LymeNet Flash: Maui help

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 » Seeking a Doctor » Maui help

UBBFriend: Email this page to someone!

Author

Topic: Maui help

Seren
Junior Member
Member # 26447

posted

Moved to Maui and became very ill with my chronic lyme. Autonomic neuropathy causing me to pass out, arrythmia, unable to digest food, sweats and chills. Can't take antibiotics due to recent terrible bout of C Diff. Any help finding someone local to administer IV glutathione or IVIG would be so appreciated. Would hate to have to leave the island, not sure I'm well enough even to travel. Living alone as I'm a recent widow at age 49l

--------------------
serendipity

Posts: 2 | From Hawaii | Registered: Jun 2010 | IP: Logged |

Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

posted

I sent you a private message, click on the flashing envelope.

--------------------
I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.

Posts: 3897 | From New Hampshire | Registered: Jun 2008 | IP: Logged |

Remember to Smile
Unregistered

posted

Dear Serendip,
So sorry to hear of your recent loses -- your partner AND your health, plus the stress of moving! Holy smokes! [group hug]

I can't help with an LLMD in HI, but plz let us know if you're still looking after checking out Siciliano's PM.

We welcome you to create additional posts in our "Medical Questions" forum so you can stay on the road to recovery thru your challenging life transitions.

Or just post in "General" and vent or whine? The moon is nearly full an we've about read it all!

Are you familiar with ILADS's Dr Burrascano and his Treatment Guidelines? The 37-pg monograph (OCt 2008, 16th Ed)? Not sure if your other doctor was a LLMD. You don't need IV tx to get into long-term remission.
[woohoo]

Wishing you well,
Smile
p.s. - I believe Dr Joseph Burrascano is the one LLMD we name on LymeNet because he now teaches & trains LLMDs all over the world.

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/