OUR INVISIBLE ILLNESS… How we deal with Endometriosis …
Ovaries, cramps and periods, … we’re talking about talking about it all and hopefully it helps you feel less alone. xo’s ~ Tati TODAY LAST CHANCE FREE …
I'm glad you posted this. Just now seeing it, but the tips…working out–what?!?! NO clue that could help with hormones.
They look like twins or are they baha
I love U both 💓
whenever erika is in a video i get so excited bc i’m currently in nursing school and i love seeing her learn makeup from tati. praying for everyone out there effected and others struggling with no support or health insurance 🙏🏻💛
Thank you for opening up. Cute necklace btw
The issues you brought up regarding insurance are so important, that’s something so many people struggle with. Not having insurance when you need care is one of the worst feelings in the world.
I am late to watching this, but I am so glad you two touched on the insurance aspect. I work in health insurance, specifically in preauthorization. Endo ablation are by far one of the most common services we see requested. So many women suffer with endo. Insurance is broken, and I can say that as someone working on the inside. They are also not the sole issue. It's the entire health care system that needs a revamp. Thank you for addressing so much in this video. You two are lovely!
Can you do a day in my life with Endometriosis
SO happy you are being so open Tati!!! You are so brave and I truly hope that all the positivity of your openness outweighs any type of negativity that I HOPE you do not receive.❤️❤️
thanks for the PSA, for real. Let's start a conversation great job ladies
Okay I love tati’s necklace like pls drop the link!
I'm from the uk and have just had a cyst out and then they found while being operated on they found I had this and it had spread to my bowels. I have been off contraception for 3 years and the ed is over producing
Endo warriors 💛💛
Love this video and the awareness you’re raising! Only thing is the definition of endometriosis is that it is tissue SIMILAR to the endometrium that’s lines our uterus, it is not the endometrium
💛
I love that yall talked about your experiences. I've had extremely painful periods ever since I was probably 14 but everyone told me it was normal, it was just cramps and that there was nothing wrong. It wasn't until I was 28 when I finally got a doctor that saw me and did tests and said okay I cant see anything from the outside but let's just treat you like you have endo because you seem to have the symptoms. We still haven't come across a great treatment but it's a start and it meant so much to be validated, to know I'm not crazy.
I have fibromyalgia. I understand that, because it's not visible, people think I'm crazy or lazy. But the pain is real and unbearable some days! Thanks for sharing your stories ❤️
I had a doctor do my routine blood tests to get cleared for college at an out of network laboratory. I was not notified and I got billed over $2000 even though I had insurance (through my parents). So now I have terrible credit out of college because I just couldn't pay for a doctors mistake. THE SYSTEM IS BROKEN!
Why not a laparoscopic surgery to remove it? I had it done in 1998. It’s one of the leading causes of infertility.
I had a hysterectomy last year from uterine fibroids and woooooow did it wreak havoc on my life. It’s not in our heads ladies! I owe a ton of money..
I know more about it now
What kind of NP? FNP right here 🙂
Have you been to a naturopathic dr? someone specializing in genes and methylation? you could both have slow gene variants… a good dr will find out and help this. I recommend Shawn Bean… total genius but in Pennsylvania. I dont know what you have done but there is always a cause… he will find it, and others like him. xx
How could I have missed this video? Thank you so much. I am in the process of being officially diagnosed with endometriosis and I have been freaking scared. And little help from family and friends. I have heard so much of the “you’re making this up”, and “it can’t be that bad”, or “if you lose a little more weight you will get better”. When I am passed out on the floor or having a seizure in the doctors office, so nauseous I cannot move, feeling as if heated ice picks and claws are trying to rip my insides , so fatigued, or bleeding so heavy I have to miss a day of work because I bled through as super tampon and maxi pad… but yet I am making it up? So glad that there is more awareness. Thank you!
I can relate I too had extremely painful periods due to adenomyosis. I didn’t get my diagnosis until my children were in middle school. I wanted to pass along a book I saw Brittany Vasseur talk about on her channel. Sending positive thoughts and prayers for you. Keep on keeping it real Love you
Thank you for being so honest with your stories. I didn’t know what endometriosis was properly until now
You both are queens! 😘🥰
👏 👏 👏
I'm sooo sorry ladies!!!
I love this vid, as I don’t suffer from Endo I have suffered from different medical issues that I had to Have 3 surgeries in one year that each one took me out of work for 3 months!! It was terrible, and yea it is a spiral. After all my surgeries where over I had a mental break down and was taken out of work for another month. I finally had to resign after I got pregnant and thank god I have a husband thAt ha allowed me to stay home with our daughter, but I completely empathize with all of what your saying, nd my women dealing with this or any medical issue. ❤️
Y'all are gorgeous!!! Y'alls eyes are gorgeous!!!
A few yrs ago I had a partial hysterectomy. My OP indicated I had endo and fibroids. A few yrs ago I've had the pain and inflammation come back. Been thru several specialists trying to find source of pain and every single time the words coming out their mouth was "we didn't find anything". Had several pelvic ultrasounds done. "We didn't find anything". Had to stop because bill's kept mounting. I do have insurance but it doesn't cover 100%. I stopped I gave up. I'm living with the pain. Some months I dont feel a thing but some well you know. I don't have a uterus but I do have my ovaries and I've read it could grow elsewhere. But YES you do feel crazy. Like "am I making this up?". Am I just whining?
Thank you so much for posting this. I’ve struggled with endometriosis for 12 years, it’s so easy to feel so alone when most of the world just doesn’t understand. It’s so nice to be reminded that we’re not alone ❤️
it’s actually a huge misconception that endo is the uterine tissue, but truly it is just “abnormal tissue” growing around the uterus and else where
Are they twins?
If you like the coffee taste look into a product from Italy called "Orzo coffee" it's roasted barley that tastes just like coffee and has zero caffeine. It's also very good for digestion. Best made with steamed milk (any kind)
Thank you for this video, sisters 🤗💞🤗 Love from Norway 🇳🇴
It took me three years to finally be diagnosed!! They kept telling me I just had bad periods….I was so frustrated
Amen!!! Sisters. I know the anguish!!!!
Hi! My mom has endometriosis…. and I always thought she was out of her mind! Complaining all the time about not getting/finding someone who could help her. She had chronic pain that would shoot down her leg… and would be in bed for days/months at a time… and then depression and an eating disorder set in. Thank you for this video and educating me! I will start an open conversation with my mom today because I know this is something way bigger then my childhood! Ty ty ty ty … both of you for being transparent and informative!!! Bless you
this was an awesome video for me! i only recently got diagnosed with endometriosis and PCOS and to have this video come out when i needed it was so helpful!!!
Took me 16 years of pestering doctors about my pain. Once in the ER I couldn't walk but was told nothing was wrong with me. My friend absolutely lost it on the doctor. Have had laparoscopy twice now and I have the Mirena IUD which helps A LOT.
I would do anything to be in a better position, but I also know there are so many that have it worse than I do. I feel this so deeply, and I hope that one day I AM in a position to make the world better, and help those people that are in the position I am in today. Thank you for this, love you guys so so much 💜💛💗
Just got an endo diagnosis ❤️
I’m a HUGE supporter and donator of Planned Parenthood. Can women go there to receive medical attention for this disease?
Erica did her makeup flawlessly wtf
I'm here to listen and learn xx
Bernie 2020 medicare 4 all now more than ever. Thanks for sharing your stories about this often overlooked condition. Brave sisters💗💗💗
I don't have endo, I have UC, but I totally relate to all the things you both were saying 💛💜 thank you for talking about the invisible illnesses!
It may be hard to believe but I went vegan and stopped using the microwave (radiation) and it helped my cramps so much. I know some people won’t believe it but it helped me by a million. Maybe it’ll help someone else.
I'm glad you posted this. Just now seeing it, but the tips…working out–what?!?! NO clue that could help with hormones.
They look like twins or are they baha
I love U both 💓
whenever erika is in a video i get so excited bc i’m currently in nursing school and i love seeing her learn makeup from tati. praying for everyone out there effected and others struggling with no support or health insurance 🙏🏻💛
Thank you for opening up. Cute necklace btw
The issues you brought up regarding insurance are so important, that’s something so many people struggle with. Not having insurance when you need care is one of the worst feelings in the world.
I am late to watching this, but I am so glad you two touched on the insurance aspect. I work in health insurance, specifically in preauthorization. Endo ablation are by far one of the most common services we see requested. So many women suffer with endo. Insurance is broken, and I can say that as someone working on the inside. They are also not the sole issue. It's the entire health care system that needs a revamp. Thank you for addressing so much in this video. You two are lovely!
Can you do a day in my life with Endometriosis
SO happy you are being so open Tati!!! You are so brave and I truly hope that all the positivity of your openness outweighs any type of negativity that I HOPE you do not receive.❤️❤️
thanks for the PSA, for real. Let's start a conversation great job ladies
Okay I love tati’s necklace like pls drop the link!
I'm from the uk and have just had a cyst out and then they found while being operated on they found I had this and it had spread to my bowels. I have been off contraception for 3 years and the ed is over producing
Endo warriors 💛💛
Love this video and the awareness you’re raising! Only thing is the definition of endometriosis is that it is tissue SIMILAR to the endometrium that’s lines our uterus, it is not the endometrium
💛
I love that yall talked about your experiences. I've had extremely painful periods ever since I was probably 14 but everyone told me it was normal, it was just cramps and that there was nothing wrong. It wasn't until I was 28 when I finally got a doctor that saw me and did tests and said okay I cant see anything from the outside but let's just treat you like you have endo because you seem to have the symptoms. We still haven't come across a great treatment but it's a start and it meant so much to be validated, to know I'm not crazy.
I have fibromyalgia. I understand that, because it's not visible, people think I'm crazy or lazy. But the pain is real and unbearable some days! Thanks for sharing your stories ❤️
I had a doctor do my routine blood tests to get cleared for college at an out of network laboratory. I was not notified and I got billed over $2000 even though I had insurance (through my parents). So now I have terrible credit out of college because I just couldn't pay for a doctors mistake. THE SYSTEM IS BROKEN!
Why not a laparoscopic surgery to remove it? I had it done in 1998. It’s one of the leading causes of infertility.
I had a hysterectomy last year from uterine fibroids and woooooow did it wreak havoc on my life. It’s not in our heads ladies! I owe a ton of money..
I know more about it now
What kind of NP? FNP right here 🙂
Have you been to a naturopathic dr? someone specializing in genes and methylation? you could both have slow gene variants… a good dr will find out and help this. I recommend Shawn Bean… total genius but in Pennsylvania. I dont know what you have done but there is always a cause… he will find it, and others like him. xx
How could I have missed this video? Thank you so much. I am in the process of being officially diagnosed with endometriosis and I have been freaking scared. And little help from family and friends. I have heard so much of the “you’re making this up”, and “it can’t be that bad”, or “if you lose a little more weight you will get better”. When I am passed out on the floor or having a seizure in the doctors office, so nauseous I cannot move, feeling as if heated ice picks and claws are trying to rip my insides , so fatigued, or bleeding so heavy I have to miss a day of work because I bled through as super tampon and maxi pad… but yet I am making it up? So glad that there is more awareness. Thank you!
I can relate I too had extremely painful periods due to adenomyosis. I didn’t get my diagnosis until my children were in middle school. I wanted to pass along a book I saw Brittany Vasseur talk about on her channel. Sending positive thoughts and prayers for you. Keep on keeping it real Love you
Thank you for being so honest with your stories. I didn’t know what endometriosis was properly until now
You both are queens! 😘🥰
👏 👏 👏
I'm sooo sorry ladies!!!
I love this vid, as I don’t suffer from Endo I have suffered from different medical issues that I had to
Have 3 surgeries in one year that each one took me out of work for 3 months!! It was terrible, and yea it is a spiral. After all my surgeries where over I had a mental break down and was taken out of work for another month. I finally had to resign after I got pregnant and thank god I have a husband thAt ha allowed me to stay home with our daughter, but I completely empathize with all of what your saying, nd my women dealing with this or any medical issue. ❤️
Y'all are gorgeous!!! Y'alls eyes are gorgeous!!!
A few yrs ago I had a partial hysterectomy. My OP indicated I had endo and fibroids. A few yrs ago I've had the pain and inflammation come back. Been thru several specialists trying to find source of pain and every single time the words coming out their mouth was "we didn't find anything". Had several pelvic ultrasounds done. "We didn't find anything". Had to stop because bill's kept mounting. I do have insurance but it doesn't cover 100%. I stopped I gave up. I'm living with the pain. Some months I dont feel a thing but some well you know. I don't have a uterus but I do have my ovaries and I've read it could grow elsewhere. But YES you do feel crazy. Like "am I making this up?". Am I just whining?
Thank you so much for posting this. I’ve struggled with endometriosis for 12 years, it’s so easy to feel so alone when most of the world just doesn’t understand. It’s so nice to be reminded that we’re not alone ❤️
it’s actually a huge misconception that endo is the uterine tissue, but truly it is just “abnormal tissue” growing around the uterus and else where
Are they twins?
If you like the coffee taste look into a product from Italy called "Orzo coffee" it's roasted barley that tastes just like coffee and has zero caffeine. It's also very good for digestion. Best made with steamed milk (any kind)
Thank you for this video, sisters 🤗💞🤗 Love from Norway 🇳🇴
It took me three years to finally be diagnosed!! They kept telling me I just had bad periods….I was so frustrated
Amen!!! Sisters. I know the anguish!!!!
Hi! My mom has endometriosis…. and I always thought she was out of her mind! Complaining all the time about not getting/finding someone who could help her. She had chronic pain that would shoot down her leg… and would be in bed for days/months at a time… and then depression and an eating disorder set in. Thank you for this video and educating me! I will start an open conversation with my mom today because I know this is something way bigger then my childhood! Ty ty ty ty … both of you for being transparent and informative!!! Bless you
this was an awesome video for me! i only recently got diagnosed with endometriosis and PCOS and to have this video come out when i needed it was so helpful!!!
Took me 16 years of pestering doctors about my pain. Once in the ER I couldn't walk but was told nothing was wrong with me. My friend absolutely lost it on the doctor.
Have had laparoscopy twice now and I have the Mirena IUD which helps A LOT.
I would do anything to be in a better position, but I also know there are so many that have it worse than I do. I feel this so deeply, and I hope that one day I AM in a position to make the world better, and help those people that are in the position I am in today. Thank you for this, love you guys so so much 💜💛💗
Just got an endo diagnosis ❤️
I’m a HUGE supporter and donator of Planned Parenthood. Can women go there to receive medical attention for this disease?
Erica did her makeup flawlessly wtf
I'm here to listen and learn xx
Bernie 2020 medicare 4 all now more than ever. Thanks for sharing your stories about this often overlooked condition. Brave sisters💗💗💗
I don't have endo, I have UC, but I totally relate to all the things you both were saying 💛💜 thank you for talking about the invisible illnesses!
It may be hard to believe but I went vegan and stopped using the microwave (radiation) and it helped my cramps so much. I know some people won’t believe it but it helped me by a million. Maybe it’ll help someone else.