Had mnd for 6years now feeling want it 2 end now
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Hi Tom and a warm welcome to the Forum. You've made a good start in making the first post, you can reach out whenever you feel up to it.
Yep, life is certainly tough with MND, no denying thatand I think it's even harder as we slowly emerge from this period of lockdown and isolation....
Hopefully you have good support?
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.
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hi tom
you could start by talking. just say what you feel i know i have. its not easy but at least you can get rid of some of it and i am sure most of us are feeling the same way. my husband was diagnosed last year. the doctor told him off for not coming earlier. i am sure he has been suffering for quite a while. but hey talk to us. perhaps it will be easier than talking to those that are close to you. its just a thought.
denise xxxwhen i can think of something profound i will update this.
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Welcome to the Forum, Bonnie, sorry you've had to join us
Is there someone who can assess you and address your pain? Often in MND pain can be caused by a change in gait, if still walking, making one use compensatory muscles; from sitting awkwardly for long periods; from high muscle tone or spasticity; associated nerve pain etc. By someone, I mean a physiotherapist, OT, GP, MND Nurse, Neuro etc.
If you know what's causing your pain, you can get the appropriate help to decrease the pain.
Our lives our hard enough without being dragged down by debilitating pain...
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.
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Hi Bonnie, I’m sorry about how you feel, especially your pain.
I’m the same with pain which is much worse at night (my spine and both hips, other pain but these ones are unbearable at times). I had to stop Tramadol recently because they were making me itchy. My GP started me on a low dose of a drug used mainly mental conditions like depression, anxiety and other things. But it’s being used to treat pain because it’s thought to calm nerve endings. I go to sleep ok but wake in severe pain in the middle of the night or very early in the morning. I get up because I can’t stand it any longer. I forget what the drug was my GP mentioned but the pharmacist gave me Duloxetine Mylan at one 30mg tablet per day. It can go up to 60mg. I’ve been told to ring my GP after a month and if I haven’t had nasty symptoms she’s going to increase the dose. I can’t wait. I’m hoping that it works but I read that it isn’t yet proven.
Maybe speak with your GP to see what they can do for you. Love Lynne xALS 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.
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Originally posted by Lynne K View PostHi Bonnie, I’m sorry about how you feel, especially your pain.
I’m the same with pain which is much worse at night (my spine and both hips, other pain but these ones are unbearable at times). I had to stop Tramadol recently because they were making me itchy. My GP started me on a low dose of a drug used mainly mental conditions like depression, anxiety and other things. But it’s being used to treat pain because it’s thought to calm nerve endings. I go to sleep ok but wake in severe pain in the middle of the night or very early in the morning. I get up because I can’t stand it any longer. I forget what the drug was my GP mentioned but the pharmacist gave me Duloxetine Mylan at one 30mg tablet per day. It can go up to 60mg. I’ve been told to ring my GP after a month and if I haven’t had nasty symptoms she’s going to increase the dose. I can’t wait. I’m hoping that it works but I read that it isn’t yet proven.
Maybe speak with your GP to see what they can do for you. Love Lynne x
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Hi Bonnie, I can’t take ibrufrofen. I have eroded top of stomach after many years of different such medications. Nor can I take anything with codeine in because it causes unreasonable constipation. It’s common to have this side effect. But I agree about it’s pain killing effect. I took it for a short time after a slipped disc many years ago.
I hope that your GP gave you something to keep your bowels ok. Nothing worked for me years ago, only coming off codeine.
Love Lynne xALS 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.
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Good morning,
Welcome Bonnie - very sorry to hear of your challenges.
Could I add another name to the list of painkillers being my old friend Indomethacin - This is an early painkiller which is used for rheumatism – including gout which I suffered from perhaps 15 years ago for the first time and for me it is really the only thing that kills that pain and I'm now using it as a rather more general painkiller although I am aware of the risks to my liver which I monitor with regular blood tests, which I also need for my other drug intake.
Lynne I have no idea whether this will hit your stomach in the same way that does ibuprofen.Warmly
Andy
Diagnosed 03/2015. One sided limb onset (arm) sporadic PMA/MND - now 90% left arm and 90% right arm, plus other bits including both shoulders and also some breathing issues – Campaign contact Winchester and Southampton branch, and trustee of the Association
"Things turn out the best for people who make the best of the way things turn out"
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