Pain letter
ajj1001
Posted: Aug 15 2009, 09:16 PM


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This was posted on Justins wonderful website (spinepatientsociety.org) and I'm not sure if it has ever been put up here. It really moved me and I thought it should be seen by everyone suffering with chronic pain.

"A Letter to Normals from a Person With Chronic Pain.

In the spirit of informing those who wish to understand: These are the things that I would like you to understand about me before you judge me.

Please understand that being sick doesn't mean I'm not still a human being. I have to spend most of my day in considerable pain and exhaustion, and if you visit, sometimes I probably don't seem like much fun to be with, but I'm still me, stuck inside this body. I still worry about work, my family, my friends, and most of the time, I'd still like to hear you talk about yours, too.

Please understand the difference between "happy" and "healthy". When you've got the flu, you probably feel miserable with it, but I've been sick for years. I can't be miserable all the time. In fact, I work hard at not being miserable. So, if you're talking to me and I sound happy, it means I'm happy, that's all. It doesn't mean that I'm not in a lot of pain, or extremely tired, or that I'm getting better, or any of those things. Please don't say, "Oh, you're sounding better!" or "But you look so healthy!" I am merely coping. I am sounding happy and trying to look normal. If you want to comment on that, you're welcome.

Please understand that being able to stand up for ten minutes doesn't necessarily mean that I can stand up for twenty minutes, or an hour. Just because I managed to stand up for thirty minutes yesterday doesn't mean that I can do the same today. With a lot of diseases you're either paralyzed, or you can move. With this one, it gets more confusing everyday. I never know from day to day, how I am going to feel when I wake up. In most cases, I never know from minute to minute. That is one of the hardest and most frustrating components of chronic pain.

Please repeat the above paragraph substituting "sitting", "walking", "thinking", "concentrating", "being sociable" and so on, it applies to everything. That's what chronic pain does to you.

Please understand that chronic pain is variable. It's quite possible (for many, it's common) that one day I am able to walk to the park and back, while the next day I'll have trouble getting to the next room. Please don't attack me when I'm ill by saying, "But you did it before!" or "Oh, come on, I know you can do this!" If you want me to do something, then ask if I can. In a similar vein, I may need to cancel a previous commitment at the last minute. If this happens, please do not take it personally. If you are able, please try to always remember how very lucky you are, to be physically able to do all of the things that you can do.

Please understand that "getting out and doing things" does not make me feel better, and can often make me worse. You don't know what I go through or how I suffer in my own private time. Telling me that I need to exercise, or do some things to "get my mind off of it", may frustrate me to tears, and is not correct. If I was capable of doing some things any or all of the time, don't you know that I would? I am working with my doctors and I am doing what I am supposed to do. Another statement that hurts is, "You just need to push yourself more, try harder". Obviously, chronic pain can deal with the whole body, or be localized to specific areas. Sometimes participating in a single activity for a short or a long period of time can cause more damage and physical pain than you could ever imagine. Not to mention the recovery time, which can be intense. Also, chronic pain may cause secondary depression (wouldn't you get depressed and down if you were hurting constantly for months or years?), but it is not created by depression.

Please understand that if I say I have to sit down, lie down, stay in bed, or take these pills now, that probably means that I do have to do it right now, it can't be put off or forgotten just because I'm somewhere, or I'm right in the middle of doing something. Chronic pain does not forgive, nor does it wait for anyone.

If you want to suggest a cure to me, please don't. It's not because I don't appreciate the thought, and it's not because I don't want to get well. Lord knows that isn't true. In all likelihood, if you've heard of it or tried it, so have I. In some cases, I have been made sicker, not better. This can involve side effects or allergic reactions, as is the case with herbal remedies. It also includes failure, which in and of itself can make me feel even lower. If there were something that cured, or even helped people with chronic pain, we'd know about it. There is worldwide networking (both on and off the Internet) between people with chronic pain. If something worked, we would KNOW. It's definitely not for lack of trying. If, after reading this, you still feel the need to suggest a cure, then so be it. I may take what you said and discuss it with my doctor.

If I seem touchy, it's probably because I am. It's not how I try to be. As a matter of fact, I try very hard to be normal. I hope you will try to understand. I have been, and am still, going through a lot. Chronic pain is hard for you to understand unless you have had it. It wreaks havoc on the body and the mind. It is exhausting and exasperating. Almost all the time, I know that I am doing my best to cope with this, and live my life to the best of my ability. I ask you to bear with me, and accept me as I am. I know that you cannot literally understand my situation unless you have been in my shoes, but as much as is possible, I am asking you to try to be understanding in general.

In many ways I depend on you, people who are not sick. I need you to visit me when I am too sick to go out. Sometimes I need you help me with the shopping, the cooking or the cleaning. I may need you to take me to the doctor, or to the store. You are my link to the "normalcy" of life. You can help me to keep in touch with the parts of life that I miss and fully intend to undertake again, just as soon as I am able.

I know that I asked a lot from you, and I do thank you for listening. It really does mean a lot."


--------------------
2009 Std meds - Gabapentin, MR Tramadol, Paracetemol, Laxatives
May PLG Fusion L5/S1 Charite in situ
March Started appealing dismissal at work. April Dismissed
2008 June MRI showed additional prolapse L2/L3
Feb Caudal Epidural, on Gabapentin since due to pain.
2007 Deterioration L5/S1 Facet arthritis, Loss of disc height.
2004 Return to Work
2002 Aug started rehab
March 2 level ADR Charite L4/5, L5/S1
2000 Broadbased disc prolapses L4/5, L5/S1
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Gilly
Posted: Aug 21 2009, 12:27 PM


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What a brilliant summary of life for so many of us at the moment,Ajj.


--------------------
1990 MRI disc protrusion level4/5 fusion offered but
declined due to poor prognosis.
Osteopathy, physio,traction,steroid injections
epidurals all tried.
2006 Muscular-skeletal back building course.
2007 Mri disc protrusions Level 4/5 level5/S1.
2008 Discograms show annular tears and bulging.
2009 2 levelADR op 23rd April by Mr Shackleford cancelled
due to anaemia.1st Oct and 15th cancelled. Now 29th
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Ruth
Posted: Aug 21 2009, 12:55 PM


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Joined: 26-November 08



I made a similar reply on Justin's site but just to say the same as Gilly really. It strikes such a chord especially with my first disc problem. I trudged through life feeling like that for 7 years before I found someone who seemed able to help me. I couldn't have put it better myself!


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1998-2001 Early degeneration L1/2. 10 admissions: discography/epidurals/facet injections/disc injections/facet rhizotomies - with little long-term effect.
2005 Successful anterior fusion at L1/2 with BMP: Mr Ross, Spire Manchester Hospital.
2008 Early degeneration L4/5 unresponsive to epidural. Discography: anular tear & bulging. Limited response to core strengthening.
2009 ADR (activ L) L4/5: 20th April, Mr. Shackleford, Spire Cheshire Hospital.
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alyssa.star
Posted: Oct 10 2009, 08:51 PM


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Member No.: 108
Joined: 8-August 08



That's amazingly written and extremely true, I think sometimes people don't necessarily need to understand or know what we're going through, all I ask is that people/my friends are patient with me and the fact that I suffer with chronic pain and can't do many things.

Thank you so much for sharing this with us,

Lyssie xx


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Lyssie, 21y/o Diagnosed with Scoliosis aged 10, August '06 age 17, had spinal correction and fusion surgery by Mr Lam, now nicely fused T11-L3! Developed pain early '08 below fusion...
-June '08, Injections
-June/July '09 Developed numbness
-September '09 Further injections, unsucessful
Attending pain management! Facet Joint Syndrome!
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tazwb
Posted: Oct 12 2009, 08:46 PM


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Posts: 153
Member No.: 119
Joined: 20-September 08



That is so true, and for the first time ever I have been brought to tears reading that and thinking about my own situation, and it feels good to let it out. I always feel I can't let this beat me and refuse to give in to it.

Reading that made me give in for a few minutes and I feel better for it.

Now, back to putting on a brave face biggrin.gif

Thank you

xx


--------------------
Mar 1989 Accident at work started back problem - Aged 16
Dec 1990 - Epidural with Manipulaton
Nov 1991 Discectomy Aged 19
May 1999 - Epidural with Manipulation
Oct 2003 MRI Scan showed DDD
Dec 2005 Epidural & Facet Joint Block
Dec 2006 Epidural & Facet Joint Block
Apr 2007 MRI Scan
Nov 2007 Discogram Positive at 2 levels
May 2008 Percutaneous Discectomy (should have been IDET but machine broke on the day)
Had ADR at 2 levels L4/L5 & L5/S1 on Tuesday 27th January 2009
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