TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
Lately I have seen a number of posts where the person asks if it is worth the money to travel to see a top notch doctor.
People need to know what distinguishes the "men" from the "boys" when it comes to lyme treatment. Then, they will see that it is worth the money.
Also, this is something to think about for those who want to save the money and self treat along with the help of a willing doctor.
I am reposting here a response I wrote to someone almost a year ago. Here is their post and mine. The thread is also listed below.
The question was:
I'd like to know what these big wig LLMD's do that is different than the lesser knowns. Like, why do people travel across the country to go see someone well known, if there is someone closer who is an LLMD but not as well known
My old post:
Hambone, I believe there are a few things that make certain doctors, like Dr. H, more successful.
From what others have told me, Dr. H. leaves no stone unturned at the first appt. He seems to be very good at discovering the cause of why the lyme patient is still ill in spite of previous therapy.
He searches into things that the lesser doctors don't look into. For example, through his questioning, he can uncover if heavy metals may be an issue for the patient, or mold. Few lyme doctors go there. He asks about childhood exposure to chemicals and various types of factories or plants that were near the person growing up as a way of gauging whether metals are causing the problem. Then, he follows his suspicions with appropriate tests.
It is a real skill for a person to uncover what is preventing a patient from getting well. Dr. H. seems to have that skill based on reports others have given to me.
It takes a very broad knowledge of everything that can hold back a lyme patient to be able to discover the cause of prior treatment failures.
It takes a lot of experience with patients to figure out what is likely going on with a particular patient.
Then, a great doctor orders tests that other lesser doctors don't order. Again, the broader knowledge of the great doctor.
A top notch doctor also knows a lot more medications that can treat any particular illness. A lesser doc knows one or maybe two possible treatments. If the patient can't take a necessary med, the lesser doctor may often not know of any possible alternative. A top notch doc knows a number of alternatives.
A top notch doc will have more complex treatment plans. He/she knows what meds can be combined and what med does not have to be taken daily. So, that doc can devise treatment plans that attack more than one disease at a time. Saves the patient time in getting to healthy.
Other tricks that top notch doctors have are things like knowing that a certain medication must be ramped up slowly or side effects will likely force the patient to have to stop the therapy. Or, knowing to add in artimesinin later after babs treatment is underway for a while rather than right at the start because that way art is more effective. These are just 2 examples.
These kinds of things aren't published anywhere. This type of knowledge comes from experience and perhaps experimenting over years of treating lyme patients. That's how Burrascano came up with his successful treatment protocol.
A top notch doc knows the possible side effects of a med, even the ones that are not published. So, for example, a third rate lyme doc will not know that Mepron can cause depression in some people and, because of this lack of knowlege, will ignore the patient's report of making plans to commit suicide while on Mepron, never realizing that the Mepron must be stopped. They will tell the patient to see a psychiatrist instead.
Lesser docs won't realize that even steroid nasal sprays should not be used by a lyme patient.
Lesser lyme docs don't realize the importance of diet and exercise to recovery from this disease. So, their patients suffer. Lesser doctors don't believe supplements are important, so they don't prescribe them. Or, they have just a very rudimentary knowledge of supplements and herbs and how they can assist the lyme patient to alleviate various symptoms that are presented.
Lesser doctors don't know much about yeast or which probiotics are the best.
Lesser docs don't know how to boost a person's immune system so that the person is less likely to relapse.
Lesser docs don't even know how to test Mepron levels to ensure they are adequate.
It all comes down to more knowledge of a wide variety of related subjects, more experience that has given more knowledge, more skill at finding the cause of the person's problems, maybe better listening skills, and the ability to tailor treatment to the particular person's allergies and reactions.
I believe it takes at least 10 years of treating this disease to develop this kind of expertise.
I also think that a doc who actually had lyme himself is in a better position in many ways to treat this disease compared to a doc who never had it. Maybe it makes the doctor take the patient's reports more seriously, or gives him understanding about the anxiety this disease causes, or understanding of herxes and flares, etc. I don't know.
I have never heard of a doctor spending as much time as the patient needs at the first appt. But, this is what I have been told about Dr. H. by his patients. A 3 1/2 hour initial appointment! That is the kind of thing that makes one doctor outstanding while another is applying a cookie cutter approach to the same problem.
Just some of my thoughts based on hearing experiences from lyme patients for many, many years.
Hope this helps you guys understand the types of things that distinguish the top lyme docs. This illness is not simple to treat.
Many doctors treat it, but only a few know how to get rid of it for a person.
That said, still some cases of lyme are rather simple, and a local doctor may be successful with these cases. More complex cases, he will not be able to get the person to wellness. The most complex cases definitely require a top notch doctor if the person is ever to get well.
The key is for the patient to figure out whether or not his/her doctor knows enough to get them well. That takes a well educated patient.
You can't just sit back and wait for the magic to happen with this disease. If you do, it may never happen. So, learn all you can about lyme treatment and evaluate your doctor's skill and the complexity of your own case. Then, find a doctor who is able to do it for you. There is a learning curve. Most don't start out with the doc who is the best for them. Be willing to change docs, as scary as that can be at first.
As I get more and more patient reports, I see more and more skills that the best lyme doctors have. For example, knowing how to get a patient who cannot tolerate high doses of antibiotics to be able tolerate high doses.
All of these things can make the difference between getting rid of lyme and never getting rid of it in a particular person's case.
Hope this helps folks to decide to go to the very best lyme doctor they can afford.
posted
Very helpful. I'll add it to the thread in Seeking about why you need an LLMD.
I'll also add it to the Quick Links to Popular Topics.
Thanks!!
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96237 | From Texas | Registered: Feb 2001
| IP: Logged |
Razzle
Frequent Contributor (1K+ posts)
Member # 30398
posted
Do any of the "top notch" LLMD's take insurance?
-------------------- -Razzle Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs. Posts: 4167 | From WA | Registered: Feb 2011
| IP: Logged |
fflutterby
Frequent Contributor (1K+ posts)
Member # 28081
posted
Very well said, bravo. I am one of the ones who thought my "not so top notch" Doc could do it for me. 18 months later and I am in awe by my first appointment with my "top notch" Doc.
The good ones may not but if you have out of network benefits, you may get some of it covered.
-------------------- "The simple things can get you through the hardest times." Posts: 628 | From Connecticut | Registered: Sep 2010
| IP: Logged |
nefferdun
Frequent Contributor (1K+ posts)
Member # 20157
posted
If ONLY I had seen THAT doctor!! I thought I was seeing a great doctor. I traveled 2000 miles each way. He was a "guru", well respected in the lyme literate community, had even come up with one of the universal test used by all LLMDs. Isn't that "Top Notch"? He was expensive; $650 an hour and we did not go over that hour. He was very careful about that!
Despite the brilliant reputation, he gave me the no brainer treatment; mepron and zithro. That's it. Period. He took me off all supplements saying they were a waste of time. He refused to talk about long term treatment or the other infections he was not addressing.
He did a lot of tests to rule out auto immune disease such as RA, even though I told him I did not have joint pain. After seeing my blood mercury was normal, he told me heavy metals were not a problem. He never mentioned any genetic mutations that might affect my ability to detox or weaken my immune system.
He refused to treat any infection that did not have a positive test result. He said I did not have bartonella even though I had responded to Levaquin. He said even though IGENEX did not test for Bart quintana, I could not have it because the test for bart henselae would cover it.
He basically shrugged his shoulders when I said I had trouble tolerating drugs. He gave me aseroquel, a drug for mental illness, to address my insomnia. It was months before I realized it was putting me to sleep but I could not wake up.
At the three month consultation, her refused to alter treatment or discuss any future options. More of the same.
I went back to treating myself and THAT is when I made progress! So that is another reason why we do not always go with the top notch doctor. It isn't always because we are cheap or broke and want/need to save money. It is because we can't find him!
-------------------- old joke: idiopathic means the patient is pathological and the the doctor is an idiot Posts: 4676 | From western Montana | Registered: Apr 2009
| IP: Logged |
posted
That's also why Lyme is the disease for the wealthy.
If you can afford the best Dr's and best treatment protocols, you have a better chance at getting your life back.
If Lyme has destroyed your livelihood, when you were just starting out in life and don't yet have a nest egg, and you don't come from a wealthy family...what then?
In this case, I scrimp, save, borrow, sell everything possible and get my family to a great ILADS educated LLMD who is knowledgeable and thorough, even if his or her name isn't Dr K, Dr J or Dr H.
(I thought I had a great Lyme Dr at the time, but after suffering the consequences of having an inexperienced, although well-intentioned, LLMD, I know I was wrong and naive when I posted this...I have since changed my tune and my LLMD)
-------------------- aperture Posts: 551 | From Louisville, KY | Registered: Nov 2011
| IP: Logged |
desertwind
Frequent Contributor (1K+ posts)
Member # 25256
posted
Great post. I agree with aperture.I am not wealthy and my credit cards keep going up and up. But I cannot imagine a life of tick borne infections.
I spent 7 years back and forth between the not so top notch LLMD and could only achieve remission.
And just kept getting worse with each flare-up.
NOT ONE LLMD I saw ever tested me for Q-Fever. Dr. H. did and it came up high positive.
I am only 3 weeks into treatment with him but am feeling, at times, better then I have in years.
Why? Becasue he is treating agressively and smart and taking all other health factors into consideration. I am on 4 different meds and tons of supp.'s.
With my back against the wall I had no choice - it was the top - notch guy or continued treatment failures.
Way too soon to tell if the tx. will be effective long term but I feel that I am in the best hands possible.
Posts: 1671 | From Tick Infested New Jersey | Registered: Apr 2010
| IP: Logged |
lymeboy
Unregistered
posted
Part of the reason the attitude towards LLMD's can be negative is that many of them are INCREDIBLY overpriced, and just not getting anyone well. After being "robbed" by one or two mediocre/ bad/ charlatan LLMD's, one begins to think the whole thing is a racket and lose faith in healthcare altogether (for good reason).
There are a few good Lyme docs out there. Literally. This is why people travel far and wide to see certain docs. If you deal with this disease long enough, you learn this. I wish it were not the case, but sadly it is.
As a poor person, I have spent plenty of time cursing the high prices. Especially when I was paying for care that wasn't going anywhere. But I finally got to someone that is helping me, and I am dealing with the money issue. For the most part, it is that initial 2 visits that wipe you out.
In a perfect world, Burrascano and Dr. H. would be sitting on government boards, and ALL docs would know what Dr. H. knows. But.... well you know the rest.
IP: Logged |
posted
Wow desertwind. I had never even heard of Q-fever before.
That is wonderful that you are making obvious progress.
-------------------- aperture Posts: 551 | From Louisville, KY | Registered: Nov 2011
| IP: Logged |
seekhelp
Frequent Contributor (5K+ posts)
Member # 15067
posted
I feel willingness to spend TIME with a patient is key. Very few do this. They are all thinking about where they need to be next. I understand it's just business, but This is getting worse and worse in medicine. It's getting old fast.
Also, way too much guessing and not enough fact-finding.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
| IP: Logged |
posted
Thank you for this post. Great info. Food for thought.
Posts: 873 | From WA | Registered: Dec 2005
| IP: Logged |
Razzle
Frequent Contributor (1K+ posts)
Member # 30398
posted
Ok so apparently some LLMD's DO take insurance and are decent doctors. Can someone PM me with these doctors contact info? I cannot afford to not have insurance coverage of doctor visits...I don't even have enough money for food, never mind treatment, but my DH makes too much money to qualify for any kind of assistance (we don't have kids, which rules us out for just about everything assistance-wise where we live).
-------------------- -Razzle Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs. Posts: 4167 | From WA | Registered: Feb 2011
| IP: Logged |
posted
Some LLMDS do take insurance. Thank goodness for them. We need more, so people can access them.
Posts: 13134 | From San Francisco | Registered: May 2006
| IP: Logged |
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149
posted
TF, I know you're cured, but thank you so much for coming back to help all of us (you're such a kind soul). Even if some of us can't afford a top notch doc, you still provide great advice that we all can use (love your posts). You rock, girlfriend!
-------------------- --Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together). Posts: 5418 | From earth | Registered: Mar 2011
| IP: Logged |
posted
I find it odd that two of the "top notch" doctors said that using Nasonex is perfectly fine.
-------------------- Faithful
Just sharing my experience, I am not a doctor. Posts: 2682 | From Colorado | Registered: Oct 2009
| IP: Logged |
TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
I agree with you.
I have heard many regular doctors tell patients that these sprays are fine to use the rest of their lives. I am really surprised to hear doctors say this and also say that THEY themselves are using these sprays daily.
I got rid of lyme 7 years ago, and when I used Nasonex daily for 3 months last year as per my primary care doc, I began catching every illness that came down the pike. I didn't know it was a steroid at the time.
I concluded that it weakened my immune system. I read the websites on both of the steroid sprays (Flonase and Nasonex) and it clearly said it does this.
So, I don't think it is fine for anybody with a compromised immune system (every lyme and babs patient) to use it regularly.
My reading of Burrascano is that he says not to use steroids in any form unless absolutely necessary and you are already on high-dose antibiotics.
I think that it would be foolish to say that steroid nasal sprays are NOT included in Burrascano's warning regarding steroids.
Posts: 9931 | From Maryland | Registered: Dec 2007
| IP: Logged |
posted
I agree with nefferdun 100%. When I did see a 'top-notch' doctor it was no different than what others were offering. In fact when I couldn't tolerate the 'normal' doses (my symptoms would go beserk to the point of going to the ER) they were initially great then lost interest in me.
"They don't leave a stone unturned". Not true at all. I asked for many tests I had heard about here and not once did they give any importance to them. Don't believe in anti-virals, parasite treatment, etc. and push their own ridiculous supplements and I was absolutely no better, only poorer.
They may be good for those with insurance and a very large pocketbook and the more 'recently' affected, ie: not severely ill for very long. I realize like any other doctors they're always watching their back. But their dedication to those who CAN tolerate meds and make headway quickly is amazing.
I know of many, many people who have been helped by them. just not me.
Posts: 195 | From - | Registered: Sep 2011
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Trubee, as for the laundry statement, I hope you told the MD in the office of the PA's error.
Not all who say that are LLMDs are actually top notch.
faithful777, you are correct: it is NOT okay to use any steroid nasal sprays. It's "Lyme 101" to know that - and exceptions.
The first step to finding a top notch doctor (but there are steps after that, too): -----------
(What ILADS is) . . . WHY you need an ILADS-educated, Lyme Literate Doctor - starting with assessment / evaluation. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- A few posts above discuss steroids. So many of us came too late to the "rule" that they are not to be used for lyme & co.
Here are the articles that explain why (and what is needed for the rare exception to that "rule"): -------------
On 2/23/12 (when I posted my original comment on this thread) I thought I was being treated by a great LLMD. He/she was knowledgeable, well-intentioned and thorough. He/she was "trained by the best". I thought, since I cannot afford to go to NY or WA, at least I am getting the same care that those patients would receive....wrong.
It hurts to have to give such an honest review of the regular LLMD's out there...but I feel that I have to.
Lyme took everything from me, my health, my ability to work, my husband's health and tried to take my baby's health. I was and am broke beyond belief.
My family has been seeing an LLMD since Nov. My husband and son were making great progress, but I kept getting sicker and sicker. My husband and I were on the same exact protocol, even though our bodies/symptoms/genes are very different.
My LLMD finally thought I had a biotoxin illness so he/she started Cholestyramine while waiting on Dr S' DVD's to arrive. I had a horrific reaction after 5 days...was stuck in a cytokine storm. At that point I was told by the LLMD "I wonder if Cholestyramine pulls toxins out of the whole body and not just the gastrointestinal tract?"
At that point, I was floored. I realized that I was a guinea pig. The knowledge that I was experiencing my Dr's learning curve was scary.
My husband was so terrified that he called the best of the best and begged for him/her to see me. They scheduled the appt, but where on Earth would we find that kind of $?
My family is broke. My relatives on my side of the family are paycheck to paycheck folks. My husband's family had reached their limit and did not want to even humor the idea of my going to NY for some Lyme Dr.
However, when it came down to life and death, my 80 year old dad who lives in a nursing home emptied his bank account..a whole $400 to help. My 72 year old mom who still has to work FT to make ends meet did the same.
The absolute worst point in my life came when my husband and I pawned our wedding rings on the way to the airport. Nothing else matters if you don't have your health.
We had a one way plane ticket and rode Greyhound for 25 hours back (both of us sick with Lyme, me carrying my bag full of supplements and heavy metal test kit the whole way).
However, it was the best decision I ever made. Of course I am not well...far from it. But I realized that my former LLMD could never have gotten me well. I had too many complicating factors.
I also learned that "being trained by" Dr.* only means they had a 2 week preceptorship...not that they had an internship or trained for months under the guidance of Dr.*
I now only have to worry about following the Dr's orders. I know I am being cared for by the best of the best. If he/she cannot get me well, no one can. I can finally exhale and have some breathing room. I don't have to spend my days researching, wondering whether I'm on the right protocol or not. I just take the medication and supplements that were prescribed and save my little bit of energy for my kids.
I know this entire post is TMI, but I wanted to let everyone know that Lyme is not a disease where only the rich can have a shot at a cure.
TF was spot on with this thread. I only wish I hadn't been so quick to dismiss it.
(BTW, all of this just happened 3 weeks ago, and now my former LLMD now posts on his/her website that he/she treats Biotoxin illness...that worries me)
-------------------- aperture Posts: 551 | From Louisville, KY | Registered: Nov 2011
| IP: Logged |
Kudzuslipper
Frequent Contributor (1K+ posts)
Member # 31915
posted
This is so great!!! thanks for the info TF.
Posts: 1728 | From USA | Registered: May 2011
| IP: Logged |
poppy
Frequent Contributor (1K+ posts)
Member # 5355
posted
Although there is a tier of lyme docs, and some are more experienced than others, it worries me that this kind of thread makes people think if they just get the right doctor, they will be cured. Chronic lyme exists, in spite of the best doctoring available.
One doctor explained to me that he could treat early and middle difficulty patients, but that third tier docs did the worst, longest running, complicated cases.
And it would help if people remembered these doctors are just mortals, like the rest of us. They get tired, burnt out, find some patients more likable than others, etc, etc.
Posts: 2888 | From USA | Registered: Mar 2004
| IP: Logged |
posted
Funny, Dr. J said topical steroids are okay.
-------------------- Faithful
Just sharing my experience, I am not a doctor. Posts: 2682 | From Colorado | Registered: Oct 2009
| IP: Logged |
canefan17
Frequent Contributor (5K+ posts)
Member # 22149
posted
I like the ones who follow a Burrascano type approach.
Combo abxs, long-term if necessary, useful supplements, anaerobic exercise, etc.
Posts: 5394 | From Houston, Tx | Registered: Aug 2009
| IP: Logged |
annxyzz
Frequent Contributor (1K+ posts)
Member # 20404
posted
I have read too many articles by LLMDs about high relapse rates for patients who are not DXed early to think that spending your last dollar is a good idea . Most of them concur that the relapse rate is extremely high and there is no cure in sight.
The people I know with lyme who have seen LLMds have not improved significantly after spending a lot of money . I am not being negative - just stating fact . I do not think years of drugs and drugs will cure me personally . I did 3 years of ABX and became free of nerve and muscle pain , but was still very ill. I could not see risking superinfection , ABX resistance , or kidney and liver issues with taking drugs forever and then relapsing after stopping the drugs . It is hard to face the fact that there is no cure for many of us with longterm lyme even with the "best " LLMD who will gladly take our money knowing he can not make a huge difference .
I am forced to self treat because of lack of insurance, but the truth is I am probably no worse off than if I had a LLMD . In my opinion , there are MANY MANY potent plant medicines that are less likely to destroy my kidneys or liver and that help keep the pathogen load down . I have read a zillion posts here over 8 years about people taking mepron and a host of other drugs for years and never improve , or who improve only to relapse .
Everything with this disease (!) is experimental , and it is a save yourself condition. The top rated docs can help those diagnosed early , but they all admit that the long term patients all relapse when drugs are removed . Does not make me want to fry my liver on expensive drugs with no tangible results except poverty .
-------------------- annxyzz Posts: 1178 | From East Texas | Registered: May 2009
| IP: Logged |
TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
I went undiagnosed for at least 10 years before a doctor figured out that I had lyme disease.
Still, I recovered. And, I know others who had the fibro diagnosis for over 30 years and it was lyme. I know at least 2 like this and they got rid of lyme.
We are all different. So, don't assume there is no hope for you just because you have had lyme for years.
Posts: 9931 | From Maryland | Registered: Dec 2007
| IP: Logged |
posted
aperture, that is a great testament to the best-of-the-best LLMD's, and there are only a handful, if that.
I see a doctor who follows Burrascano guidelines as well as the best LLMD in the country today Dr. H., who I assume is your doctor. I am 80-90% well, but my case was not complicated and treatment, aside from antibiotics, was through learning from these doctors, sites like lymenet and energy and electrodermal testing.
This illness has become so complicated that unless a doctor is on the leading edge or uses energy testing to determine what to treat and what your body needs, then it's just trial and error, and you are the guinea pig.
[ 06-21-2012, 01:15 PM: Message edited by: baileypup ]
Posts: 964 | From san diego | Registered: Oct 2009
| IP: Logged |
seekhelp
Frequent Contributor (5K+ posts)
Member # 15067
posted
annxyzz, your post sure makes sense.
Posts: 7545 | From The 5th Dimension - The Twilight Zone | Registered: Mar 2008
| IP: Logged |
Haley
Frequent Contributor (1K+ posts)
Member # 22008
posted
I think that one of the key points made by TF is that a good doc will not leave one stone unturned. That is a good doc in any field.
I have been treating for 3 years. I am not with a top LLMD but I have seen some of the best over the years. I agree with annyxx, that it is mostly experimental, but as we experiment we do find new answers such as parasites which was not considered a big factor in the past and seems to be much more important now.
I personally have come to the conclusion that this is almost like treating and entirely different disease for each person. That's why I like the term MCIDS (hope I got that right). Each tick carries a plethora of pathogens and we really don't know what they are or how they interact with each other. we can identify some of them and treat those and hope that will be enough but it often is not enough.
Posts: 2232 | From USA | Registered: Aug 2009
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Some LLMDs will work along with a LL ND (naturopathic doctor) in various ways. How to find the best in that area, too:
if at all possible - because each person & each case is different - it's best to consult with an ILADS-educated LL ND (lyme literate naturopathic doctor) (or similar) who has completed four years of post-graduate medical education in the field of herbal and nutritional medicine -
- and someone who is current with ILADS' research & presentations, past and present, and has completed the ILADS Physician Training Program (see: www.ilads.org )
Many LL NDs incorporate antibiotics (depending upon the licensing laws in their state). Some LLMDs and LL NDs have good working relationships.
When possible, it's great to have both a LLMD and LL ND and even better when they have a long-standing professional relationship.
Be aware that integrative doctors can have various levels of formal herbal &/or nutritional education, perhaps even just a short course. Do ask first. Some have learned on their own from experts in the field. There are many ways to acquire knowledge and most are eager to share basic details about their training. You want someone with a deep knowledge.
Links to many articles and books by holistic-minded LL doctors of various degrees who all have this basic approach in common:
Understanding of the importance of addressing the infection(s) fully head-on with specific measures from all corners of medicine;
knowing which supplements have direct impact, which are only support and which are both.
You can compare and contrast many approaches.
BASIC HERBAL EDUCATIONAL & SAFETY links,
BODY WORK links with safety tailored to lyme patients, etc. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
posted
I think top docs know a lot. They know what to check for. They do bloodtesting to see what our blood chemistry is like, and then often treat accordingly.
They listen very well and pick up clues from our history and our responses to anything. They know alot about products. They can tell whether we can handle a lot of treatment or not. They discover whether we can detox easily or not.
And they care. And it's great when they have good staff who returns calls promptly!
Put all that together and it's a good experience! If they take insurance, that's a plus, but many don't because they don't get paid by insurance.
Posts: 13134 | From San Francisco | Registered: May 2006
| IP: Logged |
posted
TF, I wish I'd read your post a LONG time ago! We're leaving my husband's LLMD and changing to Dr H for all the reasons you describe.
His former LLMD is a well-intentioned doctor who helps a lot of people with earlier, more straightforward cases of Lyme & co. But my husband (R), with late-stage neurological Lyme, kept deteriorating.
His LLMD seemed out of her depth. She told him that her other patients were getting better, but that he was getting worse. And she started backing away from his Lyme diagnosis--despite his +ve PCR. She suggested he go back to a regular neurologist to get tested for other diseases. Again! We'd already been through all that before he was diagnosed with Lyme.
He asked her, "Do you think I could have dementia?" His greatest fear. She replied, "Yes, that's what I'm concerned about."
So we trailed back to Mass General and the big shot neurologist we'd seen before. The one surrounded by adoring medical students who smirked dismissively when R mentioned Lyme disease. All the tests came back negative. Again. Big shot neurologist told R that he probably had depression. "I should be depressed," he replied, "but I'm not."
R was too debilitated to get up from the couch. He started hallucinating. He felt his LLMD had given up on him. He wanted to give up too. 2 years of oral antibiotics had been torture, and he'd only got worse. He told friends that it looked as if he had dementia.
What saved us was an excerpt from Pamela Weintraub's Cure Unknown in Psychology Today, on the web. Then I started reading other articles on the web by the specialists in neuropsychiatric Lyme she wrote about.
ALL of R's symptoms--the ones that had freaked out his LLMD and led her to suggest it wasn't Lyme--were in these articles as common neuropsychiatric symptoms of Lyme & co. Every one. How come she hadn't known this, I wondered?
When I quoted the article to R's LLMD, she suggested we go to NJ to see the specialist (Dr. B) for a 2nd opinion. She cared--but she just wasn't very widely read. So in NJ, after a 2-hr exam that turned into 3 hrs, Dr. B told R that he did indeed have late-stage tick-borne infections.
...And that he had neither dementia nor psychosis. His Lyme and co had caused (wait for it) a sleep disorder! That was the cause of his hallucinations. He was going into REM sleep while awake because he didn't get enough while asleep. I've never felt so grateful to a doctor!
R says this was the 1st time in 6 years that a doctor made him feel better. With better sleep, all his neuropsychiatric symptoms have gone.
If a reasonably common complication of Lyme & co like a sleep disorder could throw R's former LLMD so badly, we have to find someone with a grasp of the "unified field theory" of Lyme, CO, and everything else that piles in there and synergizes with the infections. That seems to be Dr H. There should be more Dr Hs and Dr Bs.
And I'm angry that Lyme is "the disease for the wealthy." Aperture, what you and your husband and your parents had to go through to get you proper treatment is so wrong I don't have the words for it. Sending healing vibes your way.
Sorry for the long post. And thank you, everyone, for this thread and this site.
Posts: 431 | From New England | Registered: Dec 2011
| IP: Logged |
posted
We were lucky to have an excellent doctor for my son, a LLMD rheumatologist who never gives up until she finds the reason for being sick. Being an integrative medicine doctor really helps, meaning like Dr. H in NY using prescription meds, alternative treatments, herbals and other supplements. Considering mold and toxins, all that stuff.
That said, I am THANKFUL to ANY DOCTOR who is willing to put his or her career in jeopardy to treat Lyme and/or Chronic Lyme.
-------------------- Son, 26, Dx Lyme 4/10, Babs 8/10 Had serious arthritis, all gone. Currently on Valtrex Daughter, 26,bullseye 7/11 arthritis in knees, cured and off all meds. . Self:Lyme, bart, sxs gone, no longer treating. Posts: 496 | From Washington, DC | Registered: Jul 2010
| IP: Logged |
lax mom
Frequent Contributor (1K+ posts)
Member # 38743
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
Too bad there's only about three of them in the whole country, all unaffordable for most. And even with the best their success rate is still not that high.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
lax mom
Frequent Contributor (1K+ posts)
Member # 38743
posted
My husband is living proof.
He would be dead without his LLMD but he's out working a double shift cooking on his feet all day today.
Ellen101
Frequent Contributor (1K+ posts)
Member # 35432
posted
I don't know I'm not 100% sold on a lot of these LLMD's..so manyhave seen those that are considered top notch and are still not well, or there are those that are convinced they are we'll because they saw the best, well who know maybe they would have gotten well anyway.
I for one was horrified when I saw the long list of supplements Dr H claims you need to take to get well. There is no way someone could possibly take that large of an amount and not have issues. It would be impossible to tell what was reacting with what...to me this is a large money maker for someone...
Posts: 1748 | From United States | Registered: Dec 2011
| IP: Logged |
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
It is possible to take all of the supplements Dr. H suggests. I did it years ago and continue to take many supplements till this day.
The real question is who are the LLMD's who are getting people back to functioning? We all know they are few and far between after all these years.
Too many who call themselves LLMD's are not using protocols that get results and even the very best ones still don't get a high percentage of people back on their feet.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
surprise
Frequent Contributor (1K+ posts)
Member # 34987
posted
If you've ever done a search in the past on this board, there are hundreds if not thousands of people who are no longer here,
and how many more never came to Lymenet?
You get improvements, you get better, you go on with your life. Sometimes it's hard to stay and relive the trauma you went through, too,
so you don't stay on the Internet. I think many take their improved health and move on.
-------------------- Lyme positive PCR blood, and positive Bartonella henselae Igenex, 2011. low positive Fry biofilm test, 2012. Update 7/16- After extensive treatments, doing okay! Posts: 2518 | From USA | Registered: Nov 2011
| IP: Logged |
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
I didn't say no one moved on. I've been well since 2003, since using an experimental treatment.
What I said is that there are few LLMD's that are getting high percentages of people back on their feet and even fewer LLMD's that are using the most current and effective protocols.
Yes, many have moved on but also many have been on this site for years. I've been part of the Lyme community since 1998. I would have liked to see easier access to treatment and better treatment by now.
But certainly, I understand all that stands in the way.
[ 02-18-2014, 06:57 PM: Message edited by: Abxnomore ]
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
desertwind
Frequent Contributor (1K+ posts)
Member # 25256
posted
I consider myself to be in partial remission. When I hit a year abx. free/symptom free I may claim full remission. I am back to work and back to exercise and doing the things I love. My body may always be weakened by what it has gone through but I am back to feeling like me again. Very sick for 10 years.
I do not come on here as much as I use to because I am busy with life but I still feel a part of the lyme community and want to continue checking in every now and then. It does feel like a sense of family...
I had seem 4 LLMD's before seeing Dr. H. I saw him at my worst about a year after brain surgery and 4 months of Dexamethasone steroids. Did he alone bring me back to life? Well pretty much yes.
Without his aggressive protocol I would not be back to my life again. BUT,I also modified the protocol to better fit my individual constitution. I feel that I am able to communicate well with him in terms of what I can and cannot do, what my body can and cannot do.
I like that he listens closely to my bodies response and my interpretation of my bodily cues.
I like that he tested me for things no other LLMD ever did (Q-Fever) and considers the load of environmental toxins that I have and continue to be exposed to. It is not ALL about TBI's with him and he considers much more when looking at your symptoms.
I like that he never got discouraged if I did not show improvement or never minimized my symptoms to something psychological (I'm a psychologist so good luck doing that!) or never gave up trying yet a different protocol.
Always addressing yeast and parasites. Advocated for me to get back to running once we felt my body could handle it - and that was one of my big turning points. I feel he was/is able to understand what my body needs to heal even if it is not part of some famous guideline that says no cardio.
This goes for both Dr. H. and his NP.
Posts: 1671 | From Tick Infested New Jersey | Registered: Apr 2010
| IP: Logged |
Abxnomore
Frequent Contributor (5K+ posts)
Member # 18936
posted
Certainly, Dr. H is one of the LLMD's that are included in that handful that uses a good protocol and has a good percentage of getting results.
I'm happy to hear that you had a good experience and are doing so much better. It's also great when others share information like this.
Posts: 5191 | From Lyme Zone | Registered: Jan 2009
| IP: Logged |
surprise
Frequent Contributor (1K+ posts)
Member # 34987
posted
I am also doing better, sustained improvements (knock knock knock)
and have been off LLMD antibiotics for over a year (did try some again this last summer for UTI, stomach issues, for a little bit)
and off Lyme treatment herbs, working on trying to get my gut in shape now. I treated parasites last year for a long time, too. (and before last year)
My memory is much better/ improved, I exercise daily, rarely a debilitating headache anymore, more peaceful. Some days are better than others, yes, and I've got work left to do on my gut health.
I worked with 2 LLMD's, the 2nd one we did more of a Burrascano type approach.
-------------------- Lyme positive PCR blood, and positive Bartonella henselae Igenex, 2011. low positive Fry biofilm test, 2012. Update 7/16- After extensive treatments, doing okay! Posts: 2518 | From USA | Registered: Nov 2011
| IP: Logged |
beaches
Frequent Contributor (1K+ posts)
Member # 38251
posted
desertwind, I am happy for you. Without going into detail, our experience with this doctor was the polar opposite of yours. I am glad we moved on.
Posts: 1885 | From here | Registered: Jul 2012
| IP: Logged |
Back in September 2008 I contacted you with the same question and you were so kind and patient to answer all my questions about finding the best LLMD. Without your advice my road to recovery would be much different.
Within first eight months of getting severely ill I saw 5 different LLMDs in my area.
Honestly speaking, all of them were good doctors, very knowledgeable, and ready to treat me, but I was slipping backwards in my neurological symptoms so fast that I knew I needed the most aggressive treatment I could possibly get at that point. These doctors were not offering it.
In april 2009 I found 6th LLMD and I stayed with this MD until this day. The reason why-He was the first LLMD how recognize how seriously sick I was. During first appointment my instincts were telling me that he was a doctor who would not give up on me.
And I am glad I listened to my inner voice.
TF, once again thank You for your help in 2008 and God bless.
Posts: 191 | From va | Registered: Sep 2008
| IP: Logged |
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/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
![[Wink]](wink.gif)
Printer-friendly view of this topic