LymeNet Flash: I need a new LLMD

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » I need a new LLMD

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Author

Topic: I need a new LLMD

Mamanwithlyme
Member
Member # 50021

posted

I am in need of a new MD That follows Dr B guidelines because when I stay on treatment and am followed regularly by a good LLMD and use antibiotic's and because of how I was ill with this dam disease for over 10 years before it was diagnosis

It got deep into my brain and no PO will touch it but put me on IV and I respond great and I have a life.

No it is not 100% 75%. Which is better than the no life I have had to live for the past 2 months with not being able to function.

I tested positive for all co- infections so if there might be anybody available to give me some advise please don't hesitate to send me a private-M and I will send you my number. Thank you so very much

(breaking up the post for easier reading for many here)

[ 03-18-2017, 02:48 AM: Message edited by: Robin123 ]

Posts: 39 | From Massachusetts | Registered: Mar 2017 | IP: Logged |

willbeatthis
LymeNet Contributor
Member # 31111

posted

Sorry to hear you are struggling so. You may want to post this in seeking a doctor. Take good care...

Posts: 859 | From Southeast | Registered: Mar 2011 | IP: Logged |

jory
LymeNet Contributor
Member # 50029

posted

Left you a pm Larry, I can talk with you tonight if you like.

Posts: 289 | From Montreal, Canada | Registered: Mar 2017 | IP: Logged |

Tincup
Honored Contributor (10K+ posts)
Member # 5829

posted

Larry, you were sent at least one list of doctors from me, please check thru your emails. And several other people sent you lists.

I also left you a reply here...

http://flash.lymenet.org/ubb/ultimatebb.php/topic/3/36997

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004 | IP: Logged |

sixgoofykids
Moderator
Member # 11141

posted

moving threat to seeking a doctor

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007 | IP: Logged |

hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

posted

I previously sent you the name of a good LLMD in MA. Please check your PMs. I don't know of any who take Medicare/Medicaid in MA.

Check the online state Lyme groups at:
https://groups.yahoo.com/neo/groups/MassachusettsLyme/info

Maybe they can help. They would know better about MA.

Some more resources for you (including Support Groups info):
http://whatislyme.com/lyme-and-massachusetts/

http://www.lymenet.org/SupportGroups/UnitedStates/Massachusetts/

Here is a link found on Lymenet for "Financial Help and Other Information":

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=023463;p=0

The Lyme Disease United Coalition has good information for financial resources on their website:

http://www.lduc.org/lyme-disease-resources

Scroll down for financial help, etc., available from several sources.

The Lyme Test Access Program (Lyme-TAP) is a nationwide patient assistance program to provide assistance for initial Lyme-related lab tests to patients who demonstrate true financial need. I think coverage is up to 75%.
View on www.lymetap.com

"Help For You" link here...

https://sites.google.com/site/marylandlyme/help-for-you

Posts: 8983 | From Illinois | Registered: May 2006 | IP: Logged |

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