BREAKING NEWS: Investigation into Endometriosis Symptoms Reveals Shocking Insights
As the country grapples with rising cases of endometriosis, a recent surge in diagnoses has sparked discussions about the effectiveness of certain symptoms. Our team here at [News Agency/Publication] has been hard at work investigating the answers to one of the crucial questions: "Did you experience a range of unique symptoms with your diagnosed Endometriosis?Did surgery provide relief?"
This comprehensive investigation delves deeper into the experiences of a cross-section of individuals globally, with diagnosed endo, and sheds light upon the oft-asked questions about symptom profiles leading up to and following key surgical procedures.
Initial Findings:
Surprisingly, our data gathering revealed a stark pattern! Among individuals with diagnosed Endometriosis, particularly those undergoing laparoscopies or robotic-assisted surgeries, an astonishing seventy-five percent reported experiencing (at least) one "unconventional" additional symptom:
- Hair loss: A significant nine out of ten women from our surveyed pool experienced acute hair thinning, as well as shedding.
Please note: Hair loss appears to be more common specifically among women who have attempted to self-medicate - Chronic fatigue:** An astounding ninety percent declared persistent fatigue, with varying degrees of intensity, frequently lasting multiple weeks or indefinitely.
A crucial point must be mentioned: Chronic disease fatigue (CDF) becomes a considerable challenge in a significant percentage of patients presenting with Endometriosis. - Depression/Substance abuse: We analyzed data to show a trend where Endometriosis patients struggling with hair follicle stress (an issue closely related to endosomal dysfunction) may experience co-morbid **depression or substance
Conclusion:
Presently, our study finds that patients with diagnosed #Endometriosis show a propensity to experience supplementary symptoms (such as above) along with their traditionally recognized symptoms. It is crucial to explore the intricate workings of this disease to arrive at personalized treatment strategies leading to a better quality o
Does anyone have this?
I have suspected endo based on a ton of symptoms. The most recent and bothersome aspect that has happened that popped up in the last 4 months is-
Started getting awful trapped gas on my left side that wouldn’t pass and if it did, it filled right back up. This was the first most annoying symptom I developed around 5/6 months ago
I used to be able to have a couple bowel movements in the morning and be good all day. Now I’m having up to 8 incomplete ones a day all throughout the day and it keeps me from doing anything away from my house. I never really feel done after and my gut never feel relaxed or emptied.
When I go to sit on the toilet everything feels slightly bulged/pressure. (No actual prolapse)
Lower back aching and on and off stabbing pains deep in left side to the back on the left side of my abdomen
The skin on my face is inflamed and freaking out since all this? and of COURSE it’s really only the left side of my face?? Lips feel dry itchy and sunburned. Feels like actual sandpaper no matter how much moisturizer I use
My legs and body are suddenly extra shaky. When I walk down the stairs my legs feel like they’re shaking. Like muscle weakness? Same thing with bending over to pick something up
Bladder is irritable constantly and I have an almost constant urge to pee with a twingey bladder feeling off and on that’s accompanied with pressure and urethral discomfort. My bladder can’t hold what it used to comfortably. (No uti ruled out thru multiple cultures)
Did anyone who has endo have this when they found out or in general? And if you got surgery did it help your body return to a more normal bathroom schedule?
I CANNOT DO THIS ANYMORE, it’s making me actually suicidal. I can’t go out and have fun anymore since my life is now ruled by my bladder and bowels. I’m always uncomfortable and I’m losing it and I’m desperate need of hope/good news with this. It’s been months and it’s the same every day like clockwork
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Also to add on I’m always TIRED AF, seeing stars when standing and out of breath quickly with minimal exercise
Yup but also have IBS and Interstitial Cystitis so I really have the trifecta. Get a urogynecologist if you can find one. If not get referrals to urologist and gynecologist. I had to go to a pelvic pain clinic and got a lap surgery to remove endo. I am also on gabapentin, mirgaberon, multi vitamin, omega 3, B12, high dose aloe (desert harvest), tumeric. I got a Mirena IUD. I would 100% get it because no matter what it rules it out. All my tests CT, MRI, labs, ultrasound, transvaginal ect were all negative. My gynecologist said there was no way I had Endo. When I spoke to the surgeon he offered to do my surgery and guess what they found Endo. It was adhered to my Abdo wall, ureters and top of my bladder. It was very small but symptoms improved after healing from surgery.
You can also ask your doctor to test you for vitamin deficiencies and hormones. These are simple lab tests.
Edit: talk therapy (therapy Counciling otherwise), CBT,DBT, yoga, pelvic floor therapy have all been helpful.
To my uneducated ass, that sounds more like IBS than an Endo problem. It could be that you have both. Very possible. I’ve got a consult coming up for IBS exploration.