I was wondering whether anyone plays in a brass band? I do, and I am finding it challenging to keep playing well (I was diagnosed with PD last month). I was wondering whether anyone else has had this happen, and would either like to find out if you have any tips, or just chat about our experiences.
I don't know if you are familiar with the name......
Barbara Gracey Thompson MBE
Barbara Thomson’s indomitable struggle against Parkinson’s Disease is a heart warming story, a triumph of the human and musical spirit against the odds.There was a TV doc on BBC back in April I think about this Lady.
If you Google her name you will find out more about Barbara. I believe she has also written a book.
She was awarded the MBE in 1996 for services to music. Due to Parkinson's disease diagnosed in 1997, she retired as an active saxophonist in 2001 with a farewell tour. After a period of working as a composer exclusively, she returned to stage in 2004 to replace the unwell Dick Heckstall-Smith during Colosseum's "Tomorrow's Blues" tour, and in 2005 she performed live with Paraphernalia in their "Never Say Goodbye" tour. Since 2004 she has been permanent member of Colosseum.
Maybe reading about this Lady will spur you on to bigger and greater things.
Hope this helps
All the very best to you
I will look her up. Up until now, I have felt a bit alone in this regard, and it will be so helpful to see how she has coped.
For 20 years now I've played in bands, duos and by myself in the pub / club world. But I've lost the ability to do that now. I miss it dearly but I play a bit for my friends at the end of a dinner party.
My problems lies in the essential rhythms of the music. I start ok but after 10 seconds it all goes to pot! Not good for a guitarist and bass player!I was reminded of a test my neurologist did when I was first diagnosed. He made me open and close each hand quickly and after 10 seconds, my right hand (strumming hand) stopped obeying my commands. Not good for a musician.
Yet another PD problem. Isn't this fun!!!!
Thanks for your messages. They really made me laugh when I worked out your predicament with writing “the short version of Richard”!
It is good to hear about your experiences...really good to know I am not the only one.
My main problem is my mouth, my embrasure. It works OK for a few bars, then suddenly without warning, goes to custard. Anything fast & repetitive or lovely full long notes seem to be the hardest. Our conductor has been really understanding about it, he even said he hadn’t heard me make any terrible sounds (hmmmm, I think he must have!). Luckily, my most affected hand is my left hand, which just holds the horn. I love to play Jesus Christ Superstar too – the horn section has a brilliant part in that. We play it as the finale at the Carols by Candlelight at Christmas time. Fireworks go off, and we all get so enthused that our ears are ringing at the end!
What is it like, playing the mandolin? I think they sound fantastic!
You’re right, it is a difficult bit of life to face losing, so I’m stubbornly persevering too, while I can.
Hello. Yes I am - I have started again in the last three months playing tenor horn. Hard work but great fun. I have had PD for about 5 years. I have to laugh at myself as there is too much tremolo most of the time so I have to support the instrument a lot with my right hand. A lot of emptying of water too. Early days yet but I am enjoying it very much.