Chronic fatigue
Posted , 21 users are following.
I had a massive PE in February, I'm a 66 year old female who was reasonably fit, but now I'm so tired all the time ! Will this go and does anyone else have this problem? Kind regards Linda
2 likes, 46 replies
Allexie Cocochanel2910
Posted
I had a large saddle embolism in Jan 2015 and am a similar age to yourself. I found recovery to be a very slow process....Now, nearly 18 months on and I'm pretty much back to normal but still get out of breath sometimes and get little niggly chest pains. Also I find all my energy drains away by mid afternoon sometimes. We all seem to recover at a different rate. Tiredness after 3 months doesn't sound too abnormal to me.....my pulmonary specialist said to expect 6 months to full revovery but my GP said it could be more like 18 months and I think he was right!!
Best wishes
Alex x
Cocochanel2910 Allexie
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Allexie Cocochanel2910
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Lazeedaze Cocochanel2910
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I do try to ignore it as much as poss. BW
wendy75 Cocochanel2910
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Cocochanel2910 wendy75
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scribbles65120 wendy75
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Hi Wendy, my case seems similar to yours. Also , I've had a revision hip opp a year ago and waiting for another on my right hip. Docs say this could be cause of clotting. I'm awaiting tests as the PE was only 4 weeks ago. I'm in sever pain with arteritis and taking a codine based pain killer twice daily. Now my doc says there is an antienflamatory that can be taken while on Warferan called Nabumentone. Has anyone tried it? Is it safe with Warferan?
I'm very tired all the time but can't tell if its from the medication or the PE as I still have multible clots on my lungs and my legs are barly getting my around even on crutches.
Many thanks in advance.
teristalking wendy75
Posted
THANKS SO MUCH FOR THIS INFO....had no idea there was pulmonary rehab because even simple walking is difficult-not pain-wise but tired-wise. i am not the best exercize person to begin with, but following my saddle pulmonary embolisms i realized changes must be made immediately. i am 66 a young 66 who was always on the go but about a year before i got mine 12/16/2016 i just felt something wasn't with me....i kept mentioning it to doctor who basically ignored me, but i know my body and it wasnt right. hardest thing is dealing with being slower and much more tired and feel like i cant keep up with people and it ages me and my thoughts, depressing me even more. it is a vicious cycle between pumped and ready to go and then after a short time feel frustrated and exhausted because im holding everyone up. no-one has ever said that to me, its just my thoughts.
christie2610 Cocochanel2910
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Cocochanel2910 christie2610
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terri02097 Cocochanel2910
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terri02097 christie2610
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christie2610 terri02097
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christie2610 terri02097
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carol350 Cocochanel2910
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they said I got it through having Lupus x
Wendy so interested in the group are you in the UK as I have never been told about this I am on waferin for the rest of my life I am 72 x