Daisy
Senior Member (Voting Rights)
I've been heart rate monitoring seriously for about 6 months now and found it incredibly useful. Initially it felt really restrictive because I was continually going over my AT. Now I feel lost without it.
I use a Mio Alpha 2. I chose this because it doesn't need a chest strap has reasonably big display and good battery life. It can be set to beep or flash when I go over my AT.
The last month or so I have also been measuring my heart rate variability first thing in the morning and that is also useful.
The main thing I have found is that keeping recordings over a period of time is most useful because you can see patterns of how activity physical cognitive emotional effects heart rate and heart rate variability.
I've also modified the way I do things quite considerably as a result of monitoring my heart rate. I'd say that as result I feel a bit more in control and my symptoms are a little more stable.
The way I look at it is that it has taken me many many years to get into the position I am now. I have been slowly deteriorating with occasional sharp deteriorations. So I expect progress to be slow if I'm going to start getting out of this hole to any degree.
There is a Facebook group pacing with a heart rate monitor specifically for people with ME and I find that very useful too.
I use a Mio Alpha 2. I chose this because it doesn't need a chest strap has reasonably big display and good battery life. It can be set to beep or flash when I go over my AT.
The last month or so I have also been measuring my heart rate variability first thing in the morning and that is also useful.
The main thing I have found is that keeping recordings over a period of time is most useful because you can see patterns of how activity physical cognitive emotional effects heart rate and heart rate variability.
I've also modified the way I do things quite considerably as a result of monitoring my heart rate. I'd say that as result I feel a bit more in control and my symptoms are a little more stable.
The way I look at it is that it has taken me many many years to get into the position I am now. I have been slowly deteriorating with occasional sharp deteriorations. So I expect progress to be slow if I'm going to start getting out of this hole to any degree.
There is a Facebook group pacing with a heart rate monitor specifically for people with ME and I find that very useful too.