Endometriosis Support Group
Endometriosis is a common medical condition where the tissue lining the uterus is found outside of the uterus, typically affecting other organs in the pelvis. The condition can lead to serious health problems, primarily pain and infertility. A major symptom of endometriosis is pain, mostly in the lower abdomen, lower back, and pelvic area.
No doubt that compromised immune system opened the door and STRESS invited the shingles in. Question is..."How do I get them to leave?" I don't know how I can endure this pain on top of all of my existing pain. Really...What choice do I have? Sorry...just needed to vent. Thanks, ladies...
~~Pup
This past weekend was without a doubt one of the most painful in my entire life. The usual suspects of relentless endo-related pain, along with indescribable torture of shingles in my right eye. I KNOW that this is my body's 911 CALL...but how does one "not stress" through the tribulations of this body? I spent most of the weekend in the darkness of my bedroom, with shutters closed, needing to cry...but that only makes my pain worse. The anti-virals and dose pak of Prednisone have wreaked havoc on my belly.
My actual eyeball looks as though it could bleed out. The "hot branding iron" pain sears throughout, as the blisters invade the inner lash line closest to the eyeball. The masses of "horror movie grade" mutations continue to multiply and spread across my forehead and right temple, into my scalp. I placed a satin pillow case on my pillow to ease the nightmare of my face "sticking" to the fabric and literally tearing blistered skin as I toss and turn through the night. Every morning I awaken (if I've slept at all) to my eye swollen shut and matted together. The pain and nerve meds have long-since dissipated through the long nght. I realize "Oh FUCK ME...I can't do this any more!" But what choice do I have?
My doctor said that she "hopes" we caught it in time because it can damage my cornea and cause blindness. I'm seeing my opthamalogist today @ 3:00. Oh yea...one more little happy thought...She said shingles can lead to Bells Palsy...I feel like a leper. I find myself comparing my situation to that of Job. I realize there is NO comparison to his suffering, but I find myself crying out to God..."WHY are you doing this to me...Do I not suffer enough?"
I am painfully aware that this wretched disease of endometriosis has far reaching ramifications. It robbed me (like so many others) of my dreams of having at least 2 children, creating our own little family to live happily ever after. By now those 2 children would have made me a Grandma. I'd have made a damn good mom and a wickedly wonderful Grandma=) It robbed me of my health and the ability to have a healthy relationship with my husband. It robbed me of my identity as a woman as surgery basically neutered me. It robbed me of the ability to grow old gracefully. Instead I've just grown OLDER than my years, becoming even more bitter with every passing year.
I can't justify this random babbling. The piercing pain is shooting through my head, eye, and ear. The fire pit beckons to me.
~~Pup
It is very painful and no one understand. Many people assume it is a problem with the elderly. Don't let it bring you down, stay strong! It will get easier. Strengthen that immune system - it will help.
How are you Mercy...If you were on Lupron at 17, you've suffered life long with this disease too haven't you? I guess my question is this...with "early" diagnosis (compared to most of us)...were you better able to "control" the progression? Also, has Lupron affected you adversely as you've aged? I would like to know more about your journey, if you'd share.
It took FAR OO MANY YEARS for me to be heard by GYNs, GIs, and UROs. Their neglect and apathy allowed endometriosis to consume my body and my life. I'm still fighting the good fight=)
~~Pup
I continue to suffer tremendously with SHINGLES in my right eye for almost 4 weeks now. I'm still taking Acyclovir and putting medicated drops in my eye, as well as low lose Neurontin for nerve pain. The nerve pain is like NOTHING I have ever felt. My eye, temple, forehead and scalp feel as though I have third degree burns (excruciating). This weekend I've been frightened of a facial stroke with severe tingling and/or numbness on the right side of my face. I FEAR Bells Palsy as there is danger with SHINGLES of the eye.
I don't mean to whine, but I am SO VERY SADDENED that my suffering is still so severe. With all of the GYN/GI/URO/ENDO/ORTHO/NEURO conditions that cause me life altering pain requiring PM with strong pain meds...THIS CAN BE the straw that breaks the proverbial camel's back.
I just went into the shower, so that I could bawl my eyes out without my husband knowing. THAT, by the way, makes the pain worse. I just need the release as I try to be so brave to lessen his concerns. I don't want him to know that the pain is making me consider suicide. I feel so DEFEATED in my battle against endometriosis and the ramifications of the disease. There's no doubt the stress I've endured while seeking PM contributed to the outbreak of SHINGLES.
I'm sorry for being such a baby about this. It's not like me=(
~~Pup