LymeNet Flash: night sweats

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » night sweats

UBBFriend: Email this page to someone!

Author

Topic: night sweats

adamm
Unregistered

posted

Do these start out mild and progressively get worse?

IP: Logged |

Sojourner
LymeNet Contributor
Member # 9424

posted

I think like everything else with tick borne infections symptoms vary wildly.

In my husband's case, he had a period of night sweats before dx that would come and go in frequency and severity. We wrote them off to work/life stress. They stopped all together before he entered a period of being really sick---they started up again when he was well into treatment and have been both heavy, light and non-existent since then.

The only correlation we have been able to peg is that when he is not doing so well (herxing?) he tends to sweat more at night. When he takes a break from meds they tend to lighten up.

Sorry---I am not much help--and at least I know it [Razz]

Any luck with a llmd?

Posts: 554 | From Naples, Italy | Registered: Jun 2006 | IP: Logged |

cmoc
Member
Member # 5135

posted

I have been sweating non stop for 2 months since on the antibiotics, have no idea if this is normal or not, yet, after 2 months, today, when going through a bad phase of dizziness, I have been cold.

Chris

Posts: 22 | From England | Registered: Jan 2004 | IP: Logged |

chamade
LymeNet Contributor
Member # 11472

posted

I have had these happen randomly for years before my diagnosis. Never got too much concerned and wrote them off to stress etc.
The last time I had it was 5 months ago, around the time my tingling/burning/shotting pains started.

--------------------
Why me? Well, why not me???

Posts: 411 | From San Francisco, CA | Registered: Mar 2007 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/