Whats wrong with me? // My Disabilities (Updated) [CC] 

I think your grandfather was a time traveler who saw your pain and decided to go back in time to try and help you

Thank you Jessica for acknowledging and pointing out that doctors don' t take teenage girls seriously when dealing with eating-related problems!

Wait a second her grandfather’s clinic, that was named after him got her disability wrong? That's ironic.

When I was a kid my cardiologist told me that my aorta was probably bigger than everyone else’s in my class. I was really proud of this as a kid. I feel like this is the best way to tell a kid they have an aneurysm.

💫 One thing right with me.... I watered my indoor plants today, and fed my cats. I accomplished keeping others alive.

When you said that people who have mental health issues are champions in your eyes it generally brought tears to my eyes. Thank you.

My mother suffered from multiple autoimmune disorders, including Crohn's disease and rheumatoid arthritis. She also had mental health issues, including PTSD from a severely traumatic event in her childhood (she was a witness, along with her mother and siblings, to her father's suicide by shotgun). And yet she taught me how to love, she taught me how to laugh, she taught me how to forgive. She, somehow, taught me peace of mind. She passed away nearly 4 years ago. What's right with me? I was raised by a mother who was, is, and always shall be my hero.

somethings right with me: -my eyes are pretty -i'm compassionate -i'm still alive and kicking and ain't no bitches gonna bring me down

I’m a real heathen and just grab the loo roll with my whole hand

⭐️ One thing that is right with me: My ADHD means I get far more excited about things. When I dive into something I really enjoy, the physical feeling of excitement about learning and expanding my horizons is really amazing.

Jessica: those of you who deal with mental health issues are absolute champions in my eyes Me: *sobbing*

One thing right with me: One of my recent medical tests said that my gallbladder is unremarkable...so there's that.

I was diagnosed with hEDS at 16 (7 years after the onset of pain). Mine came with the trifecta as it'a called (POTS, MCAS, EDS) as well as mild gastroparesis, hearing loss in one ear, intense migraines, scoliosis and my heart valves thickening because why not. According to three primary doctors I saw as a teen, this was all growing pains and anxiety. Well ha. Jokes on them. My body is actively trying to kill me.

My ENT did an MRI of my ear bones and found they aren't where they are meant to be and he says this is likely do to having Ehlers Danlos and why I'm deaf. That might be what people are talking about when they talk about the connection between EDS and hearing loss. One thing that's good about me is my smile 🌟

2-3 weeks ago, this video came up on my "suggested for you" page, even though I had never seen any of your videos. As you talked about your EDS, I started thinking it all sounded like what I've gone through my whole life, and doctors could never tell me why. Fast forward to this morning- I was officially diagnosed with hypermobile EDS, and I cannot believe I finally know what is going on with my body. Thank you so much for talking about this and bringing light to it! I would have never known!

Fun fact: People with hypermobility/hEDS/EDS are 3 times as likely to get a migrane and get twice as many headaches than most 'normal' people. It's not like we suffer enough though

my PTSD mixed with ADHD gives me the right amount of brakes to stop me from being too excited and hurt myself but my ADHD gives me the power to continue functioning. Somehow a better combo than I thought

🌟 one thing that's right with me: my depression and anxiety makes it easier for me to empathize and connect with other people because i feel emotions so deeply.

⭐ My autism makes me more conscious about helping others be comfortable since I'm hyper aware of every little thing going on.

You’re literally the first person I have ever seen talk about POTS. When ever I explain it people tell me I must just be out of shape🙄 even when I got medically diagnosed at 15 people said I was making it up and wanting attention. Bc I randomly fall over and pass out for fun

I've had depression and anxiety in varying degrees since high school, and even though I know exhaustion is a side effect of both I still find myself feeling almost guilty or weird that my answer to "how are you?" is always "tired." So, thanks for calling us strong. Sometimes I just need to hear someone else acknowledge my efforts to put one foot in front of the other.

My autism helps me remember stuff I read years ago in great detail.

🌟One thing right about me: Because of my ADHD, I can hyperfixate on a specific subject and retain just about everything about it! Want to know about Dallon Weekes, Furbies, or Conlangs? I'm your guy!

So because beautiful Jessica decided to share her disabilities I'm going to share mine. I've pretty much had OCD since birth. And not like the, "oh I'm so OCD" OCD. The real clinically diagnosed OCD where I constantly deal with thoughts that tell me I'm secretly a horrible person who's going to loose control and kill everyone I love in horrible ways. Also have clinical depression because of this too. Lastly, I have a condition called Generalized Vulvadynia. This makes the skin or my entire vulva, (which includes my clitoris, labia, urethra, and the entrance to my vagina) feel like it's being burned with battery acid. One thing that's right with me: I'm still alive and determined to get the care that I need.

One thing right with me: I have synesthesia, which allowed me to write a novel about a entirely unique superhero!

A round of applause for Jessica for not only dealing with all of this daily but also taking the time to explain it to thousands of people on the internet in an effort to educate. You're a rockstar!

EDS diagnosis in Germany: "Don't do Google, then you'll get better soon." This video should be shown to every doctor/physician. It's an perfect shortcut about the most important comorbidities. "You must be psycho, can't have that many exotic diseases..." 🙄 Thank you so much for your work!

"They make a rainbow and they're fun" you're adorable

'At least its interesting' Oh mood. What mystery symptoms will I experience today? Nobody knows!

⭐ one thing right with me is i remembered to take my meds and eat something

I was like "oh Jessica your eyebrows weren't that bad, that's when I started watching you!" And I went back and looked and well... Your eyebrows do look lovely now!

I have so many of the same symptoms as you Jessica, always have, and was just going through the "Omg are all my different mystery symptoms eds??" last week before I find out 2 says ago that you now are also diagnosed with eds. Always thought everyone else could do the thumb thing too lmao. I am going to try and get my doctors to rule it out or at least try and look a little bit harder for the reason I'm in pain all the god damn time and all my joints click and pop and HURT instead of them saying again to me, "that's just normal". It's exhausting trying to work out why your body does what it does.

I feel like i get sassier just from watching you. You indirectly inject me with sass.

"might be having mini strokes" she casually mentioned

My partner also has EDS, and he finally found a gastroenterologist a few years ago who’s wife actually has EDS and would take him seriously. Several other people in his family also have it, and their high levels of daily pain is often written off. I wonder if the difficulty in getting care is similar in US and UK.

I'm allergic to 6 different metals including Nickel which is in literally everything since it comes from the earth so yeah everything. Including Cobalt, the color, cheese, butter, and oil. Then there's Gold, Titanium Oxalate, Palladium, and my personal favorite... Sodium. I had no allergies to anything until 27 and became allergic to EVERYTHING! At least I don't choke and die when I cheat on my diet, I just have excruciating internal pain. It affects my nervous system as well as the connective tissue around a few vital organs. This is all long term so it's all down hill from here. 4 years later and I still can't stop eating chocolate occasionally no matter how itchy my throat gets and I want to cheese grate it lol. I can totally relate to this beautiful specimen of a woman although I believe her to be much stronger then I. She gives me hope. I've always had a similar sense of humor and I think that was to prepare me for the shit storm of my life. Now I am much more at peace with myself but as for others, I'm pretty sure everyone thinks I'm making it up as an excuse to be a size 0- 2. Even though I've been 5'2" and petite since junior high. But nonsense, I've made up an allergy and got deathly ill lost all my body mass and had diarrhea at least 3 times a day plus countless other symptoms all faked for the sake of being a tooth pick. Yup that's exactly it. This really made me not feel alone. Maybe one day my allergy will be recognized in the community and people will have a little Fucking respect. God bless xoxo

wait, not everyone can touch their thumb to their pinkie? ...huh

thank you for the shout out to us mentally ill folk. one thing we need to do better is support people with physical disabilities too, especially invisible illnesses

Glad you got the diagnosis... I know I have EDS but my local rheumatology department quote "doesn't see the point in seeing me to diagnose something they cannot cure thus wasting spaces for people actual curable conditions" that's nice 🙄🤷🏼‍♀️... Without the diagnosis I cannot get support for work or increase my likelihood of qualifying for disability benefits because my other 15 conditions don't quite cut it 🙄

⭐️⭐️⭐️One thing that is right with me: even though i cant explain things in jargon because i cant process a lot of the big words, i can explain the most complicated things in laymans terms which makes me a super easy to understand and i often am able to tell my friends about Big Issues without scientific jargon and they find me easier to understand than articles!! meaning i can probably be a good teacher

I just got an ad for “Deaf Works Everywhere” and you were in it! It was an incredible ad and I watched it all the way through (:

In literature there are different kinds of irony. I guess this would be situational irony.

Its faintly surreal learning the ins and outs of modern medicine from a model from the 1940s (I mean this in the best possible way)

"... So that means I can wrap my fingers around my wrist and do THIS with my thumb" ... Sudden concern because I not only do both of those but have a small swarm of other problems... But also, as someone with a laundry list of mental illnesses that I'm only now discovering the true depths of (thanks, Canadian health system)... thank you????

At 66 my MS diagnoses has been changed to EDS! Who knew?! Learning to walk on the treadmill is my favorite thing right now.

So glad you found someone willing to do your microblading! The eyebrows look great :D PS Apparently I've been grabbing toilet paper wrong my whole life????

One of my close friends has EDS. She's 27 now, and when she was diagnosed at 11, she was told she would end up in a wheelchair, likely by the time she turned 40. Now, 16 years later, they've changed it to 30.... She dislocates everything. Literally everything. Jaw, vertebrae, fingers, toes, kneecaps, etc. As a child they just seemed to think she was a klutz, until they realized she wasn't after she simply rolled her ankle.... And dislocated it. I worry daily about her, but she's pretty acceptant of the fact she's going to end up in a wheelchair. She is currently finishing up her master's in gerontology (her second!) and is married to a neurologist. Those of you who have EDS, the day I met her after being online friends for a good two years, I was tackled outside of a coffee shop. You'll be okay. I promise. :)

I had a brain tumor for over 30 years and chalked up the symptoms to ADD, klutziness, migraines... you name it. It's so important to get the right diagnosis, if only so that everything finally makes sense. A year and a half ago I went to a wonderful new general family doctor who said "Let's get you an MRI" and so I'm alive to tell the tale. You're an inspiration.

✨EDSer. One good thing about me...when the horse I ride fell , I bent three allll the way back. But thanks to EDS, the ER/Casualty/A&E doc said nothing was broken. Which turned out to be untrue. I had broken my pinkie finger, which I discovered a month later. But thanks to EDS, having a small broken bone was no more painful than other parts of my body. And now the hook the surgeon put in comes out on Thursday and I am very excited. Even though I have been horse riding anyway. Because when you have EDS, you can hurt yourself while doing nothing, so may as well do stuff...because horse riding accidents make for better stories than, “So there I was, doing nothing, when my rib joint ripped out with a loud pop...” So...YAY.

⭐️ One thing that's right with me: when the depression brain fog lifts up at least for a bit, I'm an incredibly apt and fast learner. I'm actually in the process of teaching myself social media marketing so that I can make my living via freelance!

Oddly encouraging to see people with lifelong chronic health issues still going through the diagnosis process! Like it's not just because I'm newly seeing doctors, it's just because doctors suck

a good thing about my autism is that i'm always excited about stuff and never bored

TITLE: "What's Wrong with Me?" ME: "Wrong"... Absolutely Nothing! ⭐⭐⭐⭐⭐ Hello Jessica. Regarding the naming of the Rheumatology institute after your grandfather - I don't know about "irony", not meaning to be rude ... but maybe it was unwelcomed foreshadowing? Um, moving on ..... I find it incredibly generous and thoughtful of you to welcome those living with EDS to interact and communicate and share their experiences with their diagnoses. A comfortable, safe space for people to know they are not alone can only be beneficial. I for one always appreciate your openness and honesty regarding disabilities and the respect with which you show not only yourself, but this community you have built. One thing right with me ... 🤔 ... well, I was diagnosed Diabetic 2 years ago. After dietary and lifestyle changes, at my most recent appointment, I was confirmed to no longer be Diabetic. Yay! Thank you for the video, Jessica! I am so sorry about your arm and having to wear that wrist brace. On the positive, your sleepwear looked fabulous! Silver lining! ... haha 😅 A pleasure seeing you. Take care!! Lovely as always 👍🤟💝

⭐️ when I smile, others will often smile back. A bit like a superpower

My new psychiatrist told me she didn’t want to minimize my anxiety or my stomach issues and I honestly don’t even think my gastroenterologists have ever said that to me. I hate how much I’ve been told, essentially, that no one can do anything for my IBS. Sigh.

As a fellow hEDS'er with Marfanoid Habitus, I almost fell out of my chair when you said you were allergic to Aloe!!!! Me too! It's one of those things no one believes. You did an amazing job with this video educating about the different types of disorders simply. I am so happy I found another person who is as "happy" and sarcastic about their lot in life and thanks for making me feel less alone. 💗

As someone who has dealt with mental health issues my whole life, and who is now on disability and unable to work because of them, I just wanted to say thank you. In the past I've dealt with friends who blamed me for me mental illnesses and recently with dear friends complaining that my "negative energy" was bringing people down. So to have you, someone I admire who has so many struggles of your own, call someone like me a champion...It made me tear up. It made feel seen. Thank you. 🌟Something good about me is that almost 31 years since my first mental health diagnosis (and there have been many more since), in spite of insurance problems and treatment failures and everything life just throws at you...I am still here. I am still trying to get better.🌟

🌟 One thing right with me: I have naturally fantastic eyebrows. I know, I know, I shouldn’t brag. Well instead how about: my super long arms mean I can reach things on the high shelf rather than getting out the step stool. Also, you’ve made me really consider how I pull off toilet paper. Evidently I just grasp it in my fist and like, twist? 🤷🏻‍♀️

⭐️One thing that's right with me: I am working through my past of being manipulated by a childhood friend and my ex boyfriend and my bond with my sister has never been stronger!

🌟 something that's right with me: uh my ADHD makes me very good at connecting the most random stuff. I'm like that guy in that one buzzfeed unsolved meme going "I've connected the two dots" only I've actually connected them. So that's a plus.

⭐ one thing right with me: I persevered through the first two year of college into finding a path that's actually really interesting to me and pays well! In about a year and a few months I should be graduated with a degree in medical technology 😁 also I have a cute nose and cute hazel eyes

I have six kids and still seem sane. ⭐️

Honestly it's always a comfort to see people with EDS talk about it. When I was diagnosed at 13 the "selfhelp" group was just 7 adults all saying they had it worse than the others, ignoring me and not actually acknowledging any way to help each other make life better. Now almost 15 years later seeing people take it in stride and talk more about it is giving me hope that other teenage girls won't feel as alone as I did when diagnosed

I’m sure most of the 1.9K comments so far say the same thing I’m about to say, but THANK YOU. It’s unbelievably comforting to hear you are not the only one.

⭐ One thing right about me: compensating for my flat feet my whole life means I have some pretty rocking calf muscles! Also thanks for calling those of us who deal with mental illness champions. I didn't know I needed that.

I kinda want a t-shirt that says "Leave Jameela Jamil and her peanuts alone!" and then wear it around for solidarity. Would that be okay?

Hello lovely. So I have only started watching you this week. I have had so many symptoms since the age of 14 and could never get an answer for them. After listening to your stories it hit me like a ton of bricks. I immediately called my mother and my aunt. One has Fibrmyalgia and the other has Rheumatoid Arthritis and low and behold my cousin has EDS.... And I am going to my doctor soon to bring him my evidence and to see a specialist. Thank You so much!!!!! I can't explain how grateful I am that you've shared your story and will continue watching you lovely lady! You're spectacular.

Kinda unrelated, but had anyone else had a PE/Gym teacher who just wouldn’t accept that you simply can’t do some things/is rude about it? Mine came to me the other day and said to me “remind me why can’t you play volleyball”, I said “because I could be hit in the head”. She then said “well don’t you have physio exercises to do?” I responded “yes, but...” she interrupted “well why aren’t you doing them?” I was on the verge of tears because I have an issue with confrontation as well as with people being upset with me, especially teachers/parents. She finished with “Remember this is your responsibility, I shouldn’t have to make you do things”. Isn’t her job to tell students to do things? My friend overheard it and said she nearly slapped the teacher. Idk, I wasn’t in the right, but damm, that made me feel stupider than I normally feel.

EDS and the dodgy mast cells that come with it make me allergic to aloe vera too! And the cold. I've never felt so seen than when I watched this video. Also in the hearing loss gang too ♥ Accurate labels matter when it comes to what's 'wrong' with your body, so I'm glad you finally have this part figured out

✨ I have Eds Fap and Hnpp, and I manage to get to medical school to become a rheumatologist for paediatric patients hopefully

Okay... I think this video is going to save my life!!! My mom has had many digestive problems, stretchy skin in weird spots, ability to wrap limbs and joints in abnormal ways, random changing allergies, unexplained migraines, weird heart arrhythmia and blood pressure control, etc. etc. and in addition to all of this, I have severe amblyopia, and that illustration explains a lot. I also have super unbalanced hearing, and my jaw does the popping thing and my mouth is crowded, so... what do you think??? No explanation for any of this...

The irony that you feel thankful your mental health is good. I as a mentally ill person always remind myself at least my body usually works (besides some fatigue and muscle tics from meds). Its a universal trait of the ill or disabled that we always think "oh it could be worse" about ourselves yet have total sympathy for others.

🌟 struggling to think of something good with me. My lungs work. That's good right?

I have bipolar, anxiety and ocd and I never feel like I’m a champion, but thank you so much for making me feel a little better about me, Jessica. You are the real champion

"They make a rainbow and they're fun!" Yes. Yes they are. Very cute, must buy for my meds!

I’m 20 and have been pushing for help since I was 16 when I started experiencing gynaecological issues. Over the years, either I’ve gotten better at noticing what “isn’t normal”, or my body is declining at a phenomenal rate (!) I’ve recently had the term “hypermobile” loosely slapped on me, and my spine has “age related wear and tear” (age related?! I’m 20!). I’ve forcibly had myself referred to rheumatology though, as the neurologist passed me to neurosurgeons, who immediately passed me to orthopaedics who referred me for physio.... Which did nothing because it was all behaviour I’ve automatically been doing for the last 10 years of my life. What’s one thing that’s good about me? 🌟 My resolve. I *will* keep going, despite what my body says, despite what the medical field says, and despite what society says! Jessica, if you see this: thank you so much. I hope one day i can meet you in person and truly express my gratitude.

⭐️ I’ve finally been able to get my depression under control, which is especially important as I recently had a baby and my postpartum depression was horrible with my previous pregnancy. I’m proud of my neurotransmitters as they have finally figured out how to let me human properly, albeit with medication, but I’m totally ok with that.

Sometimes when asked "what's wrong with me?" My instinct is "what's RIGHT with me?" Because there are so many things "wrong" would me.

This is such a good video! I have autism and struggles with a lot of stress related symptoms both on my body but also mind (like depressions, burned out for 3 years, stomach problems, bad sleep, anxiety etc) . It’s nice to see that a person you look up to can still make an functional life despite your disabilities! I’m 27 and haven’t had a real job yet but I’m gonna continue to fight to get a functional everyday. Thank you for a nice reminder!

"A standing war with garlic" are you actually an immortal vampire

I got my EDS diagnosis about 6 years ago. Welcome to the club! At least we have the silky smooth skin and looking young forever thing going for us, because most everything else sucks.

🌟 I've got a lot wrong with me (thyroid issues, migraines, anemia, asthma sciatic pain,depression,anxiety etc...) but one thing that's right with me is that I'm pretty good at remaining positive when I need to! You are inspirational and amazing and such a lovely person! Thank you for everything you do! Also your wife is fantastic and your dogs are the cutest! Love you!

🌟 something right with me - I'm still here and I'm still trying

Just watched this w my 9- and 7-year olds. Had to pause it a few times to explain things: lesbians and cats! The similarities between having difficulties w the coating on the nerves and MS, which their grandma has! How often 20 migraines a month works out to be! When you got to the bit about being amazed by people w mental problems being the 'real heroes' I got a couple hugs, because my boys know about my depression and anxiety. They did start pretending to shoot each other towards the end, because 7 and 9. What I found interesting and important about watching this w them is how easily they accepted this laundry list of, difficulties shall we say, and just tried to imagine life with them without making any major assumptions about what a person could or couldn't do. I appreciate your making this video, and am glad I got to watch it w my boys. So thank you!

A good thing about me is probably that despite having multiple mental disorders I absolutely refuse to let them run my life and try to get up every morning 🌟

🌟 when I was in the hospital, and one of my symptoms came up as “giddy”, I had to explain to my doctors that I was ALWAYS giddy. It’s not a symptom, It’s my nature! Note: they still consider it a symptom. In any case, I’d count this as one good thing about me. I think giddy is wonderful. Also, my ability to sew. I recently got a new sewing machine and it’s wonderful, because my old machine was hell on my arthritis. 🌟

⭐ One thing that is right with me - my experience with mental health issues has given me a platform to share my experience and help others

I’m 16 and I’ve never in my life met anyone besides my mom & sister who have eds. My mom didn’t know she had it until she was in her 20’s and of course she passed it down to her kids. No one knows what it is and I barely know what it is! There are so many random symptoms to it and there isn’t as much research as we need for it, so I really don’t know exactly what things it does affect. I’m hyper mobile, deal with constant joint pain, have severe migraines, chronic fatigue, terrible stomach pain, and more random ones, also my fingers are also extremely bendy like yours. Mine also came with hyperhidrosis (basically just sweating way way too much) which is the most embarrassing part for me, bc the people around me like teenagers done get it. It sucks to deal with these things so it’s nice to hear someone else having the same struggles as me. Stay safe during this time please

For the toilet paper problem: I always rip it off using my four fingers pressing towards my thumb (if that explains it well... I don't know...) and I have yet to discover to have any connective tissue disorder. I'm just clumsy. :-D

What's right with me: 🌟 I finally got all my meds prescribed since moving to the UK, and I can now pick them up once a month because the magic of repeat prescriptions. Took some time to get on order and get used to because other issues, and just not being used to only getting meds for a month at the time even if you need them for life.. 🤷‍♀️

I have hEDS, diagnosed initially in 1993 when I was in 3rd grade. Problems with hearing, tmj, my guts forgetting how to gut and digest/move things, and sudden blood pressure drops when I stand... the fun list goes on, and it can be so ridiculous. I have food allergies that are a roulette - will wheat make me sick today with wheezing/hives? Who knows! I was diagnosed with Rapid Cycling Bipolar I in 1999 - and that has been a pain because doctors see the diagnoses and ASSUME I'm attention seeking because of the Bipolar. Yeah, no, medicated and stable. It's all my body trying to kill me. /rant BUT! What's going well? I finished my 8th novel and am actually revising this one for sale, and that makes me SUPER proud of myself. :) 75,000 words is no joke, and I'm going to PUT IT OUT THERE. Terrifying.

I’ve Got Pots, IBS, fibromyalgia, and mayyybe mini strokes? Migraines too Wheeee chronic pain is a trip.

⭐️what's right with me. I'm no longer afraid of wearing crop tops

🌟 Your hair is lovely indeed! Right with me is that my HRT is finally starting to show signs of working well which I'm super happy about!

One thing right with me: I managed to escape from being a constantly emotionally distressed and bullied athlete who literally broke down every single game(almost always due to my teammates pushing all blame for lost onto me) to a happily manic artist, actor, and musician. Aka: becoming a band, chior, drama, and art kid saved my god damn heart- Aka aka: Dont force yourself to stay in things that make you miserable out of obligation kids, do what makes you happy

Going for a psych evaluation in 2 wells since after a therapist, a psychiatric facility and another therapist I still have no idea what is wrong with me. Sooooo hopefully I can finally get a compelte and full diagnosis to know what the heck I’m even dealing with aside from depression and an ambigious anxiety disorder. Funnn times today I made my teachers laugh! I’m told I’m very funny and I want to make others laugh as much as possible!

I'm finally early !! Ehlers-Danlos zebra gang 💞🦓💕🦓 I love seeing other RU-vidrs i can relate to :') also i was one of those commenters saying "lmao it's probably EDS"

a lot of this sounds uh... really familiar! like a lot! where would I go to start figuring this stuff out? also, something right with me is that I have very good color vision

*Gold Star*!! Your list of what is 'wrong' with you looks a lot like my list.I'm truly sorry about that. But I loved your idea of listing something that is *right*, so here goes. I love that I advocated for myself and got a power chair. I truly feel like I have my life back now, with some slight adjustments. So yay for my stubborn, willful streak. :)

I'm really surprised Jessica doesn't have epilepsy given her migraines, memory issues, and EDS. Then again, I have the same issues and they missed it; comorbidities are complicated and I wasnt aware focal seizures or absence seizures were a thing until I was told I had them. It doesn't help that I kept forgetting they happened either 😆 but I'd definitely look into it as some of what you're describing sounds like seizures. In that case starting epilepsy medication could help with migraines/memory issues. At least they have in my case (for the most part), but anyway, I wish you lucky on your medical journey!