Feel Good Fridays

A chain with a broken link

We made it through another week!

As you know March is Endometriosis Awareness Month, so I searched for something to do with awareness.  And am pleased I did!!  It falls right into line with my earlier post.  Today’s quote is by American author, David Foster Wallace:

“The really important kind of freedom involves attention, and awareness, and discipline, and effort, and being able truly to care about other people and to sacrifice for them, over and over, in myriad petty little unsexy ways, every day.” 

May you find the freedom from your shackles, whatever they may be.

May you learn to love yourself, as much as you truly deserve.

And may you strive to help others, unselfishly.

Have a wonderful weekend.

Yours, Lisa

Truth, Theory, or Tall Tale?

Bloomin' Uterus logo surrounded by question marks

You’ll stop having Endometriosis symptoms, pain, adhesions, and surgeries once you hit menopause.

TallTale

There have been many documented cases of women still having Endometriosis symptoms and pain even after entering menopause.  There has even been a 78-year-old woman who had to undergo excision surgery! 78!  And this woman had a hysterectomy in her 50s.  Further providing evidence that a hysterectomy will not cure your Endometriosis (although it may take away some of those monthly uterus pains).

Women who have Endometriosis and are peri-menopausal, menopausal, or post-menopausal (whether naturally or surgically-induced) will need to talk to their doctors about any hormone replacement therapy (HRT).  Some believe that the supplemental introduction of estrogen may increase your chances of recurrent Endometriosis, especially if some Endo implants remain in your body.  Some women also continue to suffer from the digestive and bowel-related issues.  It is also important to note that your ovaries are not the only estrogen-manufacturers in your body.  Your liver, for instance, manufacturers estrogen.  I repeat: talk to your doctor.  Especially if you fear your Endometriosis has returned.

Keep heart, though.  Many women report a huge decline in their Endometriosis-related symptoms once they hit menopause.  However, as you know: Endometriosis is different for every woman. Only time will tell.

Resources:

Endometriosis Association

U.S. National Library of Medicine

WomensHealth.gov

Women’s Voices for Change

~ Again, I am a layman.  I do not hold any college degrees, nor mastery of knowledge.  Please take what I say with a grain of salt.  If curious, do your own research 😉 Validate my writings.  Or challenge them.  And ALWAYS feel free to consult with your physician. Always.  Yours ~ Lisa

Reader’s Choice : Endometriosis as a Disability

medical leave request form

Many patients with Endometriosis either cannot work or miss several days of work each month due to their pain.  Others miss work due to the side effects of their treatments or medications.  Others because of surgeries and recovery time.  It’s can be a massive economic loss, and many women are reprimanded or fired by their employers due to the lost time.

What protection do we have as Endometriosis sufferers?  What can we do? Aren’t there disability laws for stuff like this?

Continue reading

Share Your Story : Lauren

black and white photo of a glamourous woman in a gown and wearing diamond jewelry

Lauren was diagnosed in 2011.   She has had ongoing battles with fertility, miscarriages, and a battle for disability benefits.  Her story is a heartbreaking one.

Lauren’s Journey: I first started going to South Jersey Fertility in February 2010, to help conceive a pregnancy. On August 4, 2011, I started to develop excruciating pelvic and abdominal pain. The pain was so bad, I had to go to the emergency room.

On September 16, 2011, I had a laparoscopy, which found classic endometriosis lesions of the left pelvic sidewall and a single band-like adhesion involving the right ovary to the uterus. There was a large peritioneal window under the right ovary. This is consistent with endometriosis.

Continue reading

Feel Good Fridays!

Solar flare in space

We made it to another Friday! I hope you’re all doing well today! And if you’re not, I hope your day improves…

Today’s quote is brought to you by American Softball player, Jennie Finch:

“Try not to get lost in comparing yourselves to others. Discover your gifts and let them shine!”

We are ALL different!  Not only in our qualities and traits, but in our mental and physical conditions.  Comparing yourself to someone else will only weaken you; cause you pain, anxiety, sorrow.  Embrace who YOU are.

Someone else’s experience will never be your own.  You can try to mimic their processes, attitudes, and desires, but will never become them.

If a medical treatment has worked for someone else, it may not work for you.  Likewise, your fixes may not be their fixes. If financial planning has worked for someone else, it may not work the same for you.  In any aspect in life, do what is best for you.  Find your way. Don’t get sad if it doesn’t work out; simply try again!

You are amazing, through and through.  Your own qualities, traits, gifts, skills, quirks, and passions need to be let loose and shine! Be yourself. Embrace who you are.

Yours, Lisa

Feel Good Fridays!

chain with a broken link

We’ve made it through another week!  And since March is Endometriosis Awareness Month, I figured I’d pick one that had to deal with awareness…and I can’t think of a better way to say it than American author, David Foster Wallace:

“The really important kind of freedom involves attention, and awareness, and discipline, and effort, and being able truly to care about other people and to sacrifice for them, over and over, in myriad petty little unsexy ways, every day.”

Thank you, David, for putting into words what I couldn’t!

May you begin to find your own bit of freedom…from whatever you’re shackled to.  Begin to love yourself as you deserve to be.  And may you reach out to help those in need.

And have a wonderful weekend!

Yours, Lisa

Endo & Liver Function

Diagram of human digestive system

Most of my blogs are started out of my own curiosity, and this one is no different.

I’ve read in numerous sources that people with Endometriosis need to keep our livers in tip-top condition; well-greased and in proper working order.  I’ve seen a few Facebook posts from other EndoWarriors that they have heightened levels of *something* when they have a liver panel blood test done, and they wonder if their Endometriosis may have something to do with that.  That struck a chord with me because I have Gilbert’s Syndrome, which is a liver disease diagnosed through heightened liver panel results.

Does my Endo affect my liver’s functions? And does that, in turn, add to or affect my Gilbert’s Syndrome? My liver blood panel test results?

Continue reading

Artichokes : MmmMmm Good!

trimmed artichokes ready to cook

Tonight I’m cooking one of my favorite meals : roasted artichokes!  I’d never cooked one before last year.  Had NO clue how to do it, and boy was I intimidated.  But with eating healthier for my Endo, I started shopping at my local farmer’s market (living in California, they’re readily available year-round), and hit the wonders of the internet : I have since learned! And it’s EASY, delicious, and oh-so-good for you!

Which got me curious : why are they so good for you? I figure they’ll be roasting in the oven for the next hour, so : Internet, here I come!

Continue reading

Share Your Story : Lisa

A red-headed pirate laughing and holding her tankard of ale

I realized that I’ve asked you to share your story, but haven’t actually put mine out there in one place (maybe a snippet here or there)….time to get everything out on paper so it leaves my head and heart (sorry it’s so loooooong…I couldn’t stop!).  I was diagnosed when I was 35 years old in 2014. 

My Journey:  I started my period when I was 12 or 13 years old.  I remember them hurting (but not as devastating as they have in my adult years), but figured it was normal.  I grew up hearing we were cursed because of Eve’s decision to sin, punished into pain and childbirth. I also heard that some of my family members had really painful periods. So again, it was normal. Classmates said they had cramps, too…so I figured mine were just normal. I became that girl in Junior High and High School that would walk around with a hoodie tied around her waist every month because I’d almost always overflow.  I had classmates come up to me during the really hard cramps, ask if I was okay, that I was white as a ghost and sweating…and I’d spend time curled up in the Nurse’s office after taking an Ibuprofen. But it was normal. Every girl went through this.  Right? My family physician had wanted me to go on birth control, but just to prevent “baby accidents” from happening, which I quickly dismissed since I had no intention of having sex. Little did I know BCP may have helped with the pain…

Continue reading