Sample community diagnosis

ADHD Women

2014.04.09 20:53 tellbaconiloveit ADHD Women

This subreddit is a space for women to find support and discuss living with ADHD. If you would like to contact the mods, send us a modmail instead of DM-ing the moderators directly.
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2008.04.09 20:05 Autism

Autism news, information and support. Please feel free to submit articles to enhance the knowledge, acceptance, understanding and research of Autism and ASD.
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2008.10.27 00:46 Peer Support: A Safe Space

We are a haven for people with Bipolar Disorder (including Cyclothymia and Schizoaffective Disorder) and those on their journey towards a diagnosis to discuss Bipolar-related issues; a community, not just a help page. Be a part of something that cares about who you are.
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2024.05.19 18:05 Celery_Worried Mum has gone into care

It's about a year and a half, I think, since her Alzheimers diagnosis. Dad has been caring for her but it was killing him. He got a stomach bug and could barely take care of himself which prompted the rest of the family to urgently seek respite care. They managed to arrange for one week, which quickly turned into two, and now dad is saying he doesn't want her back. I don't blame him one bit. She's settled in okay. My brother visited and it took her a while to recognise him. She keeps looking for her mother but I'm just relieved she's not crying for her husband - he would feel awful. Dad turns 70 this weekend and I feel like he finally has a chance at enjoying life. Which is what mam would want. I just wanted to share with this lovely supportive community. I'm sure lots of you have gone through this and understand how devastated, relieved, grief stricken and overjoyed I'm feeling right now.
submitted by Celery_Worried to dementia [link] [comments]


2024.05.19 17:59 secretlyunstable i can’t connect with people and it’s been like that my whole life

all my life i always see people form connections around me, make friendships, bond, and i feel so invisible because i can’t do the same.
i’ve literally been in a group setting where everyone met for the first time, started planning another group hangout including everyone EXCEPT me, and i was literally sitting in the middle of it while it was all happening.
i’m pretty sure everyone was thinking at the time “what’s wrong with her? why’s she so weird?” because i was literally unable to socialize so i sat there so awkwardly, not knowing how tf to socialize or make connections but watching everyone else do it so easily and it just sucked seeing how behind i am than everyone else on social skills.
i’ve tried all the advice: i’ve tried being more outspoken, being myself, being louder, being quieter, being a listener, being a talker, asking questions, blah blah blah… it seems like no matter what i do people are inherently put off by me. like everyone can just smell somethings off with me. i honestly might look into an autism diagnosis because of this. it wouldn’t help because i’ll still have this issue but it would explain a lot.
i had a joint hairstylist appointment with a friend and i really tried to socialize, but for some reason the hairstylist felt more comfortable talking to my friend instead of me, even when we were discussing my hairstyle. that really showed me just how uncomfortable people are with me.
what’s wrong with me? what is it about me that makes people shun me like this? all i want to do is fit in and have a community of people who accept me. instead, i need to learn how to be hyper independent because i have few friends i can rely on.
submitted by secretlyunstable to offmychest [link] [comments]


2024.05.19 17:47 concussed1 i would love help on understanding TBI severity rankings

i would love help on understanding TBI severity rankings, even casually, for level-setting here and beyond.
im writing this post as i have difficult looking at my screen, and the right side of my skull is lit up with neuralgia. my symptoms wax and wane, and when i am at the point of not being able to spell words or form sentences grammatically, doctors finally start to accept that i am struggling - but that feels like telling a diabetic who is ambulant that their severely low blood sugar isnt a problem because theyre not yet in a coma. i know what Fucked feels like, and i feel it all the time right now, and it doesnt make it less awful because its an acceptable facade from the outside.
i have found that my more lucid moments (of which i am having one right now!) encourage doctors to dismiss the severity of my symptoms and impact to my quality of life. like, sure, lots of healthy-brained people cant do math in their head at all and that can be fine -- but i have multiple software patents, and the lack of being able to do basic math in public or understand code syntax or even just remember my friends and coworkers names is eroding my professional capital and my sense of identity. its isolating and causes me SO much panic and anxiety, which cannot be good for my cognition.
in my first meeting with a neurologist after concussion #1, he pronounced his diagnosis that i was "extremely intelligent and extremely concussed." he seemed to think that would make my recovery difficult because my brain wouldnt 'stop trying.' um, well, ok? things only got worse: i sustained a second concussion a few weeks after the first, and also hit my head very hard on the corner of a table when bending down around the same time, and then a big big concussion several months later in a car accident (back seat of an uber, no seatbelt like a dumbass).
i was in a ton of pain starting with the first one, i lost my then-job after the second one, and i was fucked all around by the time the third one hit... but i was able to get another job after two years (albeit one which im now falling down on), and i didnt have to re-learn to speak or feed myself or some of these other major things that some folks do, which i think is part of the umbrella of brain injuries.
i dont know what that means for qualifying my TBI for other people, including subsequent doctors, and i would love help in understanding so i can be a better advocate for myself - including in this community, and when talking to others who understand this sad, hard world of TBI recovery.
if anyone has any wisdom on how to talk about this, i would love to hear it. or if youre in a similar boat and can comisserate, thats valuable, too. <3
submitted by concussed1 to TBI [link] [comments]


2024.05.19 17:00 njauf Tips on getting the right expert for your assignment

Are you a student in need of a cost-friendly (or even free), fast and quality assignment help? Here are a few tips to ensure that you get the right expert for your assignment.
  1. Do a background search on the online presence of the expert - positive reviews always indicate that the expert is good at what they do.
  2. During the introduction, check if the expert is proficient at the assignment project - You may ask for any samples related to the topic.
  3. Ask for a budget - Request for a quote from the expert on per-page or per paper charge. Always negotiate while confirming that the quality won't be compromised. It is also important to ask for the experts' accepted payment options.
  4. Be specific with deadlines - What good is a high-quality paper delivered a week past the deadline? A good practice is to fix the deadline around 20-30% earlier than your actual submission deadline to ensure there's time for any revisions.
  5. Look for additional perks offered - Request or inquire if the expert offers free: plagiarism reports, grammar checks, revisions etc. These are a plus.
  6. Request for progressive drafts - This will enable you to check if the expert is on track with the assignment instructions and confirm quality. Comment on these drafts.
  7. Matters finance - DO NOT pay before you receive the assignment, or at least screenshots of the work done. Only pay after you take a look at the work.
  8. The world is a better place with kind people :) - Appreciate good work by referring friends, leaving a positive feedback, and possibly adding a tip to the expert.
Good luck with your next assignment project! Welcome to join the community and share with your network to help as many people out there as possible.
Cheers!
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submitted by njauf to My_essayhelp [link] [comments]


2024.05.19 16:57 Cheezter TL;DR how do we find out what meditation to do & what problems to solve first [aka how to run diagnostics on yourself - or with someone]?

HOW TO RUN DIAGNOSTICS ON YOURSELF - WHICH MEDITATION TO CHOOSE
This is the 3rd time I'm posting about this but it didn't get much attention and I think it's freakin important(?): It's like learning to learn. It's this overpowered meta skill that just buffs everything else.
I'll take ownership and speak from my own experience but I feel these things must apply to many others in the community (and of course this is still with much love for Dr. K and the community)
_________________________________________________________________________
The point
Dr. K has created content and it's freaking epic, but it's overwhelming - do I deal with my procrastination first, learn how to emotions, or is it all about working with ego? I dunno!! How do we know? Many people (including myself here) don't even know what their problems are, and often end up stumbling and blindly trying things (which defo help, but god damn many dead ends could have been avoided) with about the same accuracy as playing and FPS with a Guitar Hero console.
It's the same with all the meditations. Especially those he has provided in the guide. There's too many and I for one have no freaking clue which one I need or what helps me most. And his video on How You Choose The Right Meditation For Your Problems to me said nothing more than "whichever gets you to a state of meditation the fastest and if you have ADHD speed up before you slow down" [rotating sound awareness], which was unhelpful and quite disappointing tbh.
He chooses meditations to teach those he interviewed - I think it would be powerful and very helpful if he shares how to actually do this for ourselves.
I'm hoping Dr. K will pick this up but I'm also interested in your opinions and answers.
_____________________________________________________________________________________
Fluff/context
It sounds like the Trauma guide (#notsponsored) might have some of this regarding the content, but still. The channel has imo reached a point where there's just too much content and we need some "how to navigate" - also for newcomers - to actually target the problems you need.
I'm writing again after Dr. K mentioned in The shame of ADHD that he reads the subreddit a lot and they pay attention to what's needed in the community and it aggravated me a bit because I don't see how this isn't f'in essential??
(this might smell like analysis paralysis and for me it is but I think there's also more to it: "a good solution requires first a good diagnosis of the problem")
[nerdy example: most charities don't even know if their "solutions" actually help or if it's the best idea - it's just an idea they like. Yes. Really. The best charities can make 100x more difference because of this]
submitted by Cheezter to Healthygamergg [link] [comments]


2024.05.19 16:44 nutterbuttertime Mass found in abdomen that disappeared?

I’m a 24f and in December of 2017 I had lower right quadrant pain so I went to the emergency room. CT scans showed inflammation in my LRQ so the doctor wanted to remove my appendix via laparoscopy. When I woke up from my surgery I had a drain tube in my abdomen to remove excess fluid. The surgeon said he could not see well during surgery with excess fluid. His post op diagnosis was appendix rupture.
In 2022 I started having LRQ pain again and had an exploratory laparoscopy with my gynecologist. She found my appendix fully intact and fully functioning, but I am now missing my right ovary and Fallopian tube. My post op diagnosis from the surgery was endometriosis. This prompted me to get my surgical records from my surgery in 2017 and I am shocked at how different it was than what I was told.
In my first surgical write up, the surgeon says he found a mass in my abdomen connecting my right ovary, my small bowel, and my cecum. He tried to remove the mass (also referred to as phelgmon), but it started “oozing” and he was worried about serosal injury so he just stopped and left it and inserted a drain tube to remove excess fluid. A small sample was sent to pathology which showed “non caseating granulomas”.
I’m very worried about why this mass was never brought to my attention and why I was told my appendix ruptured. My second surgeon says she did not see a mass, but how is that possible if it wasn’t removed? How is my right ovary now missing? No one can give me any answers to what happened in my body, and I am still having daily pain in that area.
I will attach my surgical write ups on my profile. Any advice as to what this may be or where to go from here would be greatly appreciated.
submitted by nutterbuttertime to AskDocs [link] [comments]


2024.05.19 16:37 Hey_86thatnow Story-what one dBPD father is like and how I survive

Story-what one dBPD father is like and how I survive
Thank goodness for this community. Reading such common experiences helps me immensely, so I wanted to share mine and see if it resonates with you all.
Dad was diagnosed about 20 years ago by a marriage counselor. She then “fired” him from her practice, saying his marriage was beyond help because of it. Apparently, this rejection is common among BPD patients…implying it's unfixable, Since then, the ICD-11 has added a category called “difficult personalities disorder” probably to umbrella in the people who don’t fit neatly into the “5 of 9 traits” required for complete BPD diagnosis. Interestingly, he’s not unfaithful or suicidal, he kept the same job for decades, he can be fun and loving. But he rants, he overeats, he splits and denies, he isolates, he ruminates and fears, he blames and attacks and projects his self-esteem issues onto others...mostly me.
First, he was a very loving father when we were kids, attentive and supportive. And then a fantastic grandfather to my sons-loving, etc.. keeping his worst traits in check most of the time with all of us when we were young. (Not with Mom, however.) It’s as if because his childhood was tough, he sees all children as underdogs who need special care. I will always be thankful for my childhood, for it laid the ground work for my self-esteem. However, he was rougher on my brother as a kid than on me, pushing, verbally abusing, etc.. This swapped as we both reached puberty. I realize this has something to do with his view of women, his wife and his own mother.
As I became a woman, I became threatening, which appears common among BPD fathers. He then let my brother off the hook, where I got the laser focused judgment and anger. This is not to say he never loses his temper with my brother, he just tends to wait until the situation is severe (like brother getting arrested for DUI.) whereas I got attacked because I had 4 framed pictures of one son and 5 of our other son displayed in my den. Dad went on a level ten verbal attack. “What kind of a mother…rantrantrant” jamming the extra picture in my face. Walking around counting them sounds irrational doesn’t it? I met a visiting high school friend at Chili’s for dinner, and asked Mom to babysit, and I hear, “What kind of a mother goes to a bar and leaves her kids, rantrantrant.” Chili’s? Meanwhile, my brother can brag about sexual conquests, even when married. I have three college degrees—Dad never says a word. My brother flunked out of college, but Dad lies to everyone bro won a free ride to a prestigious university in our state. He paints my brother with all the best traits of my mother, but projects all his worst traits onto me. The irony is, I am very like my mother; my brother is not. But I am the scapegoat now, and brother is the golden child.
This behavior and thinking is called splitting, or black and white thinking. It is so bad, that my father bought my brother a house when bro struggled financially. He has not had rent or a mortgage or land tax for over ten years. Me? Different story; everything I have, I earned and paid for. Mom kept a list of money they gave my brother over the years for cars or lawyers, etc. Not counting the free house, his column equals $64k. My column? Zero. (And I’m the “good” kid, responsible, there for my parents.) It’s taken a very long time for me to grasp that no matter how illogical or unfair it is, it won’t change—it is part of the disorder. I tell myself to be proud that I can make my own way without help.
Dad’s impulsive, hair trigger temper over things that wouldn’t bother anyone else is profound. I’m exhausted from walking on eggshells, though avoiding conflict is so much better than entering it. He never hit us, but throws things, breaks our valuables (like Mom’s great-great grandmother’s rocker), curses, yells, screams. As a kid, I watched him fracture his wrist punching the wall when angry at Mom. He has had security remove him 3 times from my hospital room (two surgeries, one illness.) once because I told my mother about Christmas present ideas for my brother (and apparently should have been discussing my niece instead.) Who cares I had just had an 8 level spinal surgery the day before; Dad jumped out of his chair, livid, “You are forgetting someone aren’t you! Aren’t you.” He lost his cool the time I’d had surgery after a bike wreck, screaming he’d never let me see my mother again, and he’d write me out of the will. All I had done was interrupt him while he was talking. Security escorted him out. It was so ugly, one son refused to talk to him for months, shocked after witnessing it. My father told him that it was no big deal—that was just how he and I related, it was just our dynamic. My son said, "My mother never behaves that way and did nothing wrong," and hung up on him.
Dad begged me to call my son and take some of the blame. IOW Dad cannot see his part in things. He sees reactions as proof that his anger is justified. Who cares how he causes these reactions. (Who cares that I was lying disabled in a hospital bed.) He is angered by the oddest things, the most innocuous things.
He once followed a woman around at a party and purposefully interrupted her everytime she opened her mouth, then bragged later that he did this. He felt she was always cutting him off at past functions. Being interrupted is his hottest button. He wants everyone to listen to every last detail of whatever he has to say. And if you listen, but look like you aren’t, that’s as bad as interrupting him. But does he interrupt you? Of course he does, all the time, bored with what you want to say.
He loves to get people’s goats, saying or doing very calculated things that he knows will annoy Mom or me or whomever. He has never physically hurt anyone, but mock something embarrassing from your past? He’s all over that. You can watch his face when he says provocative things on purpose—he’s just hoping you will ignite. When I wrecked my bike, instead of helping me up, he literally took pictures of me on the ground. Then showed the pictures to my brother, saying “What kind of an idiot rides a bike when she’s had spinal surgery” (8 years before). BPDs triangulate, and often lack compassion.
When it comes to me and Mom, his favorite hostile line is “What kind of a___________does__________”
When I went to take my mother to see my aunt and uncle, Dad tried to tag along, and my relatives said, "Please, if he wants to come, we'll have to disinvite you. We can't take anymore." he had been so hostile the last time they say him and made my aunt cry. He has no idea his behavior has this effect on people.
He talks all about himself, and if he asks you a rare question about you, it is so he can then talk about himself. It’s like he thinks the type of lunch the kid ate (whom he sat next to in the third grade) is talk-show-worthy chitchat. But will cut you off in a second if you have something more pressing or recent to discuss. He’s very emotional and affectionate verbally and physically, but if you try to share your deeper thoughts or concerns, he gets very awkward and uncomfortable, and dismissive. BPDs struggle with intimacy and bonds.
His narcissism is so bad, that when Mom died last year, he wrote her obituary, but 60% of it was about himself. When the newspaper edited out all the stuff about Dad, Dad called me fuming, accusing me of calling the paper to edit it. He still believes that. He also refused to let anyone have a memorial service/funeral-her ashes are still in the box from the crematory-- but later that summer, he started telling me what he wants me to do for his funeral. (We did a small family dinner in honor of Mom without him.)
He is mistrustful and suspicious. He tends to take the other person’s side in regards to me, never trusting my perspective. If someone is offensive to me (like a boss who was angry when I refused to work from home while I was taking FMLA/disability pay after childbirth, or my ex who wasn’t paying child support) Dad took their side. I had to be the problem. When my husband was sent to a job site out of town, Dad thinks he asked to be assigned there to get away from me. (But says, “I just worry, and want you to be happy.”) When I get a text sent by a male friend to both me and my hubby’s phone inviting us both to dinner, he thinks there’s something fishy going on there with me and the man (and funny enough, I am certain Dad never cheated on Mom.)
He throws cash around as presents, especially to the grandchildren, but even to people the rest of us wouldn’t include (ie. my husband’s brother-in-law’s niece-whom we barely know, my mother’s distant relatives whom no one has met, or my ex who hasn’t talked to him in decades, etc) It seems like a way to get their admiration or attention. He is always writing me in and out of the will, as if he’s the czar of millions. People with personality disorders are very manipulative or odd with gifts.
He has zero friends, but talks all the time about people he knew as a kid. Where are they now? I’ve never met anyone from his childhood other than family- no cards, no messages, nothing. And no one from his life as an adult is close to him. My parents’ friendships came through Mom. I can sadly say, in a crisis, if Dad really needed to call someone and talk, only family is there (and that is only because we are compassionate, forgiving people). But funny enough, when he is in a social setting, he is not shy but wants to talk and entertain and be the center of the party.
He loves to take people to task, often loudly and cruelly. Waitresses, nurses, cashiers all get dressed down and confronted for any perceived mistake. More than one doctor or service provider has hung up on him or yelled back at him. I witnessed this again in just the past two weeks, for Dad had a minor heart procedure. He wanted to tell each doctor and nurse the most irrelevant stuff, starting from the beginning of time…and would get mad if they didn’t let him. His cardiologist snapped at one point, “I need you to just give me quick answers!” so Dad yelled, and the guy walked out.
Interestingly, I found an article, advice for doctors and nurses on how to handle illnesses when the patient also suffers from BPD. The descriptions were my father, to a T. One of piece of advice said something like beware of compliments and ignore criticism. Dad has been tossing the compliments around like confetti, “OH, Nurse, so and so, YOU are my number one.” But when his demands are not met immediately, he acts like a baby. And he keeps insulting me infront of doctors or nurses, applying his faults to me; “She’s stubborn, she has nasty temper.” I can be just standing there silently, and he says this.
He said, to one doctor, “Don’t mind her, she’s very overbearing and headstrong…but in a good way.” I’d had enough, so I said, “There’s no reason to insult me, Dad.” He argued, “Oh, you didn’t hear my compliment. That was a compliment!” The doctor said, “If that was a compliment, it was a backhanded compliment." I could have hugged her.
The worst part of being raised by a BPD? If I report any of this back to him, he will swear none of it is true. Gaslighting is their favorite manipulation, suggesting my perceptions are wrong. Either that, or he is in some sort of fugue when he acts so badly.
How do I deal with all this? Often I don’t. Mom used to be a good buffer, til she developed ALZ and then Dad forced me to go through him, never allowing me to be alone with her. This hurt. Mom and I were very close, and before she lost her mind, we had many discussions about whether she should live with me instead. But BPD men get fixated on their mates, and he saw her as only his, not important to me or my brother or her grandchildren. (He even resented their dogs, because Mom "loved them more.")
Even much younger, if I called to talk to Mom, Dad would rush the phone so I would have to talk to him first. So often I’d wait til she called me first. And now that he is all alone and his son mostly ignores him, My husband and our sons are the only ones really watching out for him. I use as much compassionate thinking as I can and remember that he got this way because he had a rough childhood (and I think the disorder runs in families—I really do.) His father died when Dad was 7. His immigrant mother could not read or write and she was raising 4 young kids by herself. Neglect, food insecurity and possible social rejection made a deep scar. I know that at the bottom of all this, Dad cannot, because of BPS, really ever trust that anyone loves him. So I do what I can, take long breaks, bite my tongue as much as possible, set boundaries, and leave when need to. To help, I come here and read very similar experiences in order to remember, IT’s NOT ME.
But still, with this hospitalizing where he's milking the attention for all it's worth, I want to explode. I'm going to have a stroke if I have to spend this much time with him for much longer. During his surgery I was totally torn, hoping he would die, but very sad that he might. That’s some sucky head space. It was easier when Mom was alive and sane...
Right now, I’m finding him assisted living, but he keeps threatening to rip out his IVs and go home. He can’t. He used to say, whoever took him in when he was old, would get all the money, and I’d say, “Have fun living with my brother.” But of course, none of that is true. I’m so resentful that I’m the one solving his health crisis. But also, in honor of Mom and my childhood, I love him and won’t dump him. I won't let him live with me, but I won't dump him.
Thank you all, for totally understanding this dichotomy. Can you relate? What would you do?
https://preview.redd.it/5b7pb27vbe1d1.jpg?width=4128&format=pjpg&auto=webp&s=134bd4bbdf57fb8f83e139b42feb6459b3af79aa
submitted by Hey_86thatnow to raisedbyborderlines [link] [comments]


2024.05.19 16:37 mimi_doh (Academic) Survey on Interpretability Explainable AI (All welcome)

Hello, SampleSize community! :)
I am surveying an Explainable AI (XAI) Face Verification project linked to an academic thesis and would greatly appreciate your participation. The survey aims to gather feedback from everybody (AI experts and non-experts). Your insights would be incredibly valuable to the research.
I sincerely thank you in advance for your time.
submitted by mimi_doh to SampleSize [link] [comments]


2024.05.19 16:36 lemoraij Misdiagnosed as autistic?

Because autism has historically been underdiagnosed, many people were initially misdiagnosed with some other label before being recognized as autistic. Now that awareness has increased and many more people receive an autism diagnosis, the number of people that are falsely diagnosed as autistic has probably increased as well. I am curious whether anyone in this community has experienced such an autism misdiagnosis, how it happened and what that was like.
submitted by lemoraij to autism [link] [comments]


2024.05.19 16:24 girlisariot Dealing with mothers and the aftermath of getting diagnosed

I'm not sure whether this is the right place for this but I thought this community might be able to give some pointers. I finally received my ADHD and ASD diagnosis a few months ago and while I am relieved to finally have some answers, I did deal with a fair share of post diagnose grief (as in how could nobody tell, what could have been if there had been support systems in place etc.). With knowing I need to adjust to create a less stressful life I am trying to create new routines, masking less, communicating my different needs and just overall trying to be unapologetically me. A big stressor is my (very german) mother tbh. Think of the kind of mother that will, without being prompted, tell you you need to loose weight, your outfit is unflattering or that your haircolour makes you look ill. Last year she visited my place for the first time since I moved here around 2020 (we live an hour from each other by car) and not only did she poke jokes at how small my beloved balcony is but she would tell me afterwards that based on the state of my room she was worried I was "losing control" or could not keep up with life.
I, as so many others on here, struggle with keeping a tidy environment and had spent days using all my spoons to clean up. Sure there were some glasses etc around since I had friends over for my birthday the night before, but neither me nor my friends thought anyone should even bat an eye at it. Having depression, autism, adhd, a job, a study, some degree of a social life, going to the gym and feeding yourself and cleaning is impossible to combine sometimes and I was proud of my place. Compared to the state of my room at hers back in the day I thought she would be amazed if anything at all.
It's my birthday next week and my mum wants to come to my city and possibly over to my place again that weekend and I am not sure how to feel. I have worked so hard to build up a life that is somewhat calming and having people around me that understand and support (naturally we are all neurodivergent) but now I will have someone over that WILL judge and won't sugarcoat either. Talking to her about my feelings regarding her comments etc has never worked, not when she was criticising my weight and I reminded her I was dealing with an ED, not with anything. She will pull out the "well I am sorry for being honest" or some version of "I feel like I need to walk on eggshells around you".
I love my mum and she can be really great. In a weird way she means well or at least she thinks so. I feel like trying to change her ways will cost more energy than to learn to accept and live with them. I just can't figure out how to do that. And not speaking up and telling her how I feel makes me feel like a hypocrite. How can I stand up for myself with others but then just swallow her behaviour? I've not been able to start therapy and learn how to actually deal with the emotional dysregulation of it all, also just started dexamphetamines so my body is a overwhelmed.
Has anyone dealt with anything similar and found actually helpful things? Related to dealing with parents unwilling to facilitate or just in general the emotional part of it all? (Sorry for the long post, never been able to use little words to express myself)
submitted by girlisariot to AuDHDWomen [link] [comments]


2024.05.19 16:14 mcfraggle22 Thriving during early menopause

I'm putting this out there to document my adventures with early menopause. I'm also hoping to hear from other women who have had a positive experience. I'm grateful to this community for providing many recommendations and personal experiences which have guided me in making informed choices for my health. Background: 41 y/o, no period for a full year. Probably was going through peri since my early 30's and just didn't know it. A lot of weird symptoms the past 5-10 years make sense now! I just went through the process of getting a menopause diagnosis from an online provider called Alpha. I decided to skip the run-around with my PCP and GYN since usually the goal of the online concierge medicine apps is to provide you with meds that you already know you want/need. I plan to see my regular providers in a couple of months (the soonest I can get in) and hopefully one of them will take over writing my Rx so that I don't need to pay a monthly fee to Alpha (for now only $30, which is reasonable, but I'm afraid there might be hidden fees, so we'll see. Overall, I would recommend them for now)
Because of my age the Alpha NP still had me get my hormones checked and have a transvaginal ultrasound. This confirmed my hormones have run dry (estradiol <12, progesterone 0.5). Thyroid was normal. She did have me test FSH and prolactin too, which were inconclusive and also asked me to take a home pregnancy test despite me telling her my husband had a vasectomy 20 years ago (I get it, people sneak around). The ultrasound experience was fine and nobody should be scared to get one (make sure they let you put the probe in yourself- I did not have to ask for this, my US tech was lovely and they even warm the gel)
I am glad the Alpha provider was thorough in order to rule out anything more serious. Turns out I had a fibroid, but otherwise normal and once in the clear was given options for HRT. At first she only offered patches or oral estradiol. I requested topical estradiol gel since I've read many complaints on here about patches and they sound annoying. She prescribed the lowest dose 0.25mg. Also got 100mg oral progesterone and vaginal estradiol 0.1mg for dryness.
It took about 2 weeks to actually get meds due to waiting to get the tests etc. But I wasnt in a huge rush- it's already been over a year after all. I have high hopes, but mainly just afraid of nasty side effects, as I got MHT for long-term health (bones, brain etc) and not so much for symptom management (I feel pretty great overall).
Honestly I already feel like a superhero - went through peri while simultaneously starting and finishing nursing school, raising 2 children, working full time, went through a divorce (and many years of drama prior to that), moved 3 times, remarried and finally feel very settled the past 4 years. I am a fighter and a survivor and I want these hormones to keep me strong and loving the life I have made for myself because I'm not ready to waste away yet!
A few things that I think have helped prior to getting meds: pilates, walking and resistance training; tracking macros (aiming for 100g protein daily), low saturated fat, low sugar, high fiber diet (I got my high cholesterol down to normal levels in 8 months once I made big changes), microdosing psilocybin (yes! This really made a huge difference in mood and general outlook- look into it. I don't use it often now but it saved me during a dark night of the soul), low caffeine- just one tea daily, sunlight, fresh air and the love of a partner who truly cares (healthy relationships are a big priority, cut out the toxic people). I will update in a few weeks/months. Praying for a positive experience!
submitted by mcfraggle22 to Menopositive [link] [comments]


2024.05.19 15:08 DoGsPaWsLoVe Saturday 05/18/24: 11 Posts

Here is the recap of the 11 monetized posts from Kylea G Weight loss Journey on 05/18/24.
"Greed is a never-ending hunger, that drives people to sacrifice morals and values for personal gain." -Unknown
⚠️ Compulsive Buying Disorder (CBD), aka shopping addiction, Disordered Eating, Gaslighting, Grief, Illness, Infertility, TTC (trying to conceive) Community, and Religion will be discussed.
Disclaimers: I am not a physician, influencer, or paid content creator. I am not affiliated with WW. I am semi-retired from the healthcare field with multiple college degrees. These opinions are my own based on social media content. I wish no harm to Kylea or Joseph "Joe" Gomez.
☎️ If you or someone you know is struggling or in crisis, please call or text 988 for assistance.
Behind the Scenes Family Update: Kylea Gomez has been exploiting a life-changing medical diagnosis of a close relative (without their permission and against their wishes) to internet strangers in social media messages. She has claimed that she is supporting this relative (which is a lie) to justify her work ethic, productivity, and even basic hygiene issues. Let that sink in for a moment...
To this relative: You, your family, and your medical team are in my prayers. ✝️
To Kylea's Biological Parents: Your daughter disparages your name and relationship for personal and financial gain frequently. No concert, trip, or gift provided to you with money obtained under (allegedly) false and deceptive pretenses justifies Kylea's disturbing behaviors. Stop enabling her.
California Clarification: Kylea was rejected by a Cavapoo breeder from adopting the Original Birdie (OB) during her California trip. I am thankful to the breeders of OB for making a tough decision in the best interest of the puppy. For me, this seals the deal that Kylea falsified details of this California trip and rushed home to find Backup Birdie (BB), who is the focus of today's content.
The tagline of Kylea G Weight loss Journey is, "I changed my entire life with prayer and a playlist of songs. No surgery, no meds. Just Jesus."
DAILY STATS: 05/18/24
0/11 posts discussed prayer
0/11 posts discussed music
0/11 posts discussed exercise
3/11 posts discussed a recipe
1/11 posts was about takeout "coffee" at 5 am
7/11 posts were about Birdie Mae 🐶
📢 For our friends at Meta, that means 63% of Kylea's monetized content had nothing to do with weight loss, which is the tagline and purpose of her page. Her weight loss journey ended July 2023 per her content. Why do you continue to pay her for non-weight loss content?
⚠️ Disordered Eating- Daily WW Points Used (Data compiled from monetized content):
1 WW Point: Crazy Llama "coffee" with almond milk, sugar-free vanilla, sugar-free peppermint, and sugar-free white chocolate
3 WW Points: Taco Soup with 12 Trader Joe's Rolled Corn Chili & Lime flavored Tortilla Chips
📢 For our friends at Meta, Kylea consumed 4 WW points out of (up to) 30 daily WW points= SEVERE disordered eating. This messaging is deadly for those on a weight loss journey. Follow your policies and take action.
Recipes Shared: 1. Taco Soup: 🚨 This recipe has dangerous sodium levels. Please know your daily sodium recommendations before making this recipe. 🚨
  1. Taco Rice Bowls: The soup is drained and added to 1 minute jalapeño rice with cheese. 🚨 The sodium alert is the same as above. 🚨
☎️ Please speak with a medical professional about any questions or concerns you have about your health.
Comments: To the animal lovers, I am sending you good vibes to get through this nonsense. Here we go...
  1. Coffee at 5am: Kylea and Joe are pictured in their vehicle outside Crazy Llama Coffee with the sun shining bright. Kylea claims she was home at 5 am, and Joe took her right away to get her "favorite coffee."
⏸️ The sun rises in Joplin after 6 am. Why lie? ⏸️ Her facial sunburn that disappeared yesterday is back today. How did that happen? ⏸️ Kylea claims she does not have cravings or temptations. However, she is addicted to sweet. Her "coffee" is beige colored at best, and she needed it right away...
  1. Backup Birdie Part 1: Her airline approved pet travel accessory backpack is shown in the vehicle. "All my dog mom dreams are coming true today 💖 🐶"
  2. Backup Birdie Part 2: "My heart is so full!!! 💖 🐶 I got the cuddliest, cutest, sweetest girl. 😭 I cried when I met my puppy for the first time because I love her so much already!!"
⏸️ Kylea's followers immediately started asking to see pictures and were told they needed to wait until after Kylea's family met her first. HoWeVeR, some influencers (bestie Drue Basham, Drue's SIL Sierra, Brittany Bryant, etc.) got to see her first and comment from their influencer accounts about Birdie. I'm sorry, loyal top fans and followers, possible cross-engagement from "trusted" influencers is more important than respecting your loyalty. Welcome inside the mind of a 🐈 🐟 er. Always trying to boost engagement, the algorithm, and gain new followers...
  1. Taco Soup Recipe: 🚨 This sodium monstrosity has canned beans, jarred salsa, enchilada sauce, rotel, roasted corn, a ranch seasoning packet, a taco seasoning packet, fresh chicken, and water. 😲
  2. Backup Birdie Part 3: "Welcome home 🏠 to our forever girl 🎀 Birdie Mae 🐶 She's already following Joseph and I around and has brought us so much joy. 🌈 🎀"
⏸️ The puppy shown does not appear to be a Cavapoo, and Kylea refuses to answer follower questions about her breed. Remember, Birdie was not supposed to come home until May 20th, then May 19th.
To all individuals in the TTC Community, I know the 🌈 is a powerful symbol for you. I have experienced pregnancy loss and fertility care. My heart hurts for anyone triggered by the language Kylea uses and humanizing pets in reference to pregnancy loss. 🙏
  1. Backup Birdie Part 4: "The moment I held her, I just knew she was meant for me.🎀 🐶 She loves all of the cuddles which is good because I do too. 💖"
⏸️ Not one reference of her "sweet boy" Oliver or Alice. Where are the cats? BB is asleep on Kylea.
  1. Taco Soup Part 2: 🚨 Since it wasn't salty enough, why not put some chili & lime tortilla chips on top? Chef's 💋. Kylea held the bowl, showing her barefoot on the floor. I did NOT miss her feet content. 🤢
  2. Backup Birdie Part 5: "We already love her so much 🎀 💖" BB is asleep in a fuzzy blanket on her puppy bed.
  3. Backup Birdie Part 6: Within 30 minutes of this writer posting info in Reddit chat of how to file an animal complaint in Joplin, MO as a PSA (not a threat) encouraging Kylea & Joe to be crystal clear about Alice's whereabouts, a picture of Joe cuddling BB with Alice behind him on the couch is posted. "Joseph loves Birdie Mae too 💖 🐶 So far she loves to sleep 😴"
⏸️ 3 animals are now housed in a small apartment. Two cats with behavioral issues and a young puppy. Kylea can claim she will have no issues because "it will be fine," but she is ignorant, immature, and selfish. Wise followers will remove their rose-colored glasses and see the truth. There is a theory Alice was edited into the photo again...
  1. Taco Soup Part 3: 🚨 No more takeout for Joe! He gets to eat Taco Soup Rice Bowls for work lunches this week.
⏸️ On the recent McDonalds post, a smart follower asked what Joe eating McDonalds had to do with WW. Kylea replied it was a "balanced lifestyle." Remember, Kylea & Joe want you to believe Joe has not gained weight no matter what he eats, with photo evidence (even modified) proving differently. Kylea's chains were broken 07/05/21. No cravings, temptations, plateaus, weight gain...a perfect journey to this day (and forever). 😇 Please disregard her obvious eating disorder and mental illnesses. Seek medical care, Kylea Gomez. ☮️
  1. Backup Birdie Part 7: A 12-second video is shared of BB playing with a squeaky toy on the carpet.
⏸️ No Oliver, Grams, or Gibson content today. Kylea told her followers (in a comment) that Oliver had not met the puppy. It's good to see your "sweet boy" and subject of a ridiculous amount of monetized content is already booted engagement wise.
Final thoughts: Money reveals people's true colors. 👀 Buckle in for a nauseating amount of BB nontent.
Takeout: Crazy Llama takeout for 2: $16 est + tip;
All info from Reddit. ✌️
submitted by DoGsPaWsLoVe to KyleaGomezsnark [link] [comments]


2024.05.19 14:56 Sara-Butterfly-4711 Identity crisis BPD vs. Autism

I've another identity crisis. I thought I'm autistic, it just felt right. I got the traits. Tipps from the community worked for me. I have not been diagnosed jet, as I needed to stabilize parts of my mental health in order to get a valid diagnosis (at least that's my assumption). Now I got diagnosed with a mixed personality disorder with BPD playing a major part. And what shall I say it just fits. It explains so much. Downside is I don't know who I am anymore. Some part of me still believes I'm autistic. Some part of things there are not enough autism traits left that can not be explained by my PD. I hate that feeling not knowing who I am. I want to know. I understand questioning and not know your identity is a BPD trait. Is it just me being a pwBPD. I'm confused and can't get my head around this.
Are there others with similar experiences?
submitted by Sara-Butterfly-4711 to BPD [link] [comments]


2024.05.19 14:18 CompleteAmateur0 YouTube Music’s unreadable landscape mode

YouTube Music’s unreadable landscape mode
Text cut off, clutter everywhere and only one visible search result There isn’t even a setting to disable rotation that I can find
submitted by CompleteAmateur0 to youtube [link] [comments]


2024.05.19 13:21 thejeffreybraun Muskoka Ontario

Muskoka Ontario

Muskoka Ontario

Experience the Best of Muskoka; Activities, for May 24, 2024

Are you excited to embrace all that Muskoka offers on May 24, 2024? Known for its scenery and lively atmosphere Muskoka presents a variety of activities catering to interests. Whether you're a nature lover, a food enthusiast, or an art aficionado there's something awaiting you in Muskoka.

Outdoor Escapades & Nature

Begin your day by immersing yourself in the awe inspiring landscapes of Arrowhead Provincial Park. With its meandering trails serene lakes and verdant forests Arrowhead is a paradise for lovers. Enjoy a hike paddle across the waters or simply revel in the tranquility of nature.
For those craving a boost venture to the Ranney Gorge Suspension Bridge at Ferris Provincial Park. Feel the excitement as you cross the swinging bridge and explore the paths weaving through the gorge.

Culinary Delights & Refreshments

After building up an appetite treat your palate to a journey at the Muskoka 2/4 Craft Beer Festival, in downtown Huntsville. Sample an array of craft beers while taking in the views of the Muskoka River. It's a way to immerse yourself in Muskoka’s culinary and beverage offerings.
Don't miss out on the Poutine Feast events happening in locations, across Ontario including a lineup in Peterborough for a one-of-a-kind culinary adventure. Whether you prefer sticking to favorites or trying out innovative twists these events are bound to satisfy your cravings for this iconic Canadian delicacy.

Cultural Excursions

Immerse yourself in the scene of Muskoka by enjoying an evening filled with live music, theater performances, and artistic showcases at some of the regions well known theaters and performance venues. Let the enchanting melodies and captivating performances transport you to a world.
As day turns into night, join in the Victoria Day weekend celebrations with dazzling fireworks lighting up the sky. It's a display of community unity and happiness.
Satisfy your tooth at the Muskoka Maple Festival, where an abundance of maple syrup treats awaits you offering a glimpse into Muskokas maple syrup heritage.

Sweet Treats & Scenic Cruises

Conclude your day with a boat cruise, along the waters of the Trent Severn Waterway. Sit back and unwind. Take in the views while indulging in a special Mother’s Day brunch experience.
With a range of activities and adventures waiting for you, Muskoka guarantees a May 24th, 2024.
Get yourself ready, for a journey. Prepare to have unforgettable experiences in this captivating area.

Links;

jeffreybraun #clarkemuskokarealty #muskokarealestate #muskoka #may24weekend

https://preview.redd.it/rxy9cavxad1d1.jpg?width=1900&format=pjpg&auto=webp&s=c91590bacfe1c53bf843f23933b70323439670fe
submitted by thejeffreybraun to u/thejeffreybraun [link] [comments]


2024.05.19 13:01 Hopeful_Shit How did you know it’s Phobia already?

I am not sure if I’ve just developed a fear of needles. I had a Tele-consult today and the doctor advised me to get CBC test as symptoms are getting worse and depends on the diagnosis I might need Dextrose injections again. Hearing it made me feel terrified and nauseous.
I am used to getting shots and blood samples after getting hospitalized many times last year (a couple this year too). I have a high pain tolerance but the thought of it (needle) piercing through my skin again then onto my veins makes me feel dizzy and anxious :(. It’s as if needles make people suffer:(
How did you guys get over this fear? I know I need the test for proper treatment but I could not push myself this time. It’s ridiculous that I am even crying over this.
submitted by Hopeful_Shit to Phobia [link] [comments]


2024.05.19 12:52 AlarmedIllustrator26 Colostomy reversal surgery

Hello all, I’m writing here full of anxiety and it seems I just can’t stop crying.
In December 15th, my mom got a huge spike of fever, every time she ate, her body temperature went under the roof. She finally agreed to call an ambulance. After 16hs at the hospital we heard a diagnosis - perforated diverticulitis in several places, emergency surgery and colostomy needed. She went through it, spend 5 days not knowing she will live or die. She spend two weeks in a hospital. Seeing my mom this way, scared, hopeless, weak, was the hardest thing I had to witness. My heart shattered in million pieces, but I’m so so glad she was alive.
Once we got home, after rehabilitation, things started to go back to normal step by step. Still taking antibiotics, but she was up and about. One hell of a strong woman my mom is!. But to our surprise - temperature rise again - her incision wound got infected. Another round of antibiotics - no success. As we live in a small town, healthcare system could not do as many tests as she needed - I brought her back to my place to the capital of the country and brought her to the er - 10 cm capsule of infected puss under her surgical incision. They cut it out and took a sample - three different gut bacteria’s were living under her skin. Three different antibiotics to fight it off- for 40 fucking days. I seen my mom cry, I see her face and the words “I’m so tired of being sick” was hurting the most. But finally, April 3rd - mom crp levels were back to normal.
We found a best doctor in an area, and went to meet him. His empathy hypnotised us - mom got scheduled for a reversal surgery May 17th. As she said - it was easier the first time - all the anxiety and waiting for the surgery, thinking about complications, dreaming of shitting herself in front of the class ( she is a biology teacher) everything seemed like too much. As mom and i are best friends, we are a team, I could feel her anxiety, but not imagine what she went through and still had to go through.
She got her colostomy reversal surgery 48 hours ago. As she said, she cannot compare it with the first time, it’s much easier. Also, she passes gas every time she moves (today was the first time she stood up and went to the bathroom and passed some mucous!). Her temperature is a bit elevated, but nurses said it’s fine and expected after such surgery. but I’m so scared we have to go through the same path again - long and painful reabilitation, shitloads of antibiotics, mom losing all her hope and I’m unable to help :(
My mom is in her 60s. No illnesses apart from this situation, all her blood work is better than mine (I’m 28) 😅 she is so strong and I’m so proud of her, but also so soooo scared.
Maybe someone been in similar situation regarding this journey? How can I help my mom? Is it as hard to recover form reversal as it is from original surgery? What she can expect? I need some insights I’m so lost and want to be the best for my mom and her recovery journey.
submitted by AlarmedIllustrator26 to ostomy [link] [comments]


2024.05.19 12:40 QueeLinx Census Scam, Is this Legit? (American Community Survey)

Census Scam, Is this Legit? (American Community Survey) submitted by QueeLinx to USCensus2020 [link] [comments]


2024.05.19 12:23 jaxonjason Journal on the Importance of Treating Drug-Induced Psychosis as a Short-Term Diagnosis

Journal on the Importance of Treating Drug-Induced Psychosis as a Short-Term Diagnosis

Introduction

Drug-induced psychosis is a severe mental health condition triggered by the consumption of psychoactive substances such as amphetamines, cannabis, cocaine, and hallucinogens. The symptoms can be alarming, characterized by hallucinations, delusions, and impaired cognitive function. Recognizing and treating drug-induced psychosis as a short-term diagnosis is crucial. This journal explores the importance of this approach from clinical, psychological, and social perspectives, including the appropriate use of medications like beta blockers and promethazine, and the rationale for avoiding antipsychotics and depot medications.

Clinical Perspective

1. Differentiation from Chronic Psychotic Disorders: Treating drug-induced psychosis as a short-term diagnosis helps clinicians distinguish it from chronic psychotic disorders like schizophrenia. Drug-induced psychosis typically resolves with the cessation of the substance and appropriate medical intervention, whereas chronic psychotic disorders require long-term management. Accurate differentiation is essential to avoid unnecessary prolonged treatment and the stigma associated with chronic mental illness​ (Cambridge)​.
2. Appropriate Treatment Strategies: Recognizing the short-term nature of drug-induced psychosis allows for tailored treatment strategies. Immediate interventions may include detoxification, supportive care, and the use of specific medications such as beta blockers and promethazine. Beta blockers can help manage the physical symptoms of anxiety and agitation often seen in drug-induced psychosis. Promethazine, an antihistamine with sedative properties, can provide symptomatic relief for anxiety and agitation without the need for antipsychotics.
Use of Beta Blockers:
Use of Promethazine:
Avoidance of Antipsychotics:
Dangers of Depot Medications:
3. Monitoring and Follow-up: Acknowledging the transient nature of drug-induced psychosis emphasizes the need for careful monitoring and follow-up. Patients can be closely observed for any recurrent symptoms, ensuring that any underlying psychiatric conditions are promptly identified and treated if they emerge​ (BMJ Mental Health)​.

Psychological Perspective

1. Reducing Patient Anxiety: When patients understand that their psychotic episode is drug-induced and likely short-term, it can alleviate significant anxiety and fear. Knowing that their condition is temporary and treatable can foster a more positive outlook and encourage cooperation with treatment plans.
2. Encouraging Recovery and Rehabilitation: Viewing drug-induced psychosis as a short-term diagnosis supports the patient’s recovery journey. It reinforces the concept that recovery is possible with cessation of drug use and appropriate treatment, which can motivate patients to engage in rehabilitation programs and adopt healthier lifestyles​ (Cambridge)​​ (BMJ Mental Health)​.
3. Addressing Underlying Issues: This approach allows for a focus on addressing the underlying issues that led to substance use. Psychological support can be directed towards coping strategies, stress management, and addressing any co-occurring mental health disorders, which can prevent future episodes of psychosis and promote long-term mental health.

Social Perspective

1. Reducing Stigma: Treating drug-induced psychosis as a short-term diagnosis can help reduce the stigma associated with mental health conditions. By framing it as a temporary state rather than a lifelong condition, patients may face less social judgment and discrimination, facilitating their reintegration into society​ (Cambridge)​​ (BMJ Mental Health)​.
2. Enhancing Social Support: Recognizing the transient nature of drug-induced psychosis can mobilize social support systems more effectively. Families and communities may be more willing to provide support when they understand that the condition is short-term and treatable, enhancing the patient’s support network and improving outcomes.
3. Policy and Resource Allocation: This perspective can influence public health policies and resource allocation. Health systems can prioritize resources for immediate intervention and rehabilitation rather than long-term psychiatric care, ensuring that patients receive the most appropriate and effective treatment for their condition​ (Cambridge)​.

Conclusion

Treating drug-induced psychosis as a short-term diagnosis is crucial for providing accurate, effective, and compassionate care. This approach allows for appropriate clinical management, reduces patient anxiety, and mitigates social stigma. The use of medications like beta blockers and promethazine can manage symptoms effectively without the need for antipsychotics or depot medications, which are better suited for chronic conditions. Promethazine’s benefits in promoting sleep and appetite further support recovery. Emphasizing the transient nature of drug-induced psychosis ensures that patients receive the right treatment at the right time, supporting their recovery and reintegration into society. Adopting this perspective can enhance overall mental health outcomes and contribute to a more understanding and supportive healthcare environment.

References

submitted by jaxonjason to druginducedpsychosis [link] [comments]


2024.05.19 10:58 KaiSchtrom Assetto Corsa Dashcam Mod

Assetto Corsa Dashcam Mod
Hi to the Assetto Corsa Community,
this is my first post on Reddit and I want to share my work for free.
Weeks ago I found some gameplay videos on YouTube, where a realistic dashcam mod for Assetto Corsa was promoted. To be honest I thought the videos were all fake at first. To prove the fake videos, I investigated further into the modding process and got some unexpected results. I never thought a nearly 10 year old game can look that realistic in the year 2024!
This tutorial will show you step by step what is needed to create a dashcam modification for the sim racing game Assetto Corsa developed by Kunos Simulazioni. Because I researched many hours to get the pieces together, I will try to give away the collected info for free, in the hope that this guide maybe helpful to others.
For the full free tutorial visit https://assetto-corsa-dashcam-mod.sourceforge.io
Video samples:
Bullrun on Highway 201: https://www.youtube.com/watch?v=b1YrkvcVCds
Bullrun on Highway 201
Horizonrun at 05:41: https://www.youtube.com/watch?v=apoXvpSJz-8
Horizonrun at 05:41
Nightride on Bayside: https://www.youtube.com/watch?v=tjeTWN1_C20
Nightride on Bayside
Greets Kai Schtrom
submitted by KaiSchtrom to assettocorsa [link] [comments]


2024.05.19 10:00 AutoModerator TREATMENT Community Thread - Sun May 19 AM

Our community threads are the heart of our subreddit and operate much like a specialized support group – we share our experiences and strive to collectively support one another on the topic at hand.
Please use this space for sharing and discussing any type of treatment, trying to conceive, or family building measures. This includes, but is not limited to:
Essentially, if you mention treatment, TTC, or family building measures – it goes in this thread.

A few notes:
Above all - Science minded perspective and respect for others is important here. Please treat your fellow peers with compassion.
submitted by AutoModerator to infertility [link] [comments]


2024.05.19 09:33 Moonshademyth Everything is overwhelming.

I am self diagnosed-ish, trying to get a professional diagnosis. My PCP is all but certain I have ASD and she delivered me when I was born so she’s been my PCP for 22 years. She brought it up to my parents once when I was a kid but thanks to that great immigrant “no mental health issues” mentality they have, it was ignored and never brought up again.
Then I was excelling in school. In 8th grade I had these tics one day, my friend had just passed and I was still trucking on. I flung a pencil during one of them and hurt someone else. The school made my dad take me to the ER, he was told stress, anxiety and see someone about it. But nothing. Then I was excelling in my first full time job as a parapro for a STAR classroom. As a kid I volunteered in these classes a lot, my mom even taught one. Yeah, taught one. The adults were awful, but I was used to that. I started having meltdowns from overstimulation. At this point, I’d moved out and was living with my now husband, I was in a safe place for the first time in my life. I didn’t understand what my body was doing and why my brain was doing what it did. And then I was regressing. A lot and quickly. And now I’m realizing my entire life has been this huge lie. I come from a traumatic household, but have always been highly aware of it and have managed to process it myself. A year of talk therapy got me told “talk therapy doesn’t work for you, you have it all figured out.”
And I started a relationship pre-regression. I made friends pre-regression. Now I feel alone. My husband doesn’t understand really, he tries and all the time we’re growing together and he’s learning more and more about me and how to help me. But I have a lot of needs and I know I take up a lot of space in our lives because of it and so it feels like when I’m pushing through, knowing it’ll end in a complete meltdown, people are attentive, him included because I’m being helpful. But then I really need help, because I’ve been so focused on everyone else I need someone to focus on me. But there isn’t anyone to be attentive toward me. I feel like I’m treated like a burden when I really need the assistance.
I know I need to be the one to focus on me, but how do I do that? When people have surgeries and shitty husbands and need care, people have problems and ask for my help and I can help them. My brother is having a hard time at school. My husband works to support us because I can barely handle 14 hours a week. He met me when I worked three jobs, when I was surviving my childhood household. He fell in love with me because of my ambition and now I’m a dependent.
I’ve been battling myself to accept that I’m disabled. That before, that wasn’t me. That was a shell. I was a body. But now I have no clue who I am and it’s becoming terrifying. I feel like if I can’t just bounce back soon I’ll lose everything. Or someday I’ll become too much and just get abandoned.
I feel like my body and my brain are disconnected, I feel like I’ve got no hope. Like a diagnosis will never come, help will never be found. I just needed to speak at a community I knew would understand.
Thanks.
submitted by Moonshademyth to AutismInWomen [link] [comments]


http://activeproperty.pl/