Chronic pain - Let's talk
Are there any discussions for chronic pain?
Interested in more discussions like this? Go to the Chronic Pain Support Group.
Are there any discussions for chronic pain?
Interested in more discussions like this? Go to the Chronic Pain Support Group.
Thank you ladyjane85 for your good wishes. I like your positive attitude. So true that dressing up & looking nice can help you face the day in a better mood. I've also found that I cannot wear flat shoes; wedge heels feel better. Thanks to everyone for posting to Twokitties.
@marieh
I have had a neurostimulator for about 5 years now. It works wonders for me. The only drawback to it is that it only works for the area it has been placed for. If you have L-1 to L-5 pain and it is placed for those discs it will not work for your neck area unless you have another one implanted. Mine can be adjusted to work more on one side than the other if my pain is radiating more on one side. I can do that myself. I have also had the programmer adjust the area slightly with her device when I had hip surgery. But there are limits to what the adjustments are and they can't make it go up or down a disc. I believe it has kept my med use at the same dose for the past 5 years instead of having to have it increased. It it a gentle massaging type vibration and can be programmed with several different types of massage feelings. I can turn between them if I need a stronger one on a day where the pain is worse. It has to be programmed by the nurse who was there during my implant or a rep from the company. I just see her once a year, she loads up my controls with the ones I want and I'm set. If I wish to change anything all I have to do is call her and meet her at my Pain Mgmt office. I only wish my body would stop falling apart disc wise because I could use another one for my neck now. As far as fatigue as others have talked about, gabapenten will cause fatigue in me but the medication does help me. My Vit D level was extremely low because I'm not outside a lot. Taking a dose of that my Dr has prescribed has started to help some. It's not all perfect now but most days more than not, my pain is more manageable with the stimulator and my medication. I hope this helps some. Thank you for this site to talk and thank you for reading. ❤️
I have had several blocks, epidurals and other nerve blocks. None of mine have hurt with the exception of the steroid flare pain a couple days post injection. And like someone else had posted I find that the relief depends on who did the injections and if the actual spot was hit dead on. They are not meant to last forever. I was told they are a temporary relief to a permanent problem. I'm sorry you don't get to get in fast enough. Like you I have sciatic pain and it can be some of the worst pain I have ever felt. I go to a fantastic pain mgmt group that I can call and get a same day appt to be evaluated for an injection that day. They have a surgery center down stairs from their offices and I can go right down and get an injection if the Dr says I can. It's been a life saver.
@mlemieux
I'm so glad you brought this up. I've noticed these posts seem to all share one thing, we are all in pain, tired of it and want better quality out of life.
Like other I have tried most of the same medical procedures, some with better results than others. I enjoyed reading your post and spouted a loud YES!!
I believe no matter what I take or put on my body if my frame of mind is negative than more times than not my results are negative. So I try some things several times to rule it out completely. I have a very specific morning routine.
1. I take my morning meds with a full glass of water and refill the glass a second time and try to drink that too. My glass is 16 oz so I try to start my body off with 32 oz of water to flush out the gunk my body has tried to get rid of while restoring at night.
2. I usually lay or sit back on my bed and wait for my meds to work. But while they are working so am I. I meditate and do positive affirmations. Even if all I can do is 20 minutes of broken time and only 1 positive out of the 3 I want to do. I still think this gets me in a more positive frame of mind and I can talk myself into handling more than I normally have in the past. Some days the pain is so bad in the mornings that I convince myself over and over that I can do this. Other days I just need to go back to bed and try again after my second dose of meds. The less stress I put on myself the better I am to myself. I really don't need anyone to tell me how bad I am, because like most other chronic pain sufferers, I get depressed easily and I am my worst critic.
3. I do all I can in the day and do my very best. If it is a job, a project, or just housework I work until I need to rest and then work some more. At the end of the end I go over what I've done and I'm grateful to God for being able to do it. I try not to criticize myself on what I didn't get done, or how much or how little I've done. I say a prayer to have the strength to start over the next day and I close the chapter on that day. I try not to revisit it unless I need to keep a pain log for my doctor.
Pain isn't something that is the same for all of us. What I think is unbearable may be nothing to you or vise versa but it doesn't make it any less painful to those who are feeling it. I listen to my doctor and I work hard with him to find a plan to work for me. But mostly I try and I say TRY to stay positive. Anger, bitterness and regret lead to depression for me and it only makes my pain worse. So if I follow my 3 steps each day to the best I can I help manage my pain the best way I can.
Martin if you have other way you cope or can share more that helps you I would love to hear them.
Thank you so very much for the excellent post for discussion.
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2 ReactionsAgree. The self talk is so necessary<br>I feel then,we are whole. I too,feel<br>relaxed after meditation.<br>After that I have my cup of coffee<br>when everything is quiet.<br>Just starts me out better.<br><br>I also found that regardless of my attitude,i must do my leg exercises<br>It, has to be a part of my morning<br>routine.<br><br>Success101<br>
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1 ReactionHello @19lin<br>I am very interrested in your health<br>Condition. Is it, severe enough for hospice? I feel very much for you.<br>As I have pain,and my husband<br>has pain continuously.<br>Result of hip REVISION. IT ALL<br>WENT VERY WRONG. There<br>isn't any pain meds for him<br>As he lost an eye to gloucoma.<br>Must be very careful. Vision poor.<br>He is suffering now from side effects<br>of radiation therapy for pros<br>tate cancer.<br>Like you, he, has put this all in God's<br>hands.<br>Be strong,i believe you are.<br>Blessings on you<br>Success101<br>
Hi all! Several of you have been discussing the pros and cons of laminectomy recently. I invite you to pop over to this discussion thread https://connect.mayoclinic.org/discussion/laminectomy-recovery/ to share your thoughts and experiences, so that this important topic doesn't get buried in this long thread 🙂
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1 Reaction@bekie Welcome to Connect! We are so happy to have you here and i'm thrilled to see you are already finding the community useful. Thanks for joining us and sharing your experiences!
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1 Reaction19lin Are you able to dress yourself and do a bit each day? I went into<br>a continuing care community where I have<br> my own apartment, with light housekeeping done, and a dining room for<br>meals (or can be sent up on a tray). When<br> I get worse I will go to assisted living - the they he nursing and rehab<br>on campus, and a memory care building. Or<br>there are living facilities where you start off in assisted living. I<br>cannot believe dr suggested hospice unless you are<br> near death's door. Please look into other facilities where if money runs<br>out you will be helped by medicaid.. The very best to you.<br>ladyjane85 I am now 86, can often go up o 10 pain level in back, but can<br>still drive to drs.<br><br>
@briansr I agree, enough with surgeries. Are you living in a facility<br>where you are put either in Independent Living or<br>Assisted Living? If you are living alone one must look into a facility<br>where you can be helped. I am in a Continuing Care<br>place in an Independent Living apartment. It is expensive to get into but<br>they can never throw you out, you just move up<br> to more assisted parts. Even a spouse can live with one. Do not give up -<br>my very best, ladyjane85<br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br>