Loving Luka

F/NF words

What do I have to say here, that hasn’t been said before? It’s an ongoing battle, repetition begets boredom, boredom, depression. I’m weary from all our conversations that end up the same way, one of us hanging up on one another. I can’t do that anymore, I won’t.

I’m sitting in a coffee shop, near your apartment, trying to drink a cup of black coffee in a white mug, my hands shake, while the rain continues to flood the streets. I just think about trying to jump over the massive puddles but I don’t have any more energy in me to even try. When I was younger that was my favorite thing to do. Not now.

I feel paralyzed from pain, the pain you inflicted on me. Once, I used to be carefree, like a child, happy and silly and stomp in the puddles.  I am so ANGRY at you. In the past I cared too much and where did that get me? No where. So, instead of being disappointed like I have been in the past, I am turning into myself, safe guarding my heart and not showing it anymore, at least not to you.

Found this digging through the archives. Blurr...

I don’t WANT to care anymore, I’m past that point. I’m not lying, I have cared too much in the past, believe me, you know, I wasn’t always like this. People who have known me for years will reassure you that yes, I have changed but I have chosen that change. Why? Self protection. I’m tired of being bullied and pulled apart like a hungry street dog lunging at a piece of a steak.

You know who you are. You blame me but you never look inside yourself. You need ME? That’s not good enough. You don’t treat me well enough to be on your side. You accuse me of everything you do to me, did that ever occur to you?  I just handle it better. I don’t

need to whine and carry on the way you do, I’m an adult now.  Yes, I went through hell to get here but I survived, barely, but I survived and I am strong.

Don’t you see how your view is warped? I don’t live in the past, I do acknowledge it but deep inside YOU are the one who hasn’t moved past it. Why is it that your true emotions only come out when you were bare to the bones, out of your mind? You loved me then, you needed me then. Not since then with all your false bravado. Because if you did love me why would you be so mean to me all the time?

It’s not a big dark secret, it’s an illness. Like diabetes or cancer, get over yourself. I know you think the world revolves around you, you make it that way, you make it that way. Not everybody else does that.

I know you put yourself first, well, who doesn’t know that? You admit it with pride. ‘A great quality of yours, I’m sure you think.’ Me? You don’t care about me as much as you think. Because if you did you wouldn’t be a bully like you always have been and you still carry on the same way, even after all these years we’ve been together. You could work on a compromise instead of saying “Well, I  just can’t do it, I won’t do it. ” Maybe you can but you have never tried.

I was happy in the past to mediate to reach a solution we can both live by, I will not be influenced by your outbursts anymore. I will stay away. I don’t trust you since you have broken the rules of our relationship time and again and you know you have.  Deep inside you are a very troubled child. I can’t see our relationship continue on the way it has, not at my expense.

I need to put myself first, to care about me now. I hope one day you will be happy without making others unhappy.

 

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The Day After Robin Williams’ Died

I sit in shock even as the news about Robin Williams’ death is sweeping the country on every possible news outlet. Shock moved to sadness and even though I didn’t know this marvelously talented man or his demons, I am feeling his pain. Everyone’s pain. The world is so fragile right now, you can feel it in the the heaviness of the air, the full moon,  in the tension of the world. For some of us, called Empath Intuitives, we feel more deeply, we take on other people’s pain as if they were our own but I am trying hard to separate this one.

I wrote this in response to my friend, the great Jenny the Bloggess, aka Jenny Lawson on her wonderful post about the death or apparent suicide of Robin Williams. Please take a look at Jenny’s site (I reblogged it here if it worked) to read the whole thing, if you don’t know Jennifer Lawson, you really should. My goal in life is to be mentioned on one of her side bars one day! She will cheer you up, crack you up and has been one of my inspirations. She has really creepy (sorry Jenny) habits/hobbies like taxidermied animals but she also does beautiful things for others and that makes you want to be as awesome as she is.

Not to mention, you have never really met the true Beyonce that we, in the Jenny Fan club know. “Knock knock Motherfucker.” You’ll see. It makes perfect sense.

Jenny wrote a heart breaking and heart warming post about suicide and mental illness and all of our challenges in life. This was my reply to her:

I’m usually good for a laugh or a witty response but sorry, I just can’t this time and that’s okay. I know I will get it back but Robin Williams’ suicide hurts in a place where childhood was, we grew up with him. WHY DOES MENTAL ILLNESS STILL HAVE SUCH A NEGATIVE STIGMA, IT SHOULDN’T. WHAT IF CANCER WAS SUBSTITUTED FOR MENTAL ILLNESS? I don’t understand. It is an illness like any other illness and needs to be treated by a professional. I have an anxiety disorder and take meds for it, like Jenny, and it is treatable. Sure, there are some bad days but there are some bad days for everyone. Isn’t it time that mental illness can come out of the closet and be accepted by everyone instead of being a hushed secret? Come on, people, give those of us who struggle with something different, ( I have an anxiety disorder) an encouraging word, a smile, a chance to say “I feel sad/anxious today.”

More money is needed for mental health providers but I’m sure Robin Williams could have provided that for himself. PLEASE, talk to each other or call a suicide hotline. If not for yourself, then for your children, your mother, brother, best friend, your partner, your pet, for me and for Jenny. There’s always someone waiting to listen. I promise. Signed, your friend, Laurie F. hibernationnow.wordpress.com

Call the National Suicide Prevention Lifeline

1-800-273-8255

Search results

  1. www.suicidepreventionlifeline.org

    “Because Hope Is A Marvelous Thing” by me.

Whoever Said “Facebook Friends Aren’t Real” Is One Big, Stupid Idiot.

An American version of a fruitcake which conta...

An American version of a fruitcake which contains both fruit and nuts. (Photo credit: Wikipedia)

The holiday season is winding down and I’ve read blogs about fruitcake, go ahead, start the jokes… Pass them around like some people did (not me, kids) like a joint or bottle of beer when they were in college. I’ve heard it all, all the silly jokes how nobody likes fruitcake, and everything is artificial, ad nauseam.  My father, when he was alive, ate fruitcake joyfully and loved it; he passed that gene on to me.

I love fruitcake, I honestly do. For years I begged people if they had received fruitcake as gifts NOT to throw them out because I would happily take it off their snobby shoulders. Funny, in all that time, nobody offered me their unwanted fruitcake. Nobody, until recently, one of my Facebook Friends, Sarita, saw me talking about fruitcake and out of nowhere she offered to send me a mini fruitcake that was baking in her oven.

Sarita, is one of my group of Facebook Friends that share a common and unyielding illness. We all seem to have some sort of chronic pain disease, in my case, Fibromyalgia. Believe me, it is not limited to Fibromyalgia (Fibromyalgia generally doesn’t work alone) but comes with many other ailments. I also have an auto-immune disease, Hashimoto’s Thyroiditis and some of my friends share that as well. Others have different, chronic pain but we are connected, perhaps not in person since we live in different places but definitely in our hearts.

When I told my (adult) children that my friend on Facebook was sending me a mini-fruitcake across the country they looked at me with those critical eyes, and the “what are you crazy” stare? “Mom, they said slowly in single syllables, you. don’t. even. know. her. she. could. be. send.ing. you. An.thrax.” I had never heard a more ridiculous thing in my life. Of course I knew her, I have known her for years, we’re friends, we are here for each other, we support each other.  The fact that Sarita was a “stranger” NEVER ONCE crossed my mind because Sarita was my friend and I was hers.

“So, my observant 19-year-old daughter said,  you wouldn’t mind if I was corresponding with some random man on the internet and he baked me some cookies and sent them to me and I wanted to eat them? Well, now that was indeed different, I said. I have talked to Sarita on the phone several times, we’ve been in touch with each other for years and I am not 19 and Sarita is certainly not some stranger. However, my daughter was right, I would not feel comfortable with her taking candy from strangers but I hardly see it as the same situation.

Facebook Friends for those of us with common limitations are not only useful to us but sometimes life-saving, Who knows better what it feels like to be in a Fibro Flare than another Fibro patient? I don’t like to complain to my family or my friends at home because frankly, they just don’t get it. How could they? They don’t have the illness. I’m not saying they lack empathy (most lack it a few don’t) but my Facebook Friends understand what I feel, completely every single day.

To them, I say THANK YOU, for the love and support and the ongoing kindness. We are all here for each other and that means a lot. I need to take a break now, for some more fruit cake and with it some pumpkin bread as well. What did you say about my Facebook Friends? Yeah, that’s what I thought. It’s okay, we are all wrong sometimes……May God or Spirit or Angels Bless these special people in my Life. They are in my life for a reason.

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FWF: Kellie Elmore

Sad Little Girl

Sad Little Girl (Photo credit: Wikipedia)

everything i could never tell you

I’m sorry, baby girl, I was barely a teen then, I didn’t know there was a name for what your mama had. I just knew she closed herself in her bedroom, turned the lights off and had me babysit you every afternoon. She hid under the covers because she was really sad and all you could hear from her bedroom was her sobbing. I kept the television on to try to protect you from the sounds.

You know, back then, it didn’t even have a name, just crazy. Your mama was chronically depressed and it is like every other illness but years ago it was shameful. Thank God, now, people know more and there are medications and no shame involved.

When I would walk up one flight of dusty, gray stairs, your smile would brighten your entire face like sunshine and your cheeks would turn rosy pink as soon as you saw me. Your mama would scream sometimes, but she couldn’t control herself. Oh, I know you pity yourself but I’m sure it was not easy for her, she was very sad every minute of every day. Yes, it WAS hard for you but you are a grown-up now, can you now think about what it was like for her?

What I remember most, for some funny reason, is that she used to make two pale chicken legs in the toaster oven. Oil or butter turning into bubbles on those nasty looking legs. You must have eaten them after I left but I kept thinking “where was the rice and the salad?” Was there bread and butter to eat?  I could picture you and your mama eating one sickly yellow chicken leg each and you drinking your glass of milk.

Your mom never let you have candy so with my babysitting money I would hold your hand and take you into the candy store and let you pick out a chocolate bar and tell you it was our secret. I didn’t care about lying to your mom, she wouldn’t even have noticed. I just wanted you to have a little happiness in your life, I wanted you to be able to be a kid for a short time, anyway. Your eyes would glisten like stars on a dark night, with happiness and excitement, you were lit up like electricity in a lamp.

I met you for lunch once when we were both adults, I didn’t know you anymore. You hated your parents,  you hated everything, nothing but hate and coldness inside you. This was way before your older sister became sick too and I adored her as well. I know you were wonderful to her, you did everything for her and everyone knew that, there was the goodness in you.That sweet little girl came back to be her sister’s angel, but when she died, it died too.

We didn’t know about the funeral, no one told us. As soon as we found out we raced to your mom’s apartment where your cold, icy, blue eyes looked through us. I wanted to hug you, but you didn’t let anyone close enough to even say we were sorry. Why? You were blaming us for something we had no control over but you were the queen of control, right?

You built a wall around you of law books and court rooms and tennis-playing friends. I hope you are happy now. But, I wanted to say something that I never could say before: I missed my sweet baby for a long time. The little girl you were, the innocent, happy child that would race to sit on my lap.What happened to her? My one question is “do you even remember her, that sweet sunny child, you were?” Because if not, that would be a damn shame. A damn shame.

FIBROMYALGIA: Now With Added Trigeminal Neuralgia

English: 'A pain stabbed my heart as it did ev...

English: ‘A pain stabbed my heart as it did every time I saw a girl I loved who was going the opposite direction in this too-big world.’ (Photo credit: Wikipedia)

Hey Fibro. Can you hear me? I’m a patient, you’re the chronic illness.

Just pile it on, OK?  Not that you are asking my permission or anything, you’re not. One diagnosis after another, I figure there’s more to come, how can I not think that way? I feel betrayed by my rheumatologist who said it wouldn’t get worse. Yeah, right.  I’m an almost 57 years old, (OLD is the operative word,) woman who is utterly falling apart physically. Nope, not even plateauing. Yesterday afternoon I had an appointment with a neurologist for TMJ, I was referred by a doctor I trust. TMJ  causes a great deal of pain, daggers of sharp pain waking me up in the middle of the night, relentless pain. All a chronic pain patient needs, right?

“I don’t have ANYTHING to do with THAT” “I can’t help you at all, said the young doctor.  I don’t  know why she sent me here, he said, that is not  part of my job.” When things are down, and I am tired and feel sick already, I go down and tears started running down my cheeks. Here was my chance to take away one type of pain, I knew it wasn’t going to take away my Fibromyalgia, my chronic pain, my Imbalance, my sleep disturbances or  up my energy levels but at least I hoped that something, anything could take away one of my many types of pain I have. I asked him to call the referring doctor, really, the only doctor I trust in the world.

He was gone a good fifteen message and I took the time to “pity party,” now sobbing into my hands and getting red and swollen with a drippy nasty face. As Oprah has described it, I did “the ugly cry.” I cried  loud and hard and the people at the desk must have thought I was having  a mental breakdown which in a way I probably was. So, after my cry-fest the doctor comes in and says there has been some progress. “Really?, I thought skeptically” I was still crying and he was not acknowledging that in any way whatsoever. Not one, “I’m sorry you are so upset.” Not a :, “I know this must be difficult for you”, NOTHING. He ignored me. I found that appalling. He looked through me. Thanks, Doc. My internist did that too a long time ago. I remember it in detail, she, I’m sure doesn’t, just part of her busy day. DOCTORS:  Be human, SHOW EMPATHY. PLEASE

He then proceeds to tell me that I have another condition ( as if he forgot a teaspoon of sugar in a recipe) : ANOTHER CHRONIC CONDITION NAMED TRIGEMINAL NUERALGIA AND it has to be addressed immediately, which means another medicine, probably damaging my kidneys and liver so it has to be watched carefully. Blood tests, follow-up visits etc,

Guess what? Not only did I try it for two days but it made me MORE dizzy and light-headed. I missed a festival in town that I was longing to go to, I missed out. Again. So, tonight I stopped. I was supposed to double the dosage today and I said “No way.” I was tripping over everything and I looked and acted drunk, without have had anything alcoholic to drink. I COULD NOT WALK, EVEN WITH MY CANE. I’m taking over control. Got it?

Chuck the new medicine and call the non-empathic doctor who will most likely call in another script and call it a day. But this time, I’m ready and I WILL NOT CRY. I WANT ANSWERS AND NO MORE DRUGS IN MY SYSTEM. TELL ME WHAT TO DO WHEN I GET THE ATTACK, NOT PREVENT IT. NO MORE MEDS! I’M DONE.  I AM IN CONTROL, NOT YOU. ANY QUESTIONS? I’LL BE HAPPY TO ANSWER THEM, OH, AND I WILL LISTEN AND RESPOND BECAUSE EMPATHY IS MY STRONG POINT. LEARN SOMETHING.

National Invisible Illness Week: September 9 – 15th

Fibromyalgia Eye

Fibromyalgia Eye (Photo credit: Vinally2010)

Who am I?  Can you see me ? Over here. The woman with the curly brown hair, green eyes, the one sitting down on the bench inside Target or the supermarket. No, I’m not lazy, I’m tired. Did I sleep well? No, but I don’t usually sleep well even though I have medication for that. Do I feel rested when I wake up, eager to take on the world. Well, no but I am older. How old? I’ll be 57 in two weeks. Well, it might not sound old to you, to me it’s ancient.

I have a childhood friend who claims she has Fibromyalglia  but refuses to see a rheumatologist. What? Yes, she sees a general doctor, one who knows about endocrinology for her thyroid.Do YOU see the point? Right, me either.  I have tried so hard to help her feel better but I’ve stopped, she obviously doesn’t want to feel better, she wants to complain.I grew up with her, no other bond, my mother remembers she’s been complaining since she was five, I remember it too.

I had to go to neurologist after I suddenly fell, on my back and test after test came out perfectly normal except for one: I had no balance. He had me walk a straight line in his office as if he was a police officer and I was a drunken driver. I zig -zagged on that line as if I had an overdose of margaritas and tequila sunrises and amaretto sours, mixed together in a huge bathtub big enough to fill a college party.

“Hmm” he said, “you have no balance” I nodded my head, up and down, ‘yes, I said, I know’ but he shrugged his shoulders and sent me away and said “I was fine.” If I was fine, why didn’t I have any balance? “Oh, it’s probably your Fibromyalgia…”he said. I’ve found now that when doctors don’t know what you have and they know you have Fibromyalgia that’s the answer they give. Nobody wants to take the time to figure it out, they don’t care, half of them don’t believe in the diagnosis anyway; since we don’t have many answers let’s all lump the various symptoms together toss them into a bag and label them Fibromyalgia. That’s easy.

What’s not easy is not having a cure and there really no potential in site. I happen to have a wonderful rheumatologist in the city and he is not only incredibly knowledgeable, he also really cares and that is an amazing combination and very hard to find. I don’t have as much pain as others but I have no energy. I can do one or two errands depending on the day and I never know in advance. It’s hard to make plans. Close friends understand, others don’t, want to know who your true friends are? Oh, it’s not hard at all.

I have a handicapped parking sticker for my county, you should see the dirty looks I get sometimes when I try to get out of the car. People judge on no information, they don’t ask, they immediately judge. They don’t notice the pain in my eyes from sitting in my car trying to stand up? No. So they notice the pain in the back of my eyes so I don’t cry out?  I don’t look “sick” is that it? That’s what I thought.Do not judge me or my handicapped sticker, I don’t judge you.

There it is, I don’t look sick therefore I must not be sick? Wrong. If my legs were in casts or my arms and shoulders too perhaps you would understand, but just because my pain is in the inside doesn’t mean I’m not sick. Sometimes, I wish I could show you my pain, physically. because emotionally, you’ve already done your very best to make me feel like worse than I already do. Maybe you could stick my whole body in plaster, maybe then you would understand.

Carry on Tuesday: Once Upon A Time

Out of fog Bay Bridge and Golden Gate Bridge a...

Out of fog Bay Bridge and Golden Gate Bridge and San Francisco in fog and crepuscular rays. (Photo credit: Wikipedia)

There was a time once, not so long ago, when I was chubby, fat, or just pleasantly plump. In Italy I would have been a goddess. Men would have followed me down the cobble stoned streets, whistling and begging to touch my beautiful breasts and my bountiful behind. Unfortunately, I wasn’t living in Italy, I was here in the United States, where all I really wanted was to be slender. I thought if I was thin, all my problems would dissipate like the mysterious fog in San Francisco. I imagined the fog lifting while I watched, wearing a heavy knit red sweater and sitting peacefully on a huge rock.

A couple of months ago I was very sick, (on top of my chronic illnesses” Fibromyalgia, Hashimoto’s Thyroiditis, IBS) I couldn’t eat, I couldn’t leave my house or the bathroom for an entire four weeks. I was pale, gaunt and looked ill. People on the street would ask me guardedly “If I was okay?” Part of me, if I had a sense of humor back then wanted to say “Of course, I’m in the middle-aged super model competition” but I had no sense of humor at the time. The other part of me was scared to speak so I just said “I’m fine” which people accept with relief and don’t follow-up with questions.

All my life there was always something about me that I wanted to change and after I changed it, I thought I would be happy: my weight, my hair, my glasses, wearing make-up, dressing better, nice shoes, tinting my hair to cover the tiny amount of gray that swirled in front of my face. The gray hair that I had been so proud to have, to acknowledge my real place in the world, as someone who had already experienced a great deal of life and had earned them with pride.

Having been married for 24 years with two young adults doing well in college was proof enough and even though I did go through a time feeling sorry for myself that the kids ” didn’t need me anymore” I realized my husband and I had done a very good job of parenting. I admit, I needed to remind myself that loving and needing were two very different things, they would love me as their mom but their lives and our lives would be constantly changing. Yes, sometimes it changes so quickly it was hard to keep up, that’s when I found myself alone, crying into an old, soft, handkerchief and feeling sorry for myself. I learned to accept that too. You have no choice.

Six weeks ago I went from eating and being lively to not eating and not feeling well, I lost over 30 pounds and before you coo and ooh and ahhh and wish it was you I can tell you, you better take that back. I did not enjoy clothes falling from my body, or food flowing through me, and not being able to go outside of my house for four weeks. The doctor scheduled me for every “cancer” test known to humanity and that was not fun. The doctor, not known for his bedside matter, actually told me WHAT he was testing for when we first met him in his office. Thanks, Doc, nice touch.

I will be getting the results later this week, I’m hoping that everything will be fine, I’m ( fairly) certain that they will be. The symptoms stopped a few days after my office visit and while I haven’t gained a lot of weight back, I do get hungry and I feel better. My newest ( little ) problem is this: I went to shop for new jeans and found that there are no jeans for women of my age. They have skinny jeans, under the waist jeans and jeans for teenagers with lithe bodies. Basically, the clothes that I have are four sizes too big for me and the style out there now are for teenagers only. I have nothing to wear, I miss my “Mom jeans.” It is impossible to find them, anywhere. Suggestions?

All that I have accomplished in this quest are the lack of clothes to wear and the acquisition of numerous wrinkles. I sat outside in the sun for a few moments, noticing all the wrinkles on my knees and thighs that were not there before. As I sat, warming my face, was I thinking about the good things in my life in a delighted way? No. I was thinking about the barium test (drinking chalk) that I have to drink tomorrow morning at eight am and where to aim my projectile vomiting. That, at least, is amusing me.

Be happy with what you have and who you are. As my dad used to say “Health is the most important thing.”  It’s the only thing, be grateful.

And Now I Shake

ECG complex.

ECG complex. (Photo credit: Wikipedia)

For the last six weeks I’ve felt light-headed; I’ve often brought this up to my internist and she has always said that it’s my low blood pressure ( 80/60.) “Salt your food” she murmurs, “stand up slowly from a seated position.” Then she adds: “That happens to me too!!” (Now I’m SURE we can be best friends because we have so much in common.) My husband insists that it has been happening more often and he has nagged me to see my doctor for a few weeks now, I’ve refused.

Yesterday I had an annual physical with my gynecologist who I like but totally FORGOT that she’s a worry wart like I used to be. Notice the PAST tense. I casually asked her if she thought I needed to see my internist about this small issue. She said “yes” and “that it might be a problem with my heart “valve.” The only “v” word I expected to hear from her was “vagina”( if there are any guys reading now is your opportunity to run) valve did not make me happy. I finally confessed to my husband, tried not to look at his smug face and called to set up an appointment.

I described feeling light-headed, having to bend my head down to prevent fainting, feeling very warm, getting a massive headache but never passing out. I could reach a chair or a bed and sit down and I’d be fine in a few minutes. It never happened when driving and obviously if I felt weak, I wouldn’t go out. It did happen going up or down stairs but I always held on to the banister. It was NOT, in my estimation, dangerous.

Now that I had conceded, a nurse gave me an EKG which was perfect with the oddest exception. My whole body started shaking. Once or twice lately I have noticed that my body starts shaking uncontrollably and I can’t stop it. I have asked my husband if he could see it and he has always said “no.” I think it’s one of those “guy” things. The nurse noticed it right away, I’m sure a best friend could as well.

So now, I could add “shaking” to my long list of maladies. Along with Fibromyalgia, almost passing out, Thyroid disease, Auto-Immune disease of the thyroid,  impaired hearing, I shook. I felt like one of those bobble heads except it wasn’t just my head that bobbled, it was my body wobbling. A nurse took five or six vials of blood and then the doctor told me (wait for it…) I had to go to the cardiologist for an echocardiogram and even worse, a stress test. No, No, No! Ugh, this is sweat and embarrassment  in front of others and I hate that kind of stuff. I gave my husband the evil eye, actually two evil eyes. They scheduled me in six weeks, obviously not a crisis situation to them (Thanks, honey!)

My doctor used this new phrase at least five times during my seven minute visit: “due diligence. In my language that means ” I’m running these tests to cover my ass.” For someone who used to get anxious for days, even weeks, I only got anxious for about five minutes which for me is zen-like (and that’s when they  told me I had to see the darn cardiologist.)

As soon as we got home,  I made myself my old standard comfort food, an American cheese sandwich on soft bread with butter, some salt-ridden baked sour cream and onion Lays potato chips( for medicinal reasons only) and a cold Yoo-Hoo to drink. For dessert, nothing speaks comfort more than a dish of really rich vanilla ice cream, softly melting in a red ceramic dish. No drugs of any kind were necessary. No jelly on pizza, I required nothing else. Damn, I was proud. But, I still have to do those stupid tests unless, as my sister suggested, I cancel?! What do YOU think?

Woman in Café with Yoo-Hoo and Cigarette, afte...

Woman in Café with Yoo-Hoo and Cigarette, after William Glackens (Photo credit: Mike Licht, NotionsCapital.com)

Haiku Heights-Pain

A Pain That I'm Used To

A Pain That I’m Used To (Photo credit: Wikipedia)

A knife through my hand

crimson blood pouring out fast

A heart, numb, frozen.

*****

No contact, no love

Babies without touch, react

Doubt, afraid, for life.

*****

Your breath near mine, close

the beat of our hearts, different

Tears tell our story.

*****

Brittle bones, swollen

raw, excruciating pain

A Fibro Flare Up.

Sadness 90/365

Sadness 90/365 (Photo credit: SashaW)

*****

Alone, we will be

No guarantee in life, death

Be at peace with One.

Plinky: What’s At The End Of The Rainbow?

Rainbows

Rainbows (Photo credit: jaqian)

  • At Rainbow’s End
  • Heaven.When I die I will be reunited with my dad and my dog, Callie and so many friends that have passed. Good people, wonderful people with spirit that have died too young. I hope, also, that at the beginning of the rainbow is a cure for cancer or better yet, the clue to the PREVENTION of cancer and other terminal illnesses.