Morning of the Hawk

It was a typical Friday morning. My hubby, (who works third shift) was sound asleep, the kids were at school, the animals were fed and I was alone with the quiet. Not ready to tackle chores or a new painting I wandered through my wooded lot, stopping when I noticed something out-of-place on the roof of my garage.

I say garage, but it is actually the end of a barn whose roof if only a few feet over my head. I stopped dead in my tracks when I noticed a pair of intense eyes staring down at me. Hovering over the edge of my roof was a Broad Wing Hawk about sixteen inches tall. I froze in place, returning the hawks gaze as I took in its beauty. I talked to it like an idiot, expecting it to understand that I appreciated its beauty and that it was welcome to use my wooded lot and buildings at any time.

After staring for what felt like a frozen moment in time, I said goodbye and moved toward the back of my lot as the hawk swiveled its head, watching me from behind its lethal looking beak. Noticing a ray of sun warming the chairs surrounding the site of our campfires I scurried over and closed my eyes, reveling in the heat and healing vibes of my yard.

Minutes later a sound yanked me out of my revelry. It was like a loud rustling and flapping rolled into one. A metallic clank followed as the loose hairs around my forehead fluttered in an unexpected breeze. Springing to attention I was shocked to find that the hawk had landed on the back of the wrought iron chair next to mine, a mere twenty-four inches away.

Afraid to move for fear of scaring it off I let my eyes absorb the experience. I marveled at the size of its talons gripping the chair back. I checked out the feather pants adorning the top of its legs and the graceful curve of its body, wings and tail. I noticed it’s aroma. While not overtly offensive, it was not one I would want in my house.

I peered over the bent, wicked looking beak, into a pair of bright yellow eyes that were scanning my face. We sat like that for a good five minutes. From time to time the hawk would pace back and forth on its perch, or it would extend its neck feathers and shake its head, but it never let its gaze stray from me for more than a second.

A high-pitched screech above our heads drew the hawks attention. After emitting a few answering shrieks it took to the air to join what I assume was its mate. Just like that it was over. This was a short encounter, but one I will treasure forever.

It turns out that this pair of hawks is nesting at the edge of the Cuyahoga river across the road from my home. I often see this hawk and it’s mate glide over-head in search of dinner but there hasn’t been another “meeting.”

For that brief period of time, I felt like the luckiest person on earth.

C2012 Jane Kohler

Nancy the Great!

Nancy, such a common name for such an uncommon woman. I have my disease to thank for placing Nancy in my life. Alone, in pain and looking for help I turned to an online support group. It was here I met my long time friend “C.” “C” and I got to know each other after he threatened to boot me off the group for joking around with a few folks, something against the rules. (Not so much against the rules, but i was doing it in the wrong way)

Long story short, he and I became friends. When he founded the FMS Community I jumped on his train to help however I could. I became a moderator on the support group and began to work with both “C” and Nancy. Egad, was that really eighteen years ago?

No slacker herself, Nancy, a former financial whiz from Boston, stricken with her own chronic pain founded a 501(3) non-profit org. called the “CSSA.” She was president, treasurer, researcher and public relations. She and a small group of others collected donations, networked with medical professionals and published  a newsletter mailed to subscribers, all while dealing with her own health and family issues and…keeping up with her job as moderator for the Fibom-L online support list. She is also a talented photographer with work in quite a few collections, I am lucky enough to have one of her framed works.

I watched with cautious eyes when I realized she was caring on a “flirtation” with my pal “C.” Not out of jealousy as I am in a long-term, stable relationship, but out of concern, not wanting my friend to be hurt by a conniving woman! Worry quickly morphed from respect for a strong woman to love for a dear friend. Her and “C” met in person and never parted again. They not only joined in marriage, they blended the two organizations and we became one happy family, with Nancy handling the financial reins and legalities of maintaining a 501(3) non-profit standing.

Fast forward to 2012, my strong, intelligent, compassionate friend who wielded her computer and cell phones like weapons as she cut a swath through research, misconceptions, myths and lack of support for very real, very painful conditions, can’t even turn on her own computer.

Diagnosed with Stage 3 dementia at a young age she can’t remember how to use her computer or dial a phone. Her short-term memory is sketchy and her health is failing.

I am angry, PISSED that the universe has handed her one more blow. It’s as if taking away her health and striking her down with chronic pain wasn’t enough. The fates that be weren’t happy until they took her mind too!

I am grieving for “C.” He was a thriving musician, disc jockey and printer before chronic pain and other conditions took control of his life. He is a caring, open-minded, generous and intelligent man who had lived alone for far too long before he found Nancy. Now he struggles with her comfort and his own feelings of loss and anger.

IT’S NOT FAIR DAMMIT AND IT PISSES ME OFF!

Those who can approach their doctor and mention the term Fibromyalgia without getting laughed out of the office as the doctor tells you it is all in your head can thank Nancy. In our day nobody believed our pain was real. We were fed anti-depressants and told to lose weight and exercise more. Hell, I was 120lbs soaking wet with a highly physical job, and they STILL told me to lose weight and exercise, and maybe see a shrink.

Nancy fought day and night, shelling out thousands of personal dollars to find answers. She offered support and information to those floundering in a sea of medical professionals that thought of us as a joke. She met and worked with researchers on the cutting edge of progress. She formed friendships with medical professionals and authors who suffered from chronic, unexplained pain and fatigue who wanted to find answers. She worked with Devin Starlanyl and others, keeping up with research and funneling that knowledge to us via CSSA.

This is a personal blow for me, but I want every person who can now talk to their doctor about FM, CMP, IBS, Sjogrens and other conditions without feeling like a mental case to give credit, and thanks to this hard-working, generous, genius of a woman.

It is time to let her rest and be taken care of, but dammit, if I have anything to say about it she will be thought of as a champion, a loyal friend and dominant force in the fight against an uneducated system that refused to look for answers until public outcry backed them into a corner. Nancy stood at the front of that mob, using her phone and computers like an electronic megaphone.

I thank you and I love you Nancy. My world is better because you are in it.

c2012 Jane Kohler

The Perfect Morning

Gentle sunlight lightly tapped at my eyelids, pulling me from my slumber. Rolling onto my back I stretched the longest stretch possible, reveling in the feeling of my limbs coming alive. Wiggling my jaw back and forth I realized that for once I had not tried to grind my teeth to dust as I slept, my jaw and temples felt pretty darn good!

Sitting up in one quick move I grinned like a fool when I realized that for once, my neck and shoulders were not holding me hostage, forcing me to move and stretch before raising my head from the pillow. Instead, I swung my legs over the edge of the bed, looking forward to all I would do with my day. My feet didn’t wince when called on to hold my weight. My hips didn’t scream through the days first twenty steps. My hands, no longer numb, gripped the door knob, flinging open the door so I could greet the day.

I was going to paint, hike, cook, clean and visit people I hadn’t seen for years. I couldn’t wait to embrace the day and make up for time lost to CMP and FMS. I had WON and I was gonna make the most of it!

Then the alarm went off. I blindly slapped at the alarm with a numb arm and winced in pain as I tried to pull my head from the pillow. It seems so unfair that I can live the life I want while sleeping, but when I awaken my tortured body rules my life! I don’t want disability payments. I don’t want to stay home and not make a difference. This sucks and I am DAMN MAD that this disease, this pain is ruling my life!

Acupuncture, physical therapy, water therapy, cognitive therapy, stretching, herbs, vitamins, inversion tables, raw foods, fiber and countless other strategies have not improved my life or lessened the pain. I am sick and tired of being “SICK AND TIRED!”

I sigh, knowing that the recent rash of people addicted to prescription pain killers has doctors running into the shadows. The chance of my doctor giving me any measure of pain control is slim to none. We need help, we need relief, we need to function, make a living, raise our children, be a good spouse, help others and just live our lives.

Who is going to step up and help those stuck in the cracks, the chronic pain patients who are not dying, but they may as well be at times?

c2012 Jane Kohler