Hi, I have been falling over for about 3 years, weak 3 fingers on my right hand and speach a bit slurred for 12 months or so. I had an mri and nerve/muscle tests a couple of months ago and last week was diagnosed with slow degeneration MND. The neurologist gave me Riluzone which I'm on my second day of and no sickness so far. I was scarred to death 2 weeks ago when MND was inferred but a bit better now that it's decided it's the slow type. I have enjoyed reading others posts and found them helpful, I'm a driving instructor still. Thanks all.
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Welcome I'm an ex-carer of my mother who had a very fast progressing form of motor neurone disease
One thing I will say ask for help, I didn't ask for help quickly enough ,you don't need to be stressed and receiving help takes a lot of stress off.
If you think you don't need to do it rest! people in general get a lot of health problems because they don't rest.
Can't tell you a lot about riluzole as my mother was prescribed it but when I saw the side-effects she decided not to take it .
I'm autistic sorry about the grammar .
Only learned i'm Autistic two years ago and I'm nearly 48 .
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ccinjersey
Welcome Lynne
You found the right place for great advice, support, and knowledge from people that understand what you are your family are experiencing.
Wishing you all the best.
CCxx
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Hi Lynne and welcome.
If like me you have a slow progression MND then you will carry on doing what comes natural to you and when you can’t you make adjustments and move on. Falls can be our worst experience so my advice is don’t be embarrassed by using a stick, crutch or walker. Prevention is better than cure if you break a bone.
I’m not sure of the benefits you will get by taking riluzole and it seems like your neurologist has taken the standard default action when diagnosing MND. I say this after much discussion with my neurologist.
Best wishes,
BarryI’m going to do this even if it kills me!
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Hi Lynne and welcome, but sorry you've had to join us.
Good to hear you have a slow form of MND. As others have said, stay safe! A bad fall could be a real set back for you
Love Ellie.Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Hi Lynne and welcome to the forum;
Sorry to hear of your recent worries and diagnoses but you seem to be on the right track and are now moving forward.
Hope you can keep your job running for a while yet as a driving instructor.
Best wishes, TerryTB 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.
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I fell on the ice and sludge this morning, got soaked. Had help to get up. Not hurt. Just frustrated and a bit angry at the NHS for the sighting of this centre in a bad place for anybody like me to access. This was when going to my speech therapist for the first time. I seem to be more wobbly in the last few weeks. Over xmas I've been considering my options re when to give up working. I am going to start voice banking today. Do we sometimes deteriorate quicker for a few weeks then slow down? Or is this the pace that I must get used to? All comments welcomme.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.
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Hi Lynne,
Sorry about your fall, hope you recover quickly.
Progression tends not to be linear - often people with ALS/MND get periods of marked progression followed by a fairly benign period - but there's no rule book!
Infections, illness, trauma, stress, poor sleep and inadequate nutrition can contribute to progression too. It helps to keep on top of the game!
All the best,
Love Ellie.Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.
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Originally posted by Lynne K View PostI fell on the ice and sludge this morning, got soaked. Had help to get up. Not hurt. Just frustrated and a bit angry at the NHS for the sighting of this centre in a bad place for anybody like me to access. This was when going to my speech therapist for the first time. I seem to be more wobbly in the last few weeks. Over xmas I've been considering my options re when to give up working. I am going to start voice banking today. Do we sometimes deteriorate quicker for a few weeks then slow down? Or is this the pace that I must get used to? All comments welcomme.
As for work - carry on until you can't - helps tremendously with mental health.
Kind regards
Chas
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Hi Lynne;
It's frustrating going to somewhere that should help you and falling due to ice, etc.
Good that you are moving forward by looking at voice banking.
As Ellie says, Mnd seems to attack in waves and you could see some improvement although it could be us just getting used to the new restrictions and leaning to cope better with them.
Love TerryTB 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.
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