princessslate17

Updated Jul 04

I want to spread word about this disease I have

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I am 1 in 10. Endometriosis affects 1 in 10 women... that's way too many of us suffering from this condition. There is NO cure and not the greatest treatments for most. A lot of us will go through many different treatments/medications in hopes of finding one that helps but not all will get so lucky. We need a cure!!! #endometriosisawarenessmonth

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Women

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Yellow

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la_nav and 18 others like this

33 Comments

eregenfuss Thank u so much for speaking up about awareness. I am trying to do the same thing. I have had endo for 18 years. I feel your pain and suffering. Keep looking up and raising awareness!

Mar 04Reply

princessslate17 @eregenfuss awh im so sorry I’ve struggled with it for almost 9 years now! I’m doing my best we deserve a cure!💛

Mar 04Reply

princessslate17 @mcgraw005 awh it’s so nice to meet you endo sister! We have a pen pal group on Facebook if you’d like to join! It’s yellow love pen pals with yellow hearts between the words!!

Mar 15Reply

jenniferrose719 Thank you for what you are doing, I’ve been suffering for 15yrs and it’s been misdiagnosed until now! Counting down til 6/29 when they finally take my uterus out! Had my babies and suffering is just tooo much

Apr 02Reply

chissy77 Just finished ANOTHER treatment last week... I feel ya 😢 The pain and the suffering on many levels is oh so very real.

Jun 06Reply

princessslate17 @chissy77 I’m so sorry sweetie what are yo trying now? I have the nexplanon it helped for about a year but now I’m going in for another lap!

Jun 06Reply

chissy77 @princessslate17 they found some clusters and put me on a hormone treatment for 36 days. I had the lap about 5 years ago. The pain dropped me to my knees! I have another scan on Thursday. There just isn't enough awareness in my opinion. So thank you for bringing this out. I'm sorry to all that have to endure this.

Jun 06Reply

princessslate17 @chissy77 I am so sorry you do too!💛 if you have Facebook feel free to join “Yellow 💛 Love 💛 Pen pals” it’s an amazing support group!

Jun 06Reply

rjncache Thank you love .. I too am one in ten💛.. the scapegoat and one bullied since I was 19 (I’m 38) as no one believes nor was it heard of.. thanks to Facebook and beautiful souls like yourself who speak up and post on social media.. I finally 17 year in (now at year 19 suffering and have estrogen dominance as result of so much added stresses and toxic products (mirena iud!! Toxic friends and sorties/foods etc)

Jun 15Reply

rjncache Sorry ...validated all and every pain and issue and still my support system has left me to care for myself .. but it’s all good I have learned some of the best life lessons.. have a husband who also validated all I have endured .. we are strong we are sweet and we didn’t ask for this disease ..

Jun 15Reply

rjncache but we will find cure. Ty again makes me so happy to see women speaking up(I am starting the Endo diet and going to record it if you would like me to let you know how it goes it’s supposedly helped women detoxify and heal endo without surgery.. at very least minimize pain. I’m cool with that. I hope you are having a good day ..and have more good days to come then bad😊💛

Jun 15Reply

rjncache @janishjenn 💛

Jun 15Reply

rjncache @chissy77 💛

Jun 15Reply

rjncache @eregenfuss 💛

Jun 15Reply

rjncache @mcgraw005 💛

Jun 15Reply

rjncache @missccc oh poor thing . I’m sorry ..I’ve been have suffered since 1998 .. much love and prayers sending your way💛not one friend nor family believes or supports and shunned me.. even with facts now. This disease is crazy more then physically ♥️

Jun 15Reply

rjncache @janishjenn 💛

Jun 15Reply

eregenfuss Ladies I posted earlier about having endo for 18 years. Wanted to let u all know i am on in injection called Lupron which has helped me soo much! It basically puts me into menopause. Its been a godsend! I have been on it on and off for a few years. It stops the growth of the endo. I highly encourage you to look into it! Thought I would pass it on.

Jun 15Reply

princessslate17 @rjncache hey hun you mentioned Facebook join the group I’m in they are sooooo supportive and they will never leav you alone there is always someone who will be there to talk if not me💕 it’s called yellow lower pen pals there are yellow hearts 💛in between words love my name is Slate Pangels you can look me up love💛

Jun 17Reply

mekennalee Thank you so much for spreading awareness! I’m currently awaiting on my excision surgery as I have stage 4 endo. Sending you love and hugs fellow warrior!

Aug 04Reply

jlasich89 #endendo 💛

Dec 23Reply

kaylamixson 12 years it took me to be diagnosed. We are endo strong.

Sep 08Reply

cvm26 Good for you for posting this!! I have a support page on IG. @endosistersforever 💛

Sep 17Reply

jlasich89 I have stage 4 endometriosis & infertility 💛

Oct 31Reply

jlasich89 @holnx003

Oct 31Reply

holnx003 @tav35758... please share💕

Oct 31Reply

holnx003 My gorgeous daughter has this awful disease too. 💕🙏🙏🙏🙏🙏🙏

Oct 31Reply

vannuys77 Me and my daughter are also 1 in 10. prayers. bless you.💜

Oct 31Reply

roseybees 💛💛💛 Me too. Thank you for your message and for spreading awareness. Sending you hugs 💛💛💛

Nov 10Reply

voodoolady990 I’ve have endo for 24 years. But just diagnosed at 38 years old now. Thank you for bringing awareness! 💕

Feb 06Reply

princessslate17 @voodoolady990 I’m about to turn 22 this year and I’ve had it 11 years almost. It started when my period did and it took 5 years to diagnose. I love all my endo warrior sisters I’ll forever share my story and spread awareness. We deserve a normal life and a cure or real help/maintenance.

Feb 06Reply

caseyhunt0 I have it too!! Just diagnosed this past May ❤️🙏

Mar 01Reply

la_nav i am so proud of you endo sis for helping spread awareness. i advocate for my and all other endo warriors on myendometriosisteam.com @navita001 .I've been diagnosed for 30 years now. continue to be strong, let's keep fighting this battle 🎗

Aug 19Reply