Photo: Online search
So, someone I blocked came up with a new FB profile at some point. It’s not a common name here, so not that tough to stand out on a FB page. This person is (or was) rarely on FB. I found others with the same name but not the same photo, so blocked them as well (easy to use a phony photo). Yeah, I’m talking to you… and anyone else who is struggling with a staggering lack of integrity and/or excessive pulling of puppet strings.
Cyberstalking is a crime in the US. Even tracking my social media is a crime; we’re not FB friends. Blogs don’t fit into that category, so snoop to your heart’s content here. https://fitzpatrick.house.gov/protecting-americans-from-cyberstalking
When cyberstalking is done internationally, that is a federal crime.
https://www.stalkingriskprofile.com/what-is-stalking/international-legislation
There’s even a specific FBI page to report cyberstalking. That would involve giving out a lot of information about too many people, and I don’t want to do that. https://www.ic3.gov I still want the best for so many people, but I won’t be bullied. I doubt any of us really care about being up in each other’s business.
Are you being asked to keep secrets? Like it’s some kind of special bond? Others are told the same things. After removing myself from the ‘situation’, I doubt just about everything I was told- and that was really hard. I’d known about this person since the late 90s… I believed the fairy tale. I ended up in the dungeon.
Are you told something will happen at a specific time, and hours later it might happen? I started keeping a journal of what was supposed to happen vs. what did happen. Not a good track record for keeping to plans. I was told repeatedly that there were 10 sessions going on every day. How was there time for all of you? https://www.psychologytoday.com/us/blog/hide-and-seek/201406/the-psychology-of-lateness
Has someone else warned you about things, but you didn’t believe the person trying to alert you? Was that person then vilified by someone who disagreed with the person who tried to warn you, in order to keep you as a patient? How many people have to share the same story to be believed, or at least considered? If all of this is working for you, great. I am truly happy that you had the resources to be conditionally loved. There is no “unconditional” once finances dip, even if the fees were agreed upon. There are a bunch of YouTube comments by people who had the same happen to them, and a book full of failed treatment. You don’t have to believe anyone- and that won’t change what is. Patterns show both good and bad.
Do you know what it’s like to spend 2+ years being so desperate for something to fill the void of an absent therapist that you turned to YouTube just for SOME kind of help?
Are you told that you’re “loved like a daughter/son”? We’re all disposable. That’s pretty much all I learned between June 2022 and October 2025. It’s all for money. Before being accepted as a patient, it was known I was selling my house. I don’t think that’s a coincidence.
Are you told that ________ will happen, and it never does? One ‘rosey’ book has been ready to be published since a blog post by the author in 2013. Or the recording sessions for the website that never materialized. She told me to sell everything I could to send her $1000 USD for some investment thing for the website. I said no; I was facing 2 biopsies during that time (with financial considerations in a country without universal healthcare), and had already failed 2 other cancer screenings. That was the beginning of even more reduced contact. She’d say that isn’t true that it related to money. I have receipts and a logbook of contact (phone and messages).
https://www.psychologytoday.com/us/basics/therapy/boundaries-and-red-flags-in-therapy
Do you think that the person you admire is near ‘perfect’ and always right ? It’s easy to do when you want to get well so badly. NOBODY is always right, and perfection is a myth. Something I really respect is epistemic humility… the knowledge that all of our views are biased and limited based on life experience, point of view, etc. That there is always something to learn. I was told that my view of my experience is wrong- which is nobody’s right to put their singular point of view on me. What someone DOES with the feelings can be defined one way or another to some extent, but feelings just are. To learn from the feelings and other views is incredibly valuable. .https://pmc.ncbi.nlm.nih.gov/articles/PMC12681921/
Did you truly research the person you care so much about? Or did you wing it hoping they were who you thought they were? I didn’t read up on things I’d heard about, and it was a mistake on my part that I pay for every day I wake up. Now, I need to keep myself safe, which I never thought would be the case. It’s been one of the worst times in my life (and that’s saying something with my trauma history). I truly wanted to get well, and only with one person, because it WAS my last shot. I wanted who I thought could help. I backed up so many things online when criticism was harsh against X- you know that.
Have I made mistakes? Yup. While I don’t remember writing some things, that were on my page (I was looking for a cover photo), I immediately took them down and apologized via email to the person involved. The information was true about what I’d been told (whether what I was told was true is another matter- and I don’t believe it now), and yet I was wrong to post what was on my page ( I seriously don’t remember). I can only guess that the pain involved got the better of me, and I need to do better in the future. But I can recognize that I needed to fix something and apologize.
Imagine being told by someone who claims to have a mission of self-esteem building not to have the time to discuss a life-threatening matter when it was discussed the day before that a call would happen to talk about possible ways to make part of a second test possible (to enable the removal of a small mass that is still there because of that missed call, with other changes now also going on). That was after declining an SOS call. It was the 2nd in 3+ years, and I had permission. That call was so important because of the physical limitations from decades of restricting, and facing 8 liters of prep over 2 days when I have had an NG for fluids since the summer of 2022 just to get 2 liters in per day to protect my kidneys. It was devastating to basically be told that if I die, oh well… not important enough. But it was ‘normal’. Most calls never happened, or there would be a month between calls after being begged (literally) to stay another year (for what, I’m not sure), and messages not seen for up to a week- that little blue double check thing, ya know? When my funds ran out, so did contact, even though I was told that I wouldn’t have to pay after paying for nearly 3 years of the estimated 2 years (2 1/2 max) that I’d budgeted for based on initial conversations. On a disability income. I’ve emailed all of this multiple times to X. Didn’t matter.
Until recently, did you ever hear anything negative about me? I know she talked about me with patients in the house, and back then I was fine with that. We talked on Christmas 2024… was I a horrible creature then? I’m guessing that’s how I’m portrayed now, and would also expect the standard “borderline personality” label when I’ve never been diagnosed with that diagnosis. I’ve heard that about other people who disagreed with X.
I started in the summer of 2022… in January 2023, my time was cut drastically when new patients were brought in when others of us were still floundering, and we were left hanging while several got well in the next couple of years. I didn’t hear anything from X for a couple of weeks after getting to Snowville Hills in January 2023- didn’t know if something horrible had happened, or what was going on. Finally I got in touch with someone who had been helping me via messaging and WhatsApp calls. There are others from the past 40 years with nearly identical stories. I was never taught about the ‘core’ of the program. I was left in early stage 2, with no info on how to get my head sorted out. That’s when (or during) the time you and someone else showed up, and then later the other one in the house. Me not getting help is not and never will be your fault. Those are the choices that were made without regard to those of us left behind.
I was told you’re doing well a while back. That’s really great. I hope you go on to have an incredibly productive life and that you can do whatever job you would enjoy. You’re incredibly smart, and will have so many options when you get out on your own.
I always seem to survive (been tested enough), so I’m no victim. I’ve been on my own for 40 years. I’ve survived a lot, and now have to survive this. My mind is stronger re: boundaries and my right to my views on my experience. The restricting has gone back to pre-‘help’ levels, which has gone on for nearly all of my life, so it’s all I know. My head was never even close to being fixed. My worth was shattered with the ‘non phone call’. Everything could have been salvaged if she just kept her word. Or if she truly was having medical issues, to say so clearly, and let me know that she’d be out of contact for a while to get taken care of- I would have been so very supportive of that. Tidbits of information come across as disingenuous and flimsy.
Instead, here we are.
Author: Atypically Recovering
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More Therapy Repair
Image: Online search free downloads
Because of some creepy stuff that showed up on Facebook, I decided to do a FB search of posts related to a specific last name, and found familiar first names who mentioned people I do know of with the last name I searched. I don’t know for sure if they’re the ‘right’ person by first name only, but I don’t know them, so I blocked a few people. Those blocked with that search were NOT associated with the horrible comments for violence. If any of them see stuff here, so be it. It’s viewable to anyone, though with 3 followers in over 5000 views, this is hardly a high profile blog – LOL. And that’s fine. This is my only ‘hotline’ when I’m overwhelmed or upset. It’s one place I can write, and whether anyone else sees it or not is irrelevant. Human beings have repeatedly proven their lack of trustworthiness in varying degrees (that’s in a broad sense, not isolated to one or two people or situations; I have a trauma warehouse in my head). I don’t have family here, and don’t discuss this with the few friends I have, since I’m essentially housebound, and eating disorders/trauma aren’t great conversation topics.
I also deleted some posts I’d done as a result of being so hurt. The info in those posts was true about what I was told (but was what I was told true???), but it also didn’t need to be posted. I crossed a line about someone crossing another line. I’d completely forgotten about the posts and found them when I was looking for an old cover photo, going back through posts and photos. They came across as very vindictive, and that was not the purpose. I have very few places to ‘vent’.
Still not OK.
In the disturbing posts, the poster called for prison time and various ‘ends’ to someone’s life (I immediately reported those to Facebook). While I’m no longer in contact with the person targeted, there is no time or place for such threats. I also don’t think that prison would serve any good purpose. I know about deaths in Portugal from an article and documentary, but don’t know the details, so can’t say what was good/bad/right/wrong. Many other former patients also died or killed themselves, but that was after leaving the clinic. Others relapsed and died years after the clinic closed. The ‘violent’ person had the name of someone that was very similar to another person I’d had brief contact with, and sent a message (same middle name w/added ‘e’, last name off by one letter, first name with the same sound with the first initial, same number of syllables). They said they were getting actual help, and I wished them well, and blocked them because I can’t trust anyone associated with ‘someone’. I’m guessing the interaction was passed on.There were times when I truly enjoyed talking with someone, and hoped that I’d get through this relapse and find wellness. There were conversational phone calls at times that were quite nice, but I never learned how to get past my ‘head’. There’s a 40+ year history of other patients who have posted on various platforms about their lack of recovery with the same person I’d hoped would help me. Some of these I read about in a book by an investigative journalist on this person that I should have read before looking for them, and others I’ve seen online myself.
Were there helpful things over the years? Yes. There were, especially early on. The first six months were good. Evidently some people do get well if they’re deemed worth the time and can pay for consistent and useful help. That’s just as valid as my nightmare experience, with a fee that was agreed upon mutually prior to starting ‘help’.
I’m disabled and on a fixed income, so funds were/are limited. There is no universal healthcare. Someone knew I was selling my house before accepting me as a patient. In one request for money for a “website” (never happened that I know of in spite of reportedly recording videos all day every day for a year, which also cut down on time to help me from late summer 2023- late 2024), I was told to “sell everything” I could to send her $1000 (I have the screenshot). When I didn’t do that, phone calls slowed to one a month, with no messages being seen for days on end, up to a week, and someone wanted control over food again after more than 2 years of no food input. I’m not sure how it would work not to see messages or call, but control food. Made no sense.
Those who heard of me when I was talked about to others living with her will know that I wasn’t known as a ‘problem’. (Someone asked permission to discuss me with those in the house, which I have since rescinded in an email, so discussing me at all is against my wishes at this point). For anything they hear about me now, I wonder does it add up? Have I been turned into a villain ? I’d expect to be viewed as someone hostile at this point based on how others were talked about to me when they disagreed, asked questions, and/or pointed out problems. It’s another pattern. I don’t have that reputation. I wonder if those living with someone have been asked to keep secrets, too. I finally said that if it couldn’t be posted in Times Square, I didn’t want to know.
I didn’t get well. I felt given up on and disposed of, and intended or not, that was my experience. It would have been so much easier to just hear the truth, that things weren’t as either of us thought they were initially, and the deeper engrained mindset wasn’t going to be undone via WhatsApp ( I never even got a video call, for that important eye contact mentioned in the first Skype audio call when I was too afraid to be seen ). Someone told me I’d needed 24 hour care, but “it was always the money” that kept her from bringing me to her- but that wasn’t said until a few weeks ago, which validated that I wasn’t paying ‘enough’ to truly help. Someone finally said something to that effect in an email months after I’d left. And that’s all I ended up feeling like I was good for. Self-worth eradicated.I’m losing weight again, so that’s very good. Shrinking seems to be the best way to cope with existing. That’s my therapy outcome. I’m not sure how long my kidneys will work ‘enough’, but none of that means much.
And I will continue to wish ‘someone’ well. THAT is who I AM. -

Random Thoughts
Photo: mine
It’s been an odd week. Nothing dreadful, just a lot of fatigue and no appetite at all. In some ways that’s good because I didn’t have money this week to get fresh fruit and veg after one shop on pay day almost a month ago. I’ve got some military rations that I’ve been checking out, and wow- France takes top billing on military rations. Of course, they’re used to good stuff. I’ve tried them from Denmark, Norway, Sweden, the UK, Poland, Spain (great biscuits), Italy (too much canned stuff), Russia (not good), Germany (uh, those entrees are scary), South Korea (rice & spice), Lithuania (very good one meal rations), France, and somewhere I’m forgetting besides the US (pretty good). The US has crap food standards, and has for years, which benefits the medical industrial complex, but the MREs are improving, and some components are quite good. But France wins hands down. Lithuania has some really good dark chocolate (as do other EU countries). But I’m losing weight, so no complaints on being broke or the military food. This week, I get paid, so will be getting groceries that will be compatible with recovery after surgery next week.
I’ve noticed over the past couple of months that Canada seems to be the folks who are reading these blog posts the most (or have their VPNs set to Canada). Like by a huge margin over the 2nd place country (which varies). For a while, Indonesia was reading a lot of posts. I have no idea who reblogs my posts, but I’ll be putting those into spam and hopefully eliminating the auto-reblog thing.
The weather has been more steady, which my autonomic nervous system appreciates. It was near 90F for a couple of days, but now dipping into the 70sF during the day (cool for this time of year here), and 40sF at night. I was watching some storm chasers on YouTube, and one watched a tornado heading to his hometown (he was chasing elsewhere), but his dad had his car rigged up to film, so it was all shown live. The town got a lot of damage to property, which is always sad. I think they said it was an EF-3, so very damaging.
I was trying to find a new cover photo for Facebook, and went through that ‘album’, getting rid of some old photos, taking ‘public’ off of ones not being used, and ditching a few idiotic avatar backgrounds. There are more of those that need to go. I also ran across some old posts that are meaningless now, so those got deleted. General housekeeping. I need to do that with photos as well. The thought of going through over 3000 photos isn’t terribly enticing, but I need to get around to that, though also have stuff here in the apartment that I need to work on.There was one very odd FB ‘thing’ with someone I don’t know who was making some very disturbing posts about someone I do know, but no longer have contact with, so those got reported to FB, and I blocked the freaky poster. I’m no longer in contact, but those posts crossed a threat line that I didn’t want to make any assumptions about…. lots of lunacy, and very specific homicidal stuff that is never OK, no matter why there’s no contact. Came up on that always unwanted “people you may know” line-up that I hate. I always delete them, but hit the wrong part of the thumbnail, and was taken to their page for some seriously disturbed crap and a name that is very close to someone else’s name who knows the same person I seemingly never did know. I’m so glad I’m not their target !! It’s also annoying that the person I’m no longer in contact with still has their groupies showing up on the “may know” line-up. Humans make me miss my dog so much more. No agenda. No lies. No betrayal.
About that surgery… I’ve had the same one done 3 times before in the hospital, and at least a dozen ‘one offs’ in a MD office, ER, or urgent care. I don’t anticipate any surprises. I do have a history of blood loss with these (had to stay overnight for the last 2 ‘mass’ removals ages ago), which tanks my blood pressure, and that messes with my kidneys. Scalps always bleed like crazy, so that’s part of it. A friend is taking me and bringing me home, as long as I do OK with anesthesia and bleeding. I don’t know yet if it will be with or without being intubated and on a vent for the procedure, but at least it will be over and done. It’s not a fun surgery to recover from since I’ll have incisions all over my head. I still have some of my dog’s pee pads that I’ll use as pillow protectors for any bleeding that continues a bit, and hoping I can sleep with where the biggest incision will be. I’m not sure how the CPAP headgear will work with a wrapped up head. I’ll figure something out.
OK. Enough drivel. -

Finally To The Point of Feeling More Free From The Past Four Years
Photo: Mine
The last three of the past four years have been so difficult with not getting the help I paid for, and feeling like I was worth less than any other patient, but that has started to lift significantly after the last (and hopefully final) email with my ex-therapist. I never have to feel that level of despair and dismissal again. It’s like none of the mind games have stuck, and my head is free from the stress of all of it. But no matter what happens with the food (my head is still not OK), I feel so much stronger emotionally since I’m no longer being emotionally manipulated, and the additional food rules (more restriction) are no longer obligatory. I don’t feel the fear of not doing what she said, or potentially getting lectured about weird food rules that didn’t relate to any of my medical issues. Also, no more supplements to try, leaving me to have to Google them to make sure they were kidney disease safe; many were not. Baking soda might sound benign, but acid-base balance isn’t something to mess with. And not being asked for money for personal or family reasons, when I’m on a fixed income and have explained all I’ve had to give up for financial reasons has been amazing. When I’m strapped financially, I adjust my budget, and would expect the same from someone who is inappropriately trying to fleece others. I resented being seen as an ATM.
I’m sleeping better, and longer (I do use medical THC to sleep, though for a while even that wasn’t helping; it is working again). I don’t wake up expecting to fall short of food rules that just restricted more. I don’t wonder if yet another plan to get a phone call will let me down again with no regard to how hard that was to deal with for years after many requests to just call when she was ready to talk then. I never wanted more food- quite the opposite; I didn’t see the need to feed this body more than I had been prior to overt restriction relapse in May 2021. The ongoing, more lifelong restricting is still a problem, but no rules. My head dictates quantities, but it’s eased up on any absolute ban on foods or food groups. That might be a couple of bites of something that looks interesting, but I don’t have to finish anything that I just want to try. Some is saved for another day, or I learn whether or not I like something. Win-win.
A couple of friends came over to help me get food out of the apartment that I won’t use, so they could take them to food banks. That gives me some space to move things around my apartment, albeit slowly since I only have one speed, and it’s not very speedy. But that’s OK as long as I can make some kind of weekly progress. It takes a few days to recover from being up and active for more than 15-20 minutes, as it triggers the autonomic symptoms. I’m still not good with activity, but I’m working on it. I am mulling over a conversation with one friend about a bread/baked goods subscription I really like for their sourdough rolls and croissants that have ‘numbers’ that don’t freak me out. I have them a few times a month. My friend commented that she wouldn’t choose bread to end up on her hips, which took me back a bit (more restriction). She’s a sweet person, but that was hard to hear. Like because I have bread occasionally that’s why I’m fat. I didn’t start eating bread again until last year sometime. People in most countries have bread or a bread ‘replacement’ with every meal. I’d started regaining weight a couple of years before that, and am still struggling to get it off.
With summer, it’s going to be a bunch of grab-and-go foods that don’t take much prep or cooking. It’s too hot for that, and hot food makes things miserable. I don’t mind warming something up in a pan, but that’s about it. Nut and raisin mix is a quick dinner (prepackaged), as is any pre-fab food that requires no babysitting when it’s being prepared. I found a military MRE component that is a nice fruit flavored bar that helps when I can’t get carbs sorted out with something else.
Sleeping better has been really helpful. I still wake up worn out, but at least I’m sleeping. My hours are totally flipped around, but I like being up at night- it’s cooler to work in the garage, and nice to sleep during the heat of the day. It’s good to be able to relax a bit before surgery in 2 weeks for some recurrent scalp cysts. The chaos of sporadic “therapy” no longer being a factor has been really good. I’m still settling into my ‘old normal’, but the internal freedom of no longer being controlled in absentia has been amazing. -

Have I Gotten Anything Right Yet?
Photo: mine
It’s been nearly a year since things with my former eating disorder ‘therapist’ went far enough down the tubes to feel like therapy, such as it was, was over. Nobody had asked about my intake for a couple of years, so it seemed like it didn’t really matter if I ate or not. I knew I’d have to make myself get in enough fluids and food to make sure that my kidneys had enough on board not to get worse. It’s been hard, and there are a lot of days when I think about just going back to what was less physically uncomfortable. The emotional end of things has been much harder considering all that has gone on with my former non-therapy.
I’ve tried multiple times over nearly 4 years to get rid of the nasogastric tube that gets enough fluids in for adequate kidney function, as well as blood pressure support. The tube is back in after another try at not having it last month. I made it a few days, with lower volume food intake (tried to eat higher density foods, but I don’t like a lot of them), but then struggled for 3 days, and that’s my self-imposed limit. I can’t risk going longer since I’ve been in acute renal failure twice in the past 4 1/2 years. But I am still maintaining fluids, even if I need the tube to do so.
Food is still a problem. “Normal” eating is still something I don’t feel I deserve, and it’s physically unpleasant with bloating and feeling too full. I’m not a purger, so once it’s in, I have to put up with the side effects. I’m not as ‘avoidant’ with the types of food I will eat, but am still consumed with not eating over X number of calories per day. Tracking food is something I tried to get away from, but I have to know carbs for insulin dosing, and protein for my kidneys. It’s very difficult to get in enough protein when I have to restrict the options because of gout.
I’ve been trying to do the opposite of what my head says, and at times I can do that, but only with some types of food (single serving sizes are helpful). I’ve wanted to let myself have one meal a week or month when I just have what I want, but that hasn’t gone well for several reasons. The medical restrictions on food, only getting X amount of insulin per month, etc are hard to deal with when attempting to break some ‘head rules’ about food. The current “never restrict” goals of eating disorder recovery are hard for someone who has literally always been restricted (when I was a child) or my own active and passive restriction… For me, active restriction is when I relapse and passive restriction is eating how I did for my entire life, eating about one meal stretched over the day. For me, that was ‘normal’. And what I see in the mirror still doesn’t look like it deserves food, even though I’d give more to someone else, whether they were larger or smaller than I am.
I am starting to understand that like dogs, birds, fish, or whatever family of animals, humans have different sizes and shapes that ‘just are’. There’s no ‘defect’, just natural differences. I’m not sure what my set-point weight is (natural weight without restriction) because I’ve never NOT restricted in some way (or been externally restricted). I’ve read or heard (YouTube) that it takes time and an extended period of not restricting to get to that place, so I’m nowhere near that since I’m still restricting to some degree with the fear of going over X number of calories that are below what the dietician I saw told me is ‘normal’ for my age, activity level, and body type. I will never be a greyhound. I’m more of a Labrador retriever. And I still have the urge to be a greyhound.
I understand that repairing the damage I’ve done to myself over decades takes time and food. I know that I’ve gained muscle in my arms and legs, and that there is a difference in swelling if I don’t eat enough protein (hardest thing to get in with medical limitations). Some of that muscle gain is starting to atrophy a bit. I’m tired of most ‘safe’ protein sources, so there is a lot of forcing in of stuff just to get to the minimum, and honestly, I miss that mark many times a week. But I’m still trying. My heart rate is still wonky, and my blood pressure stays low normal unless I’ve taken trash out to the dumpster; then it goes to high normal for about 10 minutes. The higher blood pressure is probably better for my kidneys since poor perfusion is why they are damaged.
Most days I don’t feel like anything will really work to get me rid of the restricting. I still feel worth less than I did 5 years ago when I relapsed, after 3 1/2 years with my former ‘therapist’. It’s hard to feel worth anything when I’ve felt worthless for decades, and I felt kicked to the curb by someone who had no interest in me getting well even though that was the sole purpose of that relationship. I also know it had nothing to do with me personally, I was just another failed patient because I was too broke to be worth the time to get well. I’m not alone there… lots of examples online, which helps in knowing it’s not about me, but also sad that so many have been left suffering more because of that relationship that fizzled out without the decency to finish what was started. I’m working on getting past that, which is hard, but it’s not like this is the first person to be a disappointment and something to recover from. I generally land on my feet, and thankfully am as independent as I can be within physical limitations. There is no limit to my emotional independence since that’s pretty much all I’ve known. So, while I’m broken, I’m not destroyed. -

I Don’t Know How To “Just Eat” Without Shame
Photo: Mine
For something that most people never think about, food is a ‘threat’ in my head. I know it’s irrational, and I know how I’d tell someone else to view food, weight, etc- but in my head, the rules for me are different. A lot of this likely started when I was bribed to lose weight as a 6-7 year old, with literal cash for each pound lost …. I wasn’t remotely fat. I don’t believe it was malicious, but it was very damaging. My mom wanted a child who looked like kids at church who simply had different body types. I am much more like a labrador retriever than a greyhound, and trying to ‘shape shift’ me became a part of my thinking that is automatic. I want so much to change that, and have for more than 45 years.
My parents were very focused on weight and looks the entirety of my memories. I can remember the floor plan of the duplex we lived in when I was 2-3 years old, so I remember a lot (creeped out my dad). Mom was always on a diet. Dad would eat nothing but yogurt and bananas if his pants felt a bit snug. There were no snacks in the house. No desserts unless it was someone’s birthday. There was nothing in the pantry aside from some soup and cereal. The spices had purple inked prices stamped on the boxes or tins from the 60s (after I moved back home, I saw the same kind at an antique mall). I was taken to some weird womens’ workout place with those butt jiggling bands that vibrated, while my mom did her quota of butt shaking. It was all I was exposed to about food, other than holidays or school lunches for the 2 years I attended public school where neither of my parents worked.
I feel ashamed that I feed this thing I see in the mirror. And at the same time, I know that my head is lying to me. If I saw someone much larger than I am eating X kind or amounts of food, it wouldn’t even register. When I’ve watched “600 Pound Life”, I see those morbidly obese people eating huge amounts of food, and my first thought is wondering what hurt them so badly that they are destroying themselves. Not judgement like I do to myself for simply eating a ‘normal’ meal without knowing every calorie and grams of macronutrients. I have to watch carbs and proteins because of health reasons, but otherwise, I WANT to be able to “just eat” without shame. I’ve tried to ‘let’ myself eat what I want for just one day, without limits on what (need to limit quantity on some things for insulin and kidney reasons), and I haven’t been able to do it.
My head is no different than it was when I was diagnosed with anorexia at age 17, days before classes started at a good state university. I used to count curds of cottage cheese, and allowed myself 3 curds, and not the biggest ones in the container. I have gotten better about portions, but my head still tallies up calories (and I log them to have some kind of accountability, as well as knowing I’m getting minimums in- or at least close to what I’m supposed to eat). But I have never known normal eating. I’ve read that it’s about enjoyment as well as nutrition- two things that were never part of the equation in my life. I’m trying to change that, and it’s like putting me in the middle of China and expecting me to be able to use one of their computers without knowing the language at all.
I’m in my early 60s, with decades of direct and indirect chronic medical issues related to malnutrition and lifelong restriction of food. I’m getting things from the grocery store to challenge myself, and am so ashamed to have ‘junk food’ because I don’t “look” like I need food. I have been able to get single serving sizes of some foods that have ‘OK numbers’ and I am so acutely aware of how much I’m stressed by deviating from the usual stripped down options I generally eat. One meal stretched over the entire day is what I’ve had for most of my life. When I’ve been in hospitals, treatment centers, or in public where i need to look normal around food, I’ve eaten more- and then compensated afterwards for my transgressions.
It’s not about how I look, or ‘controlling’ anything (control is shot so quickly with each relapse of overt restricting). It’s about not feeling that I deserve the same as anyone else, no matter their or my size. I don’t know how to fix that, and never got any guidance on that in 3 1/2 years with my ex therapist. I’ve had to wing it with various YouTubers who have eating disorder recovery content, and it’s hard. I’ve had an NG (nasogastric tube) for fluids for 3 1/2 years because I can’t tolerate the volume of food and fluids too close together. At this point, I wonder when it becomes cruel to expect this body to consume what it never has. I’m trying more calorically dense foods to minimize volume, hoping that i can then tolerate eating and drinking without the tube.
I just want to know “normal”. -

February Update 2026: Working on Moving Forward
Photo- mine.
I’m still a long way from where I was in 2021 when this current relapse started, but without the external pressure and ex therapist’s general absence most of the time, at least I don’t feel like I have to follow her orthorexic food rules that go against any of the more recent views on eating disorder recovery. ANY restriction is discouraged, no matter the person’s weight. I’m struggling to get back to my ‘normal’ eating which was still restricting, but different. I was used to one meal spread across the day, and I know that can’t work if I want to prevent going backwards re: my body healing from decades of depletion. Five years is the longest ‘overt restriction relapse’ I’ve ever had – while under the ‘care’ of someone who claims to be the last hope for eating disorders.
https://tabithafarrar.com/2018/06/unrestricted-eating/Restriction is also felt to be the biggest reason people binge- regardless of the type of eating disorder diagnosed. I know a lot of heavy people who eat far less than others- and I have been in that group much of my life. The body is designed to survive, so if it feels it’s not getting enough, it triggers the body to eat to get its needs met. And the BMI chart was never meant for general use- it was designed by a Belgian astronomer in 1832, with no scientific vetting, even for the times. It is pointless- it’s like telling a poodle to look like a chihuahua… stupid. Every BODY is different, and has different needs.
https://pmc.ncbi.nlm.nih.gov/articles/PMC10693914/
https://www.therapeuticcounseling.org/post/breaking-the-binge-restrict-cycleI’ve been fortunate that regular bingeing left me when I left the U of IL in 1982 – where I’d pick cheese from pizza boxes in the trash room on the dorm floor, after the other floor mates were asleep. That was the end of weekend bingeing, that included cheese, ice cream, chips, dip, chocolate, and the occasional bit of ramen. During the week, I ate 1/2 potato or 1 apple per day, and took 40 laxatives PER DAY, 10 at breakfast, lunch, dinner, and bedtime- without eating. I drank Diet Rite by the 2 liter bottles- and labeled mine for the big fridge in the floor study room with “herpes”, to keep people out of it (I didn’t have it, but nobody bothered my soda !!).
I also ran the 11 flights of stairs to the top of Trelease Hall where my room was-1224 was my room. It’s no wonder I passed out in the dietician’s office just before Christmas break when I was asking how to survive the month away from school at fast food places where my folks would be stopping. I wouldn’t be where my “habits” were unrestricted or even seen most of the time. My folks never bothered to think someone could eat too little, so that helped, but the bathroom access for my laxative consumption was nerve wracking. I was thankful for young sphincters, and timing any laxatives taken between known meal stops.As far as eating goes now, I still have to pay attention to “numbers” for insulin doses and making sure I don’t have too much protein. I don’t really limit what I eat, but I’m still glued to the total numbers each day, and have a very hard time eating enough per the ‘final’ calorie goal (my former dietician gave me the ‘end goal’ for calories; protein won’t change, and carbs are only restricted by the amount of insulin I’m prescribed). With drinking again, this has caused some issues with feeling really full, so I’m eating more calorically dense stuff to avoid coming in too low on food intake or feeling too full.
I guess I’m getting closer to the “normal” restriction I’ve always done- which isn’t great, but at least I’m not bogged down by food rules that I don’t agree with, or told to eat stuff I don’t normally eat (I do keep kefir around for fast protein- but it’s not a daily thing). I tend to eat fairly dull stuff in general, but like to try new things (couple of bites). I’m eating more than one meal per day, and it’s not terribly comfortable. But I’m still eating without having a therapist lurking around (which she kind of wasn’t for a big chunk of the last 6 months I was still a patient, and prior to that, there had been the gradual breadcrumbing discussed in other posts). She hasn’t known what I was eating for years, so her ‘supervision’ was not good- and I knew it. I did eat what I said I did IF she asked, but mostly, I was invisible.
I’m glad I got the NG out (again). I kept it in for 3 days while I started drinking %100 by mouth, to help relieve some pressure to do it all at once, but I don’t mind drinking non-caloric fluids. The ones with calories take up insulin, and I only get so much per month, but I will drink a bit of soda with real sugar (high fructose corn syrup is bad for gout and triglycerides) if my stomach is upset or I have a headache- but just a few sips.
It was a colossal failure to want help from her, and even more that I didn’t read the stuff written about her in greater detail before signing on. I really liked her as a person for a lot of the time with her- but being blown off over a 2nd colonoscopy prep that was too much to handle physically, when she said she’d discuss some possible options, was the last straw. I felt more worthless by her refusal to help with something that could eventually kill me. She would deny that, but words are cheap when actions scream. She has given various odd medical accounts for her absence- but then flies to see patients in other European countries, has patients living with her, and could send photos of London, but couldn’t pick up the phone. I will never understand that kind of callous disregard for someone she supposedly “love like a daughter”. Gads, I hope not. I will also never understand needing a different name in Europe.











