Surgery Tomorrow, Health Update & Where I'll be...
ฝัง
- เผยแพร่เมื่อ 7 พ.ย. 2024
- update & where I'll be. ✖✖
If anyone's in a similar boat with chronic pain and has hit rock bottom, there are therapists (covered by most insurance) that specialize in specific illnesses/conditions that you can find by searching this database: www.psychology...
We got this, ya gotta keep goin man. Brighter pain-free days ahead, I do believe that. Love you guys. xx
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// what I'm wearing //
◇ butterfly shirt: shrsl.com/2mb6b
◇ earrings: rstyle.me/+w8X...
◇ lips: Dime Beauty Leo
◇ nails: kl polish sophie
◇ necklace: miranda frye London code "WYNN10" for discount bit.ly/360xKqO
◇ will ask the window cleaner where he got his boots and report back
◇ bucket- lowes maybe?
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Chronic pain sufferer here! If I hear “give up gluten” one more time.......
Seriously! And "are you drinking enough water?"
Or, "you just need to exercise more.".....
Have you tried...? Ugh!
So true. Migraines from degenerative disc disease in my neck and everyone try’s to tell me to work out! Ugh. Ok let’s go run on a treadmill. 🤦🏼♀️.
I agree with all of these 😂... like I'm liable to throat punch someone!
I don’t even want to hear “I’ll be back as soon as possible.” Don’t even do that! Take all the time you need. We love you 💛
Yeesssss!!!!
It’s ok to be gone for awhile! Take your time and heal! We’ll all be here when you come back! It’s ok to take a break!
Prayers for fast healing! 💕
I frickin’ feel ya man! Take care.
Please take the time you need....rest and recuperate. Then take more weeks than that!!! Your mind will probably tell you to go back sooner than what can help your body heal!!!!
1000% agree!
Yes ❤️
We need to ALL rewatch her videos. Watch the ads. Don’t skip them.
Yes! Turn on auto play on a device and let the videos run when doing chores 🤍
This is exactly what I was thinking. Let's make sure that she still has some ad revenue coming.
Agreed!!
This is a wonderful idea 🖤
Agree! Great idea ☺️
I teared up when you were talking about just wanting ONE day. I feel that so hard. I’ve had chronic migraines for over 15 years and have 3-6 migraines per week. I also go through 30-40 day spells with every season change. It just turns me into a different person - resentful, sometimes completely void of all happiness. Many nights in the ER yelling at my husband to just kill me - and I am NOT a suicidal person..the pain seems to just possess me. And even on good days, I still don’t truly know if it’s a good day because I normalize pain - I started to consider 4/10 pain as “pain free” even though I wasn’t. And I’d work my 9-5 job with that pain because the alternative is not working at all, which makes it hard to explain to people how I feel because “if I feel good enough to work, I feel good enough to do XYZ...”. Anyway, thanks for sharing. Migraine community is strong because it’s one of things that only the people who experience can understand. I hope you get some relief ❤️
I connect to what you wrote so much. Wanting to die but not being suicidal. Season change. Everything you wrote. I’m sorry you are going through this too. Not giving advice but if this can help anyone else whose at the end of their rope and tried it all... then it’s worth it to share. I came across the work of Nicole Sachs and have been doing her practice and wanted to mention her name if she can help you too. I know the fear and expectation and also the desperation and finally seeing some light in all of this is encouraging. Praying you have relief soon
Thank you for writing this. I’m crying because it describes me... I’ve felt so alone for so long.. I hope this community helps me.
That was me 6 years ago when I was stuck in a horribly stressful corporate job raising my kids alone.
I've also suffered from chronic migraines for decades. For me, they were mostly triggered by an undiagnosed thyroid problem that got 85% better once I treated my thyroid with meds. Every couple years I will have a migraine so bad I end up in the ER, but it's nothing like it used to be. I can relate to what you are saying and am sending you good thoughts & wishes.
I relate to this comment sooooo much. I have done everything to try to find a solution and I’m at a loss.
All of Taylor’s peeps should start binge watching all of her old videos while she is gone. We can help her keep income coming in simply by watching. I am so glad you are taking a break! Please take as long as you need. We will all be here when you come back.
Amazing idea!
Great idea!
That is exactly what I'm going to do! Watch some older videos to still get my daily dose of Taylor until she is back 😁💕
Share them too
Like ones that you haven't
Comment too, push her into the algorithm.
Fantastic idea! I'm totally doing this!
Yelling at my screen “YES TAKE TIME OFF GIRL” no true fan would disagree with that. Hoping for the absolute best from this surgery for you. ❤️❤️
“Doctors don’t listen”. The understatement of the century. Brutal.
Older male doctors do not listen to female patients
Tell me about it!! 🙄🤦🏼♀️
@@catnip4587 neither do the females!
When you have a chronic illness that most docs don't believe is real, it's a nightmare getting anyone to help! Even though it's a neuro-immune illness 😔
@@lindatannock I got told stuff is in my head and its aniexty...I still have no answers 😕
@@sweetiestrawberrie15 Ive been told the same thing for the last two years .
I'm only a pre-med student but your story is inspiring me to really listen and hear out my patients when I am a doctor one day.
Ok I'm dead. She added the window cleaners bucket and boots in the description 🤣🤣🤣🤣
Dead😂
😂😂😂 Thanks for pointing that out! Hilarious!
I’m so glad you pointed that out 😂😂
that is seriously hilarious. bucket - lowes maybe?? hahaha
Y'all I love her so much, like who does that. Praying for healing girl.
Well, I’m going to rewatch your older videos without skipping ads so you won’t have to worry about income while you just take care of yourself! You’ve given your community so much over the years, you’ve earned a break, for however long you need! We will miss you but we’ll all still be here when you come back!
Great idea! 👍👍
I was just thinking this!! Great idea!
me too!!!
Love this idea!
Me too!
The problem when people say that "there's always someone who has it worse" is that it diminishes what you yourself are going through. Yes, people may have a "greater" struggle, but that doesn't mean your struggle is any less. Take your time to heal. I'm so hopeful that this surgery is the beginning of an answer for you. TH-cam will always be here for you to return to, just take your time and make sure you come back when you are ready.
A-FRICKEN-MEN!! I hate that saying (someone who has it worse).
This. Yes.
YES to this!!
👏👏👏👏
I couldn't agree more! 👏🏻
Lets hear it for the boyfriend, family and friends who stand by when someone is going thru health struggles!
Right! Woohoo mystery man 🤟
Yes! Such a blessing ❤️
Let's here it for the bare minimum!!!its the least someone deserves 😅
Vanessa here🖐 I've lost "friends," Jobs, and even my older kids stay at their dads because I need too much help. I've had 2 failed surgeries and hardware in my lower back. I hurt constantly. Its so hard to survive. Being needy on other people is hard on both parties. I love this comment💖
“Doctors don’t listen” is painfully true. Seven miscarriages later, it is so painfully true...
💔💔😔❤
❤️❤️❤️❤️
Go to a reproductive endocrinologist if you can. Seriously. Sometimes nothing can be done, but sometimes it can. 7 miscarriages means there is a cause, but it has to be found. An RE will find it.
Amy and Ali my heart breaks for you. Love to you ladies
I’m so sorry 💔
Let’s all support Taylor by watching old videos during this time. If she can post 3 times a week while dealing with all that she has we can continue to watch 3 times a week till she comes back.
I actually love watching old shadow and shmoozes! So cute.
Such a wonderful idea! Let’s help keep her residual income going during the time she needs to rest and heal 💕
I've actually always been rewatching her videos lol, so I'll definitely be doing more of that!
wish i could like this 10000x so everyone sees it! def doing this amazing ides
I agree!
I absolutely can’t wait to see what this does for you. You have been so brave and such an inspiration to me, I watch you every night. one night when I was having gallbladder pain until 6AM you got me through it. We’ll be here girl, you rest and heal and drink matcha and come back when you’re good and ready!
Absolutely love seeing your sweet, lovely, supportive comments on fellow TH-camrs’ vids. So heartwarming🖤🖤
I love how supportive you always are! Such a good soul...
Love seeing youtubers being supportive of other youtubers. ❤
When queens support queens 🙌
I love everything about this comment. We love you, Taylor.
I’ve watched you for years and as a nurse, who has a daughter who suffered a severe neck injury cheerleading, I always thought “maybe it’s her neck...” I’m so happy you finally have an answer. And, as a nurse, you’re 1000% correct, you have to advocate for yourself. Finding a “good” provider isn’t as easy as it should be. ❤️
Alright Baerittos! Who is ready to binge foundation Friday playlists to help Taylor out during this time? Taylor thank you for being so strong and continuing to give us content no matter what. Take your time, good luck and I hope for a speedy recovery! ❤️❤️
My thoughts exactly 🤍
That’s such a good idea!!!! Will do!
That's where I'm starting!!
Chronic fatigue and several autoimmune disorders talking here. No judgment and no advice. Just prayers!
In the same boat
Same. Found out I had Lyme disease and now getting treatment after months of being so confused.
I don't like when people try to push a special diet on those with autoimmune diseases. It's like, "Im glad that eating solely fruits and veggies cured your ___" but that is you.
@Abi Thomason diverticulitis attacks, asthma, Hashimoto’s thyroiditis and several skin problems including eczema. I have all the stuff for a diagnosis of lupus barring the regular debilitating arthritis. I get some but it’s not enough to give me that diagnosis. Not sure if I am happy with that or not. Lots of auto immune disorders cause severe fatigue and all of them are routinely misdiagnosed at least a few times before proper diagnosis and treatment such as it is. Most people with 1 auto immune problem have several others as well. They travel in groups.
Same here!!!
Honestly don’t know that I’ve ever cared about a person I’ve never met more ♥️♥️♥️
Right? 💔🖤
Same here! She’s such a good person!
This comment totally sums up how I feel as well! 💜
Same 💜 I cried for this girl.
Same!
I’m actually in healthcare and I spend time with and frequently speak with doctors and I still couldn’t find out what was wrong with me. I ended up diagnosing myself and then telling my doctor what I’m pretty certain I have. And I was right. You know yourself better than anyone.
Cat M: What was it?
Taylor-I’m unsure if you will ever read this but I feel so strongly about want to share with you. I have struggled with migraines for years-(NO: I’m not giving you migraine advice, lol) I found you years ago when you had under 200k subs. I have watched you and learned with you, through you.
I have an appointment of some kind every day-I have other pain issues as well. I could tell you my whole story but the short and dirty version is-in the darkest times you have saved me. When I was in the hospital for a week with migraine pains that had me crippled your videos were my light. I know you don’t share all your struggles and that your life is so much more than what we see, but what I see I love, admire, and truly look up to.
When you do share with the world your struggles your vulnerability makes me feel as though I too can vulnerable in a time and place where that can be viewed as weak or complaining. Your struggles are your strengths and you are beautiful for that. ❤️
“Doctors don’t listen” so true and hit me so hard as someone with an autoimmune disease. I can tell I’m not the only one in the comments either
Same here - ME/CFS
Same doctors don’t listen
Yep me too hEDS/HSD
Same here CRPS. Took entirely too long for diagnosis
My boyfriend just got diagnosed with an autoimmune disease in his 30s and dealing with doctors who just want give you an injection that costs thousands of dollars even with insurance instead of answer questions related to extensive research we’ve done about other treatment options has been so frustrating. I’m a nurse, I work with doctors and have for a long time, I don’t think I’ll ever get over how little they actually care or do.
Just one more comment because I have to make sure you know we will be here. Take a week off, take a year off, whatever you need. Rest and recover. Eat some burritos. Hang with your peeps. Watch some Christmas movies. Soak in your tub. Shop online. Post if and when you want (just please post a quick update somewhere because we are all thinking of you and hoping the surgery is helpful!)
Deep breaths. One day at a time. We are here.
My mom has fibromyalgia, and this story sounds so familiar to hers. It’s very hard being someone where all you can do is watch, not knowing fully the burden that they deal with, and having people assume that she must feel fine because she doesn’t “look sick”. You’re so strong and I love that you’re speaking up about chronic pain, because it’s so misunderstood by those who don’t experience it, or have a loved one who experiences it. Sending you good vibes 💛
Audrey Randolph: Look up "Dr Eric Berg fibromyalgia" in youtube & read the comments.
Every single person with chronic pain just felt your struggle so deeply when you said “just one day,” while your voice cracked and tears filled your eyes. I can’t tell you how many times I have begged to have “just one good day.” One day without migraines, stomach issues, arthritis pain, fatigue, lightheadedness, anything. What a relief just one day would be. To feel like a “normal” human. To feel like my own body isn’t my worst enemy. To feel like there’s a better solution than a whole head transplant to a different, working body. I wish you a lifetime of good days. I hope you have the ability to wake up in the morning not fearful of what pain awaits you for the day, not praying that you’ll make it through, that you have so few bad days that they are a distant memory. Best of luck. I hope this surgery brings you long needed relief.
Liz Herring I agree with everything you said. I've been bedridden for so long I don't think I even know how to be with people even if I could. The moment I open my eyes I start counting the hours until I'll be able to fall asleep again. This is not a life. I'm so thrilled that she has found a possible solution to at least part of the problems. It's all about hope. I have been amazed at how many similar stories I've been reading in the comments. Chronic illness is so isolating that you think it's rare for a person to be so debilitated by their own body. All these invisible illnesses were named really well. People literally disappear from their own lives. Sadly, I agree that most Doctors just seem indifferent when a patient starts talking about pain. I've only met a few that seem to have any compassion. Lol! Sorry for the ramble. The brain fog is strong today. ❤
Amen hun! ❤️
Ugh, I feel this so much 😔
TH-cam is strange- know we’re not “friends” but I just wanted to give you a hug the whole time. Thank you so much for sharing this, I know it’s so hard to be vulnerable on the internet. For those of us who deeply care for you, being in the loop and being able to pray for you and send encouragement is such a gift. So thank you for letting us love on you! And thank you thank you thank you for taking a break. Less output, more input. Soak it in, be cared for. I’ll be thinking of you, and have a merry holiday season if we don’t see you before then! 🥰🥰
This. You said exactly what’s in my heart 🖤
Yes, so well said. ❤
Yes this! Very well said
You summed it up perfectly! Everything I wanted to say. ❤️❤️
I am reading that doctors don’t listen .. super true ! I wonder if she should go see a doctor in Mexico ???? Trust me they listen !!
See you when your ready, don’t cheat yourself. There’s millions of “us” in the world there’s only 1 of you.
I also battle a “Silent disease “ and no one will ever understand what we battle unless lived it. I’m praying for you everyday ❤️
TAKE YOUR TIME. DON'T WORRY. TAKE THE TIME FOR YOU. WE WILL ALL BE HERE WHEN YOU ARE READY. Fingers crossed for your recuperation!!!
People who don't experience chronic pain will never truly understand that hopelessness and the "is this really all there is" feeling. You have a lot of people in your corner, we will be here after you take as much time as you need. We love you.
So very true!
Yes!! 😘💋❤🌺
Your comment really hit home.
We sure do! People just don't get it (or even try to understand) 💖💖
trying to come to terms with “this might just be my life now” sucks so, so much
"Will ask window cleaner where he gets his boots" in the description is hilarious. Good luck tomorrow, keeping you in my thoughts ❤️
I would’ve never seen that! 🤣
Same here! 😆 She's thorough.
Heya Taylor!!!
I just found your channel through Seeking Alexandria... I, too, suffer from chronic illness & have daily pain, so I completely understand your trepidation & hesitation to talk about this... Not everyone does understand it & I've lost friends over the years due to not being what they consider "normal," i.e., going out to the bars to party (yeah, not high up on the priority list when having pancreas problems, lolz)...
YES, advocating for yourself is #1 when you have health issues!!! Doctors don't always listen, sadly, so whenever I've felt unheard, I've gotten other opinions... In fact, one doctor said I was putting "too much faith" in blood tests!!! A BLOOD TEST!!! It's not a matter of faith, my dude, it's actual science!!! That one blew me away...
I have a similar situation (not as severe) where I got my first migraine at 6 years old, so I've pretty much had them lifelong, but they started really ramping up the past couple of years... They accidentally found the cause of that: bulging disc in my neck, when doing the MRI I needed to get a spinal cord stimulator in... So I might need nerve injections to help with that or surgery in the future... I just thought my migraines were progressing on their own, but now I can tell when it's because of my neck as opposed to other things that might trigger it, because of the location of pain...
I'm so sorry to hear that you're going through all of this!!! I hope that you have the BEST outcome!!! I'm off to watch your latest update, so I guess I'll find out there... Just know you aren't alone in the chronic illness/pain world!!! Thank you for a great video, even though I know it was hard to share all of this... Sending love!!!
🖤🖤🖤
~Casey
Well I’m going to go to sleep but put on an auto play of all her videos - want to make sure she gets more views on past videos to hopefully contribute as much as I can
You’re vulnerability is incredibly brave. You don’t know how many hearts you’ve touched and how many minds you’ve empowered by sharing your struggle. Thank you for helping people like me feel less imperfect and more human. I wish you all the best and am so happy that you’re surrounded by people who love you! I wish I could send you a get well card . Here is a virtual hug from San Francisco California. “For when I am weak, then I am powerful “
Let’s just take a moment and be in awe of what Taylor can accomplish when she is free of some pain?! I’ve watched what you have done over the years and to know that behind the scenes you have suffered so much is honestly gobsmacking. My fingers and toes are crossed for you. Dear Universe : take care of our girl ❤️👍🏻
Completely agree! PS thank you for introducing me to the word “gobsmacking!” 🤣
Sadly, many doctors see female on the chart and begin dismissing or tuning out the patient in many instances. The frustration and effort to be heard is daunting. I am so glad you have finally found a solution and some answers. I feel for you. I get the full aura experience, photo sensitivity and violent nausea. Sending continuing healing energy to you.
I’m currently in medical school, and hearing your story about how doctors don’t listen to you and haven’t been able to help you made me so sad. I hope that when I’m a doctor I’m able to do better. Wish you a speedy recovery and some relief❤️
doctors never listen.
Anastasia, I'm so glad you want to make a difference! 💜
I am and was in Taylors position, over 30 years of chronic pain and other symptoms because doctors didn't listen. I had to advocate for myself too and if I had not read medical papers and books in different languages after a spontanous paraplegia I wouldn't have been able to get any diagnoses yet. (My body likes the rare illnesses, I collect them like sticker lol)
Since then I met many doctors who don't care and who shy away from complex cases but there are some gems who want to help and those give many hope!!
One advice I have is: don't be afraid to tell patients you don't know something, you are always able to help if you are honest. Just don't let them down, help them to figure out a plan B, find somebody who does know what's to do and tell the patients "if you don't get help there, I'm still here to support you in finding help". Because too often we get referred to somebody else who's rude and we don't know what to do (yes, even if they're nice to you, they can treat patients like trash). Sorry for the rambling 💜
@@nataliaalfonso2662 I hope you don’t ever waste a doctors time
@@immadiva94 I was quarantining.
Then I had to spend 2 weeks in the goddamn hospital IN THE CENTER OF COVID IN NYC BECAUSE DOCTORS DONT LISTEN.
Exposed to covid. For 2 weeks. On an IV.
This was after going to ERs 5 different times.
I was dying. I was dying. I was DYING.
I had strep c induced epiglottitis. Due to my congenital heart defects, I am at very advanced risk of endocarditis. I was manifesting symptoms of meningitis and not seeing out of my eyes.
DURING A PANDEMIC. One that would kill me immediately. I hadn’t left my house for anything other than doctors appointments Since lockdown. And they WOULDNT LISTEN.
I kept begging for help. They kept telling me it was in my head.
I kept begging and they kept discharging me.
Finally a hospital admitted me. Presbyterian.
9 days.
I was on an iv for 9 days without any treatment. I couldn’t even swallow my own saliva.
I kept begging to please check my throat, TO SWAB MY THROAT.
They kept sending psychiatrists in suggesting I was psychotic or had an eating disorder. I am 5’3 and 140 pounds of curvaceous cuban foodie.
I wasn’t even able to swallow my own saliva, and they were sending rudest doctors SO YOUNG....
That DOCTORS I HAVE TUTORED....
Have been their attendings.
9 days.
9 days without even water. Hearing them talk despicable dehumanizing shit about me.
Absolutely narcissistic personalities that fetishize their own ethos over FACTS.
Well la di da. Before even giving me a throat swab, they put me under, despite my telling them I have a mast cell activation issue and will be sick for months if I go under.... I told them they could do endoscopy without a aesthetic as I’ve had it done before...
No. They do the endoscopy and ALL OF A SUDDEN it’s every doctor in the hospital apologizing to me because SURPRISE. Fucking DUH. Literally fucking DUH.
I had EPPIGLOTTITIS. It is a MIRACLE I am alive.
So then I tell them..
Ok. This is very rare I. Adults and can be viral bacterial or possibly fungal. If this is BACTERIAL...
I have 3 regurgitating valves in my heart and a PFO. SWAB MY THROAT. SWAB MY THROAT.
They kept saying if it were bacterial I'd have a higher fever. I'm explaining to them.my fever threshold got all out of wack a few years ago from a really serious illness.
Deaf ears.
They DISCHARGED ME AFTER 2 WEEKS.
Without treatment.
Within the first few days I was back in the ER 3 times. I kept BEGGING for antibiotics or SOMETHING.
They all kept saying that if I needed antibiotics, the other doctors would have given them to me.
I finally went to a freaking city MD Urgent care. I hadn't swallowed in WEEKS and I was surviving in the hospital On an IV. How was I gonna survive WITHOUT ONE?
Simple fucking throat swab done by an assistant under the city md's doc supervision proved LITERALLY EXACY WHAT I HAD SUZPECTED FOR WEEEEKKKSS.
Strep type c. It had started to progress to meningitis which is why I was losing my sight.
So then the city MD prescribed me antibiotics! FINALLY.
Freaking LEVOQUIN. LMFAO. For someone with co genir heart disease who has had a history of tendonitis? Thank God I'm not as dumb as medical professionals and as soon as I read the pamphlet I knew it would kill me.
I ran back to the ER at the hospital that nearly killed me. I SHOWED THEM the result of the throat culture. I explained I can't take the levoquin. I ask them how they could have had me there for WEEKS during a pandemic when a simple throat swab and a day or two of IV vancomycin would have saved me! They dismissed me and said they sent me the new antibiotics.
I get to the pharmacy and it was zithro.
Even though the RESULTS I SHOWED THEM FROM THE CITY MD CLEARLY SHOWED THE STREP WAS RESISTANT TO ZITHRO.
I had to wait a whole other week to FINALLY get the linezolid that cured me. I had to have multiple bottles of blood drawn at my cardiologist. He, and my congenital cardiologist and the immunologist and the entire all agree that I was going to die.
And wait! Get this! Unbeknownst to me, Lovely Cindy, the NP at my cArdiolofist ALSO WORKS at Presbyterian. Where I also died.
She's the one that insisted I write about it and make sure to bring up lawsuits because she told me she has seen them kill more patients than she can count. That they've tried to tell her she's just "aNxIOuS" even though she's a cardiac nurse whose full time boss has diagnosed her with SVT.
I grew up as a miracle child saved by a rockstar of pediatric cardiology. In a family of doctors and nurses.
I say this from the bottom of.my heart: I respect murderous psychopaths that dismiss anyone who doesn't talk to them Inna coddling ring-kissinf fashion as far as I can throw them.
The exceptions that's prove the rule??? The incredible amazing doctors that know that just because they went to school for 8 ty ears does not.mwan they know a body more than a patient who has had it for 34??? The ones that believe a patient? They prove just how disgusting and ubiquitous empathy impaired doctors are. So. Do your job.
Oh this was just THIS TIME. LMFAO.
I've had broken bones for WEEKS bc doctors kept telling me I'd be in more pain if my whole hand was broken. I've had anaphylaxis ignored. I've been offered drugs that I had said I was aeefic too. LMFAO MY ROOMMATE AT THE HOSPITAL WAS DIABETIC! On dialysis! She was there for diabetic kidney failure and they gave her IN JELLO WITH SUGAR. LMFAO.
The thing with doctors is that they really believe that just because they have ETHOS it means they can't be wrong. Or that someone who isn't a doctor's can't know more about something than they do.
Some of us were born brilliant into medic families and chronically ill! My own brilliant surgeon uncle was misdiagnosed when he was being stricken down in the prime of his life with MS. plleeeeeaaasseee.
I'm from Bayside queens where doctors have killed more kids anditerslt jump started the opioid epidemic.
Please. Spare me. I respect nurses and the janitors at hospitals and the REAL ACTUAL MEDICAL RESEARCHERS and the expert diagnosticians and humble residents that become brilliant by knowing they don't know it all than some Podunk JERSEY resident who demands respect from folks who literally almost just died at the hands of nincompoop residents.
I dont know if you were home sick during the chapter of medic PTSD? Or malpractice? Or the lingering effects of having survived bacterial meningitis? But I'm having NONE of your demands for idealization.
Yeah, you're working during a pandemic. But while doing so, how many people with mold exposure or strep or manifesting heart failure or liver enzymes imbalance or peritonitis or ruptured ovarian cyst or early stages of cancer did you just dismiss to go home to die bc some textbook told you it isn't common?
If anyone else is reading this and has chronic pain, chronic illnesses or whatever you have going on I only wish you the best and good days! ❤️
Honey, we can all hear in your voice, your nervousness and hesitation in telling your story. Clearly not comfortable in talking about your life, medical issues. You certainly do not owe to us who follow you but I'm sure we all appreciate that you did. I wish you nothing but the best in every aspect of your life. Ive only watched the video a few minutes in and my heart hurts for you. I suffer from migraines but not on your level. I cannot imagine what you have been through. We all care about you. Thank you for sharing. In my prayers beautiful lady.
I've had debilitating, chronic migraines for over 30 years. Everything you are stating is true. Hang in there! I've lived it & am living it.
Side note- my ex is a high rise window cleaner in Seattle and there’s a good chance that was him cleaning your windows 😂
Nearly laughed out loud at this comment oh my gosh 🤣
Did he see the craziest shit? Because I'm just like... what if I was walking around in my birthday suit 🤷🏽♀️🤣
😂🤣
@@whitneydukes8029 seriously! Half the time I’m not wearing pants at home 😂
@@nlyb3167 Oh same!
Beginning of video thoughts: Yes, Taylor! Speak that truth! I still remember walking around ASU at 19 years old with literal sheets of my skin peeling from my arms, face, and scalp. My neurologist didn't want to believe that I was allergic to a medication. I walked in my doctor's office and the first words the nurse said was, "Oh honey, what happened?!" I burst into tears. My doctor and his nurse sat and listened to me for at least 30 minutes before helping me find a new neurologist THAT SAME DAY. People ask why my doctor is close to 50 miles away from me. Simple answer: He always listens to me.
Middle of the video thoughts: "Not gonna ugly cry. Not gonna ugly cry." Also, Taylor is like a teacher. I remember teachering for through strep throat, the flu, severe sciatica, and every other plague those little people gave me while smiling, laughing, because it is my passion. In January, I had a month long sciatica flare up. I pushed myself to work through it. I don't know how Taylor does this.
End of video thoughts: Why are you putting a time limit on your recovery? TAKE AS MUCH TIME AS YOU NEED! My heart broke for you when you said you felt let down by your body. I felt that in my soul. Please take all the time you need to recover. 💖
This will give us time to rewatch your back catalog, so don’t worry about us.
Something to bear in mind is that people have staggered returns to work, so it’s also totally fine not to jump straight back into three videos a week.
Take your time. We’ll be here when you get back.
My dear I will constantly keep you in my prayers. I too have suffered with low back problems for almost 15 years. A bulging disc with a hernia tear pain is no joke, so many other health issues which I will not go into prayer is the only solution and a good doctor's you say You must have someone who listens to you I totally agree with everything you say God bless you and keep you.
"Just because you carry it so well doesn't mean it's not heavy".
You carry it so well Taylor, too well. I hope this surgery gives you relief and time to heal.
That quote just got me right in my feels ❤️
This quote is outstanding. Thank you for sharing.
I loved that, because I always have to explain that just because I don’t show it doesn’t mean I don’t feel it.
I feel like the window washer was a necessary comedic relief. 😅
In all seriousness, debilitating pain is something nobody should have to go through. We’ll be sending love, positive vibes and we can’t wait to hear how you’re feeling afterwards. ❤️
The details may differ but this is so many of our stories.
Taylor, I so completely empathize with you, not because I have chronic pain but because of my husband. He too has suffered chronic pain for over 10 years. He had an accident when he did construction and a 10 foot wall fell on top of him and another worker, crushing them. As a result years later, he’s now sufferings excruciating pain in his neck and shoulders to the point he can hardly function and it’s gotten worse. He’s seen so many doctors and specialists and like you said a lot of doctors just don’t listen. I’m so happy you have found a doctor who is helping you. I pray one day my husband finds a doctor who will be able to help him. For now he can barely function day to day even with all the meds he’s taking. Your story touches me on such a personal level as your story sounds so similar to my husbands as how you are feeling and dealing with this. I love you and your videos and I pray for the very best for you. I truly hope that you get relief and recover quickly. Sending you the very best ❤️🙏🏼❤️🙏🏼❤️
I cried watching this! I struggled with chronic Illness for 8 years straight. So many doctors, so much money, so many meds and none could figure it out. I HAD to be my own advocate and keep fighting for my health and my life and finally in 2017 I was able to receive my healing 😭😭😭 im praying that this is the answer for you and that you’ll have 100% relief!!! God bless you!
Girl, we ain’t going anywhere. Life has a pesky little way of interfering with...life. Take the time that you need to heal. If you don’t have your health, then nothing else matters. ❤️❤️❤️
So well said. Life always seems to get in the way of *living*, lol
Exactly. It’s important to plan, but at the end of the day, the universe couldn’t care less about your plans. We’ll be here, patiently waiting for the good news ❤️
I would give anything to give her a pain free life!
Seeing you tearing up and hearing you say "I can't do this anymore" absolutely broke my heart. I've been an avid viewer for so many years now and it is so good to hear that you're taking time off to take care of yourself. I wish you the most luck with your surgery! We will all be here waiting for you whenever you return ❤️❤️❤️❤️
Nothing but love and support being sent your way. Please do what's best for you and take care of yourself. I have seen you struggle through so much in the past 4 years of being subscribed. I hope this surgery gives you all the best! You deserve it
Sending you all my love and healing thoughts for a successful surgery and full relief from your chronic pain. That you post 3X a week living with that is beyond amazing. You're an inspiration and I'll miss your videos but will go back and watch from the beginning to do my little part to help you. xo ~angie
As a mom I can't imagine how your mom, especially living in another State and not being able to wrap her arm around you, was feeling during that phone call. It's innate for us to want to take our children's pain away and make things all better! So God Bless your mom.. And your dad for being with you virtually at the consultation. You have amazing parents. God bless you, too, Sweet Girl. My prayers for a successful surgery and wonderful outcome. Take all the time you need for YOU, Taylor. We will still be here. 💙💜💛💚
Girl, I have chronic migraines and I have Multiple Sclerosis, and I TOTALLY UNDERSTAND AND EMPATHIZE WITH U ON EVERY ASPECT THAT YOU'VE EXPLAINED HERE.
I also UNDERSTAND when people try to explain dumb shit like taking a multi vitamin or Motrin, and stretching as a means of getting rid of the pain. Urgh! People think they are helping, but unless they KNOW it's gonna work, then they are just making things worse for us...because TRUST ME, IF IT COULD BE CURED BY SOMETHING SIMPLE, THEN WE'VE ALREADY BEEN THERE, TRIED THAT! 🤦🏻♀️
I AM SOOOOO HAPPY FOR U TO BE GETTING THIS SURGERY!!!
HOW EXCITING!!
ITS BEEN MONTHS NOW, BUT I'LL LOOK FOR YOUR UPDATE VIDEO TO THIS VIDEO.
MAY GOD BLESS U GIRL...MAY GOD BLESS BOTH OF US DOLL.
WE LOVE AND ADORE U GIRL, AND WE WILL WAIT HOWEVER LONG U N3ED US TO WAIT FOR U!!
YOU'RE GONNE BEAT THIS AND LIVE A HAPPY, PAIN FREE LIFE, I KNOW IT!!!
P.S. WE ARE ALLOWED TO BREAK DOWN, I GEET THAAAAT, BUT... WE DONT EVEEEER "GIVE UP" LOVE.
XOXO
I lost my boyfriend through suicide in August. When you said that you couldn’t do this anymore on the phone to your mum, it broke me. But it was good to cry along with you. We will be here when you come back. Will go back through and catch up on videos I’ve missed/haven’t had time to watch. Take care, love from Scotland.
Ahh, girl I'm so sorry for you 😥it must have take a toll on you...stay strong.❤
So sorry for your loss 🙏🏻🙏🏻🙏🏻
I’m so sorry for your loss. Grief isn’t linear. But I’m so happy there are still things you can find comfort in there. My thoughts are with you ❤️
I am so sorry for your loss. Sending love from WA state. ✨🙏🏾✨💖
@@nikoletthorvath7376 thank you, I really appreciate that.
I just want you to know that you've brought me, a nurse dealing with surgical patients daily, such a dose of empathy. I wish you the very best with your health journey, channel your strength into being with your loved ones and physically healing. Continue advocating for yourself, I know it's hard and our healthcare system is a mess, but your well-being is worth the fight.
Your strength is admirable, but even the strongest of us need breaks. Take your break Taylor we’ll miss you and we’ll wait for you. Stay safe.
Have a safe procedure! Chronic pain is absolutely a beast. I’m 34 and I have Eosinophilic Granulomatosis with Polyangiitis. I have a lot of nerve issues, asthma, arthritis, skin damage, and a host of other minor issues. Nothing compares to when it’s coming from the head! I hope this procedure resolves a lot of your pain ❤️
the part where she was saying how she felt like her body defeated her.... i felt that. living with RA has been very similar to this.
Yes! I have RA as well and I felt her pain. It’s so incredibly frustrating to have a body that doesn’t match your spirit or your age. I was diagnosed at 28 and it had completely changed my life.
Same! RA freaking SUCKS!!!
Yup! Same!
I was diagnosed with JRA at 4 so this script is very familiar to me. At 50 I’ve been baptized by pain over the years. My new found mantra is that my immune system is brilliant and has made no mistakes. It’s just taken a long time to clear out what it was after.
Thank you all for your responses! I was diagnosed at 18 and I’m 22 now. It’s so encouraging to know that there are other people out there who understand!!!
That moment when a doctor is kind, listens, takes you seriously and you just about fall into a pile of tears on the floor because you went in with armor ready for the same crap and you were caught completely off guard.
As a physician, I’m so sorry to hear you and so many people in the comments say you weren’t listened to. I hope you finally find the help you need.
Thank you for this comment. Chronic pain is so hard to deal with everyday and it's hard when your medical professionals don't hear what you're saying to them.xxx
@@shinystarsimmy I agree. I’m currently in pain management. I do have a great doctor but it took me 2 other “doctors” before finding him. The first said I was lying and I just wanted drugs even though I had 10 years of MRIs. She told me to just take ibuprofen even after me telling her multiple times I cannot take NSAIDS. While being her patient I ended up having surgery to remove a softball sized ovarian cyst and she said I just had surgery to get pain meds. This cyst was so bad I would be doubled over in pain crying. My husband (then bf) made me go to the ER and they acted like I was trying to score drugs. They didn’t even run bloodwork. I even told them my medical history which included a RNY 2 years before and how my surgeon said if I had any abdominal pain to go to the ER. Luckily I had a checkup with him the next week. He made me go to his ER to rule out a hernia. They diagnosed me with the cyst. Funny enough they even tried to give me morphine while in the ER but I declined. Mainly because I drove myself and was 3 hours from home. I have also had at least 40 kidney stones in the past 8 years and I refuse to go to the ER because I know how they will treat me. My husband tried to get me to go 2 weeks ago when I had one of my bad migraines that lasted 8 days. I told him they won’t do anything. It isn’t right that someone who suffers from chronic pain (with actual documentation) gets treated like a junkie.
@@angelamorrow8973 I'm so sorry you're going through this. We should never be dismissed in this way. It makes me so angry that so many doctors treat those of us with horrific chronic pain this way. I think before they make comments they should read a patient's notes. They would see a pattern of people who are drug chasing. Unlike people who don't want more drugs but generally just some support and reassurance and help to manage that pain and some understanding that life is a challenge. 😢
Thanks for your comment. Took me 7 years+ to get taken seriously and diagnosed with autoimmune diseases. Even with family history and obvious symptoms...
As a nurse (and patient advocate), near future FNP, and a sufferer of chronic pain and autoimmune diseases that are “invisible,” please know that it happens WAY more often than any providers would like to realize. Take it to heart and use that knowledge in your practice to see and hear what your patients are really trying to tell you. 💕
I’ve got chronic pain as well. I’ve got trigeminal neuralgia followed by pseudo tumor cerebri. Good times! I’ve been dealing with this for 20 years. There is only so much a soul and body can take and I know it drains you in every sense. I’m down to praying for good hours a week and make the most of it when I get them. However they are few and far between. I tell my husband whenever we go see people, go to dinner, visit friend and family, I constantly have to wear my social mask to avoid showing anyone my pain and then having to answer questions about it. I feel like I truly have no idea who I as a person am anymore, because the pain has forced me to become someone I don’t know or recognize. So each day I get up and I pray I’ll be ok. I’ll be praying for each of you who have chronic pain. I’ll be praying for your surgury sweetheart, I’ll be praying that you finally find your own way back. God Bless you.
C5-C6 titanium fusion here, and it also took many years to get a doctor to take me seriously. I was 26, and they kept saying I was too young for the problems I described. That surgery helped me so, so much! I pray you also have a positive outcome, and that you finally get the peace of mind and body you deserve. I hope you have a speedy recovery, for your sake. Don't push yourself, take your time, and then take time just for you. We'll all be here when you're fully recovered and ready. 💜
When Taylor was talking about 'not remembering a pain-free life' I was sympathizing, but for a different reason. I've had major depressive disorder my entire life - was even suicidal/crippling apathy as a little kid, for no discernable reason (great upbringing, good parents, safe town, etc.) other than I was just born with it. I've learned how to manage it over the years, but, man, Taylor, I feel you on the 'no good days' thing.
This is not meant to equate my experience with hers, in any way. I get migraines too, and I can't even begin to imagine the amount of pain she's gone through.
My husband had a herniated disk in his lower back when he was 21 and he was in so much pain, could barely walk, and BEGGED several doctors for over a year to take him seriously. Finally that one special doctor did, got him in surgery and he immediately felt relief. Not pain free but so much relief. I pray this is the same for you. He overheard this video and just felt for you Taylor, we are excited for you and hope this is the first solid step in the right direction for your health!!
@sarahp My husband had the same issue!! He even had a chiropractor tell him maybe his pain is all in his head. Finally a coworker’s mom worked at a Spine center and told him to go immediately to get an MRI. After surgery he felt a million times better.
I have issues with my neck too and doctors do nothing. My neck feels so freaking hard. I just feel so tense. Im glad to finally be watching this video. I hope you start to feel better after your surgery xx
“A pain free life is not an option”...this breaks my heart for you, but also, thank you for saying this. I’ve had chronic pain since 2018 and I basically put my life on hold, waiting for pain free days to come back. They likely never will, and I need to start to live my life again, pain and all. (Well, you know, post-rona. 🙄) Thank you for this reminder. You truly help people both by talking about this, and by giving us a way to relax and unwind, as well. You’ve got this, we are all thinking happy thoughts for you! We’ll be here when you get back, and I truly hope you find some relief.❤️
Take care. We'll be here when you're back. Sending good vibes.
Go heal. We’ll be here when you return. We gotcha girl.
I’m praying your surgery blesses you with the relief and comfort you are looking for. I’m so sorry for all the pain you’ve gone through and doctors not listening. As a type 1 diabetic for 43 years, I know the aggravation of them not caring for you. I look forward to seeing you when you return and catching up on older videos. Love you!
“Doctors don’t listen” I FEEL THAT IN MY SOUL!
Okay last comment lol. From the wise Dolly Parton, "don't be so busy making a living that you forget to make a life!!" I think that's some advice everyone can use.
Dolly is the best 💙
I love Dolly. She's a sweetie.
Not even a minute in and I am about to cry. Feeling for you Taylor!!!
My mom suffers chronic migranes. I have had a couple no way I could do what she does. Immatrex puts you down for the day. I just want to hug her and make her some iced coffee
Bout to, I was.... :) I have minimal pain and whine I couldn't even imagine pain like she has had
Same
You are a beautiful lady, please take care of yourself. Don't hurry through your recovery time. I understand about docs not listening! It took 5 years for a doctor to find a huge clot in my abdominal area. They kept thinking it was my legs, when I would tell them it was in my pelvic area. Since my femoral bypass in 2010 I have felt soooo much better. Thanks to ONE doctor that listened, and did testing for that area. I wish you relief beautiful girl!!! Sending hugs over the miles!!!
"Doctors don't listen". Truer words have never been spoken. Praying that she gets the relief she so desperately deserves and needs. Please read the comments further down about watching older videos for Adsense. It's one small thing we can do to let her know we care.
You saying “a pain free life is not an option and that’s ok” breaks my heart for you. If you take any time away nobody that loves you and supports you will ever question your absence. Take care of yourself because you deserve some relief ❤️
When my coworkers have time off we chat them “have a good break” so HAVE. A. GOOD. BREAK. We will be here when you come back! Thank you for being here for your community through some of your toughest times in your life. You’re amazing. Sending you all the love and good vibes for your surgery. ❣️🌯
I am so glad your doctor could find the exact source of your pain. I have chronic migraines 7 times per week all day since I was 12 years old, and I am now 54. I tried everything and more.
"Doctors don't listen"...YES...so true.
As a nurse I’ll just say it’s so important to advocate for yourself and your body. I’m so sorry everything you’ve gone through. Sending lots of love❤️❤️❤️
The whole you can’t race with a broken rocket ship part hit me like a ton of bricks. I’m 27. I’ve had chronic migraines since I was 5. But within the last two years I’ve had increasingly worse chronic body pain. To the point that I cannot stand long enough to take a shower. If I try to, my whole body involuntarily shakes from the pain. Five years ago I was doing 5ks and lifting weights 3-4 times a week. I mentally beat myself up so much for not being able to keep up. I don’t think I’ve ever heard someone else put that into words.
@Heather....it hit me hard too!! I'll be praying for you & @Taylor. A painful life is no joke. I get pain so bad at times tears just roll down my face uncontrollably because I hold EVERYTHING IN!! Love & Healing hugs, Steph ❤😘💋🌺
I'm gonna leave this here knowing full well that you may never see this but I felt compelled to say this. I feel you on every single level. I won't go into all of my health conditions, cuz there's a lot, but I too suffer from chronic illness, chronic pain and chronic migraines. I started watching your videos because I was watching Jessica Braun and she spoke very highly of you and I trusted her opinion so I thought I'd check out your videos. You are like heaven sent to me, it inspires me everyday how you have all of these health issues that would normally stop a person in their tracks but you just deal with it and keep going. I'm so glad that you shared this video with us, I cried with you, I get it I understand and I thank you for inspiring me each and every day to just keep going. ❤
I know this is difficult for you to talk about and even more difficult to live through. You’re in my thoughts and prayers. Do what you must to get from today to tomorrow ❤️
It’s really important to remember that we only know part of the story, so giving medical advice is not only pointless, but also a little dangerous, given that we don’t know Taylor’s entire medical history.
I had chronic migraines as a child and it was absolutely miserable. I would hurt so bad that I would bang my head on the floor because that split second of relief was worth it.
Taylor, I’m holding you close to my heart during the surgery and recovery.
My heart hurt watching this. I hate that you are in so much pain, and I’m REALLY praying that this surgery helps!!! I would love to see you completely pain free!!! We will all be here when you are ready to return! Please take your time and recover completely! You desperately need the downtime, and your channel is so good- Taking care of yourself will not end in you losing everything you’ve worked for! We love you so much and we want to see you feeling your best! ❤️
I felt “doctors don’t listen” in my soul. I don’t understand why it’s so hard to find a doctor that will actually listen. It took me 5 years for me to find a doctor that would even refer me to a specialist.
It broke my heart when you talked about how there are days where you feel like you can’t do this anymore because I have absolutely been there. My chronic condition is not migraines so I don’t know what you’re going through, but I do know what it’s like to feel like your body is betraying you.
I truly hope you find some relief. You are an inspiration to many of us. I often watch your videos when I’m having flare ups because you are so calming and it gives me something to focus on. You constantly remind me that I am not alone and that I need to look forward to and take advantage of the good days. ❤️
My heart goes out to you, Taylor. I have fibromyalgia and chronic migraines. MS runs in my family too so I’m currently going through a bunch of other tests. I’ve also been in 3 car accidents and got whiplash and severe concussions each time. I, too, have never had a pain-free life. Usually I can suck up the pain and put on a face but so many days are lost to being in unbearable pain. It’s an “unseen illness” so it’s very hard to get people, including doctors, to take you seriously. There is nothing in my life that has made me feel more defeated than trying to manage intense chronic pain. I’m only 33 and otherwise in great health and it’s terrifying to think I might have to live my entire life this way. I hope your surgery went well. I will be checking in on your next video to see how you’re doing. ❤️❤️❤️
I got to the “I can’t do this anymore” point with my endometriosis in 2009 after dealing with debilitating pain for 6 yrs. it breaks my heart to see someone else going through something similar. Sending prayers that you heal soon.
I have been surgically pain free from endo for 5 years now. ❤❤❤
I saw a quote recently that spoke to me: "Good health is a crown on the head of a well person that only a sick person can see."
It's so true. We don't know that we have health until we lose it.
Also, this is random, but I started taking Ubrelvy this year too!! I love it. Triptans would stop my migraine from progressing, but Ubrelvy actually makes me feel better!
Sending you all the love, the hottest heat packs, the coldest ice packs, the coziest pillows, and extra spoons.🥄 🖤🖤🖤
Edit: I also have the same headache patches, and the same neck ball squeezer in your thumbnail!! If you ever do a video sharing your migraine/pain tools, I would buy them all!!
I keep seeing Ubrelvy commercials and now that people are commenting success with it, maybe I should talk to my doctor about it!!
@@kirasthebest it's so exciting that there have been so many new options available the last couple years! I hope you find the right meds that help you. That has been the key for me. 😊
Yes! I have had migraines for a long time but I haven’t seen anyone for it. So anything besides my heating pad and vicks and excedrine would be like Take My Money!💰 lol
Love love love my ubrelvy!!! I had an allergic reaction to immatrex and nothing was working until ubrelvy
@@liznotslow thank you! I hope so too 💛
I've been living with chronic pain for 26 years - longer than some of Taylor's viewers have been alive. I spent my child's life in pain every single day. What Taylor has been able to achieve with her channel while living with her medical conditions is a testimony to her drive and talent. I join with those who are praying for Taylor to have some relief. May God guide your medical team and bless you with healing. 💞
When I was a teenager, I had chronic migraines, accompanied by throwing up and chronic vertigo. Days on end of migraine headaches. I said to my mom “I can’t do this anymore”, we skipped school and ended up in the ER for the whole day. They did a cat scan and found water on my brain. We went up to a different hospital immediately and they diagnosed my with hydrocephalus. I waited two years to have surgery and when I woke up, the change was immediate. Best wishes. I feel very lucky to have had a team of neurologists who heard me and were able to find the route cause. It was a long road!
I am so happy to hear you're feeling better!! 💜💜💜
Was this caused due to an accident? Glad you’re better :)
As an ER nurse, sometimes it’s just easier (emotionally) to forget that there is a story behind each chief complaint. Thank you for the reminder of how important each patient’s story/life experience truly is.
I’ve been watching your videos for years and I absolutely wish you the best ❤️.
New schedule: focus on yourself and healing!
Good luck for surgery and recovery! Thank you!
“JuSt UsE A CoLd COmpReSS”- my number one comment on my chronic migraines 👍🏻 I know how you feel girl. Chronic pain for 10+ years here too.
I just found your channel. I have Rheumatoid arthritis and Lupus. My pain is never under a seven. Thank you for making this video. You are not alone in your chronic illness journey.
Taylor, just wanted to say that I pray that this procedure gives you relief and healing!
Let's come back every M W F and tell Taylor about our day, a funny story or leave a nice little message either under this comment or under her video so she can come back and read these if she's feeling down. Love you taylor u deserve the world, be kind to yourself 💕
I love your idea! Another person suggested that we have Flashback Taylor Video during her recovery. Watch her older videos, Like and Comment. This will help her AdSense, which will keep her videos in recommendations. It's a great way to help Taylor. Let's do both!
@@VeroSCIA I will be doing both because I love her sooo much she's the only youtuber that I actually keep up with
Hey Taylor, just checking in, I hope everything is doing okay and I hope that ur feeling well after surgery. Can't wait to see you! But take all the time that you need💕🦋💖
Hey Taylor, today i got a promotion at work! And I finally enrolled in health care so I can go get my issues looked at! Much love and be kind to yourself 💖
No pressure either way. Just good luck and lots of love, Taylor. Sincerely.
Take care of yourself!! I also suffer from chronic debilitating pain daily for 10 years now after multiple back surgeries and I can relate. I pray this brings you relief from pain and betters your quality of life! It's something so difficult to talk about because unless someone suffers from it they can't understand, even if they sympathize or want to understand it's only possible to a certain extent. I wish you the very best, and send you the good positive thoughts and energies for healing and a wonderful outcome! Looking forward to your return as you always brighten my day! Love from California!!
Rest. You'll heal faster. Don't worry, we'll still be here when you're feeling up to YT again.
After 14 surgeries, and constant 24/7 pain the last 15 years, I found myself nodding in agreement with so many of your statements about how you mentally feel. Wishing you a complication free surgery, and a swift recovery. Hugs!