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Helping my white middle aged husband understand privilege.

Please ask as anonymous if you answer this one on the pod, as some people could identify hubby from my following post 💜 Hey Em, bit of a heavier question than some of the other recent ones, but let me tell you, I live for the Shmyson update and content 😂 Background context: My hubby has come a long way in understanding his own neurotype which is impressive as he can’t remember his own pass to get into his building at work most of the time. He accepts that he probably has inattentive type ADHD, alongside autism. I would suggest he would meet the diagnostic criteria for a level 1 presentation, which he agrees with. He has come along on the journey of yours since your press club address, and I have been exposing him to more of you in general over the last 12 months or so. And by exposing, I definitely mean aggressively putting an AirPod in his face and making him listen to your pod with me 😂 He was very involved in discussions with me about our house dynamics when you released the Marriage Diaries, and you are a standard topic of conversation in my house. Thank you for the ongoing content that I can use passive aggressively 😂 I digress! He really enjoyed the first episode of Anomalous, and shared the link to me of the yesterdays episode enthusiastically when it dropped (Like I hadn’t already listened to it, but props for trying 😂😍). Last night when we were dissecting the episode, there was a lot of defence on his behalf in your bringing attention to the trans/queer community. He felt as if the pod wasn’t the correct place for this info to be spoken about, and wasn’t reflective of the ND community as a whole and “why being attention to something that doesn’t need attention on it in terms of ND? I’m listening for ND content, not LGBTQI+ info. I attempted to engage him in dialogue around the fact that intersectionality is important when discussing these things, and it’s crucial to discuss/highlight the oppression marginalised communities experience in general. You can’t separate them. It was like trying to explain quantum physics to a cat. He wasn’t able to understand what I was putting forward to him. Clearly I am not communicating in a way that allows him to grasp concepts of intersectionality and I suppose privilege more broadly. He also is very defensive when it comes to mentioning systems of oppression being rooted in heterosexual, white, middle aged men. “Why does it always come back to that?” His argument is that he feels he specifically doesn’t represent that stereotype, and as such feels as if he isn’t entitled to his opinion and will be shut down immediately because of this. Ironically, that’s the point 😂 My question after all that is this: can you please articulate in greater detail the reason why discussing intersectionality and systems of oppression is important when addressing ND? And provide your definition of privilege so that he may understand it better? Because let’s face it, I fucking can’t 😂 It’ not that he’s opposed to understanding these important topics. He does ‘try.’ Ironically it’s his privilege and neurotype preventing him from grasping these concepts in full 😂 He has a lot of respect for you and your articulation of things, so hoping you can bless his ears with your wisdom. I’m just his wife, ya know?! (Ps - I am also combo type ADHD, and suspect I am autistic as well. Just in case you didn’t get that from the huge explanation haha!)

AITA - WARNING - Long Post Ahead!!

AITA !!!WARNING!!! Long Post Ahead!! (with a couple of small side quests unintentionally added in for good measure) Also trigger warnings for infertility, medical trauma, parental trauma etc Backstory: My Mum and I have a very up & down, challenging and arduous relationship (she is undiagnosed ADHD & OCD and at 31 after the birth of my second child I was diagnosed with ADHD & 18 months later added ASD to my long list of acronyms (C-PTSD, OCD, Anxiety & Binge Eating Disorder)). We are ‘close’, however she is not someone I consider emotionally supportive, nor is she a safe person for me to unmask around. It took her a while to come to terms with my diagnosis (as most mothers’ of late diagnosed daughters generally are); however sending her Em’s speech at The National Press Conference and a few other posts from when Em was first unpacking her initial ADHD diagnosis helped her understand me a little more, and also let go of some of the shame, guilt and ableism she was experiencing. Sidenote: I went into labour with my eldest daughter at 23 weeks and gave birth to her 4 weeks later; she was born at 27weeks weighing 1070grams, had lifesaving surgery at 3 days old and was diagnosed with a rare form of cancer at 8 months old (don’t worry, she’s now in remission and a completely healthy, happy, Neurodivergent AF 5 year old)) During those 4 weeks between my waters breaking and her actual birth, I was an Inpatient ‘on bedrest with toilet privileges’ at Canberra Hospital (4hrs away from home), and requested a copy of Em’s book ‘Try Hard’ (which she picked up from the bookstore for me). That same year I was DEVASTATED I couldn’t see Rage and Rainbows as I had only just gotten home with my micropreemie, so it didn’t feel right to leave her. I say all of this to help you (Benjamin Wasley who is probably proof reading this!!!) get an understanding of how deep my connection to Em and her work, and also the importance of how much Em’s advocacy work (both direct and indirectly) has helped my Mum understand me a little more and at the very least, drop SOME of her judgment towards me. Sidenote: I subscribed to Emsolation the day it first dropped as I was in NSW, in my first trimester with my 2nd child, but in complete lockdown due to my eldest daughter’s compromised immune system thanks to her being a micropreemie with a rare form of cancer. I also became a paying Emsolator the week it became available, as I love everything that Em does and although I couldn’t afford much, that $9.95 a month was my irrefutable ‘self-care’. Now in a complete plot-twist, on Mother’s Day this year, I was on the phone to Mum, and she said she had seen Em’s show OUTGROWN advertised and if I’d like, she would buy me two tickets to the Canberra Show. Of course I said yes without hesitation, as I had been going in to see the seats and ticket prices ever since Pre-Sale tickets became available to us subscribers, however never had the money to purchase any myself. Now for as long as I can remember, whenever my Mum has gotten me a gift (especially a thoughtful one), it has ALWAYS either come with some random set of rules & demands, or as an attempt to apologise without her having to actually say the word ‘sorry’ (generally for her shitty behaviour towards me or insensitive remarks on my body, parenting, weight, house cleanliness (or lack there of) etc. OF COURSE I jumped at the opportunity, expressed my deep gratitude and even told her how I had been looking at tickets for over a month when Pre-Sale became available to us subscribers. I was (and still am) GENUINELY impressed with her seeing the ad for Outgrown and thinking of me instantly. She said it’s because she knows how much I love Em (I listened to Em when she was on Radio with the first 2 dickheads she had to put up with, and have followed along with everything she has done since); and that our diagnosis journey’s were so similar and happening around the same time, having me send her stuff that I thought would help her understand, she knew I would LOVE to go to one of her shows. Now OF COURSE I immediately called my best friend since I was 16 and asked her to be my plus one (Mum bought me two tickets for my birthday, knowing that my anxiety would NEVER allow me to go alone - no matter how much the other Emsolators felt like ‘my people’). However upon reflection, should I have asked my Mum to come with me, as I’m sure she’d love it also, and we haven’t spent any time together since I was 16 and only a few months away from moving out (to the Gold Coast of all places!!!). It’s probably important that I add here that I am a recovering people pleaser, and it’s only been in the last 2 years that I have been setting firm boundaries with my Mum (that she still crosses ALL THE TIME). I would love to hear your opinion team, on whether I made the right choice by asking my best friend to come along with me, or if I should have asked Mum first if she wanted to join me, as it could be a really lovely bonding experience (but also probably VERY triggering for me as we would be sharing accommodation for the night and she is NOT a nice drunk and will not be able to attend without atleast a few sav blancs under her belt, which will absolutely turn into an argument at some stage. To give you an idea of the depth of her nastiness when a bottle of cheap white deep, when my baby cousin died at 25 from suicide, she told me she wished it was me and not him (according to her she ‘merely meant that she wished she could take her sister’s pain away); when I called her to tell her I had gone into early labour she screamed so much that I had to hang up on her and call my Dad so I could give them all of the information; when I was 6 weeks postpartum (from an emergency cesarean) she took me shopping to ‘cheer me up’ while my daughter was in NICU and after trying afew different things on, she told me “everything would look so lovely on you if only your stomach wasn’t so huge”, and most recently she dropped over unannounced while I was in the middle of a panic attack and as a way to ‘calm me down’ asked me to describe what was going on, when I started rattling off all the things that have recently gotten ontop of me and she responded by rolling her eyes and declaring that “everyone has problems mate” - I could go on for days!! I apologise for the ridiculously long AITA (complete with backstories nobody asked for and sidequests that probably hold zero bloody relevance (that’s what happens when I’m classified as an extra, EXTRA at anything (subscriber or whatever else)! Love everything you guys do over there ‘Down The Hill’, and am SO excited to see you in August (with my people pleaser guilt tagging along with me in my handbag no doubt!!!).

Toowoomba girly

Hello Em, I am a Toowoomba girly and coming to see your show here. I have been sharing your show, and I have mustered up a few friends plus my husband to come along. I don’t have a very big social media following so I’m possibly not getting the word out there much. My question is, do you have some flyers I could be posting around town or something like that?! I am (clearly) very excited to see your show and would love to help get more people on board! This is probably not the place to ask this but I thought it would reach you anyway 😂 I’m rambling now. Much love, Maddie

FOR GOOD? or something bad

Hi Em, long time lurker, first time caller 😂. I have lost contact with my best friend from high school. We had several big arguments and I always felt that she was immature. But we had this song, For good (wicked obvs) that we always promised that we would sing at each of our weddings. I’m not getting married yet. But I just played the album in preparation for their trailer release of Wicked! And I sobbed like a baby. She never got along with my long term partner and we are still happily together. But I’m feeling really lost after such an emotional outburst from our old song. I also never replaced that friendship. I don’t have a Michael in my life. My best friend is my partner. But I’m missing having a sister like figure in my life. Should I reach out? See if after several (3+) years we are in different place. Last time we saw each other we both were pretty horrible to one another. Please help.

ASD, Stem Cells & Rabbithole!

Hey Em! I was scrolling on TikTok this week and came across some content of a family flying to India to get their son stem cell therapy for his regressive ASD! I’m not sure of the science or anything whatsoever but weirdly the whole thing seems pretty off and like the family are trying to cure their kids ASD! How do you deal with the feelings that this kind of things bring up? I’m currently unpacking my internalised ableism but this whole thing just seemed so off base and really upset me! Have you come across anything or any content that just seems to make you uncomfortable and make it seem like ASD needs to be ‘cured’?