LymeNet Flash: NH Lyme Patients

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 » NH Lyme Patients

UBBFriend: Email this page to someone!

Author

Topic: NH Lyme Patients

tdtid
Frequent Contributor (1K+ posts)
Member # 10276

posted

When I first came to Lymenet, I was so disoriented and lost, but yet so many came to hold my hand through this process.

I still have a long way to go, but I just had my port removed a month ago and think I can go the rest of the way on orals.

Now that I am feeling better, I am getting actively involved in the advocating side. NH is trying to pass a law much like CT did so we can protect our doctors.

We need Lyme testimonies or warm bodies or both to make them realize it isn't just a few people being hit with this horrid disease.

Any help would be beneficial to start this ball rolling for all patients and the doctors that are running scared to treat us.

http://kettmann.com/LymeLetter/

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | Registered: Oct 2006 | IP: Logged |

purplemom
LymeNet Contributor
Member # 21064

posted

Cathy, I am from NH but feel that my testimony would not be worth much with CDC negative tests.
I do hope it goes through though.

Posts: 207 | From NH | Registered: Jul 2009 | IP: Logged |

MariaA
Frequent Contributor (1K+ posts)
Member # 9128

posted

WOW, I'm so happy to hear that you're doing so much better now. You've come so far in the past year!

--------------------
Symptom Free!!! Thank you all!!!!

Find me at Lymefriends, I post under the same name.
diet: http://lymefriends.ning.com/group/healthylowcarbrecipes
Homemade Probiotics thread
Herbal Links Thread

Posts: 2552 | From San Francisco | Registered: Apr 2006 | IP: Logged |

tdtid
Frequent Contributor (1K+ posts)
Member # 10276

posted

This is NOT about being CDC positive. It's to protect our doctor's in this state so they can treat clinically with long term antibiotics if they see fit.

Too many are running scared and we need all the help we can get.

MariaA, So good to see you again. Yes, it was a LONG bumpy road. I did have my port removed about a month ago after 16 months of IV. It was rough, but we all know how that goes.

Still a way to go, but compared to where I started, this is a huge jump.

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | 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/