LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




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.

LymeNet Flash Discussion
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 Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » hormones and lessening of lyme symptoms??

 - UBBFriend: Email this page to someone!    
Author Topic: hormones and lessening of lyme symptoms??
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
this is absolutely crazy or at least i think it is...

my obgyn put me back on cenestin pills and premarin vaginal cream..

the sweating was driving me crazy and he said this would help...

the sweating has really gone down, the joint pain is not as bad, some of the twitching is reduced....

so why would hormone pills reduce these symptoms? i guess i'm trying to decide what's lyme and what's not...

still, hope springs eternal...

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
TheTruth
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Are you in menopause? Joint pain is very common in menopause. Maybe your joint pain was never from lyme disease at all. Or, at the very least, the pain was multifactorial. By taking exogenous hormones to treat the symptoms of menpause, you improved your symptoms. Therefore, it would seem logical to me that at least a portion of your symptoms are related to hormonal dysregulation.
IP: Logged | Report this post to a Moderator
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
well i had a hysterectomy at about 45. the really heavy sweating and all started about two or three years ago and i would have been about 55 at that time.....

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
TheTruth
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
A hysterectomy (assuming it was a TAH/BSO) is the exact defintion of "surgical menopause". In medical menopause women's ovaries shut down...in surgical menopause women's ovaries are removed. The end result is the same.
IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sex hormones will usually give you some kind of charge. The only danger is in potentially masking lyme symptoms, which I guess isn't a bad thing...

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
northstar
Frequent Contributor (1K+ posts)
Member # 7911

Icon 1 posted      Profile for northstar     Send New Private Message       Edit/Delete Post   Reply With Quote 
I ran across this article on hormones and MS:


http://www.msassociation.org/publications/summer08/cover.story.asp

quote:
Sex hormones: Estriol is an estrogen-like hormone that may have both neuroprotective and anti-inflammatory properties.

A small pilot study with 10 non-pregnant women showed a significant reduction in inflammatory lesions as well as cognitive improvement.

Based on these results, seven medical centers in the United States are conducting a two-year trial, enrolling 130 women with RRMS to receive daily Copaxone injections along with a daily estriol pill or a placebo.

Additionally, a recent report of four women, whose MS symptoms remitted during infertility therapy, adds weight to the concept that sex hormones may be a viable anti-inflammatory therapy.


Posts: 1331 | From hither and yonder | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I know testosterone works as an anti-inflammatory of sorts. It also helps general sense of well-being so I would imagine estrogen would do the same for women.

I've read studies though that suggest T may actually help lyme spread or something along those lines. I'll have to get the citation.

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
hurtingramma
LymeNet Contributor
Member # 7770

Icon 1 posted      Profile for hurtingramma     Send New Private Message       Edit/Delete Post   Reply With Quote 
I will be waiting for Lymeorsomething's next post. My OB/GYN recently suggested Testosterone for me. When I asked my LLMD about it, he made the remark that it does mask lyme symptoms and that I would feel better, and he had no objection, but suggested I get to the root of the "lack of libido" instead.(read romance needed) He didn't say anything about it spreading lyme faster.

--------------------
"Few of us can do great things, but all of us can do small things with great love". Mother Theresa

http://www.facebook.com/profile.php?id=1629665573&ref=name

Posts: 938 | From Northeast Kingdom Vermont | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
gemofnj
Frequent Contributor (1K+ posts)
Member # 15551

Icon 1 posted      Profile for gemofnj     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am also interested.

I was reading that Intrinsa, which is testosterone, is available in the UK, but only recommended for women who have had a complete hysterectomy.

I'm 54 and still not in menopause!! At least if I am, I have very few symptoms and low libido is one of them (besides the lyme trauma).

What are the choices out there for those that still have all their parts?

Maybe I should ask my gyno specialist? He probably wont agree, since I am on birth control at the moment to prevent an ovarian cyst problem.

[Frown]

Posts: 1127 | From atlantic city, nj | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'll try to find those articles tomorrow. I think that the little bit of T that women use would not be immunosuppressive.

The studies I've seen dealt with males and/or male animals with higher levels of T.

However, there are studies that suggest postmenopausal women are more susceptible to reinfection/relapse with lyme. Let me find the citation.....

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.