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Ivan

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    Ivan

    Hello all,

    My wife has been diagnosed with this disease within the last 6 weeks. I have watched her over this last year go from nicely shaped woman to skin and bone, with now all the signs of mnd. We didn't know why she was losing weight.

    No doubt this has been asked by others but, as we are told there is nothing to be done about the disease, has anyone tried CBD? I know it's a contentious subject but, if it helps in anyway then it's worth it.

    Best wishes to all.
    Ivan Pearce

    #2
    Hi Ivan,

    I'm so sorry to hear about your wife. We wouldn't wish another person to have to join us here . I've used CBD; for me I thought it helped a little with some symptoms, but had no impact on the progression of the disease. Others may be more enthusiastic.
    Best wishes, Kate

    Comment


      #3
      I'm so sorry about your wife's diagnosis, Ivan.

      It sounds like her first symptoms were swallowing difficulties?

      By all means try CBD oil but is the hope to relieve specific symptoms or for her to take it as an overall 'supplement' type product? There are various strengths available and they can range from a few quid per bottle to quite eye-watering prices! Do your research though and buy from reputable vendors/sites as it's not a regulated product, i.e. just because it says 5% on the label, doesn't mean it is. (BBC's "Trust Me, I'm a Doctor did a segment on CBD Oil if you want to watch it https://www.bbc.co.uk/programmes/m000dbdm )

      If you feel up to it, perhaps tell us how your wife is but she can help herself live a better quality of life by getting an appropriate amount of calories & fluids, through a feeding tube if necessary, managing her symptoms with meds or physical interventions and using non-invasive breathing assistance if needed.

      I hope you have good support yourself.

      Take care.

      Love Ellie.
      ​Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
      Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user
      .

      Comment


        #4
        Hi Ivan

        Welcome to the Forum. I was so sorry to read of your wife’s diagnosis.

        Based on recent personal experience, may I pick up on one aspect of it: weight loss.

        To an extent, loss of weight is inevitable in MND. As our neurones die, the muscles they served shrink and wither away. But it is well recognised that every attempt should be made to keep weight loss to a minimum.

        I have monitored my weight regularly for decades, so months ago it was easy to detect a significant downward trend. I contacted my MND clinic who moved very swiftly, calling me in for a consultation with a nutritionist as well as my usual doctors. MND is known as a “hungry” disease. Paradoxically, despite shrinking muscles, lack of mobility and loss of appetite, MND places high demands on our metabolism. Additional calories are needed.

        I was prescribed high calorie drinks, specially formulated to contain also essential vitamins and trace elements and designed to help patients at risk of medical malnutrition. A typical dose is three 125ml bottles a day. There are several makes, such as Ensure:

        If you're looking for meal replacement drinks and shakes that can give you a boost in nutrition, turn to Ensure, the #1 Dr. Recommended Brand. Ensure was introduced into the market in 1973 and has been providing people with complete, balanced nutrition ever since. Learn more today!


        Talk to your MND team about whether they might help your wife. Your GP can prescribe them.

        Good luck, stay safe!

        Doug
        Diagnosed April 2017

        Comment


          #5
          Hello Ellie,
          Many thanks for your advice. My wife Alison, is swallowing fine, the disease is not that bad yet, she has just wasted away which I understand is typical of MND. She is still up and moving around although some days she is very dizzy and stays in bed. As she is an ex midwife she understands the medical problems that she will have to face. I just hope I can help her.
          Best regards to all
          Ivan

          Comment


            #6
            Hello Kate,
            Thanks for your response. As Alison is ex medical background I doubt I could get her to try it anyway, but thought the question was worth asking.
            My heartfelt best wishes to you.
            Ivan

            Comment


              #7
              Hello Ivan, dizziness isn't usually directly associated with MND. I don't mean to pry but could it be due to medication side effects, inadequate nutrition, dehydration or an infection? I know your wife has medical knowledge so will know more culprits which can cause dizziness.

              Love Ellie.
              Last edited by Ellie; 11 May 2020, 14:31.
              ​Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
              Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user
              .

              Comment


                #8
                Welcome Ivan. There’s a lot to get your head around in these early days but Please don’t hesitate to ask questions- there’s usually someone who will be able to give you an answer or point you in the right direction.

                Comment


                  #9
                  Hi Ivan

                  Just a quick update on high calorie nutritional drinks.

                  The link I included in my 20.31 post yesterday is not appropriate. It goes to the US site. Here is the specific Ensure product I've been prescribed:



                  Thinking of you both.

                  Doug
                  Diagnosed April 2017

                  Comment


                    #10
                    Originally posted by Doug Carpenter View Post
                    Hi Ivan

                    Welcome to the Forum. I was so sorry to read of your wife’s diagnosis.

                    Based on recent personal experience, may I pick up on one aspect of it: weight loss.

                    To an extent, loss of weight is inevitable in MND. As our neurones die, the muscles they served shrink and wither away. But it is well recognised that every attempt should be made to keep weight loss to a minimum.

                    I have monitored my weight regularly for decades, so months ago it was easy to detect a significant downward trend. I contacted my MND clinic who moved very swiftly, calling me in for a consultation with a nutritionist as well as my usual doctors. MND is known as a “hungry” disease. Paradoxically, despite shrinking muscles, lack of mobility and loss of appetite, MND places high demands on our metabolism. Additional calories are needed.

                    I was prescribed high calorie drinks, specially formulated to contain also essential vitamins and trace elements and designed to help patients at risk of medical malnutrition. A typical dose is three 125ml bottles a day. There are several makes, such as Ensure:

                    If you're looking for meal replacement drinks and shakes that can give you a boost in nutrition, turn to Ensure, the #1 Dr. Recommended Brand. Ensure was introduced into the market in 1973 and has been providing people with complete, balanced nutrition ever since. Learn more today!


                    Talk to your MND team about whether they might help your wife. Your GP can prescribe them.

                    Good luck, stay safe!

                    Doug
                    Hello Ivan just to echo the comments by Doug I currently use https://www.fortisipdrink.co.uk/
                    These are made available through my nutritionist on a repeat prescription

                    Comment


                      #11
                      Hi Ivan, I’m sorry about Alisons diagnosis. I see that you’ve had good advice already so I won’t bore you. I’ve heard that people who have MND struggle to keep on weight. That isn’t my experience so far. I’ve put on lots of weight since my diagnosis (due to my good diet but loss of mobility) but I will keep my eye on it.

                      It’s good that Alison is still mobile. I hope that her dizziness is sorted out quickly so that she can enjoy her mobility while it’s still there.

                      Look after yourself, 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


                        #12
                        Hi Ivan,

                        Sorry about your wife’s diagnosis, I agree with Doug about the calories drinks and puddings. Even though last
                        year I was still eating quite normal amounts I lost a stone in weight and now with calorie drinks and having had a RIG tube fitted I’ve put most of it back on, feel fitter and better. I’m now back to an average weight I’ve been for the last 10 years. Had to laugh today when the nurse came to change the tube I’ve had 4 months and as I opened my shirt she said “blimey, you’ve put a load of weight on!"
                        Weight and fat are so important to survive and fight this disease for as long as possible. By the end of last year I was struggling to get 1500 calories a day in due to the swallowing and eating difficulties that developed, now with the feed tube and some drinks I’m averaging 2200 calories a day.
                        I was offered CBD but never tried it, just wasn’t sure.

                        Regards

                        David R

                        Comment

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