Baclofen

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  • Terry
    Forum Member
    • May 2012
    • 1917

    #16
    Hi Boiler;

    Does your husband suffer from back trouble normally and did it start with a twinge in the lower back?

    Just asking because I can suffer from lower back spasms that put me out of action for a few days each time. I used to take a strong relaxant like what Ellie suggests, but now I dose up on Ibuprofen and after a couple of days I can start to move.

    I don't think that it is directly related to Mnd but it is another one of the lovely side issues, perhaps caused by weakening muscles and poor posture. I hope he can relax them, heat and just rubbing the area can help.

    Love Terry
    TB once said that "The forum is still the best source for friendship and information."

    It will only remain so if new people post and keep us updated on things that work or don't work and tips.

    Please post on old threads that are of use so that others see them and feel free to start new subjects and threads.

    Comment

    • Boiler68
      Forum Member
      • Feb 2018
      • 82

      #17
      Hi Terry

      He hasn't had a bad back like this before where it makes him gasp and double up. I guess poor posture and sitting all day is a major factor. He said earlier it had eased off a bit but not longer after asked for some painkillers! Currently filling hot water bottle and he's straightening out with a lie down.
      Thanks for your reply. Hope your back doesn't give you too much trouble this year..

      X

      Comment

      • Kayleigh
        Forum Member
        • Nov 2018
        • 1227

        #18
        Hi Boiler,

        Sorry to hear about Mr Boiler's back pain - not a pleasant way to start the new year at all! It is bad enough coping with things without being in pain as well.

        I have recently been advised by my nurse that if I get any cramps or pains, I should take ibuprofen (like Terry does) or for longer periods of time to take paracetamol, because apparently prolonged use of ibuprofen can cause stomach ulcers.

        She also told me that if I need stronger painkillers, I can get them prescribed by my GP.

        Might be worth asking his GP, if pain doesn't clear up with 'standard' painkillers, what can be prescribed so that it can get sorted asap - as I can't imagine either him or you are getting much sleep or having a very pleasant time at the moment, if he is in severe pain.

        Hopefully, Mr Boiler will be feeling better soon.

        Also, I hope you and your family are ok too.

        Best wishes,
        Kayleigh x
        Last edited by Kayleigh; 5 January 2019, 19:08.

        Comment

        • Lynne K
          Forum Member
          • Nov 2017
          • 2614

          #19
          I'm sorry for all of you struggling with back pain due to spasms. I hope that you all manage to sort it out one way or another.

          I'm the same, in terms of severe back pain every night, but no spasms. My pain is not an MND symptom (it's because of my severely degenerated discs) but caused by my MND because in the past I could reduce or even eliminate it by walking and if pain not too bad fast paced walking. Now I cannot walk off the pain. I knew that this would happen when I got diagnosed.

          I cannot usually take ibuprofen because I already have stomach issues since years of taking anti-inflammatories. I don't take them now despite various pain issues because I get heartburn most days and reflux sometimes. I was told by my GP that the top of my stomach was eroded.

          I get my husband to rub in ibuprofen gel in to my lower back before bed sometimes. I wish I could have it every night. But even the gel can cause heart burn and reflux.

          Too many paracetamol, even taking the recommended safe maximum dose can damage your liver. Anyway if we take any pain killer too often our bodies get used to it, they have less effect. Some people crave more and hence addiction can result. That's with codeine-like tablets. It isn't worth taking them in the first place.

          I take paracetamol rarely, despite being in pain 24/7 because I want them to work when I'm at my wits end with pain. I'm getting close to that now. Maybe paracetamol by mouth tonight and ibuprofen gel on my back. I might then get a few decent hours sleep for a change.

          I had low dose amitriptyline for insomnia related to pain about 15 years ago for a few months. It did help but I had a dreadfully foggy head until about 2pm next day so stopped taking it. My ex husband had a higher dose when he had a breakdown. Even at the lower dose that I was on I felt really chilled out, and not my usual then self who couldn't sit down for long of felt I had to get up and do stuff, anything. So, if ever I felt down about this disease and was still losing sleep because of pain I'd take a low dose of amitriptyline.
          Lynne
          Last edited by Lynne K; 5 January 2019, 17:22.
          ALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.

          I'm staying positive and taking each day as it comes.

          Comment

          • easter19
            Forum Member
            • Dec 2018
            • 18

            #20
            hi lynne
            have you had your new mattress and topper delivered yet ?
            does anything help with the pain
            hot/cold heatwraps etc
            love
            emma x

            Comment

            • Kayleigh
              Forum Member
              • Nov 2018
              • 1227

              #21
              Hi Lynne,

              Sorry to hear about the problems you experience due to long-term pain.

              Hopefully, when you get your new mattress it will help you sleep better.

              I agree with you about the painkillers - there are the benefits v. side effects to consider, especially if being used long-term. However, we have got enough to cope with without being in pain. It is a personal choice to make. I always used to be extremely cautious about their possible side effects, but my life has changed and not being in pain is much more of a priority for me now. Being in pain affects our quality of life, and so I want whatever life I have left to be as pain-free as possible.

              I would never take 'stronger' painkillers unless I had got advice from my GP first and, hopefully, I would only need them for a short amount of time. I have taken codeine tablets for one or two days in the past and they have stopped the pain, with no side effects and no addiction.

              Best wishes,
              Kayleigh x
              Last edited by Kayleigh; 5 January 2019, 19:21.

              Comment

              • Lynne K
                Forum Member
                • Nov 2017
                • 2614

                #22
                Hi Kayleigh. We got the new mattress and memory foam topper on Thursday. I'm still in severe pain every night. Some pain and or discomfort I'm my back every day. I turn with great difficulty on to my side when I'm at my wits end with the pain when my back is in contact with the bed. But after a while on my right side my left hip gets seriously painful so I have to go back to my back, so square one pain wise. In a way I'm looking forward to 3 days back pain free from Monday. When the do my op' they plan to put a pain killing epidural in and keep me in bed 3 days. I'll have a physio to work my legs, so they don't cease up. Lynne
                ALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.

                I'm staying positive and taking each day as it comes.

                Comment

                • Lynne K
                  Forum Member
                  • Nov 2017
                  • 2614

                  #23
                  I do have the new mattress and topper thanks Emma. I just posted a reply to Kayleigh about this. I have a tens machine that I sometimes use during the day. I wouldn't leave it on at night. A heat pad might work because running hot water on my back in the shower is lovely because lessons pain. I look forward to my shower every day. Lynne
                  ALS diagnosed November 2017, limb onset. For the 4 yrs previously I was losing my balance.

                  I'm staying positive and taking each day as it comes.

                  Comment

                  • Catsparkle
                    Forum Member
                    • Jun 2018
                    • 83

                    #24
                    Ive started on 5mg Baclofen and loved it! My legs wallked normally again. From what Ive read it has a short life so you take it through the day? Because of the severe withdrawal reactions my doctor wanted to see if I had any adverse reactions before upping me. I'm using it before i need to go out at the moment.

                    Comment

                    • Ellie
                      Forum Member
                      • Oct 2012
                      • 12572

                      #25
                      Hi Lisa,

                      Baclofen is "usually" taken 3x per day, but sometimes it's only taken for when spasticity will cause problems, e.g. in bed or before a physio session.

                      Some spasticity (high muscle tone) can be a good thing for maintaining a degree of function - in your case reducing tone in your legs enough so you can bend knees and move feet allowing you to walk, but not resulting in low muscle tone which wouldn't allow you weight bear - that's why I say it's a balancing act to find the right dose.

                      If you think you'd benefit from a 2nd or 3rd daily dose, ask your Dr.

                      I take Baclofen 3x daily and add Tizanidine, another antispasmodic, for bed as that's when my already-high leg muscle tone goes even higher!

                      Good luck,

                      Love Ellie.
                      ​Diagnosed 2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
                      Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user
                      .
                      ​

                      Comment

                      • matthew55
                        Forum Member
                        • May 2020
                        • 5794

                        #26
                        I swear by Baclofen, it's even part of my exit plan. I've never considered Botox as it is a poison at the end of the day. I know I'm conflicted but that's just me init? πŸ˜πŸ€—πŸ˜‚πŸ˜xx
                        Bulbar started Jan 2020. Mute and 100% tube fed but mobile and undefeated. Stay Strong πŸ€—πŸ˜˜πŸ€—πŸ˜xx

                        Comment

                        • Ellie
                          Forum Member
                          • Oct 2012
                          • 12572

                          #27
                          matthew55 Yeah, me too mate - in fact it's so good that I spent all morning washing my own windows πŸ˜‰πŸ€£πŸ€£πŸ€£πŸ€£
                          ​Diagnosed 2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
                          Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user
                          .
                          ​

                          Comment

                          • matthew55
                            Forum Member
                            • May 2020
                            • 5794

                            #28
                            I never thought of you as a washer woman. Live and learn eh? πŸ˜‰πŸ˜πŸ€—πŸ˜xx
                            Bulbar started Jan 2020. Mute and 100% tube fed but mobile and undefeated. Stay Strong πŸ€—πŸ˜˜πŸ€—πŸ˜xx

                            Comment

                            • Ellie
                              Forum Member
                              • Oct 2012
                              • 12572

                              #29
                              Anything for a few bob, me πŸ˜‰
                              ​Diagnosed 2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
                              Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user
                              .
                              ​

                              Comment

                              • LindaB
                                Forum Member
                                • Jun 2021
                                • 2710

                                #30
                                Window [email protected] talented πŸ˜‚πŸ˜‚πŸ˜‰πŸ˜˜
                                Initial diagnosis 7-4-2021 'suspected MND' confirmed by 2nd opinion 4th June 2021 ALS. Began with R foot limp and lots of falls. NIV overnight. Generally weak. Mostly terrified.​​​​​​

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