LymeNet Flash: Started Treatment, Finally

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 » Started Treatment, Finally

UBBFriend: Email this page to someone!

Author

Topic: Started Treatment, Finally

rhpress
Member
Member # 4679

posted

I finally (after 9 months of searching and Four years of pain) I was able to have my voice be heard in a real LLMD's office. Traveled from Georgia to NC to see Dr. J. thank you all for your support and encouragement. He put me on 750 mg of Zithro and 100 mg twice a day of minocin. It felt great to finally talk to someone who knew what Lyme was and was willing to do something to help me. I know I am in for a long road to recovery, but being able to take the first steps feels great.

Hillary

Posts: 51 | From Locust Grove, Ga US | Registered: Oct 2003 | IP: Logged |

smiles
LymeNet Contributor
Member # 5635

posted

Hillary,

Glad to hear your 'on the road to recovery'!

It must feel awesome to finally take action and have some 'sort of control' over what must have been a frustrating experience over the past four years.

Smiles

Posts: 160 | From MD, USA | Registered: May 2004 | IP: Logged |

Corgilla
LymeNet Contributor
Member # 4066

posted

Hi Hillary,

Isn't it great to have that justification? I'm not nuts! There is something REAL wrong with me. I'll tell you what, when I was first dx'd, I was so relieved.

Here's the other reason I'm posting this. During the Olympics down there, I had a hotel in North Carolina and made the commute every day for a week. ARGH! I only went to Conyers for the equestrian stuff though. Only made it to Atlanta once and stayed with a friend over night.

That was a very tough trip. I'd do it over again though.

Congratulations,

Corgilla

Posts: 694 | From PA | Registered: Jun 2003 | 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/