Good evening all.
So we got Dad in front of a neurologist this morning. Onward referrals now to SALT, a headscan, an EMG and he has had today’s obligatory blood test.
( to recap Dad is 89, his legs have now stopped working and he has deteriorating bulbar signs in his speech- his arms and hands still work).
What was really interesting was that his tongue fasciculations were not on display today. But obviously she respected previous attendant’s observations of them to refer him on for an EMG.
So whilst we wait on those tests and a final review I’d like to say I’ve learned a lot from the association and much more from the forum. Even if my Dad has not got ALS/MND we are another family aware of the impact of the disease and will be doing what I can going forward to support research, care and understanding.
I’ll be back with final diagnosis at an unknown date- I reckon about July, we could draw lots!
In the meantime best wishes to you and on behalf of my Dad and family thanks for your help and advice.
So we got Dad in front of a neurologist this morning. Onward referrals now to SALT, a headscan, an EMG and he has had today’s obligatory blood test.
( to recap Dad is 89, his legs have now stopped working and he has deteriorating bulbar signs in his speech- his arms and hands still work).
What was really interesting was that his tongue fasciculations were not on display today. But obviously she respected previous attendant’s observations of them to refer him on for an EMG.
So whilst we wait on those tests and a final review I’d like to say I’ve learned a lot from the association and much more from the forum. Even if my Dad has not got ALS/MND we are another family aware of the impact of the disease and will be doing what I can going forward to support research, care and understanding.
I’ll be back with final diagnosis at an unknown date- I reckon about July, we could draw lots!
In the meantime best wishes to you and on behalf of my Dad and family thanks for your help and advice.
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