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A warm welcome to the forum Aidan in Shrewsbury. Im sorry for your diagnosis. Its such a shock isn't it ?
You made me smile with your comments about Cardiff winning the premiership. At one of my early appointments I asked the neurogist if I would live long enough to see Leeds promoted. He smiled a wry smile and said Debbie I dont think any of us will live that long. I did see Leeds promoted but the way we're playing atm I think I might see them relegated.
Take care,
Love Debbie x
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Originally posted by Deb View PostA warm welcome to the forum Aidan in Shrewsbury. Im sorry for your diagnosis. Its such a shock isn't it ?
You made me smile with your comments about Cardiff winning the premiership. At one of my early appointments I asked the neurogist if I would live long enough to see Leeds promoted. He smiled a wry smile and said Debbie I dont think any of us will live that long. I did see Leeds promoted but the way we're playing atm I think I might see them relegated.
Take care,
Love Debbie x
Love Aidan
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Hello Aidan, sorry you had to come on here, I've found as the carer that you just adapt to this whole saga without particularly realising that's what you are doing, I have lost count of the "New Normals" we have had.............for me its only looking back and realising just how far down this road we have come which can be alarming at times,
I'm not one to live for today or the hour I love a good bit of analysis and try to look at whats coming our way next before it actually does - better to be forewarned is my motto and Alberts OT agrees!
Best wishesHusband Albert diagnosed PMA Feb 21
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My husband (age 58) started in a similar way, he was being investigated for left hand carpal tunnel initially Jan 2021 which coincided with left frozen shoulder. Nerve conduction tests were carried out Feb 2021 which concluded that as four fingers were affected it wasn't only carpal tunnel going on and referred to neurologist. By the time neurologist was seen in April 2021 the right hand was also similarly affected and a limp had developed in left leg. GP suspected a brain tumour.
This seems a fairly quick diagnosis compared to some on here - and health services have been amazing, despite the pandemic.
Upon diagnosis of ALS (Apr 2021) GP's comment was " well at least its not a brain tumour".
He now has an attendant operated power wheelchair, uses head operated Ipad for communication, no speech (voice banked Sept 2021 when speech started to be affected), PEG fed and now advised to use NIV overnight as breathing is now compromised. Not yet a year from diagnosis.
With hindsight, early symptoms were a few years ago when he had symptoms with his tongue which felt "funny" and swollen on one side and he kept biting it as it didn't move as it should. ENT couldn't find anything wrong and advised that his teeth may need attention.
We read up on everything as we took the view that forewarned is forearmed, and discovered that the only guarantee is that everyone's journey is different - there is no set progression path or timeline. We are 10 months in and it is difficult to comprehend how quick the progression has been for him.
Fortunately we took advice from the various experts about having things done before anyone thought they would be needed - eg adaptations, PEG, voice banking. As it happens voice had started failing by August, voice banking completed September. Voice completely gone by Christmas. PEG fitted mid November, now 100% PEG reliant.
Hope your progression is much slower - wishing you well xxCarer for husband diagnosed with ALS April 2021. Hand onset. PEG fed, completely immobile, communicates with eye gaze.
Respiratory and blood gases still within normal range.
No speech but sense of humour still fully intact.
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Originally posted by Aidan in Shrewsbury View PostI too often have a poor appetite and simply don’t want to eat a big meal. Try to make up for it by grazing between meals but don’t even want to do that much of the time.
If not, a Dietitian can help advise you how to maintain your weight, which might include some nutrition drinks. I know that sometimes we almost need to force ourselves to eat but eating can make us feel heaps better, improve our mood and how much sleep we get. xx
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 Aidan in Shrewsbury View PostI have even put on a bit so the grazing on cakes is working.
At the risk of being a Party Pooper 🙄 try to make sure you get a decent amount of protein too - our bodies really need it. xx
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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Had a productive day today. Saw my neurologist this morning to get a prescription for Riluzole. Had to go to Telford to see him which was a bit annoying but when I get it it will come from the neurology dept of my local hospital hope to start it by next week. Stopped at a place in Shrewsbury called Ableworld which sells all sorts of devices for disabled people.
Got myself a walking stick with prongs which is quite good but what I found really good was a rollator I could whizz along at nearly normal speed with that. Will definitely get one am seeing a OT soon who might help. Could actually whizz along to the shops with a rollator. Was reluctant about them before as it’s saying to the world I am disabled but of course I am.
Actually going to the pub tomorrow for a lunchtime putting the world to rights session with my cronies. Should get the Ukrainian situation solved.
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Great you've had a productive day Aidan in Shrewsbury. The pub sounds more enjoyable, however, than a trip to see the neurologist although both are necessary !🍻
Your OT should advise and then source any equipment you need so I wouldn't buy anything ( unless of course its an emergency!) . Mine tended to look ahead which i found upsetting at the time but she was right.
You may notice that I'm not talking about football today 😩😩
Love Debbie x
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