LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




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.

LymeNet Flash Discussion
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 Post New Topic  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Seeking a Doctor » looking for an LLMD in MD, VA area

 - UBBFriend: Email this page to someone!    
Author Topic: looking for an LLMD in MD, VA area
Peggy in Maryland
LymeNet Contributor
Member # 10480

Icon 1 posted      Profile for Peggy in Maryland     Send New Private Message       Edit/Delete Post   Reply With Quote 
I spent the day on the phone trying to find someone. All I found was waiting lists clear into the summer, and "we're not taking any new patients right now." Help, please?

Thanks.

Peggy

Posts: 143 | From Maryland | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
northstar
Frequent Contributor (1K+ posts)
Member # 7911

Icon 1 posted      Profile for northstar     Send New Private Message       Edit/Delete Post   Reply With Quote 
1. Could you get on their waiting list ? And call once in a while for a cancellation check?

Also, if you are within driving distance to Pa., there are some in Pgh, and the Phillie area.

Unfortunately, there is always a wait time, and it is at a time where you can least afford to wait. I had to wait 3 months, and I was in bad shape by the time I got in.

2. I have not read your previous postings, but could your primary help in the interim?

3. Herbal Route: do a search for Buhner here, get his book, and consider that route. It is helping many who could not do the abx, or chose not to. This may tide you over until you get to a llmd.

Northstar

Posts: 1331 | From hither and yonder | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
I SENT YOU A PM.

also, go to left-hand side, support groups for your state, click on closest one to you.

if leader has shown weather to call or email them, do as they instructed; they know who is good, etc [Wink]

IP: Logged | Report this post to a Moderator
Peggy in Maryland
LymeNet Contributor
Member # 10480

Icon 1 posted      Profile for Peggy in Maryland     Send New Private Message       Edit/Delete Post   Reply With Quote 
Northstar--I put my name on 2 waiting lists. Philly is 3 hours away, but I'll go that far if I have to. Too sick to drive--my husband has become chauffeur for the past few months.

My primary has been working with me since October. I've done orals, IV for a month, now weekly bicillin injections. Nervous system problems are improving, but I now have GI problems and suspect co-infections. He doesn't seem to know how to deal with that. I'm losing weight and the list of things I can eat is shrinking rapidly.

I have all the Buhner herbs but have not been able to tolerate the protocol. I hope I will after things calm down enough.

Betty G--thanks for the info. I've spent the week on the phone with support group people, but have so far been unable to find a doctor who can see me soon. I've printed your PM and will begin calling those names today.

Thanks again for everything.

Peggy

Posts: 143 | From Maryland | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
valymemom
Frequent Contributor (1K+ posts)
Member # 7076

Icon 1 posted      Profile for valymemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Peggy

I know someone you can see within the month (probably) I will send you a PM.

Posts: 1240 | From Centreville,VA | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
YorktownNL
Member
Member # 7657

Icon 1 posted      Profile for YorktownNL     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Peggy

I sent you a PM. But then noticed you GI comments. If your GI problems started with the abx make sure you consider yeast.

Take a lot of acidophillus and consider a prescription antifungal like nizoral.

Whenever my belly acts up, its because I messed up my yeast control meds.

I had GI problems way back before the lyme meltdown fixed themselves when I eliminated sugar...low carb atkins style for about a year. Now I still keep my carbs low and the problems didn't return.

Mike

Posts: 87 | From Yorktown VA USA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
Peggy in Maryland
LymeNet Contributor
Member # 10480

Icon 1 posted      Profile for Peggy in Maryland     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Mike,

I just replied to your PM then noticed you had sent the info about the yeast. I've been on probiotics since before I started abx. I take Kirkman's PB Gold twice a day and Culturelle once a day. Both of them are expensive. I just added one more after reading your post, but I have to go slowly or I'll blow up like a balloon. I'll try increasing by one a day.

I've been on a prescription antifungal since day one. First diflucan, then nystatin till today-- I eliminated it to try to narrow the field of what could be causing the GI problems.

I haven't eaten sugar for years, and have a very clean, high-quality diet. To avoid yeast, I also eliminated fruit once I started the abx. I don't eat much in the way of carbs, except vegetables. Now I don't seem able to tolerate grains at all. So I'm really feeling the need for help--can't eat much at all now, and losing weight fast. And the GI problems did start with the abx.

Peggy

Posts: 143 | From Maryland | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 5 posted            Edit/Delete Post   Reply With Quote 
peggy, have you been tested for food allergies?

i never had until last 4-06. MERIDIAN LABS did testing on 95+ foods; cost was $95.

guess what? i'm allergic to following:

GLUTEN -- wheat and rye items

CASEIN -- cow's milk, cheeses, egg WHITES, and garlic

they really upset my gi system; so that is MAY be happening to you also .... gluten!


NOTE: hospitals can now do a CHEEK TEST reasonably to test for gluten sensitivities! a local woman here w/2 celiac sons got our hospital to do this just late last year! [Big Grin]

IP: Logged | Report this post to a Moderator
northstar
Frequent Contributor (1K+ posts)
Member # 7911

Icon 1 posted      Profile for northstar     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sorry you are having trouble. You are lucky though that your primary is doing as much as possible.

Some other alternatives to the GI problem are

a. bartonella, as has been mentioned here many times. The test is even less accurate than lyme, from what I read. I have heard it mentioned as affecting mucosa.

b. malapsorption: this is a syndrome, with causes such as fungus (candida), parasites, other bacteria (including bartonella), and reduced enzyme production by the body.

Allopathic doctors scoff and take notes if you mention it.
So, the problem has to do with nutrient absorption.

So, I have read here that people have tried these (based on memory so I assure you there are more)

anti fungals,
check body pH,
work with parasite cleanses,
take enzymes, boost supplements (amino acids , minerals, vits, omegas, etc.),
or attempt metal detox (which are tied up with the candida),
adding nutrient dense foods, and even fatty foods such as nut butters, avocadoes, butter, bananas sparingly, to pack in some extra calories.

There has been some discussion of muscle wasting here, too. Maybe there is something of help if you do a search.

Northstar

Posts: 1331 | From hither and yonder | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
Peggy in Maryland
LymeNet Contributor
Member # 10480

Icon 1 posted      Profile for Peggy in Maryland     Send New Private Message       Edit/Delete Post   Reply With Quote 
Betty G--I was tested for food allergies about 5 years ago, and the only things I was allergic to was stuff I never ate anyway. And I'm eating so little now (vegetable broth, for example) that I doubt that's the problem. But it's worth checking, so I'll ask whatever doctor I decide to go to. I don't eat gluten or dairy or eggs anymore.

Northstar--Yeah, those allopaths are good at scoffing, huh? I was on antifungals till today, but now have eliminated all prescription drugs (except for the bicillin shot I got yesterday) in an attempt to narrow the field of what's causing the problem.

I take enzymes with every meal, and more supplements than I can count (Burrascano's guidelines). I'm taking lots of chlorella for detoxing, and have been for awhile.

The only nutrient dense food I can handle right now is a Metagenics protein bar. That's supplying me with most of the calories I consume. It works for me because it seems to be not so much a question of what I eat, but how much. The less the better--my stomach just won't handle more than a minuscule amount. So the protein bar gives the most nutrition with the least bulk. Frequently I can eat only half of one. Don't know what I'd do without it.

Peggy

Posts: 143 | From Maryland | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.