Sunday, September 18, 2016
She - An Inside Look at What It's Like to Have PMDD
I can sense she is coming, as my world starts to blur, she climbs into my body and claims it as hers.
Nobody sees her, she causes such pain. She is nothing like me yet goes by my name.
It's like a possession no priest could exile, she's taken me over, she's stolen my smile.
My body is hurting, I'm wrecked and alone. For two weeks a month, my body's her home.
Her rage has no limit, she's hurtful and cruel, she says things I wouldn't, and I look like a fool.
She drags me by force to the depths of despair, until I don't know myself, I am no longer there.
She damages my friendships and destructs my work, has me laid up in bed, exhausted and hurt.
And when I'm broken and lost and she's had her fun, she climbs right back out, I've survived another month.
And I take back my body, my mind and my heart, I repair all the damage, I make a new start.
I'm back and I'm happy, I'm thankful and free, though I know in good time she'll return for me.
Maybe one day I'll be free from her hell, she will no longer own me, and I will be well.
Until that day, I will swim the rough seas.
I won't let her drown me, for she isn't ME.
by Nicola James, 2016
Hello! It’s Not Just PMS. PMS and PMDD Are Not the Same Thing
Sunday, March 20, 2016
PMDD Quote of the Week
~I wasn't always easy to get along with and I used to be less under control, but now I will warn the people in my life that I have PMDD and take responsibility for it but I still get harassed about it, like they think I'm making things up, like when it makes me irritable, or cold, or cry for no reason. I make sure that they know it's that time and nothing is personal, yet they still act surprised when I show symptoms. They try to debate me about my emotions, which after years I have come to accept I have less control over, but they don't trust me about my own experiences.~
Saturday, June 27, 2015
Living with PMDD: Why Every Woman Should Be Practicing Hormonal Self-Awareness
One line that caught my eye was: What a hormone surge does is it gets rid of a woman's ability to numb herself to the quality of her environment.
With their permission, I have reposted the beginning of the article. If the opening intrigues you, please click on the link to finish reading the article. Well worth your time.
I had a client once whose boss insisted on using positive-only language in the workplace. So, when giving feedback about mistakes and areas for improvement, he’d say, “You have a great opportunity to practice your communication and organization skills here” instead of “You’re awkward and messy.”
Sunday, August 3, 2014
The Voices of PMDD, A Guest Post on Shattered Dreams
No one intentionally judges someone with bi-polar disorder or depression. It is a slight shrinking away from the unknown and the unstable. PMDD is similar to being bi-polar. The difference is the consistency. PMDD will hit every two weeks like clockwork. About every third cycle, in my case, it is so severe I have to talk myself out of suicide. My muscles and joints hurt so bad I feel my bones will crumble if I move too fast. Typing hurts. Rolling over hurts. The sadness is so deep there is no hope, no joy, no future. It is only darkness for days and days. And right as the pain is going to consume my mind and body, my cycle begins and the world is turned upright again as if the previous two weeks never happened.
It is vicious. It is destructive. It is painful and it is never ending.
I am told by those around me I am outgoing, extroverted and can do anything I set my mind to to. That is until they see me fall and wonder what happened.
I was just as confused until September 2011, when it became clear there was a pattern to the insanity.
My husband and I were in the middle of trying to start a photography and real estate business when it became clear we were facing something much bigger than we could have ever imagined. I would soon discover my ambitions would be pulled out from under me like a ugly, worn out rug.
Up until then, I had hope I would one day shake whatever it was that tripped me up so much. We thought it was connected to the abuse from my childhood or maybe my walk with God was really weak or maybe I was just a weak person in general. Maybe, just maybe, if I tried harder, or prayed harder or exercised harder or ate better or something!!!!! There had to be something I was doing wrong.
After we narrowed the diagnosis, I began facing the fact, I couldn’t do everything I dreamed of doing….and that pain is another post entirely.
I knew something was wrong, but I had no idea the symptoms grew worse and worse as you get older. It made sense though, as I was moving into my 40’s, why the intensity was growing.
Friends only see me when I can leave the house. I venture out when I have energy and drive. This causes so much confusion when I meet new people. I am vibrant and joyful at first and when I am pressured into social situations during the “luteal” phase, they see a quiet, sad often “sick” stranger they don’t recognize.
I can’t imagine how it is interpreted.
I cancel coffee dates, go two weeks without answering my phone, drop out of obligations I make during my good weeks. I’ve since learned the crash will come and I have no business volunteering, working, serving or reaching out to anyone.
I’ve lost jobs, quit jobs, started and quit businesses, started and quit homeschooling over and over, lost friends, went on uncontrolled spending sprees, started arguments and walked away from relationships to save them from myself.
I wish at times, I had a physical ailment. A limp, a scar, a broken bone or even cancer. At least then, when someone met me they would have evidence of my disease. They would be able empathize and process the injury in their own mind.
Instead, the injury is inside my mind. It is not visible unless you live under the same roof.
It is hidden behind a mask I wear everywhere I go. I can’t escape from the betrayal of my mind and body every month. It is always taunting me…always waiting silently to paralyze me yet again and destroy everything I begin to build.
I’ve learned not to build anymore. That is what hurts the most.
Sunday, May 18, 2014
The Voices of PMDD, A Guest Post by Alice
Saturday, March 29, 2014
PMDD, Prostaglandins, Pain, and YOU
Tuesday, April 12, 2011
Taken By Surprise...
This has been an odd month for me. After a couple of years of only experiencing PMDD symptoms every few months--due to the onset of menopause--for the past two cycles I’ve been back to my regular clockwork schedule of symptoms and a refresher course of how miserable PMDD can be.
But now, I also know how to manage and minimize it. I now know I am not my PMDD, and my PMDD is not me. After nearly forty years of cycling through it, being buffeted by first regular, then random storms of PMDD, I have finally learned to separate myself from my PMDD.
To do that, however, takes a great deal of self-attention and self-awareness. You have to listen to everything your body tells you. The body never lies.
But a PMDD body does lie. Imagine that. Your own body lies to you.
No wonder you feel like you’re going crazy sometimes.
I am a very much a positive thinker. Calm, creative, goal-oriented, and optimistic. Generally I sail through my days without a problem. I don’t sweat the small stuff, and half the time don’t even sweat the big stuff. Life has a way of working out for me, and for that, I am grateful. The more it happens, the more I learn to trust—to trust in myself and my higher power—that all choices made from that quiet place within me can be trusted and will lead me to good and positive outcomes.
So imagine my surprise last week, when a day I had willingly chosen to give over to helping a loved one get the medical help he needed, for me turned into an endless loop of mental frustration. What is this? I kept asking myself. This day is no surprise, and I chose to spend it this way, and yet….
And yet I can’t seem to stop the thoughts of anger, resentment, and frustration from welling up inside of me.
I did not let them out. I knew well enough that the person I was spending the day with was not the problem. But Lord, how I wanted to. Just wanted to let loose with every negative thought on my mind. We even joked about it.
Did you catch that? I was able to joke about my feelings in the midst of a PMDD episode.
And I didn’t even know I was having one. I just knew something was “off.”
It wasn’t until the following afternoon that I began to suspect it was PMDD. Thursday morning I procrastinated until it was too late to leave for my Qigong class, which I absolutely love. There’s no reason for me to miss the class, as everyone there knows about my PMDD and accepts me as I am. They welcome my arrival no matter what my mood, which I often announce upon coming in the door.
“Brain’s not working right today,” I will say, and everyone will know I’m a little off my stride.
So I skipped class—all the while asking myself, “Why would you skip something that brings such good things into your life?”
Remember, PMDD doesn’t make sense. It just is.
That afternoon, I found myself unable to focus on what I needed to be doing. My handwriting was off, and I kept getting distracted by the latest shiny thing—a new email, a new link to explore, a phone call to answer, a note to write, a snack to make.
Speaking of snacks, suddenly, for the first time in weeks, I wanted chocolate.
Should have been another clue, but I wasn’t thinking PMDD yet.
Not until the next morning, Friday morning, when I literally did not want to wake up. I swear to you, it felt exactly like when I woke up to a carbon monoxide leak in my house last November. Debilitating, bone deep lack of motivation and fatigue. All I wanted to do was sleep.
The phone rang and I dragged myself out of bed. An hour and a half later, I’m still yawning, yawning, yawning. It took extreme effort to keep my eyes open. Coffee didn’t help. At all. I don’t normally drink coffee, so if I do have a cup, the effect is immediate.
Not today. Not a blip of relief. I felt like I had an iron band around my head, my tongue was made of cotton and was also thick and swollen (which is one of my PMDD symptoms—allergy aggravation), I couldn’t get enough water to drink, and I was ravenous both before breakfast and less than an hour after.
I finally realized I wasn’t truly hungry…I just wanted to eat. Believe it or not, there is a difference. My stomach was full. But my brain was sending distress messages. What those messages were, I have no clue, because there was nothing distressing that I know of going on in my life—you know, like the kind of situation that spurs emotional eating…
I just know the signals my brain was sending were manifesting as a nearly overwhelming desire to eat.
It was hard, but I didn’t succumb. My food charting (another experiment I hope to share the details of some day) told me I had already eaten as much as, if not a little more than, I had on any other day. So this was not true hunger. This was my PMDD talking, not me. I was not hungry. The chart clearly showed that on any other day, I wouldn’t have been the least bit hungry…and believe me, I am not one to deprive myself of basic nutrition, because I learned long ago that it will only make my PMDD worse.
So I compromised with my PMDD, and spent the day sipping my favorite chocolate drink, because suddenly all I wanted was chocolate.
I did, however, go to bed really early that evening, in deference to my fatigue. Added to that was now a strange aching in my legs, all the way down into my arches.
What had happened? Had I pulled/strained a muscle somewhere? Somehow? How could I, when I’d skipped class on Thursday? It didn’t make sense.
I woke up 12 hours later, still sleepy. Still ravenous. Still wanting chocolate. Still aching.
Okay…by now I am beginning to realize what is happening here. It must be my PMDD. By noon it was confirmed. I started spotting.
Suddenly everything that happened the previous three days made complete sense. The strange and unreasonable irritability on Wednesday, the clumsiness, disorientation, and inability to stay focused on Thursday, the lack of motivation, intense lethargy, fatigue, and ravenous appetite on Friday. The chocolate craving, the sensation of an iron band tightening around my head, the urge to weep, the dull ache in my legs.
I continued to eat normally, despite the ravenous hunger, sip my favorite chocolate drink, and headed off to the gym to walk around the track, even knowing it was the last thing I wanted to do. But exercise had helped before, and I wanted to experiment, wanted to see if there was actually something I could DO to make it better.
The first twenty minutes I felt like I wanted to vomit. No lie. Around the half hour mark, I started to feel a little better. By the 45 minute mark I was heading back toward an even keel. Came home, made a healthy, carb-laden supper, then went to church.
Things weren’t completely right, however, until I went out for a salty bowl of chicken noodle soup afterward.
Go figure. But for some reason, after the soup, I came home full of more energy than I’d had in three days. I was psyched, ready to take on the world.
Instead I rested and read and had a cup of tea. The storm wasn’t over yet; that was just the eye of it. Been here, done this enough times to know this thing comes in waves.
Sunday morning I was dozing again when the phone rang and woke me up. I didn’t have nearly as tough a time waking up as I had on Friday morning. Huge difference between then and now.
Why? The menstrual blood was flowing.
And because of that, I made it to my next Qigong class and the grocery store and was able to focus on a couple of creative projects I needed to complete.
The first wave of the storm had hit, and I weathered it. Mostly by repeating this is not me, this is my PMDD. I am not angry, resentful, mad—that’s my PMDD talking. I am not hungry, that’s my PMDD talking. I have no reason to cry—that’s my PMDD talking.
Unfortunately, there was not much I could do about the fatigue. But getting out for a walk definitely helped with that.
The good news is (except for one cup of coffee) I managed to avoid the quick-fix stimulants that so many of us use to get past our fatigue, stimulants that only make our PMDD hit back even harder. Tobacco, alcohol, caffeine, sugar, energy drinks.
You, too, can weather the storm, whether yours comes in waves, or all at once. It just takes an enormous amount of effort to do so. Not everyone has the time or energy or circumstances to be able to do it. I understand that. I accept that. You need to accept that too, and simply start wherever you are right now.
Start with what you have, start with whatever symptoms present themselves. Try to sort them out like tangled threads. This part is me, this part is my PMDD. I am not my PMDD. I am better than my PMDD. I am stronger than my PMDD. I will not allow my PMDD to define me.
And I will not allow anyone else to define me by it, either.
Because they have never slogged through the storm in my shoes.
Until you know how it feels to have a brain and body that sends basic biological signals contrary to all conventional wisdom and common sense, you will never understand.
To those who do, you deserve to be congratulated and applauded--not dismissed, discounted, and ridiculed.
We are the strong ones, we are the survivors, and we are not our PMDD.
