Halsey Part 1: Endometriosis, Lupus and The Unfiltered Truth About Living With Chronic Illness

[@Hatsinahat]

Seeing this doctor be so validating about how someone with chronic illness knows their body and how she’s trusts their judgement is truely amazing

[@ironiceilidh]

ash is my comfort person for a reason

[@helenogbonna3361]

I love her

[@ishathompson8439]

Same

[@VeganBambi]

"ASH" like you know her lmaooo

[@kimberleygliddon]

@@VeganBambi grow up

[@meidson12]

Only people with chronic illness will understand why Halsey knows so much about medicine despite not being a doctor. It's sad, really. If we don't advocate for ourselves, we might get sent home to die. If I didn't know better, I'd be dead, thanks to a doctor who took me off treatment without checking anything.

[@juliahall4359]

Hearing her share her experience with endometriosis and thinking to myself “oh my god, is that what’s wrong with me?” They just described every symptom I’ve experienced (even the “my mom and all my aunts have heavy periods”) and I’m feeling so heard…

[@GrotesqueSilence]

Go get diagnosed! Don’t allow them to just do ultrasounds and dismiss you when they don’t see it. You NEED to get the laparoscopic procedure (exploratory surgery) to actually see it in most cases. Don’t allow anyone to tell you no. I was told no from my first doctor and she just wanted to stick me on birth control and pretend that would solve it. I found a new doctor and told them that I will NOT bother trying birth control or anything until I got that procedure done, he agreed and I have now had 2 of them (which the second one helped more than the first, so don’t be deterred if the first time doesn’t seem to do too much) and I’ve never felt better! Will actually be scheduling a 3rd soon more than likely. Which do not worry that you’ll always have to have them cause it’s not the case for everyone, it could be a one and done or multiple. I’m good every 2-3 years but I also get it on my bladder, so it does change the frequency for me. But please, go and advocate for yourself and have it looked at! Best decision of my life and I’ve even been blessed to have a baby through it all. ❤

[@kayredhawke1522]

i found out i have endo from a podcast too! the cycle podcast shares patient stories and i learned what was wrong with me it genuinely changed my life

[@crazylaydee_]

Nobody in my family had it aside from aunts who aren't blood related. My grandmother & aunt both had tumors or fibroids which can be related to endo, but I'm the first of my blood line with endo. It's wild, but, you go many many years being brushed off with "that's a normal period" 😢 When it's really not

[@NattyByNature-]

@@GrotesqueSilencenow you’re saying this I’m wondering if they missed it

[@GrotesqueSilence]

@@NattyByNature- they do! I had both an external and internal ultrasound done and they were like “nope can’t see it, you don’t have it.” Like 90% of the time you CANNOT see it that way, only times you can is if it is so bad and thick that it overpowers everything. You need to get the exploratory procedure done. It’s very simple: a cut in the belly button, a cut above the pubic area (generally at the c-section area, and if they need to get a look around or there is more in other areas they will make 1 more (or more if it’s severe) by your hip area. They are no bigger than an inch and recovery was fine both times. Only issue I had was not even with the cuts, I had air trapped in my chest the first time which hurt.

[@Seschal]

yeah, I totally relate to the "playing doctor" because as a person with chronic illnesses who's constantly dismissed by doctors, I ended up turning to the internet to try to find out what my symptoms were matching to, and learned about alot of other conditions on the way ❤

[@RebeccaJoArt]

@@Seschal Thank God for the Internet, right?? Without it, many of us would be in big trouble, lol 🙈

[@teltomo5862]

you know how dr. a complimented halsey and then halsey went back and give dr. a a lot of compliments, too. That's how you know halsey is deeply kind person.

[@jadelyngrace]

As someone with adenomyosis, endometriosis and another suspected autoimmune disease, this episode is so dear to me. Thank you Halsey, Dr. A, and Mary for spreading awareness on important topics like chronic illness.

[@SHEMDPodcast]

So sorry to hear you are suffering! Thank you for listening, big hugs to you🤍

[@a_lost_lover]

It means so much that the doctors actually acknowledged that Halsey know so much about their body and their health ! As disabled people we gather so much knowledge about body, about our illnesses, it's important that doctors recognise that and work hand in hand with us !

[@doomsday1980]

I was diagnosed with lupus at 15. Got pregnant when I was 25 and my lupus went into remission. I felt amazing. It lasted till my son was around 7. Then it hit again, with a vengeance. It was insane how sick I got. And the pain was unbearable

[@SHEMDPodcast]

Thank you for sharing. I hope this episode made you feel less alone and gave you some more knowledge on how to care for yourself. Thanks for listening!

[@mariakqueen6574]

As someone who is also chronically ill, Halsey is such an inspiration. Being completely honest and still being so strong really makes a big difference. I love Halsey for always being true to herself and opening up about this!

[@lamb83]

I couldn't agree more with Dr. A that she is one of the kindest, most generous, and loving people on the planet. I have no doubt that her son will recognize what an amazing Mom she is. I am so deeply sorry for all she has been through, including the cruel dismissals of her health struggles; I am so glad that she has Dr. A in her life. Sending her SO much love and wishing her a healthy future full of joy and blessings. ❤❤

[@tuberyarik]

Halsey's If I can't have love, I want power album helped me to cope with my emotions, my extremely hard breakup and tuberculosis treatment. And seeing them talking openly about their health issues made me respect Ash even more than I already did. We need more people to talk about their medical journeys, and bring this subject and speak out bc medical trauma and gaslighting is no joke. Esp for women, poc and queer people. Lots of love and hugs to you, Ash. You're a real fighter.

[@sararussenberger8469]

The relationship between you and Doctor A is SO precious. Protect these people.

[@Briana-Mars]

Chronic illness is so difficult to deal with, and it breaks my heart Ashley has gone through this. I appreciate them bringing awareness to these issues. It can be helpful to see other people surviving chronic illness and feeling better.

[@SirenASMR_]

Breaks my heart that all of us who have no funds and no one listens to us

[@Briana-Mars]

@@SirenASMR_ True

[@lafytaffy1220]

Amen 🙏 ❤

[@brooklynnoelle]

I was just diagnosed with Lupus a couple weeks ago. It's been a 4 year journey trying to figure out what's wrong. My previous docs telling me, when I brought up autoimmune diseases, that "we don't think it's that", and when I asked them to test my blood just in case, they said no. So I went elsewhere and in less than a month got diagnosed. Joint pain, skin inflammation, tiredness, always sick/not feeling well, hair falling out, rapid weight loss (I lost 22lbs in about a month) and I've since lost more. Halsey coming out and talking about her Lupus diagnosis is what pushed me to seek help and advocate harder for myself. I was at the point of not wanting to be on this Earth anymore. It's so validating to hear, so I wanted to come back and say THANK YOU for this interview and her talking about her symptoms which made me push harder for the help.

[@SHEMDPodcast]

Thank you so much for sharing your story! I am so happy that this episode helped you. I hope others can learn from your advocacy, too! We wish you the best!

[@444caitlyn]

as someone with dysautonomia conditions, including endo, sjogrens, and eds, having halsey speak about and raise awareness for these conditions is incredible and so appreciated!!! the medical gaslighting and neglect we all experience is truly traumatic and worsens our health. i have ptsd bc my doctors never helped me, and i was a kid too. nobody’s safe lol

[@abbied]

So I’m just now looking this up, but is eds just another word for Ehlers-Danlos syndrome? (Just asking)

[@BetteFoord]

​@@abbiedyep! Just shortening it

[@abbied]

@@BetteFoord Thank you 👍🏻😌

[@BetteFoord]

@@abbied no worries!

[@abbied]

@@BetteFoord 😌💕

[@RebeccaJoArt]

A page like this give me faith towards women’s health education! It’s been hell trying to figure out all of my chronic issues and so many doctors just write it off as “Oh, you’re young. It’s gotta be this super common thing.” And when you try to stand up for yourself to tell them: “This isn’t normal.”they don’t believe you. I hope to find a decent doctor one day so I don’t have to figure it all out on my own.

[@SHEMDPodcast]

Thank you for listening! We are so happy to have you as part of our community.

[@thatboyblair]

As a guy, I found his fascinating. First we almost don't understand the true magnitude of the illnesses women deal with and how they actually affect their day to day life. Also as someone that's been dealing with health issues for the last couple years with doctors telling me it's all in my head, it is nice to see doctors that listen and show up for their patients and find solutions.

[@tiffanymoore5632]

I really feel like the Halsey's music coincides with whatever my life dealt me at the time. This year I've had two breast biopsies which were negative, however breast cancer runs in my family. My aunt was diagnosed last year even though she tested negative for the BRCA gene. So this weekend I'm getting an MRI and later this year I'm getting a lumpectomy. When "The End" came out I couldn't stop crying because I felt so seen.

[@prarthanabajaj1090]

Same. I got my official endometriosis diagnosis in October 2023. And then recently in April 2024 I had tests for ovarian cancer (tested negative but got asked to start planning a family soon because my endo got bad) & she came out with ‘The End’ right after. It feels like she’s my soul singer.

[@MushroomFae444]

I’ve been diagnosed with Lupus and Endometriosis too 😭 I didn’t know I could relate to you and your music anymore 🥺

[@andreavides5532]

this episode was incredible. halsey is so strong and inspirational and i am so glad that she has someone like dr. a in her corner. can’t wait for part 2!

[@SHEMDPodcast]

Thank you for listening!

[@kellygosa7438]

Women don’t know enough about their health at any age. Happy to see some improvements.

[@BetteFoord]

We're actively discouraged and gaslight

[@GlamwithKendall]

This makeup look is everything on her!! The hair and everything is giving Marilyn Monroe. 12/10 obessed 🥰

[@arolamichelle]

I have immense love and gratitude for Halsey as a human, artist and advocate for women, chronically ill and disabled people and survivors. i’ve been sick for 10 years now and this episode made me feel so seen ❤

[@SHEMDPodcast]

So happy you got something out of this episode. Thank you for watching!

[@andromedastrike1505]

This is the first time I've come across your podcast. I'm so impressed by Halsey's decision to share this time of information - she is elevating awareness. It takes a strong person to share this type of information especially a popstar who is scrutinized for everything. Halsey is so well poised, knowledgeable and well spoken. And this podcast's host are so impressive. I'm a new fan. I'm officially following every post and getting all those notifications. Thank you!

[@SHEMDPodcast]

Thank you and we are so happy you found us! x

[@calistagarrard1597]

Been listening to Halsey since I was 14 and was also diagnosed with endo at age 20. H gives me such strength

[@justbecauseican1410]

I wish I had this doctor. I have been unwell for quite some time. I also have a toddler to look after which i am unable to do. That is the most heartbreaking thing for me. I want to be healthy so i can play with my son. I have been looking for answers but the doctors i have been seeing are not that educated. You are really lucky if you have the wealth to see these doctors.

[@JULIANLUCIA]

try and see a derm if you can. i had been fighting to be heard and just now i am able to get tests done bc of her listening!

[@SoniaMinden]

I’m so sorry you’re struggling, sending hugs. That sounds hard.

[@swm3638]

My baby girl was born on September last year and I started experiencing headaches on November😢... I've had panic attacks, numbness on left side of the face, tingling left eye, pulpitating left temple nerve and just generally unwell... I'm not working and a single parent😢... You are not ALONE. My symptoms are scary but I can't do nothing about them so I'm just waiting for the big day🙌😞

[@KatjeKat86]

​@@swm3638 Just let you know, not to diagnose you but all the symptoms you mentioned except the panic attacks are migraine symptoms.

[@SeeWonderHaveLive]

Why would you need wealth to treat autoimmune or other probs? All Dr's should warn ppl to remove dairy. I'm in remission from IBD. I've known about dangers of dairy since I was 16! I blame it for causing many problems in western society. Healing can start in the kitchen. Can you tolerate organic legumes? Look at the cookbook Meals that Heal by Carolyn Williams. I'm Middle class and very much mad how expensive it is to find healthy alternatives. PS We all evolved on meat. Don't fall for Hollyweird plant based crap

[@LilLibra]

As a fan of Ash for the last decade I’m so proud of her and her journey. I appreciate her being so open about her health because many of us are also going through the same things or have experiences with them. I love her and glad she’s doing better ❤

[@AleinWonderland]

I have Lyme disease, brain damage, seizures, Tourette syndrome, and a lack of an immune system. I’ve been sick since the day I was born, and I’ve been looking for a doctor like Dr. A for so long. I’m so so glad my idol found her and is getting better! So happy for you Ash! don’t ever stop advocating for yourself and I won’t either.

[@KardoNewman]

This! ✨✨✨

[@scotty2hottie759]

I hope and pray you find your Dr. A too!!

[@glaoss]

Not me crying at 4:00 because that’s exactly how I see her 😭 love you so much, Ash! I’m glad you are alive and wish you the happiest life ahead ❤

[@tjluv13]

that’s EXACTLY how my PCOS diagnosis happened

[@fairytaleviola]

Same my mom would just say her aunt had periods and she was even passing out from the pain and calling ambulance that same lady miscarried in the past too apparently I found out late( now she’s 70) but basically it was considered normal Or whatever

[@aprilshades]

I have just NOW AT MY ALMOST 29 YO been possibly diagnosed with ENDOMETRIOSIS cause none of the other gynecology related conditions matches with all my symptoms.... Hearing Ash talking about her IUD make me realize how much pain I went through at my 25s when I had one placed for 15 days and gave me one of the worsts pains of my life... Now I see it.

[@fairytaleviola]

Btw can’t they see during the exam ? They can see mine

[@SHEMDPodcast]

Thank you for sharing. We are so happy to hear you finally got some clarity with your diagnosis.

[@DanielleCobb-b7g]

I love how Halsey is so open about her journey. It's a blessing to have women with a platform speak about their experiences in the hope that it can help others. I had severe endometriosis and lived with excruciating pain for years. I was dismissed and treated poorly by doctors. I dealt with unsupportive teachers and managers while I was dealing with this chronic issue for about 15 years. I was told by many doctors that I should take birth control or get an IUD and that I probably had PCOS. When I finally decided I couldn't handle the pain anymore, I had a laparoscopy. My left ovary and fallopian tube had to be removed because they were glued together. I had been to several doctors and gone to the ER twice and knew something wasn't right. Always listen to yourself, trust your gut, always fight for yourself, and get answers!

[@SHEMDPodcast]

Wow. Thank you so much for sharing your story. We applaud you for advocating for your health and getting answers. I am sorry you had to go through all of that pain to get there. We wish you the best.

[@heatheralice4572]

I'm so greatful for this interview. I am not only a huge Halsey fan, but I have spent the last 6 years going through an organ transplant, battling ulcerative Colitis flare ups and now I'm currently being diagnosed with endometriosis at age 35. I have followed Halsey's advocacy for endometriosis and women's health and women's rights, and most of all I am truly touched by her recent songs The End of the World, and Lucky... there just aren't many songs that truly express wjat it's like to be sick. Chronic illness is so hard and I just really appreciate hearing about the experiences of someone I already respect. I truly hope she continues to get the help she needs and wish her all the health and love in the world.

[@JaeLynn2121]

❤❤❤❤❤

[@SeeWonderHaveLive]

Colitis can start with a virus. I began to cure chronic SIBO finally after 3 years with Oil oregano. Now I use soil based PRO Biotics. I know someone always sick can't absorb their food with terrible medications from Colitis. They don't eat normally, then got worse coughs.. it is always negative gram bacteria. Research it.

[@KatelynDiAnn]

Ash is easily, hands down the kindest and most personable human I’ve met (aside from my own mom and aunt). I met Halsey at a cd signing for the Room 93 ep and I think first show in Houston. This was right after I had all 4 of my wisdom teeth taken out lmao I got the procedure done and picked up my Vicodin so I could stand in line for the meetup. Ash noticed the ice packs on my face and made me feel so special and comfortable. So much more to say just about that moment but God bless this person. I’ve got soooo much love and respect.

[@CreativeArtandEnergy]

I appreciate the public spotlight on this topic.

[@TheanneChan]

I’m a 44 year old women it’s so sad I’m going and have been going through all this almost since i had menstrual I keep trying to diagnose myself and doctors literally turn their head on me Always pain Bleed so much so much pain Bloated threw up I wish they listen to us more

[@SHEMDPodcast]

We are so sorry to hear this. I hope these episodes can help you gain clarity on your health journey. We wish you the best.

[@BaileeLaducer]

Love Halsey for her music but love her more for being relatable and speaking up about her experiences. Having autoimmune disease is hard! As a person with Sjrogrens, RA and fibromyalgia, plus several family members with Lupus I feel so seen!! Nothing means more to someone battling their body daily than someone who understands the struggle!

[@SHEMDPodcast]

Thank you for sharing and listening to this episode. We wish you the best in your medical journey!

[@Chips185]

She's so multi talented. And sounds awesome live. Love her and her music, can't say that much about other artists in her genre.

[@chayo4537]

Because you don't even know them 😂

[@Chips185]

@chayo4537 because other pop artists' music is not my cup of tea. Halsey is great, though.

[@LaJurado]

I was diagnosed with endometriosis 2 years ago, like 2 months before my 30th birthday and the part were the doctor said it can be a 10 years late diagnosis hit me. I've been spending all my fertile life with issues and terrible pain, even before getting my period for the first time, so I do get it.

[@kellyanncoveny8425]

I just got diagnosed with lupus and it’s very overwhelming, but watching Halsey be so honest about her experience makes me feel like I’m not alone ❤

[@meidson12]

Being in the process of being diagnosed with a chronic illness has been the hardest experience of my life. The isolation and feeling of loneliness is devastating. I'm so glad I live in a time where Halsey exists. No popstar talks about these horrors of being sick and having to fight doctors to be taken seriously. We have to learn so much medical stuff by ourselves because that can mean the difference between life and death.

[@SHEMDPodcast]

We are so happy to hear you got something out of this episode. Thank you for sharing.

[@laurah674]

To everyone involved in making this, I sincerely can’t thank you enough. Especially to Halsey for sharing such a difficult experience publicly. I was diagnosed with lupus in April and started treatment in May. I’ve been fighting through a really rough bout of fatigue this past month, and other un-fun symptoms the past few days. Anywho, I was feeling down on myself and this just really helped to watch for some reason. I’m so appreciative of the work Halsey’s doing for lupus awareness and research 💜

[@SHEMDPodcast]

Thank you so much for listening! We are so happy to have you as a part of our community.

[@rouxpatterson3709]

i am so incredibly grateful to Halsey for being so open and vulnerable about this, her bravery makes it easier for others to be brave, too. i wish her the best of luck and only good things for the rest of her life ❤

[@LYS-hq1jv]

She’s very fortunate to have these drs at her finger tips. Happy for her and her story will touch many.

[@arontamas5639]

I love how much awareness she brings about all of these topics...... I was so happy when she could have his first child! She was so on the way of becoming a mum!

[@jr-eo5be]

thank you so much for this. as a halsey fan it has been heartbreaking seeing her deal with her health issues. halsey means so much to me and so many others who grew up with her. thank you Dr. A for saving her life

[@fernandamunoz2637]

She so strong and kind, amazing human 🩷 we love you Ash

[@jm52hz]

ash is an angel, and i’m so glad she has such amazing people in her life that inspire her as well.

[@torid3023]

I love seeing this side of h. she’s so insightful and been an inspiration of mine since I was 15! This podcast was so informative and wholesome at the same time ♥️ Can’t wait to see the next part!

[@SHEMDPodcast]

Thank you for listening!

[@GreenGiant96]

I've been diagnosed with hashimoto's for 4 years, and what Halsey said made me realize my face skin issues are because of hashimoto's. I know my dry and sensistive skin all over my body was from that, but i didn't know my "rosacea" and "acne" flareups were hashimoto's flares. The only two doctors to take my issues seriously were gynecologists. Other doctors had all said my labs were in range and we'd monitor, but the one gyno said even if it's in the range, it's not where a 20 year old should be. She also pointed out that many of the issues i had then (acne and rosacea, endometriosis, allergies, ibs, etc) were all inflamatory conditions and that something had to be causing the inflammation. A gynecologist obviously diagnosed my endometriosis and the same one years later found my pituitary brain tumors. My male endocrinologist had dismissed my concerns about breast discharge, but she took me seriously. Struggling now with getting doctors to take my joint pain seriously, but still coming up against the "your labs are in range"

[@SHEMDPodcast]

We are happy to hear you got something out of this episode. Thank you for sharing your story and listening.

[@samsidedown]

Miscarriages are so painful, I've had an extopic at 9 weeks and it was even more painful than the miscarriage i had two years later.. what a WOMAN! Only a super hero would go on the stage through a whole misscarrage yo not let ither peoole down. I'm so proud of how aware she is, not many people are on this level anymore ❤

[@emilyonizuka4698]

I've been grilled by my doctor too about my low weight and whether it's because of an eating disorder. I even started to wonder if I really did and was just in denial. I'm also an East Asian woman and there's the stereotype about us being small. turns out, I had a congenital heart condition and needed surgery. I'm so glad to hear others talk about their health problems as well. we all have some kind of health problems at some point in life and I think it would be helpful to actually talk about it more.

[@SHEMDPodcast]

Thank you for listening!

[@Sarahhhhhhhhhhhhhhhhhhhr]

Incredible! I definitely cried a few times. It is so difficult to know something is wrong and not have the answers yet. Having inconsistent access to healthcare is so incredibly frustrating. I just want someone to run a test on me for once so I can figure it all out and start healing. Halsey you are an angel I wish you the best.

[@SHEMDPodcast]

Thank you so much for watching! We hope our episodes can help you advocate for your health and start healing!

[@angelanabozny83]

Ugh , i can so so so relate ,i am 52 i have had a miscarriage and i know that pain ! But god has a plan for each of us and at 48 yrs old i was blessed with a baby ! ❤

[@SHEMDPodcast]

Thank you for sharing and spreading this positivity! We wish you the best.

[@kaylahevans873]

This is such a special episode. Thank you so much to all of you for your transparency and honesty.

[@HelleWeston]

Thank you for this heartfelt, honest conversation. It was so insightful and I love seeing intelligent, empowered women supporting each other like this! ❤️

[@SHEMDPodcast]

Thank you for listening!

[@spookygiggles]

This was such a beautiful interview! I wish nothing but the best to Ash and any other people out there struggling with chronic illness. Can’t wait for part 2, hope it’s soon ❤

[@nugabug0219]

i thought i already had the utmost respect and admiration for Halsey, yet they managed to raise that bar even higher!!! can’t wait to hear pt 2! and definitely subscribing to SheMD. thank you for raising awareness around women’s health!!! after struggling with my own endo journey for the past two years, i’m glad to say i found my own Dr A and am feeling better than i have in many years just ten days out from a proper endo surgery:) thank you so so much for being advocates and activists for women🙌🏻🙌🏻🙌🏻

[@143purple]

Where is part 2

[@SHEMDPodcast]

Thank you so much for listening! Happy to have you in our SHE MD community!

[@toriferguson5]

I relate so hard to the guilt when it comes to being a mom who’s sick. 😩😩

[@petrichoriver]

This is such an important and wonderful episode! Halsey is such a sweet & inspiring person. I hate to know she's had to suffer so much. How much bravery does it take to share your experience in front of so many people? Wow. Big hugs to her! The End & Lucky were so personal, this new album will be phenomenal, I can tell and I'm very excited! I'm glad you're in this world, Ashley. You're a gift 🩷

[@BetteFoord]

As a fellow chronically ill musician, I'm so thankful for Halsey speaking up and spreading awareness 💖

[@Lin-wp2wr]

God I love Halsey so much. Even them talking about how she offered the IVF to someone else instead of taking it. The fans know who she is. We've seen what she's done over the years and how selfless she can be. I wish her nothing but the best, even if there comes a day where we, as fans, cannot be a part of her life anymore. I want her to live fully and happily because god damn does she deserve it.

[@DahshonJahzer]

I do not know, there is just something about her that I love and adore so much. I remember dance class being choreographed into the first Halsey song I ever heard which we had a dance to Ghost right. I started listening to all her albums after and have been following ever since! My favorite songs from her now are Angel on Fire and Control and obviously many many others but stay strong. You are so brave and I love you for that. I am sorry to hear this but I am so glad you caught it early in your life. Your existence is so valued, you shine so bright. From Dahshon 👽🏐

[@alyssarose2468]

Halsey literally is incredible.

[@jessieg1313]

What a bunch of beautiful women! My heart feels so happy knowing that they really exist! And Halsey is amazing!

[@tassirina]

I love Halsey so much, you can tell that she has a beautiful soul ❤

[@Haileycartero]

As someone with Sjogren’s and struggling to get a diagnosis, I needed this interview. I was already a huge fan of Halsey, and now I have even more respect for you. ❤️

[@lafytaffy1220]

So true... The chronic illness is hard enough but then to slowly learn that nobody really cares, it changes your view of the world and your view on everyone you've ever known. Great episode! Thank you for sharing your story! ❤ Thank you for creating this podcast, women need this hands down! 🙌❤

[@SHEMDPodcast]

Thank you for listening!

[@roguelogan50]

Wish I could have doctors like Dr. A

[@nessiequin]

Halsey, thank you for your story. I’m going through the same thing right now. I have been receiving medical testing for possible lupus. Going from doctor to doctor and the increasing medical bills is getting exhausting, but I have hope that I will eventually find out what is going on in my body. I am happy for you that you were able to get to the bottom of your illnesses with these amazing doctors!

[@Wendisoph]

Ash’s story means so much to me as someone who has been misdiagnosed for 10 years. Less than a week ago I was diagnosed with chiari malformation, my cerebellum has grown into my spinal column. I have had headaches for 10 years, was told by a pediatric neurologist at 11 that it was psychological, (this doctor also put me on over 10 medications within a few month period. Never giving them enough time to work. Even amatriptaline (powerful antipsychotic) that gave me bloody nightmares) I’ve been misdiagnosed multiple times. Since it’s been a decade I was so hard on myself why I couldn’t do so many things without getting a headache and my body feeling weak. I thought “wow am I really this sensitive as a person? Am I that out of shape” it’s so reassuring to know that I really do have something wrong with me because I knew something was wrong. My headaches have almost always been brushed off as stress related, and I’m sure that plays a part, but I’m glad finally a doctor decided to look at my cervical spine along with my brain which showed chiari on the mri. Hopefully I can finally get some relief.

[@SHEMDPodcast]

Thanks for listening and sharing your story. We wish you the best in your medical journey.

[@tiabella9516]

Thank you Halsey! I’m from Australia and I’ve been a fan for yearssss, I appreciate you talking more on these subjects, I have endo, and possible other illnesses, but doctors won’t listen most of the times, but I feel as though it would be a bit easier to get through to our drs if we have this information, A big thing that got me is how good you felt while pregnant, and I was the exact same, I fell pregnant 2 months after surgery, and I was taking contraception, at the start I was in pain but after the 12 month mark and afterwards I felt amazing, literally never better, I could eat everything and no issues, it’s made me think twice about sweeping these problems under the rug, having a young child can make this harder as we want to put them first, but we forget that due to our babies we need to get better first. Thanks Queen you don’t realise how much we appreciate this 💝

[@Monkeylover4ever77]

It’s amazing how much your medical journey is almost exactly like mine word for word. I also could tell you more about my body and diagnosis’s than any doctor. And can also identify others issues. I have fibromyalgia, hashimotos, narcolepsy, endometriosis, and other things. I so appreciate you bringing all this awareness. Love you Halsey 💜

[@SHEMDPodcast]

Thank you for listening! I hope these episodes help you get the clarity and care you need to heal.

[@Livedreams9]

The way I would do anything to talk to Halsey and Dr. A. I beg the universe with my entire soul. I wish I had that kind of care, instead of being brushed off and slowly losing all of my light and hope.

[@SHEMDPodcast]

I hope these episodes arm you with ways to advocate for yourself in doctor's offices. We wish you the best.

[@MrsDelenax3]

Thank you for using your platform to talk about these important topics, h❤

[@n.k.pierro]

i am so grateful to halsey and their transparency on their health and wellbeing journey. I've been a fan since room 93 days (even met her at a music festival years ago, coolest sweetest celeb I've encountered hands down) and when they talked about their endometriosis I looked it up and realized I fit the description to a T. So here we are 5 years and two surgeries later with a third one on the books for later this year, which would make three surgeries under 30 yrs old for me. I just hope now that endo is a more known and recognized condition young women can go to doctors and be taken seriously and not just told they'll grow out of it or just put on pain treatments without investigating or addressing the cause. I hope research can find new ways to diagnose endo without surgery because right now thats the only 100% for sure way to know. It is weirdly gratifying though to put a name to and see other people with the same thing that felt and was treated like it was all in my head for most of my life. My best wishes to Halsey and all the endo girls out there

[@olivia.groves]

Just got an ultrasound to see if I have endometriosis. Bc I’ve been dealing with these symptoms for almost a decade. ALWAYS ADVOCATE FOR YOURSELF. Thank you all for talking about this and all the work you three do. Definitely do not feel alone and will take it day by day once I hear the results. Shoutout to the nurse practitioner who ordered me that ultrasound and listened to me. My gyno that I used to go to DID NOT.

[@thesacramento_chef]

I’ve had adenomyosis and had a hysterectomy and was also diagnosed with stage 4 endometriosis. I’ve had 5 excision surgeries by world renowned endometriosis specialists and it’s come back again….and now I’m currently dealing with severe endometriosis pain and am currently being tested for RA and Lupus. It’s so debilitating and hearing her explain the extreme fatigue and hair loss that comes with the symptoms of lupus really resonated with me. I just got my blood test results that are all pointing to lupus and RA. Everything she said about what she’s experiencing is exactly what I’m currently going through. I hope there is light at the end of the tunnel for me as well.

[@Me_1983-]

I'm glad you are going thru all the testing. Our stories are so much alike, I had a full hysterectomy at 38 with the same issues. I also have lupus, RA, and fibromyagia with complications from each. The sooner you get in with good specialist the sooner you can feel relief. Prayers and good energy your way

[@sspiker]

I wish I could have seen this interview when I was a new and young parent. The difference it would have made... especially with the guilt.

[@Philoishness]

So much respect for halsey for being open about these struggles!! I have just started the process of trying to figure out my own health issues i've been having for half my life after i had been dismissed and misbelieved so heavily that i have extremely bad perception of my body now. Hearing them speak about their own body with so much understanding and knowledge is very inspiring!

[@haannnaah]

So, so unbelievably proud of you Ashley. I'm so, so glad that you're alive. I've been here since the start, and I'll always be here. You're an incredible, strong and brave person and an amazing mother.

[@JaclynK.]

37:45 so rare for a doctor to go to bat for you 🎉 I applaud this team work between patient and doctor here❤❤

[@AbigailColeman-l4j]

I’ve been a Halsey fan for a while now and though I don’t feel heard I’m currently trying to figure out what’s going on with me. Thank you She MD I’m not giving up 😊

[@SHEMDPodcast]

Don’t give up! Always advocate for yourself🤍 hugs to you!

[@tarynb2287]

I love how real halsey is, Ive watched her music videos and listened since the beginning, also I connect with her about having endo(its brutal, I had surgery for it in 2009), bipolar, my step mum has lupus and I have so much sympathy for her also she's just such a inspiring woman and Ill always be a fan. Xx

[@Ash_Ley925]

Ahh when does part 2 come out?!? I need it now hahah

[@ishathompson8439]

Next week Tuesday

[@Seschal]

They didn't go into what Halsey said at the end about Ketamine therapy, but if you struggle with medication-resistant depression or addiction, PLEASE research it and find a clinic in your area to get on the waiting list (it's a multi-month therapy and clinics don't have alot of spots).

[@Rohpink]

there's a part 2

[@SHEMDPodcast]

Find more about Ketamine therapy in part 2! Thanks for listening.

[@wayviay]

I learned a lot. Glad that this was recommended to me.

[@SHEMDPodcast]

So happy you enjoyed! Wishing you all the best

[@sammiejo163]

Currently having intestin and kidney pain but I can't go to the doctor because I know I'm just gonna be told, take this and see if it works, and when it doesn't, I'll be sent to the next doc that says "you're fine". I don't have the money to be going to the doctor just for them to write me off to the next. I just went through this not too long ago with a tailbone issue. I saw 3 doctors! Months before that I had hand foot and mouth disease and I was misdiagnosed with strep throat. The felling of being helpless and hopeless never ends.

[@SHEMDPodcast]

So sorry to hear this. We hope these episodes can help you get some clarity. We wish you the best.

[@SashaC23]

Holy smokes! I'm not the only one that does the, "Have you had your thyroid checked?" thing all the time. Researching medical terminology and diseases is so interesting. It's like putting a puzzle together about how each human body functions. Also, a hashis girl here. 👎 Autoimmune diseases suck. Not trying to be a "fan girl" but Halsey and I would definitely hit it off as friends irl. Maybe her aura and soul is why I've always been drawn to her and her music. 🤷‍♀️ A Halsey docu would be sweet, btw. Waiting patiently for the new album and hoping her health and strength continues to improve more each day!

[@SpaTherapyRain]

Thank you for this interview! I was diagnosed with endometriosis and it’s definitely a struggle. Appreciate Halsey for sharing your experience and to the doctors for their help with understanding this diagnosis.

[@SHEMDPodcast]

Thank you for listening!

[@elisabethpatterson9417]

Great video! Thanks for sharing, I'm so glad Halsey is feeling better. xoxo

[@TheKatarinaGiselle]

The same is true for all women who have any autoimmune disorder and are pregnant. The best I ever felt in my life was the times I was pregnant. My sister also has severe health issues similar to mine, and she ended up having five kids. I wanted to have more because I wanted more kids..but also because I felt better pregnant. Like a super hero! Actually healthy, every time my sons weaned from nursing, my health got progressively worse fast. My sister is 6.5 yrs older and like I said she had five. I stopped because it seemed after each pregnancy, her health got worse and worse ONCE she wasn’t nursing, at this point, she doesn’t want to live and says she has plans to end her life this fall. I don’t buy the threats, but I understand completely because if she is worse off than me, and most days I’m in so much pain that I feel like dying..then I can only imagine how she feels. I am 36 now and if I could, I would get pregnant.

[@SHEMDPodcast]

Wow- that you for sharing this story. These disorders can be so debilitating. We wish you and your sister the best. I hope these episodes can help you not feel less alone and help you advocate for answers.

[@morrigansmagikalmakings]

Can't wait for part 2! I had adenomyosis and still have some undiagnosed issues and it means so much to see conversations like this ❤

[@Damanique]

Halsey is such a beautiful soul and she's gone through so much s***... I have struggled with my health a lot too (6 surgeries, PCOS, ovarian removal, early menopause) so I can really relate to what she's gone through. Halsey really shows that being a musician and a pop star is just one facet of her life and she's a human with flaws and all. Many of us suffer the same illnesses without the fame, and it's not easier or harder. It just sucks and it can happen to anyone. And I admire her for being open about it, pop stars are not perfect, they are people, and they try to live their dreams and have their career just like us.

[@SHEMDPodcast]

Thank you for listening! Dr. A has started a PCOS paltform (ovii.com) and a PCOS support facebook community if you're interested in joining. facebook.com/groups/oviipcossupport/

[@fani437]

I'm so glad I clicked on this video 27:21 || 29:50 This is exactly what I felt 3 years ago, the organ pain. It would start in one place and travel down through different parts of my body. It was very painful and just strange. I just kind of dealt with it up to this point, especially the fatigue and bone(?) pain/ stiffness. I had an mri, X-rays taken but nothing out of the ordinary, so I kind of lost hope in knowing what was going on. plus, it happened around the time I got COVID so it was just kind of lumped into maybe it was post covid symptoms, but I knew there was something different going on. To this day, I haven't been diagnosed with anything. Watching this video, gave me some sort of hope, I'm almost 29.

[@SHEMDPodcast]

Thank you for listening! We wish you the best in your health journey.

[@tarastone4417]

Thank you! Us women need to share these stories! This was so interesting and inspiring.

[@SHEMDPodcast]

Thank you for listening!

[@georgettecastillion]

So0o.... ncredibly relatable. I have experienced very similar issues. Currently, I am searching for a new doctor that cares like Dr. A does! Thank y'all for sharing such imperative information & Ashley for always being so vulnerable. I pray that she finds a way to not be so hard on herself and give herself grace! She always utilizes her voice and experiences for good! This helps more than y'all realize! -xo

[@JaeLynn2121]

Halsey is my everything ❤ hoping hearing her struggles helps many women out there suffering as well. She is absolutely the kindest, sweetest, most authentic genuine person & is so incredibly talented. I dont even kno where'd id be without her music & poetry ❤ cant wait for the 2nd half! * & her NEW ALBUM!! 🎉 🌟 #luckyforhalsey

[@Monkeylover4ever77]

Oh my gosh! I felt the same during my pregnancy!!!! And I have lupus markers, but not a diagnosis’s I fight extreme fatigue. Man I wish I had your doctors