LymeNet Flash: Best Advice Poll

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 » General Support » Best Advice Poll

UBBFriend: Email this page to someone!

Author

Topic: Best Advice Poll

LisaS
Frequent Contributor (1K+ posts)
Member # 10581

posted

Just wanted to hear some of the best advice you've gotten from a fellow lymenetter or llmd or anyone regarding lyme and coinfections that has really helped?

For me it was Johnlyme & Mike who got me hooked up with my llmd

And Lymetoo when she said

quote:

"As mentioned, if these positive blots are found by specialty labs, over 99% of those patients will respond to antibiotics.

Now I don't even fear whether it is the right diagnosis or not.

--------------------
https://www.facebook.com/profile.php?id=1660435643

Posts: 1078 | From Lake Geneva WI | Registered: Nov 2006 | IP: Logged |

AZURE WISH
Frequent Contributor (1K+ posts)
Member # 804

posted

hearing that it took others here on lymenet a signifigant amount of time to start feeling better with babs treatment has helped.

Also hearing others say that the babs herxes were worse for them than the lyme ones cuz i certaintly think that it has been true for me.

And of course knowing people got better after treating babs.

So my long rambly post is trying to say the best advice on lymenet has been -

hang in there. it will get better.

--------------------
multiple chemical sensitvity group:
http://www.lymefriends.com/group/multiplechemicalsensitivities

Group for artists. All media welcome:
http://www.lymefriends.com/group/creativecorner

http://groups.yahoo.com/group/Lyme_Artist

Posts: 3860 | From nj,usa | Registered: Mar 2001 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

I'm glad that helped you, Lisa!

I learned this from someone who used to post here many years ago....don't remember who it was:

"The only way out is through."

Boy, does THAT apply to Lyme treatment!! [Razz]

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96227 | From Texas | Registered: Feb 2001 | IP: Logged |

Geneal
Frequent Contributor (5K+ posts)
Member # 10375

posted

There are so many words that have become the staple of my existence.

Slow and steady wins the race. (Thanks Lymetoo [Smile]

)

Another favorite is that God hears all prayers.

Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006 | 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/