life tremendously.

I keep perseverating on her long-term care plan, but "support" doesn't come from nowhere. Locked-in Canadian lady up there had a husband and kids, and presumably the rest of the family too. We know so little about CVA Pooner, and can only hope she didn't alienate her family. Best case scenario she has her parents managing her care, and Aiden, Milo and Leaf visiting on different days to read her the latest fanfiction and spending enough time with partner-assisted scanning to help her really communicate. Best case.

Government's going to pay to keep you alive; keep your butt dry and your weight stable and at least one bath a week. A state-appointed guardian, if the legal family isn't involved, has a lot on their plate and isn't going to advocate for more than that.
 
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Screening like, "Is she a woman?" and "Is testosterone harmful to women?"
Right- these days I am getting increasingly annoyed with the number of semi-enlightened ex-libs who say this kind of thing. As though there could ever be real "consent" to having your arm chopped off and stapled to your crotch. As though there was a kind of female for whom it would be safe and sane to prescribe high doses of male hormones.
A young pooner got an unwanted dose of facts and truth… She reacted in the most manliest of ways: Blocking, crying and then posting an essay on Reddit:

View attachment 6320713
A sober moment of silence to respect the massive bullet that the brother in this story dodged by making this crazy pooner his ex. This was a near miss as epic as if he'd turned his head to consult a chart on immigration.
 
A young pooner got an unwanted dose of facts and truth… She reacted in the most manliest of ways: Blocking, crying and then posting an essay on Reddit:

View attachment 6320713
While I agree with his sentiment, I always saw "deformed" as something someone was born with, that they can't help.
This Pooners arm is "mutilated".
Hello bois, yall keepin it skibidi rizz up in this function?
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Pooner phenotype is real. Is it the Testosterone that causes that round face so many of them seem to have?
Bloat from water retention from trying to piss through strictures?
Seriously go pick a random Pooner, the chances are she will have a similar look.
 
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While I agree with his sentiment, I always saw "deformed" as something someone was born with, that they can't help.
This Pooners arm is "mutilated".

Pooner phenotype is real. Is it the Testosterone that causes that round face so many of them seem to have?
Bloat from water retention from trying to piss through strictures?
Seriously go pick a random Pooner, the chances are she will have a similar look.
There is a little fluid retention/moon face type effect, from the steroids. And there is a little bit of chubbiness probably due to eating above her paygrade due to testosterone making her as hungry as a 6 foot teen boy while being a 5 foot cat lady. But most of it is just the uncanny valley effect of seeing an unremarkable but definitely female face and features, with the coarsened skin and facial hair from the steroids. If you smoothed her skin back out and took off the pube beard, she'd just like like a normal pudgy girl.
 
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