I am so, so, so tired! Advice for fatigue?
2 posters
Page 1 of 1
I am so, so, so tired! Advice for fatigue?
Hi folks,
I had a HM on June 15th and have been on disability since. Can't return to work yet but am trying really hard to build up my mental strength. Have just started volunteering at the local Veterans Hospital and at the public library BUT I am so bloody tired! After 1-2 hours of mental effort, I feel like I am in a fog, so while it is good to be getting out into the community, it is so draining! I would love to hear from others how they deal with fatigue. I am sleeping well but just not having nay mental stamina for more than an hour or two.
Thanks,
Tracy
I had a HM on June 15th and have been on disability since. Can't return to work yet but am trying really hard to build up my mental strength. Have just started volunteering at the local Veterans Hospital and at the public library BUT I am so bloody tired! After 1-2 hours of mental effort, I feel like I am in a fog, so while it is good to be getting out into the community, it is so draining! I would love to hear from others how they deal with fatigue. I am sleeping well but just not having nay mental stamina for more than an hour or two.
Thanks,
Tracy
TWORTHIN- Posts : 7
Join date : 2011-07-22
Re: I am so, so, so tired! Advice for fatigue?
Oh Tracy, fatigue is a way of your body to tell you to slow down, A HM attack takes times to get over, it is not like any other migraine type.
You WILL get there, but you need to pace yourself and maybe doing both is too much.
I was exactly the same, after a big HM I had to sleep every few hours. I would have a nap for 2 - 3 hrs during the day and still sleep 10 hrs at night. In the very beginning I was like you I fought it and would not give in, but I did learn in time that it did not work. You need to listen to your body and rest.
One doctor told me that pushing it- was when you did something for 1 min today - you do it for 2 mins tomorrow.
I know this will be frustrating to read, but I have been there and totally understand.
One thing I did find helpful on the old 'get your brain back plan' was the brain trainer on the DS. I only did it for 5 mins to start with but over a course of a year I got that up to an hour. I am not sure if you are like me, but if I over do it I get brain fog and numbness? When this starts I know it is time to stop and rest - this sounds easy - but it was a very hard lesson for me to learn - I was a completer finisher at work and hated to leave things half done................. my thinking has now changed.
And that is half the battle with HM. You have to change.
xxx
You WILL get there, but you need to pace yourself and maybe doing both is too much.
I was exactly the same, after a big HM I had to sleep every few hours. I would have a nap for 2 - 3 hrs during the day and still sleep 10 hrs at night. In the very beginning I was like you I fought it and would not give in, but I did learn in time that it did not work. You need to listen to your body and rest.
One doctor told me that pushing it- was when you did something for 1 min today - you do it for 2 mins tomorrow.
I know this will be frustrating to read, but I have been there and totally understand.
One thing I did find helpful on the old 'get your brain back plan' was the brain trainer on the DS. I only did it for 5 mins to start with but over a course of a year I got that up to an hour. I am not sure if you are like me, but if I over do it I get brain fog and numbness? When this starts I know it is time to stop and rest - this sounds easy - but it was a very hard lesson for me to learn - I was a completer finisher at work and hated to leave things half done................. my thinking has now changed.
And that is half the battle with HM. You have to change.
xxx
Similar topics
» Chronic Fatigue? Vitamin B12 Injections Might Be the Answer
» Chronic Migraine, neck issues and visual issues? Any advice more than welcome!
» Advice needed regarding Botox
» Headache/Migraine in Fibromyalgia & Chronic Fatigue Syndrome
» Carers UK is a charity with some great advice on benefits
» Chronic Migraine, neck issues and visual issues? Any advice more than welcome!
» Advice needed regarding Botox
» Headache/Migraine in Fibromyalgia & Chronic Fatigue Syndrome
» Carers UK is a charity with some great advice on benefits
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum
Thu Mar 30, 2017 9:04 am by Sarah
» Facebook group - now set up
Fri Feb 24, 2017 7:43 am by Tee
» cluster headache
Wed Feb 15, 2017 3:51 pm by Heregailing
» Your view on migraines and social media
Fri Feb 10, 2017 4:17 am by Tee
» Fats and Chronic Pain/Headaches
Thu May 19, 2016 10:52 pm by Sarah
» National hospital - London
Sun Jan 10, 2016 3:18 pm by pīwakawaka
» Just saying Hello
Sun Jan 10, 2016 3:12 pm by pīwakawaka
» Botox for harmeplegic migraines
Thu Sep 24, 2015 10:59 pm by Robyn17
» Hello and thank you
Mon May 25, 2015 12:55 am by ajdesq