LymeNet Flash: neurologist in MA?

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 » neurologist in MA?

UBBFriend: Email this page to someone!

Author

Topic: neurologist in MA?

bystander
LymeNet Contributor
Member # 11893

posted

Hi.
My partner has Lyme (9 years before diagnosis; 4 years of treatment). She's done oral abx; then IV; she's now back on orals. She has a lyme friendly doc and a lyme friendly neurologist, but things have been getting worse rather than better.

Anyone have any feedback (positive or negative) on lyme literate neurologists in Mass? Would especially like feedback on Dr. LR.

Thanks.

Posts: 204 | From ma | Registered: May 2007 | IP: Logged |

bettyg
Unregistered

posted

never heard of him; not on our list.

try this also!

People seeking doctors might be able to get help from their state online information and support group. Nearly 3,400 people belong to state groups. Some of the groups are small but more than 20 of them have 50 or more people and seven have over 100.

To find your state group, go to
http://health.groups.yahoo.com/group/statenamelyme

Type your state name and lyme as one word, like this -
http://health.groups.yahoo.com/group/newyorklyme

South Carolina is the only state that needs a hyphen between the statename
and lyme, e.g. http://health.groups.yahoo.com/group/southcarolina-lyme

The groups are moderated and you have to apply. Most don't allow doctor names, but once on the group, you can ask for doctors in a certain area and ask people to email you privately.
*******************************************

IP: Logged |

22dreams
LymeNet Contributor
Member # 17846

posted

Hi bystander,

Check your PMs. Hope it helps in some way.

Posts: 571 | From Massachusetts | Registered: Oct 2008 | 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/