Night sweats - coping strategies

[Rich316]

Hi All,

I have Relapsed CLL - ALC probably in 70’s + by now (bloods next week). I am now starting to get night sweats for the first time ever (I think) as I never seemed to suffer them during my first 7 year W&W and 4 year remission - even though my Lymphocyte count peaked at 270. I guess that this means I am even closer to treatment, but there are things I need to get sorted first (Heart meds and Cardio rehab after a MI heart attack in August). I will report these new symptoms to my Haematology team in a couple of weeks time, but are there any tips anybody can offer as a way of dealing with them? Or lessening the sweats?

Thanks

[lankisterguy Volunteer]

Hi Rich316,

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I quickly scanned through the "Related Posts" box on this page and found one interesting reply: healthunlocked.com/cllsuppo...

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another healthunlocked.com/cllsuppo...

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And this posting:

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Its been a popular subject- here is a link to the 452 times it was mentioned in the past.

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I hope you can find some ideas to explore.

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Len

[Rich316 in reply to lankisterguy]

Thank you Len, I will have a read through this evening. Very much obliged to you.