i live on the opposite end of the country (nyc), im a black girl with super curly hair and brown skin, i don't even wear makeup except for eyebrows, but you've been one of my favorite youtubers for like 6 years now and i watch every foundation video and makeup haul and vlog cuz you're simply the best 💓
Hey, I'm a 70 yr. young woman who loves her too! I can't do makeup like she does bc it's full-on glam for a young woman, but I get inspiration from her. Hevk, she's just entertaining!
Totally agree! I’m a huge fan, curly, curvy, 47 yr old gray haired Glamma and you are my go to when it comes to foundation. I know I’m going to get an unbiased and unfiltered opinion. Your personality is really what makes everything so enjoyable. I know the struggles of migraines and remember getting my 1st one at age 4. My mother putting me in a shallow tub of cool water with the light turned off in the bathroom and just floating till my teeth started chattering.🥶 I just started Emgality took my first shot 2 days ago. I’m praying for some relief.......I wonder if those rocks are an allergic reaction of sorts.🤔 I hope that someone can figure it out for you even if it’s a voodoo priestess because not being able to get relief from that pain is such agony. I think about you and Kristi all the time. In my head we’re friends so I say a little prayer for you guys and all the migraine/cluster headache sufferers out there. Only thing mine are good for is getting a foot massage out of my hubby.😜
I'm almost 53 and am in Virginia. I do love makeup but Taylor has me interested in different foods I would never think of, house decorations and other random stuff. She just seems like such a cool lady! Unfortunately, I now say super cute all the time😂😂😂😂
Can't put it in stores in bad areas or who's primary shopping demographic is low income. The tablets WILL get stolen I live in studio city which is a relatively good part of LA and people's cars get broken into all the time inside our locked garage
I am so sorry for your pain. I have pain from a crushed heel. I wish I could help you cause I know what living with pain is. Watching your channel while I was doing learning to walk again helped take my mind off the pain. I never thanked you for that. Thank you Taylor ! I will be praying for you and I want you to share with us your pain and struggles. People love you and that includes me.
I save her videos for the evenings! I have chronic migraines, and a variety of other chronic issues - She helps distract me from my pain well enough that I’m able to sleep post-video ❤️. Taylor is a chronic pain superhero🦸♀️ .
I have the same issue and even have it happen by my under arms and cleavage area of my breast but mainly through out my neck. I have fibromyalgia and a hypothyroid. I have chronic pain mostly in my shoulders and neck but all over my body. I have asked my doctor about the lumps and have gotten no answers.
Girl, if you're talking about pain and asking for suggestions, it must be baaaaad. 😔 Love you so much and hope you find some answers ❤️🙏 You're beautiful!
She’s the only ads I actually look into because she has ALWAYS been truthful. So thankful I’ve been watching for years now and to see her just being herself makes her my absolute favorite always😭
Love your videos! Have you ever had those lumps biopsied? A biopsy would be a way to figure out what cells/tissue makes up the lumps, and hopefully point you in a direction as to what is causing it.
Taylor's comment section is the best 👍👍 I love all of you notification squad peeps!!! Taylor thank you for inspiring your audience members that live with chronic pain!!! Bless the baeritto fam 😭🥰🥰🥰
When I go to the mall because I need clothes, I find nothing. When I'm at the mall because I'm bored, I can spend hundreds :) Oh, and the truffle flatbread is the BEST!
I don't get chronic migraines like you do, but when I get a migraine it's normally caused by knots in my neck. It's myofacial pain, which means my entire back and neck are literally covered in hard, pea-size (or bigger) lumps all the time. If it was myofacial pain, I'm sure your physio/doc would know that though. I really hope you can get some answers soon! It's obviously some form of knot that's pressing on nerves, but it's weird your medical team can't figure it out! From one spoonie to another, I'm sending hugs 💖💖
Yes!! I commented as well but wanted to copy paste my comment here since there are so many comments 😊 I do agree that it's weird that her doctors wouldn't suggest myofascial pain syndrome 🤔 but anyway, here's my comment in case she happens to read yours and mine gets drowned in the hundreds of comments lol Google Myofascial Pain Syndrome!!! It sounds exactly like what you're going through. It causes pain throughout the body, mostly in neck, back, and muscles. And it causes rock hard muscle lumps in these areas. In college, I had neck lumps and lumps down my spine and lower back. They were super hard and painful and obviously, I was freaked out. I had biopsies done, blood work, etc and the only thing that really came up was my abnormal autoimmune panel. I was referred to a rheumatologist and he diagnosed me with lupus and myofascial pain syndrome. The MPS causes muscular knots that are super painful to the touch. I have found that as long as I keep my autoimmune issues under control, the lumps stay away but that's not true for everyone. I hope you find some answers soon!
❤️🥄 ❤️ If only there was a way to borrow spoons, lol. On my off days, I’ll let you borrow a couple of mine if I can borrow a couple of yours for when I’m at work! 😂
Zebra Strong if there was anyway to actually borrow spoons, that would be amazing. I’m doing better here in MI, because the weather is warm. Really not looking forward to winter. This past winter was my first without major pain meds since 2008 & I could not function. Since my last doctor retired, all my new doctors want to try every single thing before they put me back on meds. I’m thinking death might come from shock because of how much pain I was in Dec-May. It’s horrible. Everyone that deals with chronic pain/illnesses has my empathy. It effects every aspect of your life.
Jenna Frazier, maybe that’s the perfect middle ground. Down here in MS, I’d kill for some just plain cold as opposed to our humidity, lol. I’ve been told from family that live up north that our winter is a worse feeling cold than up there because of the humidity... I’m really lucky to have an amazing doctor that thinks EDS is cool, so he is constantly doing his own research and working with me to learn what works best for my body. Lol, it’s not every day you find an orthopedist willing to take over as a primary care provider. If I could recommend him to the entire world, I surely would!
@@jennajune2101 I'm so sorry you had to go through the winter with no pain meds! That's ridiculous!! I have fibro, M.E and recurring shingles, and permanent myofacial pain. It depends where the lumps are, as to how painful it gets really. I'm in Scotland so the cold, damp winters are a killer. I hate winter-time!
I would recommend going into see a rhuematologist. I did a couple of years ago for some very random symptoms and told the doctor that I wasn't even sure if I was in the right place. The doctor told me that they actually deal with more than autoimmune diseases. She did a big battery of tests and did not give up without a result. I've learned through family history that many many autoimmune diseases do not always show up in blood tests for a decade or more. I have every single symptom of RA and respond to infusions for it but I am negative on every blood test. It's a starting point and all they can do is tell you somewhere else to go! Best of luck!
You looking so out together to run errands and chill at home is so motivating. I've been in such a rut since COVID, but these vlogs remind me to look good for yourself
I know you asked about the May clinic on your other video but I HIGHLY recommend them. My mom was given practically a death sentence cave diagnosis when she reached out to Mayo. She's been in remission for seven years in October. My mother in law also went to them, she has unfortunately passed but she had been given a month to live by another practice and thanks to Mayo's guidance and compassion we had her with us for almost 18 months. She got to spend precious time with us and our boys and we made a lifetime of memories! I'll be praying for you! 💗
Sounds like possibly lymph nodes. Maybe ask for an ultrasound. I’m a tech and we can see nodes whether they are normal or abnormal around the neck and other areas. - maybe see an ENT specialist if they are appearing more around your throat as well.
nicole fedorko I have this too, a string of hard pea sized lumps going up the back of my neck on one side and they never go away. Got an ultrasound, they were lymph nodes. Ultra sound deff helped ease the worry.
Yes! My son gets these! The doctor says that it’s his way of fighting off anything that shouldn’t be there. They come and go. Not sure if they are the same, but I would bet they are
I said the same thing. I’m a nurse and wondering if it may possibly be an allergen. I have a pt that has to have weekly infusions because of her allergies and she has lymph node changes with exposure to certain triggers.
I’m going through a really hard time with my boyfriend right now and I’m not sure where we stand at the moment so I’m really not in a great mood and I’ve been crying off and on for the past 24 hours but I just wanted to let you know that watching your video brightened my mood a little and made me feel a lot calmer and took my mind off of what’s happening, thanks taylor💜
Bless your heart for putting up a long vlog when you're dealing with such difficult health Taylor. I know you're used to it but still know how much we appreciate all your effort. I hope you get some idea of what to do about your neck rocks, it sounds awful. Sending you so much love. 💕💕💕💕💕💕💕💕💕💕
My mom has dealt with migraines for years and I always send her your videos because she is always talking about the same symptoms! She has the bumps too and she believes they play a factor in her flair ups too!! I pray they find answers to migraines soon ❤️
So grateful to have an extra video from you this week! I’m sorry you’re not feeling well, though. I hope you figure out what’s going on soon! Love and light ❤️
I watch ALL your videos. You are so relatable but for some reason this specific video made me so calm & felt like I was legit talking face to face to a best friend. I had no idea that even 31 minutes passed
Something similar happens to me. My cervical nerves (back of the neck) flare up and it messes with my sinuses and I literally spend hours throwing up. No medicine helps, I just have to wait for it to go away. No doctor I’ve spoken to believes that my vomiting is not caused by medicine (they think I take too much medication when really all I do is wake up and throw up). I’m no help at all, sorry, but when my cervical nerves flare up I get hard lumps around my neck and especially behind my ears. You’re not alone and thank you for sharing how you feel. Love you Taylor 🖤 and yay for the bonus vlog!!!
I’m a little late to the game but I tried everything for neck spasms and tension that lead to headaches. After exhausting all natural options, and after about 3 years, I ended up going on Lexapro for anxiety and Xanax as an emergency treatment. Their ability to relax and chill me out has helped me tremendously. Obviously not a good option for everyone, but after a lot of research, I gave them a try and finally have my life back. Much love. Xoxo
Loved that striped shirt, was super cute and your tan looked amazing! I already bought the St. Tropez one after seeing you recommend it, which has changed my life. It does come off pretty quickly within the week so I just ordered the Loving Tan one to try out. Thanks for the best recommendations! But seriously, anyone who is super pale (like see-through) try the St. Tropez one!
Love you Taylor! I’ve had headaches my entire adult life. NOT comparing to what you go through but sometimes they get really bad. It’s so weird cause if I don’t have a headache all of a sudden I’ll notice and I’m like oh my gosh my head doesn’t hurt! Mine involve my neck too. I just wanted you to know I understand (sort of) what you live with. Take care 👍🏻💖
Taylor, I’m a nurse. Have u seen an rheumatologist? They deal with the immune system. When u said, “inflammatory response” I immediately thought of autoimmune system. You may want to get a consult my dear. Good luck and keep us posted!
I immediately thought of autoimmune diseases. I have one. Sadly, they tend to like to visit in pairs. I hesitate to make suggestions to Taylor because I don't know all if her symptoms, how many years they've been there, etc.
Taylor you are my favorite. Thank you for just being you. The surprise vlogs are always my most watched! It's fun seeing how you live your day to day lol
Taylor, I am not sure if you will see this but, are the lumps on other parts of your body as well? My boyfriend had lumps like you are describing randomly throughout his body. He was diagnosed with MAC (in his case of the lung). He didn’t have chronic pain but the lumps were very similar to the way you described yours. Also I want to say thank you so much for sharing your story/journey of chronic pain. I have suffered from chronic migraines since I was 12. It’s great to hear that I am not alone. Stay positive and I hope you get the answers you are looking for. Thank you!
I’ve been using the Just for Men dark brown on my blonde eye brows for a year and I swear the longer you use it the longer the colour lasts. It’s amazing!
me omg!! i thought my youtube feed was playing a trick on me, like maybe it was an old video recommendation, but...nope! Can't wait for winter tho seriously!! lol
My situation is so similar to yours. You perfectly described it. I will spend hours rubbing those muscles in that area around my neck. (To the point that they’re sore the next day) I’ve seen neurologists, chiropractors, & pain specialization. And they can’t figure it out for me either :( You’re not alone girly. We will overcome this!
I think what you’re talking about in your neck is a swollen chain of lymph nodes.. I also have neck pain and I have jaw pain that gives me headaches and my lymph nodes get swollen during flare ups too.. there are lymph nodes all over that area so even if it isn’t in the typical place your lymph nodes are, that could still be what it is.. my physical therapist said that muscle spasms and tightness can flare up lymph nodes and make them swell like that
I don’t really comment on vids but I really appreciate that you list everything you mention with links. I know it’s probably time consuming to list everything, but know it’s very much appreciated!! Love videos like this 👏🏽
I know you said it wasn't a lymph node situation, but I had a weird autoimmune issue in college called Kikuchi Fujimoto disease, and I would have flares of hard and painful lymph nodes, but it was not just my lymph nodes, but up and down my neck like you're describing. I had another flare back in 2016, and was given an ultrasound on my neck to check the size and shape... Could you request an ultrasound of your neck?
Verochka_Moya she mentioned in an older comment she’s going to an ENT for an ultrasound on Wednesday. My mom has the same issue as well and is going to see an ENT for an ultrasound. I haven’t heard of kikuchi fujimoto, only Hashimoto’s which is what we think my mom has.
@@EdgyEspresso Awesome! Glad to her she's going to an ENT. I'm sorry about your mom. Is she doing better? Kikuchi is similar, but attacks just the lymph nodes. It took a while to get diagnosed, but once the biopsy came back negative for lymphoma, there were only a limited number of things it could have been. The hospital actually had a doctor from Japan who had seen it before... It's more common in Asia, and it also effects females more than males. I was lucky for such a dedicated team. Eventually it went away on its own a year-ish later.
Sorry to hear you’re having unexplained medical issues... ☹️ I have chronic pain and it was so frustrating switching doctors all the time trying to find out what is wrong with me... I’ve pretty much given up for now and hope more research sheds light on things. Really hope you’re able to get an answer and solution ☺️ much love for your channel 💛
Yes, Taylor! I get those lumps too. I too have chronic intractable migraines, which I get daily. Nothing has worked thus far. I have always assumed that those lumps are in the muscles. I have read comments and see that some have suggested that they are Myofascial Pain Syndrome. That sounds very likely to me. I was also diagnosed with Carotidynia at one point, which is inflammation in the carotid artery. This caused pain/swelling up the neck and into the jaw/ear area. I hope that you find some answers. There are so many issues related to the migraine syndrome that they are just learning about. I was first diagnosed at the age of two, so I have been around this block more than a few times!
I NEVER comment on videos, but when you started talking about the bumps in your neck, I knew I had to. I also get those hard bumps along my jaw and throat. I used to think they were my lymph nodes, but my neurologist doesn’t think it’s them. I take a lot of medication for epilepsy, and I’m wondering if they are the body’s way of dealing with and metabolizing so much medication. Either way, I’d be curious to know if you figure out what they are. Please keep us updated!
Hey! I also have epilepsy(15yrs+). This happened to me a couple of times with a change in a new medicine- the lumps would appear. After a couple weeks I would get off of the meds. It was almost like my body was telling me not to take it. The side effects aren't worth it. Finding medicine that works with your body is a never ending story. Just like T says appreciate the good days & go with your gut.
The one super hold curl product you need is gel! A big blob of gel in super wet hair to create that gel cast. Then let it dry and scrunch out the crunch!!! It took me forever to actually apply the product to super wet hair but it's a game changer.
I use ghost hair oil by verb. But I def want something that is going to hold my natural curls. Maybe for a video idea you could compare the curl products you have been testing. Also look into the "plop method"
@@lala_bee I love it. Been using it for a year now. I use garnier whole blends maple shampoo, and the shea butter and coco(the brown one) and then right after my shower I add the ghost oil on top then I put it in a turbie twist. I get 4 days hair out if it. The verb ghost oil line is great but expensive. I tried to rebuy it off Amazon but it was fake and did not work the same.
@@athenaphelps6688 Thank you! I'll have to try your combo. I did not like the Verb shampoo because didn't do anything for my hair, but I kept the conditioner.
@@lala_bee the conditioner I feel like is amazing with all type of shampoos. It does great things. I'm a blonde (more hair per square inch) with wavy frizzy thick dense hair. I dont brush it and only run my fingers thru it. I dont wash my hair but maybe 2 times a week if that. I use the Maui vanilla bean dry hair oil for in between and and taming frizz for morning hair. I dont use heat in the summer. Use whatever shampoo and conditioner you feel works best and add the ghost hair oil. I've trained my scalp to tolerate the no brushing, 4 day hair system I use for the past 4 years
Taylor I used Yon Ka moisturizer years ago and had to banish it to the back of the drawer, completely broke me out and I have normal/dry skin. I guarantee that is what caused your breakouts. Love your videos ❤
I’m so sorry about your pain. I would recommend seeing a rheumatologist. I’m not sure if you already do. My daughter sees one in San Diego. He is amazing. A good rheumatologist can really help you with pain and inflammation.
I am an extremely blonde girl with CLEAR eyebrows. I started dying mine with Just for Men a few months ago after seeing Jenna Marbles try it and I'm not kidding when I say it's changed my life. I now feel 10000x more confident without makeup on since my eyebrows are visible for the first time in my life!
Oh yeah, yonka is a no no for me as well.. all the products I’ve tried from them broke me out badly.. I have sensitive break out prone skin, btw.. also I hope you get some answers on your health issues.. good luck ❤️
That Fabletics store is A+! Totally wish there were one closer to where I live! For the "rocks" in your next, my best friend was getting small ones for over a year along with severe migraines and fatigue. After about a year we all convinced her to get them checked out fully, ENT biopsied them and it turned out to be the beginning of thyroid cancer. She had her thyroid removed within a month and is "rock" free now since January. The doctor who did the surgery said that basically her body was trying to fight it on its own and sort of crystallized around one of the nodules in her neck to prevent it from spreading. Hopefully you get some answers, I read below that you're seeing an ENT which is amazing. Sending love and good health days your way ❤️
Just to add, nix the antiperspirant asap! Reading up on it, it can cause all sorts of issues with the lymphatic system and wreak havoc on your body with prolonged use!
Definitely sounds like an inflammatory response. You should try to get an ultrasound during a flare. They also might want to biopsy depending what they see especially since it's causing you a ton of pain. I have something called Mast Cell Activation which makes my body attack everything good or bad and I get major inflammatory responses. It can be Histamine related. Because you had too much Histamine that Day from high histamine foods (you'd be shocked - look up a low Histamine diet) and the sun can cause Histamine release as well as stress and then I react anaphylacticly or with rashes and hives but it causes inflammation and everyone reacts different. So maybe it's Mast cell? It sucks when doctors don't know and they just kind of give up. That happens to me all the time but we have to be our best advocate and keep pushing for whatever test or doctor referral or anything that we think we should do for our health. Lots of research on our part which sucks but we are left to suffer the consequences it we don't.
Wowwww it's like you're reading a page right out of my book. I'm being tested for mastocytosis. I had never heard of it before but was going to the ER every other week from anaphylaxis. Unfortunately, the doctor was a jerk and made me feel guilty/had me in tears for not keeping track of each episode from the last 1.5 years and what I ate/was doing at the time. I haven't had an episode in months, but now my scalp is having major issues with sores. Seeing your comment has motivated me to pursue my mast cell research again. Hope you're feeling better 💕
Melissa If i can help in any way let me know!! Definitely watch your Histamine intake at this time. I take supplements for it at every meal. Other things can set me off too though like scents. Like cleaning supplies and perfume. Any scents and MOLD is a big one!. I've had to change all that in my house but otherwise I carry and epi pen and a face mask if I'm out. Mast Cell is hard to diagnose so I had to seek out a specialist in Washington (I live in Canada) and she looked at my genes which had a lot to do with my Mast Cell flare up. Keep pushing with the doctors. They get used to the day to day and can't see past that sometimes. Having an invisible illness is so hard. Wishing you the best xxxx
Do you take maxalt for your migraines?? That’s the only thing that resolves mine. Granted you still get the migraine hangover but the massive head pain is gone.
I had to switch to Naratriptan from the Maxalt because I couldn't handle the hangover. The Naratriptan has worked wonders for me. Hate knowing you're in pain 💔 sending healing vibes your way ❤
ZX6R Unicorn, i used to take the first one you mentioned before this as well same feeling i guess hangover-y since i had migraines still and im on topomax to prevent migraines as well.
I have autoimmune diseases mainly Sjogrens and I suffer from migraines as well. My rhemo said that it usually starts from the inflammation of the neck lymph nodes which we do have multiples up and down in the neck. I've noticed that when i get cortisone shots in the back of my neck my neck pain goes away along with the swelling and it prevents migraines. Hopefully this helps! Feel better!
In your cleansing balm video you mentioned you were hoping Elf would come out with one. They do have a melting balm. Just used it last nigh and loved it. Washes off completely, no fragrance and no eye fog.
This is going to sound a bit crazy but it could be your jaws. I was getting intense pain in my throat, temples, head, neck and shoulders.. three Dr's in and I'm diagnosed with TMJ, I'm a teeth clencher, it's very stress related. You can get enormous inflammation in your jaws that affects EVERYTHING.. including running low grade fevers.
since u mentioned yesstyle, can u do a full face of korean products video? makeup but maybe even with skincare bits, it would be interesting! love you!
OMG!! I didnt know Fabletics had an actual store girlfriend!!! I love them and JustFab!! I was an ambassador for JustFab, love them both so much!! Great items!!
Have tests done for sarcoidosis, which is an auto-immune condition of lymph that causes nodules to form in many places internally. The lymph thinks there is a foreign object in the body, but when it doesn’t find one, it attacks itself. I have nodes in my lungs which are asymptomatic, but people get them on their spine, behind their eyes, in the neck, and in other internal organs. It’s worth looking into and also, I agree with the others, lupus. Good luck!❤️
Taylor my old manager had lots of migraines also and they found nodes on her thyroid the area your showing is where your thyroid is so I would definitely consult and endocrinologist
The Paul Mitchell Wild Ginger Awapuhi mousse is great. I have curley hair and love this product. I make a cocktail of about five things to keep my hair in check. 🌺
I just have to say your fitness progress is noticeable, your legs look more toned and you look leaner overall. You’ve always looked great, just wanted you to know it looks like your work is paying off. ❤️💪🏻
I really don’t think she needs any medical suggestions or advice from randoms in the internet. Also naturopathy is an entire scam so not a great suggestion anyway
Those sound like lymph knodes in your neck. And usually they flare up when you have an infection or it’s fighting something? But have they looked into lymph nodes issues? I had Hodgkin’s lymphoma and we have lymph nodes in our neck, armpits and pelvic. I started writing this before you said something about lymph nodes. But it’s still worth looking into. Hope you feel better and can figure it out. I suffer from extreme migraines also. But not near as bad at yours. Love you girl
It does sound like lymph nodes. We actually have lymph nodes all down our neck. A quick google image search shows where they are all located on our throat/neck/collarbone area. Mine flare up during a migraine, but not as bad as hers :-( Taking steroids reduces inflammation, and a short course of steroids can sometimes help the pain. They clear up my neck stiffness too. Chronic pain sucks.
Missy Maria I had lymph node cancer! I’d think I’d know about lymph nodes , thank you. And have you ever heard of second opinions? They never hurt! I also suffer from migraines.... if I could mentions anything to help Taylor not suffer as badly I will. But again thanks for your incorrect input.🤷🏻♀️🤦🏻♀️
Have the doctor's done a thyroid ultrasound? The lumps sound like thyroid nodules. If it's a nodule, please have them do a fine needle biopsy to rule out thyroid cancer. Hope you feel better soon. ♥️♥️♥️
Taylor, the neck thing is a neurologic response. My primary care put me on Flexeril, and butalbital because my migraines were causing my whole body, neck, shoulders to lock up. Especially after my heart surgery & stroke in 2016, they keep close eye on my amount of flare ups. I try to take CoQ10, and cbd oil for pain which has helped.
![Blox Fruits Dragon Rework Update [Full Stream]](http://i.ytimg.com/vi/EqDAp8udhm0/mqdefault.jpg)
i live on the opposite end of the country (nyc), im a black girl with super curly hair and brown skin, i don't even wear makeup except for eyebrows, but you've been one of my favorite youtubers for like 6 years now and i watch every foundation video and makeup haul and vlog cuz you're simply the best 💓
Hey, I'm a 70 yr. young woman who loves her too! I can't do makeup like she does bc it's full-on glam for a young woman, but I get inspiration from her. Hevk, she's just entertaining!
Ah thanks for watching for so long!!! That’s awesome.
Awwww, what a great story!
Totally agree! I’m a huge fan, curly, curvy, 47 yr old gray haired Glamma and you are my go to when it comes to foundation. I know I’m going to get an unbiased and unfiltered opinion. Your personality is really what makes everything so enjoyable. I know the struggles of migraines and remember getting my 1st one at age 4. My mother putting me in a shallow tub of cool water with the light turned off in the bathroom and just floating till my teeth started chattering.🥶 I just started Emgality took my first shot 2 days ago. I’m praying for some relief.......I wonder if those rocks are an allergic reaction of sorts.🤔 I hope that someone can figure it out for you even if it’s a voodoo priestess because not being able to get relief from that pain is such agony. I think about you and Kristi all the time. In my head we’re friends so I say a little prayer for you guys and all the migraine/cluster headache sufferers out there. Only thing mine are good for is getting a foot massage out of my hubby.😜
I'm almost 53 and am in Virginia. I do love makeup but Taylor has me interested in different foods I would never think of, house decorations and other random stuff. She just seems like such a cool lady! Unfortunately, I now say super cute all the time😂😂😂😂
Tayolor, the crow thing is obvious: You're tiny, and with all that shiny black hair they no doubt have decided you are their Queen!
April Nelson Aww! That’s so cute!
That change room technology! 🤩 That should be everywhere!
Can't put it in stores in bad areas or who's primary shopping demographic is low income. The tablets WILL get stolen I live in studio city which is a relatively good part of LA and people's cars get broken into all the time inside our locked garage
I love that you do your vlogs as a bonus video. It's nice to have a little extra Taylor during the week.
We are so lucky!
Glad to see that just for men(and jenna) actually CAN work for your brows
That's exactly what I thought of too 🤣🤣
I’ve used it because of Jenna and it really works so well!!
how long does it last with face washing and stuff? :)
Bought this tonight to try, wish me luck
Yessss
I'm so glad you did this announcement about the Just For Men!!! I can't live without it now!!
you are the most dedicated youtuber that ive been following so far...and yes! i love ALL ur vlogs...
Whoever came up with the idea for using men's hair dye to tint your eyebrows is GENIUS! Loving your earring collection sooo much! 💗
I am so sorry for your pain. I have pain from a crushed heel. I wish I could help you cause I know what living with pain is. Watching your channel while I was doing learning to walk again helped take my mind off the pain. I never thanked you for that. Thank you Taylor ! I will be praying for you and I want you to share with us your pain and struggles. People love you and that includes me.
I save her videos for the evenings! I have chronic migraines, and a variety of other chronic issues - She helps distract me from my pain well enough that I’m able to sleep post-video ❤️. Taylor is a chronic pain superhero🦸♀️ .
My boyfriend just came home and said “we get a bonus vlog tonight!!”
😅
omgg so cute!!
Bless
Awe, I love him already!
Tell him welcome to the family!
Taylor in those gold glasses is literally the cutest thing!
I have lupus and I have the same lumps during a flare. Couldn’t hurt to ask for a blood test to check for autoimmune disorders.
Yes I was going to say this my friend has lupus and she has these little rocks when she gets a flare up.
Me& my mother have fibromyalgia & we also get the same rock like bumps...during flares or after over exerting ourselves
I also get hard lumps during a flare! Not alot but sometimes 2 or 3 that can feel...and because I know they are there I'm constantly feeling them
Helshira I have Sjogrens, doctor says I don't lupus, but I also get these weird lumps in my neck when I get migraines! I thought I was crazy lol
I have the same issue and even have it happen by my under arms and cleavage area of my breast but mainly through out my neck. I have fibromyalgia and a hypothyroid. I have chronic pain mostly in my shoulders and neck but all over my body. I have asked my doctor about the lumps and have gotten no answers.
Drinking game - take a shot every time Taylor says "super" or "cute" - two shots if she says "super cute." 😂 You'll be hammered in no time.
Lmfaooo.. She said "super cute" as I read ur comment, and 4 more times as I was writing this😂😂😂
Truth!! 😂😂 She's so addicting though..
I cracked up with the footage of the tanning drops! Your face was priceless 😂😍
Girl, if you're talking about pain and asking for suggestions, it must be baaaaad. 😔 Love you so much and hope you find some answers ❤️🙏 You're beautiful!
She’s the only ads I actually look into because she has ALWAYS been truthful. So thankful I’ve been watching for years now and to see her just being herself makes her my absolute favorite always😭
Love your videos! Have you ever had those lumps biopsied? A biopsy would be a way to figure out what cells/tissue makes up the lumps, and hopefully point you in a direction as to what is causing it.
Really good idea
I’m getting a biopsy and ultrasound Wednesday!
@@taylorwynn Good luck! I hope that you are able to get some information on the swelling.
@@taylorwynn Hoping you find some answers!
thataylaa hope they figure out what it is💜💜💜
Taylor's comment section is the best 👍👍 I love all of you notification squad peeps!!! Taylor thank you for inspiring your audience members that live with chronic pain!!! Bless the baeritto fam 😭🥰🥰🥰
❤️❤️❤️❤️
When I go to the mall because I need clothes, I find nothing. When I'm at the mall because I'm bored, I can spend hundreds :)
Oh, and the truffle flatbread is the BEST!
You’ve convinced me, I need to try Fabletics!!! Your vlogs are my favorite, it just feel like I’m talking to my friend and catching up lol.
I don't get chronic migraines like you do, but when I get a migraine it's normally caused by knots in my neck. It's myofacial pain, which means my entire back and neck are literally covered in hard, pea-size (or bigger) lumps all the time. If it was myofacial pain, I'm sure your physio/doc would know that though. I really hope you can get some answers soon! It's obviously some form of knot that's pressing on nerves, but it's weird your medical team can't figure it out!
From one spoonie to another, I'm sending hugs 💖💖
Yes!! I commented as well but wanted to copy paste my comment here since there are so many comments 😊 I do agree that it's weird that her doctors wouldn't suggest myofascial pain syndrome 🤔 but anyway, here's my comment in case she happens to read yours and mine gets drowned in the hundreds of comments lol
Google Myofascial Pain Syndrome!!! It sounds exactly like what you're going through. It causes pain throughout the body, mostly in neck, back, and muscles. And it causes rock hard muscle lumps in these areas. In college, I had neck lumps and lumps down my spine and lower back. They were super hard and painful and obviously, I was freaked out. I had biopsies done, blood work, etc and the only thing that really came up was my abnormal autoimmune panel. I was referred to a rheumatologist and he diagnosed me with lupus and myofascial pain syndrome. The MPS causes muscular knots that are super painful to the touch. I have found that as long as I keep my autoimmune issues under control, the lumps stay away but that's not true for everyone. I hope you find some answers soon!
❤️🥄 ❤️ If only there was a way to borrow spoons, lol. On my off days, I’ll let you borrow a couple of mine if I can borrow a couple of yours for when I’m at work! 😂
Zebra Strong if there was anyway to actually borrow spoons, that would be amazing. I’m doing better here in MI, because the weather is warm. Really not looking forward to winter. This past winter was my first without major pain meds since 2008 & I could not function. Since my last doctor retired, all my new doctors want to try every single thing before they put me back on meds. I’m thinking death might come from shock because of how much pain I was in Dec-May. It’s horrible. Everyone that deals with chronic pain/illnesses has my empathy. It effects every aspect of your life.
Jenna Frazier, maybe that’s the perfect middle ground. Down here in MS, I’d kill for some just plain cold as opposed to our humidity, lol. I’ve been told from family that live up north that our winter is a worse feeling cold than up there because of the humidity... I’m really lucky to have an amazing doctor that thinks EDS is cool, so he is constantly doing his own research and working with me to learn what works best for my body. Lol, it’s not every day you find an orthopedist willing to take over as a primary care provider. If I could recommend him to the entire world, I surely would!
@@jennajune2101 I'm so sorry you had to go through the winter with no pain meds! That's ridiculous!!
I have fibro, M.E and recurring shingles, and permanent myofacial pain. It depends where the lumps are, as to how painful it gets really.
I'm in Scotland so the cold, damp winters are a killer. I hate winter-time!
I would recommend going into see a rhuematologist. I did a couple of years ago for some very random symptoms and told the doctor that I wasn't even sure if I was in the right place. The doctor told me that they actually deal with more than autoimmune diseases. She did a big battery of tests and did not give up without a result. I've learned through family history that many many autoimmune diseases do not always show up in blood tests for a decade or more. I have every single symptom of RA and respond to infusions for it but I am negative on every blood test. It's a starting point and all they can do is tell you somewhere else to go! Best of luck!
First post!! I know you’re not but every time you say “pacific” I always hear “6pm specific time”. 😂
You looking so out together to run errands and chill at home is so motivating. I've been in such a rut since COVID, but these vlogs remind me to look good for yourself
Crows and ravens are really smart and they remember faces and tell their friends if your friendly or not so you must have been nice to some
True!
I know you asked about the May clinic on your other video but I HIGHLY recommend them. My mom was given practically a death sentence cave diagnosis when she reached out to Mayo. She's been in remission for seven years in October. My mother in law also went to them, she has unfortunately passed but she had been given a month to live by another practice and thanks to Mayo's guidance and compassion we had her with us for almost 18 months. She got to spend precious time with us and our boys and we made a lifetime of memories! I'll be praying for you! 💗
Sounds like possibly lymph nodes. Maybe ask for an ultrasound. I’m a tech and we can see nodes whether they are normal or abnormal around the neck and other areas. - maybe see an ENT specialist if they are appearing more around your throat as well.
Ya I’m getting a ultrasound done next week from an ENT- thanks!
thataylaa awesome. Hopefully they figure it out! Good luck
nicole fedorko I have this too, a string of hard pea sized lumps going up the back of my neck on one side and they never go away. Got an ultrasound, they were lymph nodes. Ultra sound deff helped ease the worry.
Yes! My son gets these! The doctor says that it’s his way of fighting off anything that shouldn’t be there. They come and go. Not sure if they are the same, but I would bet they are
I said the same thing. I’m a nurse and wondering if it may possibly be an allergen. I have a pt that has to have weekly infusions because of her allergies and she has lymph node changes with exposure to certain triggers.
I’m going through a really hard time with my boyfriend right now and I’m not sure where we stand at the moment so I’m really not in a great mood and I’ve been crying off and on for the past 24 hours but I just wanted to let you know that watching your video brightened my mood a little and made me feel a lot calmer and took my mind off of what’s happening, thanks taylor💜
Bless your heart for putting up a long vlog when you're dealing with such difficult health Taylor. I know you're used to it but still know how much we appreciate all your effort. I hope you get some idea of what to do about your neck rocks, it sounds awful. Sending you so much love. 💕💕💕💕💕💕💕💕💕💕
My mom has dealt with migraines for years and I always send her your videos because she is always talking about the same symptoms! She has the bumps too and she believes they play a factor in her flair ups too!! I pray they find answers to migraines soon ❤️
Bonus vlogs for the win! Always such a great surprise!
❤🌯❤🌯❤🌯❤🌯❤
So grateful to have an extra video from you this week! I’m sorry you’re not feeling well, though. I hope you figure out what’s going on soon! Love and light ❤️
A surprise Taylor video always makes my day!! 🖤🥰🖤
I watch ALL your videos. You are so relatable but for some reason this specific video made me so calm & felt like I was legit talking face to face to a best friend. I had no idea that even 31 minutes passed
Please do a tutorial on your make up in the striped shirt! Gorgeous! 😍
Something similar happens to me.
My cervical nerves (back of the neck) flare up and it messes with my sinuses and I literally spend hours throwing up. No medicine helps, I just have to wait for it to go away.
No doctor I’ve spoken to believes that my vomiting is not caused by medicine (they think I take too much medication when really all I do is wake up and throw up).
I’m no help at all, sorry, but when my cervical nerves flare up I get hard lumps around my neck and especially behind my ears.
You’re not alone and thank you for sharing how you feel.
Love you Taylor 🖤 and yay for the bonus vlog!!!
“Low rise is high rise if you’re short” 😂😂🤦🏻♀️ truth!
I’m a little late to the game but I tried everything for neck spasms and tension that lead to headaches. After exhausting all natural options, and after about 3 years, I ended up going on Lexapro for anxiety and Xanax as an emergency treatment. Their ability to relax and chill me out has helped me tremendously. Obviously not a good option for everyone, but after a lot of research, I gave them a try and finally have my life back. Much love. Xoxo
Loved that striped shirt, was super cute and your tan looked amazing! I already bought the St. Tropez one after seeing you recommend it, which has changed my life. It does come off pretty quickly within the week so I just ordered the Loving Tan one to try out. Thanks for the best recommendations! But seriously, anyone who is super pale (like see-through) try the St. Tropez one!
Love you Taylor! I’ve had headaches my entire adult life. NOT comparing to what you go through but sometimes they get really bad. It’s so weird cause if I don’t have a headache all of a sudden I’ll notice and I’m like oh my gosh my head doesn’t hurt! Mine involve my neck too. I just wanted you to know I understand (sort of) what you live with. Take care 👍🏻💖
Taylor, I’m a nurse. Have u seen an rheumatologist? They deal with the immune system. When u said, “inflammatory response” I immediately thought of autoimmune system. You may want to get a consult my dear. Good luck and keep us posted!
I immediately thought of autoimmune diseases. I have one. Sadly, they tend to like to visit in pairs. I hesitate to make suggestions to Taylor because I don't know all if her symptoms, how many years they've been there, etc.
Taylor you are my favorite. Thank you for just being you. The surprise vlogs are always my most watched! It's fun seeing how you live your day to day lol
Taylor, I am not sure if you will see this but, are the lumps on other parts of your body as well? My boyfriend had lumps like you are describing randomly throughout his body. He was diagnosed with MAC (in his case of the lung). He didn’t have chronic pain but the lumps were very similar to the way you described yours.
Also I want to say thank you so much for sharing your story/journey of chronic pain. I have suffered from chronic migraines since I was 12. It’s great to hear that I am not alone. Stay positive and I hope you get the answers you are looking for. Thank you!
The Just for Men beard dye is so good for your eyebrows. It ends up fading but it fades so pretty.
You were looking even more beautiful than usual when you were doing a haul after San Diego trip.
I’ve been using the Just for Men dark brown on my blonde eye brows for a year and I swear the longer you use it the longer the colour lasts. It’s amazing!
Who else got EXTREME christmas vibes from the thumbnail?
me omg!! i thought my youtube feed was playing a trick on me, like maybe it was an old video recommendation, but...nope! Can't wait for winter tho seriously!! lol
Yess! That's exactly what I thought when I saw it, too!
Yes!!
me!! lol i wanted to comment this but i thought maybe i was crazy.
Same!!
can i just say how much i appreciate the effort you put into your description box? even linking things you only just mentioned. love u!
My situation is so similar to yours. You perfectly described it. I will spend hours rubbing those muscles in that area around my neck. (To the point that they’re sore the next day)
I’ve seen neurologists, chiropractors, & pain specialization. And they can’t figure it out for me either :(
You’re not alone girly. We will overcome this!
Crows are actually a sign of new beginnings and good things to come.
I think what you’re talking about in your neck is a swollen chain of lymph nodes.. I also have neck pain and I have jaw pain that gives me headaches and my lymph nodes get swollen during flare ups too.. there are lymph nodes all over that area so even if it isn’t in the typical place your lymph nodes are, that could still be what it is.. my physical therapist said that muscle spasms and tightness can flare up lymph nodes and make them swell like that
I don’t really comment on vids but I really appreciate that you list everything you mention with links. I know it’s probably time consuming to list everything, but know it’s very much appreciated!! Love videos like this 👏🏽
Could you do a video on different/best SPF's please.. I trust your judgement! and good SPFs are so hard to find. Love your vlogs!!
Dr Dray’s channel. No nonsense dermatologist.
Vlog moooooore!!! love all the mini hauls and recaps and catching up with u!!
Yes!! We love a nice extra long bonus vlog! 🌯💛
Sorry you're not feeling well Taylor 😢 I hope you're able to find what's causing your pain so you can start feeling better. Love the vlog💕
I was waiting for the private video and I was hoping it was a vlog and it would go up today!!
okay so you’re always gorgeous but at 15:30, I LOVEEEE this look on you! The shirt, the hair, the makeup. Perfectionnnn! Loved this vlog💛🌯
I know you said it wasn't a lymph node situation, but I had a weird autoimmune issue in college called Kikuchi Fujimoto disease, and I would have flares of hard and painful lymph nodes, but it was not just my lymph nodes, but up and down my neck like you're describing. I had another flare back in 2016, and was given an ultrasound on my neck to check the size and shape... Could you request an ultrasound of your neck?
Verochka_Moya she mentioned in an older comment she’s going to an ENT for an ultrasound on Wednesday. My mom has the same issue as well and is going to see an ENT for an ultrasound. I haven’t heard of kikuchi fujimoto, only Hashimoto’s which is what we think my mom has.
@@EdgyEspresso Awesome! Glad to her she's going to an ENT. I'm sorry about your mom. Is she doing better? Kikuchi is similar, but attacks just the lymph nodes. It took a while to get diagnosed, but once the biopsy came back negative for lymphoma, there were only a limited number of things it could have been. The hospital actually had a doctor from Japan who had seen it before... It's more common in Asia, and it also effects females more than males. I was lucky for such a dedicated team. Eventually it went away on its own a year-ish later.
Sorry to hear you’re having unexplained medical issues... ☹️
I have chronic pain and it was so frustrating switching doctors all the time trying to find out what is wrong with me... I’ve pretty much given up for now and hope more research sheds light on things.
Really hope you’re able to get an answer and solution ☺️ much love for your channel 💛
Isolated nerve dysfunction? Have you had MRI when the knots are active? That’s so bizarre really hope you’re feeling better chronic pain sucks 🙏🏻😭
Yes, Taylor! I get those lumps too. I too have chronic intractable migraines, which I get daily. Nothing has worked thus far. I have always assumed that those lumps are in the muscles. I have read comments and see that some have suggested that they are Myofascial Pain Syndrome. That sounds very likely to me. I was also diagnosed with Carotidynia at one point, which is inflammation in the carotid artery. This caused pain/swelling up the neck and into the jaw/ear area. I hope that you find some answers. There are so many issues related to the migraine syndrome that they are just learning about. I was first diagnosed at the age of two, so I have been around this block more than a few times!
I always tinted my eyebrows with my current hair dye. But I used a spare eyebrow spoolie. I only left my eyebrows on for about 10 mins.
Same!
I NEVER comment on videos, but when you started talking about the bumps in your neck, I knew I had to. I also get those hard bumps along my jaw and throat. I used to think they were my lymph nodes, but my neurologist doesn’t think it’s them. I take a lot of medication for epilepsy, and I’m wondering if they are the body’s way of dealing with and metabolizing so much medication. Either way, I’d be curious to know if you figure out what they are. Please keep us updated!
Hey! I also have epilepsy(15yrs+). This happened to me a couple of times with a change in a new medicine- the lumps would appear. After a couple weeks I would get off of the meds. It was almost like my body was telling me not to take it. The side effects aren't worth it. Finding medicine that works with your body is a never ending story. Just like T says appreciate the good days & go with your gut.
Scrolling trying to find a video to watch, then you upload unexpectedly! YAS
Same!!
The one super hold curl product you need is gel! A big blob of gel in super wet hair to create that gel cast. Then let it dry and scrunch out the crunch!!! It took me forever to actually apply the product to super wet hair but it's a game changer.
I use ghost hair oil by verb. But I def want something that is going to hold my natural curls. Maybe for a video idea you could compare the curl products you have been testing. Also look into the "plop method"
I have straight hair but will Google the plop method because now I just have to know!
How do you like the Ghost oil? I have fine, frizzy, wavy hair and was going to try it once I finished up the Bumble +Bumble serum.
@@lala_bee I love it. Been using it for a year now. I use garnier whole blends maple shampoo, and the shea butter and coco(the brown one) and then right after my shower I add the ghost oil on top then I put it in a turbie twist. I get 4 days hair out if it. The verb ghost oil line is great but expensive. I tried to rebuy it off Amazon but it was fake and did not work the same.
@@athenaphelps6688 Thank you! I'll have to try your combo. I did not like the Verb shampoo because didn't do anything for my hair, but I kept the conditioner.
@@lala_bee the conditioner I feel like is amazing with all type of shampoos. It does great things. I'm a blonde (more hair per square inch) with wavy frizzy thick dense hair. I dont brush it and only run my fingers thru it. I dont wash my hair but maybe 2 times a week if that. I use the Maui vanilla bean dry hair oil for in between and and taming frizz for morning hair. I dont use heat in the summer. Use whatever shampoo and conditioner you feel works best and add the ghost hair oil. I've trained my scalp to tolerate the no brushing, 4 day hair system I use for the past 4 years
Taylor I used Yon Ka moisturizer years ago and had to banish it to the back of the drawer, completely broke me out and I have normal/dry skin. I guarantee that is what caused your breakouts. Love your videos ❤
I’m so sorry about your pain. I would recommend seeing a rheumatologist. I’m not sure if you already do. My daughter sees one in San Diego. He is amazing. A good rheumatologist can really help you with pain and inflammation.
Taylor never asks us for help and I hate it that she’s hurting enough that she has to. I’m sorry for all of you pain doll ❤️
I enjoy your vlogs so, so much!!! 😚
I am an extremely blonde girl with CLEAR eyebrows. I started dying mine with Just for Men a few months ago after seeing Jenna Marbles try it and I'm not kidding when I say it's changed my life. I now feel 10000x more confident without makeup on since my eyebrows are visible for the first time in my life!
Oh yeah, yonka is a no no for me as well.. all the products I’ve tried from them broke me out badly.. I have sensitive break out prone skin, btw.. also I hope you get some answers on your health issues.. good luck ❤️
That Fabletics store is A+! Totally wish there were one closer to where I live! For the "rocks" in your next, my best friend was getting small ones for over a year along with severe migraines and fatigue. After about a year we all convinced her to get them checked out fully, ENT biopsied them and it turned out to be the beginning of thyroid cancer. She had her thyroid removed within a month and is "rock" free now since January. The doctor who did the surgery said that basically her body was trying to fight it on its own and sort of crystallized around one of the nodules in her neck to prevent it from spreading. Hopefully you get some answers, I read below that you're seeing an ENT which is amazing. Sending love and good health days your way ❤️
Just to add, nix the antiperspirant asap! Reading up on it, it can cause all sorts of issues with the lymphatic system and wreak havoc on your body with prolonged use!
Go watch Jessica Braun’s hair video. She has good recommendations for curly hair products !!
I was thinking the same thing!
as someone who works at Trader Joes, it’s very funny when youtubers i love do trader joe hauls. also that mushroom flatbread is the best
Taylor just used your code for Bryan Anthony and I got my mom the sweetest pair of earrings thank u so much
NYM texture spray is life! It makes my curls look so beachy and tousled!
Definitely sounds like an inflammatory response. You should try to get an ultrasound during a flare. They also might want to biopsy depending what they see especially since it's causing you a ton of pain. I have something called Mast Cell Activation which makes my body attack everything good or bad and I get major inflammatory responses. It can be Histamine related. Because you had too much Histamine that Day from high histamine foods (you'd be shocked - look up a low Histamine diet) and the sun can cause Histamine release as well as stress and then I react anaphylacticly or with rashes and hives but it causes inflammation and everyone reacts different. So maybe it's Mast cell? It sucks when doctors don't know and they just kind of give up. That happens to me all the time but we have to be our best advocate and keep pushing for whatever test or doctor referral or anything that we think we should do for our health. Lots of research on our part which sucks but we are left to suffer the consequences it we don't.
Wowwww it's like you're reading a page right out of my book. I'm being tested for mastocytosis. I had never heard of it before but was going to the ER every other week from anaphylaxis. Unfortunately, the doctor was a jerk and made me feel guilty/had me in tears for not keeping track of each episode from the last 1.5 years and what I ate/was doing at the time. I haven't had an episode in months, but now my scalp is having major issues with sores. Seeing your comment has motivated me to pursue my mast cell research again. Hope you're feeling better 💕
Melissa If i can help in any way let me know!! Definitely watch your Histamine intake at this time. I take supplements for it at every meal. Other things can set me off too though like scents. Like cleaning supplies and perfume. Any scents and MOLD is a big one!. I've had to change all that in my house but otherwise I carry and epi pen and a face mask if I'm out. Mast Cell is hard to diagnose so I had to seek out a specialist in Washington (I live in Canada) and she looked at my genes which had a lot to do with my Mast Cell flare up. Keep pushing with the doctors. They get used to the day to day and can't see past that sometimes. Having an invisible illness is so hard. Wishing you the best xxxx
Gosh the clip starting at around 15:30 of your sit down haul you look soooo good! Love the top, simple makeup, & curled hair!🤩
Do you take maxalt for your migraines?? That’s the only thing that resolves mine. Granted you still get the migraine hangover but the massive head pain is gone.
I take maxalt!!! It works wonders i take that and two tylenol and poof my migraine is GONE! Miracle.
Ya I take it about 5 times a week, wouldn’t survive without it
I had to switch to Naratriptan from the Maxalt because I couldn't handle the hangover. The Naratriptan has worked wonders for me. Hate knowing you're in pain 💔 sending healing vibes your way ❤
ZX6R Unicorn, i used to take the first one you mentioned before this as well same feeling i guess hangover-y since i had migraines still and im on topomax to prevent migraines as well.
I have autoimmune diseases mainly Sjogrens and I suffer from migraines as well. My rhemo said that it usually starts from the inflammation of the neck lymph nodes which we do have multiples up and down in the neck. I've noticed that when i get cortisone shots in the back of my neck my neck pain goes away along with the swelling and it prevents migraines. Hopefully this helps! Feel better!
Trader Joes has hair and skin care products. I've been impressed with every one I've tried (I have curly hair)
In your cleansing balm video you mentioned you were hoping Elf would come out with one. They do have a melting balm. Just used it last nigh and loved it. Washes off completely, no fragrance and no eye fog.
This is going to sound a bit crazy but it could be your jaws. I was getting intense pain in my throat, temples, head, neck and shoulders.. three Dr's in and I'm diagnosed with TMJ, I'm a teeth clencher, it's very stress related. You can get enormous inflammation in your jaws that affects EVERYTHING.. including running low grade fevers.
since u mentioned yesstyle, can u do a full face of korean products video? makeup but maybe even with skincare bits, it would be interesting! love you!
OMG!! I didnt know Fabletics had an actual store girlfriend!!! I love them and JustFab!! I was an ambassador for JustFab, love them both so much!! Great items!!
Have tests done for sarcoidosis, which is an auto-immune condition of lymph that causes nodules to form in many places internally. The lymph thinks there is a foreign object in the body, but when it doesn’t find one, it attacks itself. I have nodes in my lungs which are asymptomatic, but people get them on their spine, behind their eyes, in the neck, and in other internal organs. It’s worth looking into and also, I agree with the others, lupus. Good luck!❤️
Taylor my old manager had lots of migraines also and they found nodes on her thyroid the area your showing is where your thyroid is so I would definitely consult and endocrinologist
The Paul Mitchell Wild Ginger Awapuhi mousse is great. I have curley hair and love this product. I make a cocktail of about five things to keep my hair in check. 🌺
I highly recommend you do research on sweat shops and sustainable fashion!!
Oh. Kackie Reviews Beauty just did a video on sustainable fashion. 😁
I just have to say your fitness progress is noticeable, your legs look more toned and you look leaner overall. You’ve always looked great, just wanted you to know it looks like your work is paying off. ❤️💪🏻
Have you tried seeing a Natropathic Dr.... Or an endocrinologist? Would love to know if they have any avenues that you haven't tried before. ❤️❤️❤️
SouthernStar I was also going to recommend seeing an endocrinologist
EXACTLY!! Naturapathic endocrinologist. Not reg endo...they only know diabetes pharm.
Let us know about ur journey. Healing grace sweet girl!
I really don’t think she needs any medical suggestions or advice from randoms in the internet. Also naturopathy is an entire scam so not a great suggestion anyway
Meagan Garrison she literally asked for advice...
@@meagangarrison9066 Hope saying 'randoms in the internet' brings the feeling of superiority you're looking for... God Bless Meagan.
Once youve worked out the curly hair products you really like, would you do a video about it/mention them in raves and rejects?
Those sound like lymph knodes in your neck. And usually they flare up when you have an infection or it’s fighting something? But have they looked into lymph nodes issues? I had Hodgkin’s lymphoma and we have lymph nodes in our neck, armpits and pelvic. I started writing this before you said something about lymph nodes. But it’s still worth looking into. Hope you feel better and can figure it out. I suffer from extreme migraines also. But not near as bad at yours. Love you girl
sammysamala09 Lymph nodes are not that far down your neck. Also, she mentioned that her doctors ran tests and ruled out her lymph nodes.
It does sound like lymph nodes. We actually have lymph nodes all down our neck. A quick google image search shows where they are all located on our throat/neck/collarbone area. Mine flare up during a migraine, but not as bad as hers :-( Taking steroids reduces inflammation, and a short course of steroids can sometimes help the pain. They clear up my neck stiffness too. Chronic pain sucks.
Missy Maria I had lymph node cancer! I’d think I’d know about lymph nodes , thank you. And have you ever heard of second opinions? They never hurt! I also suffer from migraines.... if I could mentions anything to help Taylor not suffer as badly I will. But again thanks for your incorrect input.🤷🏻♀️🤦🏻♀️
Yoo I loved the video! I love how it is multiple days and you show us your life and can let us know what's going on with you!
Have the doctor's done a thyroid ultrasound? The lumps sound like thyroid nodules. If it's a nodule, please have them do a fine needle biopsy to rule out thyroid cancer. Hope you feel better soon. ♥️♥️♥️
Taylor, the neck thing is a neurologic response. My primary care put me on Flexeril, and butalbital because my migraines were causing my whole body, neck, shoulders to lock up. Especially after my heart surgery & stroke in 2016, they keep close eye on my amount of flare ups. I try to take CoQ10, and cbd oil for pain which has helped.
Watch jessicas hair care routine, she mentioned some curly hair products i think you might like =)
I actually just tinted my brows the same way last week! My brows finally match my dyed hair. I’m obsessed