I did a search of the forums and couldn't find this topic being discussed anywhere. But I am curious if any of our members who have been diagnosed with PD and continue to swim might share any tips or advice with regards to training.
Two friends of mine here in the Pittsburgh area have recently been diagnosed, and both are determined to continue swimming despite slowing down. It seems to me that aquatic exercise could be a great way to exercise and perhaps even slow down the progression of the disease. Surely, there must be within the greater USMS ranks more than a handful of swimmers who are currently contending with this disease.
I told my one friend, who isn't a USMS member, that I would post an inquiry on his behalf here on the forums and share any results it might turn up.
Thanks in advance!
Parents
Former Member
Hi Jim,
thanks for posting this topic. My doc suspected PD in December 2017 and I started swimming later that month. I've been putting a mile in each night. I was formally diagnosed with PD in June 2018. In December, I joined a local USMS team and swam in my first meet in Feb. 2019. I swim 6 days a week, rain or shine. Unless I have an ear infection.
My MDS says the swimming is keeping my PD symptoms at bay and mixed with the L-dopa (synthetic dopamine) I take 4 times a day, I'm doing pretty well. He has prescribed daily exercise for me and I don't plan on stopping.
I've found that Swimming with PD leaves me feeling better than when I walked in. Also, when I miss a day, I have a hard time getting 6 hours of sleep - which is the most I can manage even on my best days. I am pretty stiff, but that's a reaction to PD and the constant exercise (I also walk about 3 miles a day). I generally try to get massages once every 10 days.
-S
Hi Jim,
thanks for posting this topic. My doc suspected PD in December 2017 and I started swimming later that month. I've been putting a mile in each night. I was formally diagnosed with PD in June 2018. In December, I joined a local USMS team and swam in my first meet in Feb. 2019. I swim 6 days a week, rain or shine. Unless I have an ear infection.
My MDS says the swimming is keeping my PD symptoms at bay and mixed with the L-dopa (synthetic dopamine) I take 4 times a day, I'm doing pretty well. He has prescribed daily exercise for me and I don't plan on stopping.
I've found that Swimming with PD leaves me feeling better than when I walked in. Also, when I miss a day, I have a hard time getting 6 hours of sleep - which is the most I can manage even on my best days. I am pretty stiff, but that's a reaction to PD and the constant exercise (I also walk about 3 miles a day). I generally try to get massages once every 10 days.
-S
