livinlyme
Frequent Contributor (1K+ posts)
Member # 3773
posted
have been seeing one in nY but they no longer accept medicare i know this is almost impossible to ask does anyone know of an LLMD who accepts medicare still in the state of PA preferably the north eastern area ? entire family dealing with this and it is too costly out of pocket to afford the treatment without insurance everyone we start to see ends up telling us 300 per visit and no more insurance ,, which to me sounds like since the gov has gotten involved in our health care they are given full license to kill us slowly because we are being prevented from seeking care by doctors we have been seeing for years and the ones we are forced to seek who accept insurance will not treat the main problem but only the systems - death
-------------------- "Hatred paralyzes life; love releases it. Hatred confuses life; love harmonizes it. Hatred darkens life; love illuminates it." Posts: 1389 | From who knows, who cares, but somewhere over the rainbow | Registered: Mar 2003
| IP: Logged |
You should call the LLMD's office to ask if the information is current.
Btw - please break up your post into 2-3 sentence paragraphs, as there are people on Lymenet who cannot read large blocks of text due to neurological problems from Lyme.
To do this, click the pencil/paper icon, make your changes, then click "Edit Post". Thanks.
Posts: 8981 | From Illinois | Registered: May 2006
| IP: Logged |
livinlyme
Frequent Contributor (1K+ posts)
Member # 3773
posted
ty but it no longer valid not n service as most are not any more
-------------------- "Hatred paralyzes life; love releases it. Hatred confuses life; love harmonizes it. Hatred darkens life; love illuminates it." Posts: 1389 | From who knows, who cares, but somewhere over the rainbow | Registered: Mar 2003
| IP: Logged |
posted
Perhaps he retired? I tried googling it, but got the same phone number I sent you.
We who voluntarily send out information and dedicate a considerable amount of time in doing so don't always have up-to-date info unless someone lets us know or if we do the research ourselves (which is very time consuming).
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,
NJ08534USA http://www.lymenet.org/