Saturday, April 30, 2016

To the Person Who Thinks Chronic Pain 'Can't Be That Bad'

I have a friend. A poisonous friend.

When she is angry, she makes my days hell and my nights sleepless. She attacks me when I least expect it, especially if I’m lulled into a sense of security. She follows me everywhere, every day to the point where I truly cannot remember a time that I lived totally out of her clutches.

She is cruel. She cares little for family occasions, first dates, social events and the like. She perhaps forces me to stay home, or she makes sure she is right there with me, ensuring I don’t forget her presence for a moment.

She’s been a silent witness to some of the most remarkable and agonizing moments of my life.

She’s always here.

Her name is Pain.

There are many who live with her, just like me. We do our best to keep on living despite her glowering presence. It doesn’t matter how long you live with her, you never become immune to her.

Yes, we learn to continue our lives, even the mundane daily stuff that keeps it “normal.” Yes, we smile, laugh and make jokes. We make love, shop and eat, despite the anger it causes her to display, and we relish and appreciate anew the simple joys that take much to remove or lessen. Cuddling my grandbaby. Looking into her eyes. Laughing with my children and hearing them say, “I love you Mama.” They all make life with her worth living.

But let me tell you a secret. It hurts! It never stops. You wake, it hurts. You rest, it hurts. You do some basic physical activity, it hurts. You eat, it hurts.

See, constant and chronic pain isn’t something you magically get “immune” to. If I kicked you in the shins wearing my boots every 10 minutes, you would not be desensitized after the hundredth kick, would you?

You don’t get magically used to pain.

Let me tell you another secret.

I don’t have a “low pain threshold,” and neither do the huge majority of my pain family — those others I know and love who suffer daily alongside us all.  On the contrary, whenever it’s possible to physically do so, we do things like go to markets, gatherings, the park and shopping with our babies. Yes, like “normal” people! But you see, we often do it in such pain that if anyone else experienced it, they would demand pain relief at the closest emergency room.

Normally, pain is your body’s sharp and intense warning that something is amiss. You are meant to feel it, and the amount of pain allows you to determine how serious the injury may be. With chronic pain, the pain is no different. It screams at you to notice it. It rends your heart and mind with its incessant demands to be noticed and treated. However, no matter what the pain relief is, unless there is an urgent or acute injury or illness on top of that pain, then the aim of the medical profession is to relieve it to a degree. The aim is not to take away pain. It is not necessarily realistic to do so long-term unless we are palliative. So that’s the next secret I have for you. Despite often hefty pain-relieving medications, pain is diminished to the point that we can push through it and attempt normal function, but she is still right there

Please, the next time you think to yourself about someone with chronic pain, that it can’t be “that bad,” that we are being hypochondriacs or that we are just being a baby or just trying to get out of some activity, give yourself a forehead slap!

Here’s another secret.

It’s rare for someone who lives with pain to actually tell you that she hurts so badly she fights the urge to bash her head against a wall, or scream, or just cry about the unbearable unfairness of it all. While you look on, we  protect you from our pain. “Nah , it’s fine, just a twinge.” “It’s OK, I’m just a bit sore.” Or the automatic response, “Fine thanks, how are you?”

We learn fast. To tell you of pain, and the misery she brings, often eventually creates anger, resentment, ill-treatment, impatience, and out and out rudeness. At first it’s all sympathy. But I don’t want that! Empathy! That’s what I need. Not the (not-very-discreetly) rolled eyes and mutterings.

This is why I protect you. Because to one who hasn’t experienced chronic, disabling pain, to show that I hurt appears to diminish me, to be a weakness, a failing. It’s humiliating to justify my pain, so I seldom choose to do so.

The best thing that you can do for a friend or loved one who also lives with pain is to realize that pain hurts! If we are exhausted, sore or unwilling to do some activity, it’s because we hurt, badly. Even at the moment that you helpfully attempt to change the subject, that hurts, too. When you chatter brightly about your toe or that sore back you had once, you diminish our reality and you diminish your capacity to hold anything nearing empathy for us. Instead, ask what tangible thing you can do to help. Or say truthfully, “I don’t know how that must feel, but I’m here if you need me. I believe you. I love you.”

Remember that I invariably almost over-respect any pain that you have. I will often fuss relentlessly if you are even mildly sick or hurt, because your pain is one that I feel I can help, unlike mine.

Most important, here is the final secret I will share with you.

Pain moved in uninvited. We didn’t ask for her or welcome her. She is something inflicted on us entirely against our wishes. So please don’t punish us for something we have zero control over. And learn to listen to us, and hear what may be underneath our “just a bit sore” and “It’s OK.” That means more than anything.

By
Krissy Purcell
Contributor
I write about Chronic Pain
04/14/16

Sunday, April 24, 2016

Don't Flinch From Prescribing Pain Medications

http://www.painnewsnetwork.org/stories/2016/4/21/dont-flinch-from-prescribing-pain-medications

Friday, April 22, 2016

The Weight of Grief


THE (MODIFIED) PALEO-MEDITERRANEAN DIET






BY ALEX VASQUEZ, DC, ND, DO

This is my interpretation of the Modified Paleo-Mediterranean Diet as
 described by Alex Vasquez, DC, ND, DO. I have reformatted this in a
 table form, and use this as a handout in the office. This is available in 
table form within the downloadable handouts page.
Vegetables, (5-9) servings daily: choose from a wide variety of fresh, in season, or
frozen vegetables, brightly colored, lots of leafy greens, collards, broccoli, 
green beans, Brussels sprouts, cabbage, lettuce, chard, kale,bok choy, avocados. (Limit)
tubers like yams. (Severely limit) starches like corn, white potatoes. Avoid canned goods.
Fruits, (2-3) servings daily: a wide variety of fruits, (especially fresh locally grown
fruits in season) fresh, frozen, or dried apples, pomegranate, melons, kiwi, plums,
pears, pineapple, mango, citrus fruits, figs, dates, raisins, cranberries. (Limit) the
sweeter and dried fruits like dates, raisins, prunes, grapes and bananas due to the
higher sugar content (they are to be used as sweets).
Protein (2-3) 3 oz. servings (deck of cards size) prepare grilled, steamed, stewed,
sautéed over low heat: lean, free range, all natural, antibiotic free, growth hormone
free proteins, game, chicken, liver, poultry, turkey, lamb, lean beef,
(limit to once a week) fish (2-3 servings per week, including) small, low mercury,
cold water, wild caught fish, such as sardines, mackerel, herring, salmon).
(Excluding! farm raised, unless organic) fish. Also, excluding tuna, swordfish,
Atlantic salmon, bottom dwellers like catfish. (Limit) shellfish. Eggs
(limit 4 per week) also tofu, soy and whey protein.
Legumes, (including up to one serving daily) lentils, beans of all kinds,
kidney beans, navy, pinto, black beans, chickpeas (hummus),
black eyed peas, peanuts) also soy milk, tofu. (Limit) to one serving per day
non GMO, organic soy.
Seeds, including sunflower, pumpkin, sesame butter (tahini).
Nuts (in order of richest in omega 3’s) including walnuts, macadamias, Brazils,
filberts, pecans, cashews, almonds, also almond milk.
Berries (including) blueberries, raspberries, blackberries, currants, etc.
Dairy (including) yogurt with abundant live cultures like greek yogurt, kefir
also cultured soy or coconut milk. (Severely limited) cheese. (Excluding)
milk, butter, ice cream, sour cream.
Grains (severely limit, or exclude all) whole grain brown rice, oats, quinoa
barley (exclude) all wheat flour.
Fats (including) olive oil, canola, coconut. (Severely limiting, excluding!)
seed oils like sunflower, corn, safflower. (Excluding) lard, all Trans fats,
(shortening, margarines, deep fryer oils), peanut, brominated vegetable oils
(used as preservatives).
Sweeteners (including) honey, agave nectar, stevia. (Severely limiting, exclude)
raw cane sugar, molasses, (excluding) sugar, aspartame, NutraSweet, Splenda,
saccharin, acesulfame-K.
Beverages (including) 64 ounces of clear filtered water daily, teas,
(include 1 serving green tea) and (organic) coffee in moderation, 4 oz wine
(optional, limit). Excluding all types of soda, fruit juices, Kool-aid, artificially
flavored and bottled drinks, imitation juice, caffeinated energy drinks. (Excluding)
all distilled alcohol and beer, malt alcohol beverages.
Excluding ALL commercially made foods, frozen meals, fast foods,
convenience foods, artificial foods, chemical food additives, artificial flavorings
and all artificial sweeteners.
Number and size of portions and also amounts of carbohydrates consumed
should be directly related/proportional to overall calorie requirements, and
whether weight loss is desirable.

    Tethered Spinal Cord Syndrome

    What is Tethered Spinal Cord Syndrome?

    Tethered spinal cord syndrome is a neurological disorder caused by tissue attachments that limit the movement of the spinal cord within the spinal column.  Attachments may occur congenitally at the base of the spinal cord (conus medullaris) or they may develop near the site of an injury to the spinal cord.  These attachments cause an abnormal stretching of the spinal cord.  The course of the disorder is progressive.  In children, symptoms may include lesions, hairy patches, dimples, or fatty tumors on the lower back; foot and spinal deformities; weakness in the legs; low back pain; scoliosis; and incontinence.  This type of tethered spinal cord syndrome appears to be the result of improper growth of the neural tube during fetal development, and is closely linked to spina bifida.  Tethered spinal cord syndrome may go undiagnosed until adulthood, when pain, sensory and motor problems, and loss of bowel and bladder control emerge.  This delayed presentation of symptoms is related to the degree of strain placed on the spinal cord over time and may be exacerbated during sports or pregnancy, or may be due to narrowing of the spinal column (stenosis) with age. Tethering may also develop after spinal cord injury and scar tissue can block the flow of fluids around the spinal cord.  Fluid pressure may cause cysts to form in the spinal cord, a condition called syringomyelia.  This can lead to additional loss of movement, feeling or the onset of pain or autonomic symptoms.

    Is there any treatment?

    MRI imaging is often used to evaluate individuals with these symptoms, and can be used to diagnose the location of the tethering, lower than normal position of the conus medullaris, or presence of a tumor or fatty mass (lipoma).  In children, early surgery is recommended to prevent further neurological deterioration. Regular follow-up is important: retethering may occur in some individuals during periods of rapid growth and may be seen between five to nine years of age.  If surgery is not advisable, spinal cord nerve roots may be cut to relieve pain.  In adults, surgery to free (detether) the spinal cord can reduce the size and further development of cysts in the cord and may restore some function or alleviate other symptoms.  Other treatment is symptomatic and supportive.

    What is the prognosis?

    With treatment, individuals with tethered spinal cord syndrome have a normal life expectancy.  However, some neurological and motor impairments may not be fully correctable.  Surgery soon after symptoms emerge appears to improve chances for recovery and can prevent further functional decline.

    What research is being done?

    The NINDS conducts and supports research on disorders of the spinal cord.  The goals of this research are to find ways to prevent, treat, and cure these disorders.

    NIH Patient Recruitment for Tethered Spinal Cord Syndrome Clinical Trials

    Organizations

    National Organization for Rare Disorders (NORD)
    55 Kenosia Avenue
    Danbury, CT 06810
    orphan@rarediseases.org
    http://www.rarediseases.org External link
    Tel: 203-744-0100; Voice Mail: 800-999-NORD (6673)
    Fax: 203-798-2291
    Spina Bifida Association
    4590 MacArthur Blvd. NW
    Suite 250
    Washington, DC 20007-4266
    sbaa@sbaa.org
    http://www.spinabifidaassociation.org External link
    Tel: 202-944-3285; 800-621-3141
    Fax: 202-944-3295
    American Syringomyelia & Chiari Alliance Project (ASAP)
    P.O. Box 1586
    Longview, TX 75606-1586
    info@asap.org
    http://www.asap.org External link
    Tel: 903-236-7079; 800-ASAP-282 (272-7282)
    Fax: 903-757-7456
     


    Prepared by:
    Office of Communications and Public Liaison
    National Institute of Neurological Disorders and Stroke
    National Institutes of Health
    Bethesda, MD 20892


    NINDS health-related material is provided for information purposes only and does not necessarily represent endorsement by or an official position of the National Institute of Neurological Disorders and Stroke or any other Federal agency. Advice on the treatment or care of an individual patient should be obtained through consultation with a physician who has examined that patient or is familiar with that patient's medical history.
    All NINDS-prepared information is in the public domain and may be freely copied. Credit to the NINDS or the NIH is appreciated.
    Last Modified September 28, 2012

    Wednesday, April 20, 2016

    Let Me Introduce Myself

    Dear Brians brother (or whoever you may be)

     A little birdie has told me that you don’t know who I am, so let me introduce myself to you, quite simply put my name is Arachnoiditis. ... I lurk in your brothers and other peoples spine and I’m a sticky gooey mess, I stick the walls of the dura, I’m inflammation but so much more than that. I hurt people, and make them squirm in their seats, I don’t allow them to walk far and I send shooting pains throughout their body, I give them burning stinging pain and shock like knife stabbing jolts, why not, I like to play. Oh and forget a good sleep, I'm there lying in their beds with them too. They all take medication but I catch up to them pretty quickly and stump the doctors into oblivion. I’m pretty sure they’d like to name me Hell at this point. You know, some of these people still even have jobs, I don’t know how on earth they do it with me in their spines because my goal is to stop them in their tracks. Problem is, they have will power to shut me out. I don’t have a clue how they do that – that’s not fair. I’ll tell you all about me as we go along and a few more people who are affected by me, ha! I’m not like the flue though, I NEVER go away, even though these people think they’re having a good day. It’s my goal to make each and every day as miserable as possible so here goes. Firstly I need to mention that I’m really selfish, so trying to forget about me for most of these people isn't going to happen!! So I make Dawn have bladder infections that put her in bed for days, I make sure she stings and burns, she even wets her pants which I jump up and down with glee for – my job is done. I'll tell you about my buddy who causes that in a little bit. I make Melanie's body stings so bad all she wants to do is run away or worst for me, - die!! , but I chase right after her, where is she running to, there's nowhere to go. Sharon gets twitches so bad she had to stop driving her car, so then she had to move because she's no longer self reliant, ha ha good, that means she can’t go places by herself now, besides she was never alone, I am there every day without fail causing fatigue so bad she can't even walk from the kitchen to the bathroom, I give a whole new meaning to exhaustion. I make Taras toes curl, I wish I could say it was from a pleasurable experience on her part, but I only create havoc so no game Joe. I cause spasticity so she can’t even wear shoes any more. She gave me a funny name though in her big toe and that upsets me. She calls her big toe her penis toe!! I make these people sweat, get cold and clammy with goose bumps, some of them have stinging legs, they buzz like a bee and fizz like a soda pop, I make some even have what feels like water trickling down their legs, that must be fun - NO, I know it's not because they complain about it a lot - good, that is another goal I have and it too, is done. I should have a checklist here because so many things are caused by me like severe headaches, dry and blurry eyes, tinnitus (must be fun), the frequency for some of these people sounds like the aliens are landing. I'm pretty sure Ruth says this often, and noises from across the room sound like they're in her ear, I know that's uncomfortable because she says so - so again, see, she's never alone, the noise is there lurking in her ears 24/7. I also have a buddy too, he's called cauda equina syndrome, the one that's playing heck with Dawn, well that's this guy - and he causes diarrhea and constipation, bladder retention and infections and usually drop foot too. Saddle pain is also his goal, but heck it's mine too, move over CES I want to cause that, just give me one more chance to rule !! So I hope you're getting to know me a bit by now? I could go on, really I could but before I do, I'll just say a few more choice words and then be done. So yeah, I forgot about those who can't swallow properly and have to eat a diet of liquid foods, it doesn't happen to everyone, but my goal is to get there as well. Why not, I'm allowed to roam free, oh yeah, I play heck with any part of the spine, I forgot this part, from neck to lumbar, I make hips hurt so bad, a vice would be easier for them to deal with. I pull on things these people didn't even know existed until I showed up. Oh the one thing I like to do is cause heck with hands, after all, who needs those? Oh I forgot to tell you how I got here. Well, there's a few ways - surgery was done on so many of these people, a multi billion dollar industry that is supposed to help people, well, it's a free for all for me, so why not. I didn't cost a thing, only to make matters worst, what were they thinking, I was going to make it all better? And then there are those who have epidural steroid injections, I wasn't even lurking in the needle, but you know, the off label depo medrol can melt a polystyrene cup in about 6 hours, so my job is to stick and glue together the spinal nerves for the rest of their lives - depo medrol is my friend. He does a pretty good job I think. Then there are moms to brand new babies, thinking they did it all the right way in getting an epidural to help the pain of labor. I guess by now they realize after all, labor pain is nothing to what I cause them daily, because I'm there for the rest of their life, of course, they can't even take care of baby like they wanted to because I'm lurking in their spines, and I won't let them forget. Some people have had meningitis, then I show up, some have even fallen, and then there are those who have lumbar punctures and need blood patches after. The blood introduced into the spine created me, and I certainly won't let them forget about me. The one thing that I'm upset about now as it was stopped were myelograms with the oil based dye, darn, I have to find more creative ways to find my way into peoples lives. So, now you know me a bit better, maybe you can't forget about me either. Forget spreading the word, I mean, I want to survive after all. So adios Ember Fin
     Written by Ember Fin - July 2013


    Sunday, April 17, 2016

    Not By Might Nor By Power But The Holy Spirit

    I woke up with this scripture in my mind this morning as I was struggling to just sit up when my husband brought me a cup of coffee. I will be the first to admit that even though I remember scripture I have a hard time remembering the verse in the Bible where it comes from. It is Sunday and my daughter asked me was I going to church as she was getting ready. I knew that I was not able when tears fall as I try to move and I hold my breath as I situate myself in an upright position. I attend a wonderful church that I love and my Spirit is renewed when I am able to attend. The devil has tormented my mind and body that only some can truly understand. It is time that the Lord brings balance. This Scripture that laid heavy on my mind reminded me that I have every reason to be encouraged, to be hopeful, and to rejoice. It is not by my might, nor my power, but by the HOLY SPIRIT. I was becoming discouraged and my trust had swayed. I allowed fear, anxiety and worry to  come into my life. If my readers do not mind me sharing transparency in my life, you then will be able to see I am human, I fail everyday and I do have to allow the Holy Spirit to show me what is actually going on past what I see in the natural. By God's grace I am allowed to see that all power belongs to God not me. God is worthy to be praised and God is worthy to be trusted.

    God knew me in my mothers womb. He created me. He knew what I would face in life and he gave me a purpose. I have questioned this and asked: What purpose does a woman have who has lived a life of hurt, torment, shame and pain?  I have a testimony from my experiences that other women need to hear. The devil has tried to steal my life in so many ways to stop me from helping someone else who may need to hear it and today I will share my story. It will not go into great detail due to the ages of readers who may read this. I refuse to let the devil continue to steal from me and as you read let me first say that I am sharing this in hopes it blesses someone's heart. I want it to let you know that you are not alone. This is not to be taken by anyone to have pity on me at all, but to give God the glory for allowing my to share with you.

    I was born in August of 1975 with one sister who was one year older than me. At the age of one month my mother left us. My father was addicted to alcohol, sex and did not provide for his family. My mother did not have anyone to help her. She lived in abuse with no where to turn. My sister and I went to live with our Aunt and Uncle. My aunt became my mother and my uncle became my father as I will refer to these two as such in the following. My mother had four children and my father had three. There were nine of us all together. My mother was not raised to be loving nor affectionate and my father did not lead our home. At a very young age I was molested by a family member and I will not elaborate on which one, but I was told that I smiled all the time that the person who done this probably thought I liked it .I was around the age of 6. Later in life I found out my sister was also molested. It did not stop there as later around age 8 I was molested again by a person that our family knew. I can recall at the same age sitting behind my dresser with a bottle of baby aspirin and taking them trying to end my life. I recall today the tears that fell down my checks begging God to let me die.
    We went to church almost every time the church doors were open because one of my mother's children had married a Pastor. I would get slapped right in church in front of people. My mother seen no wrong in this. My mother's children are my now my siblings. The Pastor, my brother in law did not teach this behavior and did not agree. He tried to speak with my mother, her reply was for him to mind his business. I was taken to the alter every time I got in trouble and was made to say the sinners prayer again and again. Even though some of my family will be angry by me saying this due to shame, but I was abused physically by my mother. She would slap my face, she slapped me off the porch for dancing and would get on top of me on the floor and hit me saying every word that came out of my mouth was a lie. I had one agenda as a teenager and that was getting out. I succeeded. I got married at the age of 16 and had my first child at the age of 17 and my second child at the age of 19. My husband abused me, cheated on me and finally left me alone. I was physically dragged out of my home in the winter by my feet. I was hit in the face by him for not pulling a trigger on a shot gun that he had his mouth on. I was held down while he had sex with me during times of abuse.
    I remember on Thanksgiving going to the bathroom and taking an overdose. I later spent two weeks in the State Mental Hospital due to my attempt of suicide. When I went back home his girlfriend had wrote her name on my bed mattress. I had a painful miscarriage during this marriage. He left me and moved in with his girlfriend at one of his family member's home. I had two babies no job and the Mortgage company coming to my home. I left that town and moved in the next town. I went to work for a furniture company and my job was collections and repossessions. This is the time that I turned to alcohol. Every night I would drink until I passed out and then get up and start another day. Unable to feed myself everyday because I had to make sure my children were fed. I finally went to work in a loan company and in a short time became a manager of that finance company. Working two nights until nine and working sometimes six days a week. I met my third child's father who had such a smooth way about him. He worked in another loan company. Later I became pregnant with my third child. Her father would drink and was addicted to cocaine later becoming very abusing. This abuse was different. I would have to hide under neighbors beds for my life. He cracked the sheet rock on a home we were renting at that time from ceiling to floor by throwing me into the wall. My life had become a cycle and every time I tried to escape by suicide, it failed. My second husband was not physically abusive but I will be very vague in saying just only he wanted to practice sex that is not natural. Alcohol was used in excess in this marriage that ended because I then had learned to harm before harm came to me. My husband now that I thank God for, came into my life and he was just as damaged as I was. He had a bad boy past and was facing prison. I remember coming home and the sheriffs office surrounding my home. My husband was being locked up for his participation in a crime. When he was released on bond we were sitting on the back porch intoxicated with alcohol and smoking marijuana and he said he wanted to go to church that Sunday. My comment was I wanted to go also. We did not know where to go and I had resentment towards the church from childhood. We ended up at our current church VWOC. It was so loud in there and one of the Pastors started to blow a horn and then I seen another Pastor run around that church. I looked at the back door because I thought for a second that was the way out. I had never in my life seen anyone run in a church. Seven years later my husband and I become deacons at VWOC. So many people passed my husband and I up for damaged goods. My husband did not go to prison and he paid his restitution for his crime in another way. I will not leave out that in 2013 I did walk away. I walked away from my home, my church, and my faith and my husband. I then put myself in danger but my life was spared again. My husband and I reunited and I repented of my sin. I had people passing judgement and at times found it hard to raise my head much less walk with it up. Shortly after repenting and getting back to where I knew God had placed me I was in an automobile accident in which a driver had ran a red light and hit me. This accident took the life of that driver. I underwent surgery on my spine and have had complications from the trauma and surgery that were considered to be rare. I was diagnosed with Chronic Adhesive Arachnoiditis, Post Laminectomy Syndrome, Lumbar-sacra Spondylosis,  Radicular Syndrome. Chronic Pain Syndrome, Spinal Fluid Obstruction, Post Traumatic Stress Syndrome, Colitis, Bradycardia with tendency to PVC, Syncope, Cervical Kyphosis, DDD cervical, lumbar and sacral and now Premature Ovarian failure( Premature Menopause.) I have experienced Pain so extreme that I have literally felt not connected to my body. Suicide consumed me after this accident. My Husband has had to get off from his job to come home to hold me during this time. He would rock me like I was his child.
    It took all this to happen to know that I know that I was loved. Honest love that had no motive. Is it easy? No it is not. The devil attacked our marriage, our children, our finances and most of all he started attacking our mind. Recently the attacks have been so strong that it had become so hard to see past the natural. The scripture reminded me that God is about to bring back balance if I just hold on and trust in him as he so deserves.
    I hope that my trials give someone else hope that God Can and God Will.


    Saturday, April 16, 2016

    Today I am struggling with pain that has not been relieved by medications or limiting movements. My leg feels like I have pliers squeezing it. My spine feels like it is broken and the fire is raging.  I have slept maybe two hours. I have decided to share my day today instead of posting just articles of self-care and tips because I wanted you to know that I am right here with you in your daily struggles and on your days where pain is all you can feel that you are not alone. As I looked at my messages I seen where someone very dear to me and my family had sent me a message with a song. Send Me Jesus. God knew what I needed today. I needed to feel Jesus and to reminded that he is here with me through the good and the bad days. Pain doesn't care about anything else you are facing. It doesn't care if the bills are high and the teenage children are acting up or even about you relationships. I wanted you to know that today will pass as I too am hoping for a better tomorrow. My mind has wondered as everyday stress and pain has tried to overcome me. Today I will fight! I will fight through this for there will be a better tomorrow.

    Romans 5:3-5
    More than that, we rejoice in our sufferings, knowing that sufferings produce endurance, and endurance produces character, and character produces hope, and hope does not put us to shame, because God's love has been poured into our hearts through the Holy Spirit who has been given to us.

    If I ran a poll and I asked;  What is one thing that pain has shown you? You would be surprise at the number of people who list HUMILITY.  Yes it is easy to say ANGER,  but there are stages of grief that also apply to pain. Anger is one of the beginning stages. Humility is one of the last stages. I will not loose hope. I can honestly say that there is true power in pain. It will make you or it will break you. Before my accident I never thought that I would be writing a blog about PAIN and I have never heard of the word Arachnoiditis. We will fight together each day for we were made to have purpose.


    By Michell Freeman

    Thursday, April 14, 2016

    How Pets Help People With Chronic Pain


     It can be hard to get up in the morning, do daily chores and give 100% at work. Pets are beneficial to our health in many ways, and they can help people with chronic pain.
    We all experience pain at some point in our lives. Whether it’s chronic pain or acute pain from an injury or medical issue, pain is a normal sensation in the nervous system that says pay attention. Acute pain is generally something that can be treated. Chronic pain is much different, and defined as pain that lasts for at least three months or longer. The impact of chronic pain can range from mild irritation to life changing restrictions that can affect a person’s emotional and social outlook as well as physical health.

    It can be difficult for doctors to find the cause of chronic pain, and managing the pain becomes an ongoing challenge. Constant pain can make it hard to get moving in the morning. Some people are forced to give up a job they love. It can cause a person to withdraw from family and friends, become depressed, feel isolated from the world, and even lose their sense of identity. It’s hard to explain how debilitating chronic pain can be to people who have never dealt with it. You can’t always see someone’s pain, and it’s an invisible disability.
    Pets can be lifesavers for people with chronic pain. Caring for a dog or cat helps distract the mind from pain and shifts the focus onto another living being who needs attention, food, grooming, walks and playtime. Teaching a dog basic commands not only makes him easier to control, it can help someone with chronic pain train their pet to help them with some everyday chores such as retrieving dropped items and fetching things. Pets can also help by simply laying next to an aching joint to provide warmth and relief.
    A feeling of isolation is common among people with chronic pain. It’s hard for family, friends and co-workers to empathize when they don’t understand how you feel, but a pet is always there to provide emotional support and much needed companionship. Pets give their love unconditionally and don’t cast judgment. Sitting and talking to your dog or cat can help decrease feelings of loneliness, depression and isolation. Cats especially are said to have a calming effect on humans – more than any other animal, in fact. A pet will listen to you talk as long as you want to, and petting your dog or cat while talking to them helps loosen up stiff joints and muscles.
    Pet owners with chronic pain understand that no matter how much they may hurt, their animal still needs to be cared for. The simple act of petting a dog or cat releases endorphins, the body’s natural pain and stress relievers. Interacting with a dog or cat causes an increase in oxytocin levels for bonding, and serotonin levels that modify sleep, mood and pain. Spending time with a beloved pet also increases dopamine levels that provide a feeling of happiness, and decreases cortisol levels which reduces stress, anxiety and depression.
    Cats and dogs can remind people with arthritis that it’s time for a good stretch. It’s important to keep moving, and low-impact aerobics and stretching helps build muscle, improve endurance and relieve pain by maintaining range of motion in joints so they don’t stiffen up. When you see your pet stretch, join him!
    Pets are sensitive to when their owner isn’t feeling well, and sometimes one of the best things you can do for yourself is to take the dog for a walk or toss a ball for him to fetch. Exercise takes your mind off your pain and helps maintain a healthy weight, which can also help reduce pain.
    Chronic pain can wear a person down over time, but it’s hard to ignore a cat gently touching your face with her paw or a dog resting his head on your lap as if asking, “Can I help?” Both are sincere gestures that say you’re not alone. Pets help ease chronic pain by making us laugh, releasing endorphins. Laughter is one of mankind’s best medicines, and our pets provide plenty of reasons to laugh every single day.

    Monday, April 11, 2016

    50 Ways to Encourage a Chronically Ill Friend

    1. Ask, "What events in your life are changing and how are you coping with the changes?"
    2. Understand that she lives in a constant state of making decisions for which there is no guarantee that she is making the right choice.
    3. Put meals in disposable containers and attach a note saying "This doesn't need to be returned."
    4. Add stickers to envelopes for a cheerful touch.
    5. Arrange for your friend's kids to have a night with your children.
    6. Don't make a person into a project.
    7. Ask, "Would you be willing to talk to a friend of mine who has recently been diagnosed with a chronic illness and offer her some encouragement?" It makes one feel good to know that her experience can offer someone else hope and that God still has a purpose for her life. 
    8. Wash his car and put a little note inside for him to find later. Remember important anniversaries, both the good and the bad. No one else will
    9. Ask, "Do you want company the day that you wait for the test results? I could come over for a couple of hours."
    10. "No matter how little you have, you can always give some of it away." ~Catherine Marshall. Just listen . . . until it hurts to not say anything. And then listen some more. 
    11. Ask her, "How do you feel God is working through-or despite-this illness in your life? I'm interested." 
    12. Ask, "What do you wish people understood about your illness?" 
    13. Don't make her feel guilty about things that she cannot do. 
    14. Treat her to a gift of movie rentals via postal mail through a service ($7-15 a month). 
    15. Ask, "Would you be comfortable with having your name on a prayer list, so that others can pray for you?" Don't assume. 
    16. Instead of saying, "I will pray for you," say, "I'd like to pray for you right now, if that's okay." 
    17. Mop the floors. 
    18. Ask if she would be interested in writing something for the church newsletter, maybe even about the subject of living with chronic illness. 
    19. Buy a brightly colored umbrella as a gift. 
    20. Ask, "Do you have an errand I can run for you before coming over?" 
    21. Ask her to do spontaneous things, like go to a concert in the park, or just for a picnic. She may be more likely to participate since she knows if it's a good day or a bad day. 
    22. Don't say, "So, why aren't you healed yet?" or "I wonder what God is trying to teach you that you just aren't learning!" 
    23. For a unique gift, provide brightly colored paper plates, napkins, and utensils in a gift bag with a note that says "For when you don't feel like doing dishes." 
    24. Get her a pretty box to keep all of her notes of encouragement. Remind her to get it out and read things when she is feeling down. 
    25. Be her advocate. If you are at an event and walking/seating is an issue because of her disability, ask her if she'd like you to take care of it. If she says you can, be firm but not rude. Don't embarrass her by making accusations of discrimination or by making a scene. 
    26. Ask, "Would you be interested in a prayer partner from our church?"
    27. Purchase matching coffee mugs for you and your friend, and then commit to pray for one another each morning while using them.
    28. Say, "While you're in the hospital I'd be happy to take care of your pet." 
    29. Don't tell her about your brother's niece's cousin's best friend who tried a cure for the same illness and. . . (you know the rest). 
    30. Find out which charity is most important to her and then give a donation in her honor. 
    31. Ask, "What are your top three indulgences?" and then spoil her soon. 
    32. Hold the door open for her. They are heavy! 
    33. Don't tease her and call her "hop along" or "slowpoke." Comments you mean in fun can cut to the quick and destroy her spirit. Proverbs 18:14 says, "A man's spirit sustains him in sickness, but a crushed spirit who can bear?" 
    34. Say, "I know you must need someone to just vent to occasionally. I may not fully understand how you feel, but I'm here to listen anytime." 
    35. Ask your church youth group to come over and clean up the yard during seasonal changes. 
    36. Don't ask her, "How are you able to make it financially?" If she wants to share a burden she will. 37. Ask, "What would you advise me to look for in a new doctor?" 
    38. If your friend has a disabled parking placard and you are driving, allow her to tell you where she wants to park. If she's feeling particularly good that day, she may not want to park in the "blue space." Don't be disappointed that you'll have to walk farther. 
    39. Don't gossip about others. She'll wonder what you say about her. "Do not let any unwholesome talk come out of your mouths, but only what is helpful for building others up according to their needs, that it may benefit those who listen" (Ephesians 4:29). 
    40. Proverbs 25:11 says, "A word aptly spoken is like apples of gold in settings of silver." Be kind, gentle, and respectful. 
    41. Accept that her chronic illness may not go away. If she's accepting it, don't tell her the illness is winning and she's giving in to it. 
    42. Don't say, "Let me know if there is anything I can do." People rarely feel comfortable saying, "Yes, my laundry." Instead pick something you are willing to do and then ask her permission. Try the coupon in back! 
    43. Ask her to share her testimony at an event. 
    44. Buy a magazine subscription for her on her favorite topic. 
    45. Plant a rosebush to view from a window. 
    46. Understand that you don't need to know all of the details about the illness in order to be helpful. He'll share with you what he's comfortable with you knowing. 
    47. Don't ask, "Why can't the doctors help you?" or insinuate that it must be in her head. There are millions of people who are in pain with illnesses that do not have cures. 
    48. Avoid having gifts be "pity gifts." Just say, "I saw these flowers and their cheerfulness reminded me of you." 
    49. Send tapes of church services your friend misses to her with a copy of the bulletin and a note. 
    50. If she doesn't have a cordless phone, get her one. Phone headsets are also nice

    Reprinted from Beyond Casseroles: 505 Ways to Encourage a Chronically Ill Friend by Lisa Copen

    Using chronic pain as an opportunity for personal growth

    Using chronic pain as an opportunity for personal growth | painACTION.com

    Sunday, April 10, 2016

    She is a Survivor!

    She is a Survivor!


    She lived it 
    She felt it 
    She was brought to her knees 
    She cried She trembled 

    She could not believe what happened to her
     She took it
     She hid it 
    She turned it away
     She went into her shell
     This was where she would stay 
    Writhing with pain Senseless with fear 
    Turning inside her 
    It was her lot to bear
     She lived it
     She felt it 
    She was brought to her knees 
    Until One day
     She could bear it no more
     She looked into her innermost core 
    She felt the latent strength 
    She saw the unused courage
    She made a choice that day 
    She would no longer be the victim
     She would take back her freedom 
    She would do all that she could to find a way
     Freedom for her dreams,
     Freedom for her body,
     Freedom for her soul 
    She decided She made a choice that day
     She would be a Survivor 
    She has seen hardship and conflict. 
    She has felt shock and trauma.
     She has experiences that she wishes no one else to have. 
    She has felt pain in every part of her physical,
     emotional and spiritual being.
     She has become stronger and wiser and by being a
     survivor she has empathy and compassion pouring 
    from her.
     She will do everything in her power to stop the pain.
     She will do everything in her power to protect those who 
    need her. 
    She will do everything in her power to educate the
     world in compassion and harmony.
     She has survived the past and she will survive what
     may come.,, 



     © Alexandra Gold 2014 www.awomanonpurpose.tv

    To the People Who Question My Daughter's Chronic Pain

    http://themighty.com/2016/04/when-people-dont-understand-my-daughters-complex-regional-pain-syndrome/?utm_source=Facebook&utm_medium=ChronicIllness_Page&utm_campaign=ChronicIllnessTia Rago

    The 7 Psychological Stages of Chronic Pain


    The 7 Psychological Stages of Chronic Pain
    September 14, 2015
    By Jennifer Martin, PsyD, Columnist

    Have you ever wondered if other people with chronic health conditions feel the same way you do?

    Throughout my years with chronic pain and illness, along with the hundreds of patients I have counseled, I have found that, while everyone copes in their own way and experiences their condition uniquely, there are common feelings that most of us share.
    When I first began counseling chronic pain patients, I often used Elizabeth Kübler-Ross’s “Five Stages of Grief” to help them understand what they were going through.

    But as time went on, I reflected on what I experienced with my own chronic conditions and also on my patients’. It seemed that these stages, while very helpful, didn’t fully explain the broad range of emotions that people with chronic illness experience.

    After all, Kubler-Ross developed them to explain the responses to grief and loss. Having a chronic illness can be viewed as a type of loss, but they were not developed specifically to explain the emotions of people experiencing chronic conditions.

    I used Kübler-Ross’s stages as a model to develop the Seven Psychological Stages of Chronic Pain and Illness:

    1. Denial

    In this stage, we are in a state of shock and refusal. We wonder how our life is going to change and how we are going to live with those changes. Denial and shock help us to cope and make survival possible.

    This stage can be dangerous for people with chronic pain and illness because if they are in denial about their condition, they may not take the necessary steps to get themselves the treatment they need.

    Example: “It’s not a big deal, it will go away” or “The doctor is wrong, I don’t have diabetes.”

    2. Pleading, Bargaining & Desperation

    This is the stage where we want more than anything for life to be what it once was. We become fixed on anything that could make our illness and pain go away -- or anything that could give us some semblance of the life we once had.

    We may find fault in ourselves and what we think we could have done differently. We may even bargain with the pain or illness because we would do anything not to feel them anymore. Guilt is common when bargaining.

    Example: “Please just don’t let this ruin my life” or “If you make the pain go away, I promise I’ll be a better person.”

    3. Anger

    After we conclude that our pleading and bargaining is not going to change the diagnosis, anger sets in.

    Anger is a necessary stage of the healing process. Feelings of anger may seem endless, but it is important to feel them. The more you truly feel anger, the more it will begin to subside and the more you will heal.  Your anger has no limits and it may extend to your doctors, family, friends and loved ones.

    Anger is often felt later on when the illness and pain progresses, or holds us back from doing the things we would like.

    Example: “This isn’t fair! I didn’t do anything to deserve this!” or “Just give me something that will make me feel better!”

    4. Anxiety and Depression

    Feelings of emptiness and grief appear at a very deep level.  This depressive stage feels as though it will last forever.  It is important to understand that this depression is not a sign of mental illness.  It is the appropriate response to a loss or a life-altering situation.

    We may withdraw from life and wonder if there is any point in going on.  Depression after a loss is too often seen as unnatural or something that needs to be snapped out of.  Being diagnosed with a chronic illness or experiencing chronic pain is a loss – a loss of the life you once had.

    Having a chronic pain or illness may also bring up feelings of anxiety; anxiety about what the future holds, anxiety about not being able to live up to expectations, anxiety about social situations, anxiety about medical bills, etc.

    Example: “I’m going to be in pain forever so why even bother?” or “I’m going to be in debt forever.  How am I ever going to pay off these medical bills?”

    5. Loss of Self and Confusion

    Having chronic pain or illness may mean giving up some key aspect of what made us who we were.  It may mean an inability to be physically active like we once were.  It may mean not being able to be as sociable as we would like or it may even mean giving up a career.

    You may wake up one day and not recognize the person you are now.  You may question what your purpose in life is now.  This stage may occur at the same time as anxiety and depression, or it may be separate.

    Example: “I don’t even recognize myself anymore.” or “My career was my identity.  Who am I without that?”

    6. Re-evaluation of Life, Roles and Goals

    Having a chronic condition often means giving up a lot.  We are forced to re-evaluate our goals and futures.  We are forced to re-evaluate who we are as a husband, wife, mother, father, sibling or friend.  While we once had a successful career that gave us purpose, we may find ourselves beginning to question what we can do for work in the future and how we can contribute to our families.

    While we were once able to do it all, we are now re-evaluating what absolutely has to get done during our days and how we can accomplish these goals while still remaining in a positive mood.  Re-evaluating your life, roles and goals is a crucial first step in accepting your condition.

    Example: “I may not be able to be a nurse anymore but maybe I could teach classes a couple times per week.” or “I can’t be as physically active with my husband anymore so what else can I do to show him I love him?

    7. Acceptance

    Acceptance is often confused with the idea of being “OK” with what has happened. This is not true.  Many people don’t ever feel OK about having to live with pain or an illness for the rest of their lives.

    This stage is about accepting the reality of your situation and recognizing that this new reality is permanent. We will never like this reality and it may never be OK, but eventually we accept it and learn to live life with it. It is the new norm with which we must learn to live.

    We must make adaptations and alterations to our lives. We must find new things that bring us joy.

    Example: “I’m not going to let this define me. I will learn to deal with this the best I can.”

    It's important to remember that these stages are not linear.  While some people begin in the denial stage, move through each stage and end with acceptance, many people jump back and forth throughout the stages.  I hope that these stages give some comfort to those who are experiencing chronic conditions.

    Jennifer Martin, PsyD, is a licensed psychologist in Newport Beach, California who suffers from rheumatoid arthritis and ulcerative colitis. In her blog “Your Color Looks Good” Jennifer writes about the psychological aspects of dealing with chronic pain and illness.

    Jennifer is a professional member of the Crohn’s and Colitis Foundation of America and has a Facebook page dedicated to providing support and information to people with Crohn’s, Colitis and Digestive Diseases, as well as other types of chronic pain.

    The information in this column should not be considered as professional medical advice, diagnosis or treatment. It is for informational purposes only and represents the author’s opinions alone. It does not inherently express or reflect the views, opinions and/or positions of Pain News Network.

    Saturday, April 9, 2016

    Pain Is Real


    PAIN IS REAL BLOG
    Perspectives on life-altering pain. Current issues, purposes and consequences of pain relief policies, guidelines, and laws affecting the accessibility of safe, effective, and affordable health care.




    Pain is Real Blog
    28 MARCH 2016 In CDC Guidelines
    An unexpected and major "aha" moment had my attention.  Something strange happened after I read the introductory paragraphs of the CDC Guideline for Prescribing Opioids for Chronic Pain, United States, 2016. My body immediately and strongly reacted before I could logically consider the guidelines and their implications.  I could hardly breathe.  Hot tears dripped onto my cheeks, and my stomach felt like someone had grabbed it and twisted hard.  The unfamiliar and strong gutteral reaction lasted for hours.
    Was it despair or fear or deep concern for the people with chronic pain who would be negatively affected?  I knew how and why the guidelines were created.  What was this new and uncomfortable sensation that rendered me inarticulate and with no appetite for the rest of the day?  Was it foresight that in the future people would look back at the guidelines and wonder why it was acceptable for our government to stigmatize, denigrate, and torture people with chronic pain?
    21 MARCH 2016 In Stigmatization
    grey haired woman holding headsmallToday a woman with fibromyalgia frantically searching for legal guidance called my office. In the midst of a contested divorce, Julie (not her real name) was experiencing fibro flares exacerbated by a car accident two weeks earlier. Earlier that day, she was seeking a delay from the court for the divorce proceedings while she recovered. After explaining that she had fibromyalgia and was in more pain since the accident, the judge asked her, “How did you get to court?” “I drove.” “Since you were able to drive, and you look just fine to me, I deny your petition to delay the divorce proceedings.” And the judged closed her case, changing her life forever.
    Through her tears on the phone, Julie told me what she had wanted to tell the judge. “Your honor, I didn’t sleep last night because I was afraid if I used my prescription sleep medication, I’d sleep through my alarm to wake me for this hearing. And then I drove here two hours early and waited in the parking lot so that I wouldn’t be late. I am not able to defend myself and cannot afford an attorney to help me with the divorce.”

    NEWSLETTER

    Join our newsletter to stay updated on breaking research, advocacy and relationship news in the FM Community!

    CONTACT US

    • Phone: 801-200-3627

    CONNECT WITH US

    We're on Social Networks. Follow us & get in touch.