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HealingWell.com Forum > Diseases & Conditions > Lyme Disease > Oh no! LymeMD is in trouble!
Veteran Member
Date Joined Sep 2014
Total Posts : 1204
Posted 5/12/2015 5:01 PM (GMT -6)
Please read: I need your help.
I have been writing this BLOG since 2008. It has been widely read with over 1.2 million page views. I hope it has been helpful.
I have intentionally tried to keep this BLOG non-political. But alas, Lyme is a political disease and this is an inescapable fact.
I am in trouble now and asking for help.
I have been investigated by the medical Board 3 times since 2008. The first two investigations were dropped. I am no longer under investigation; I have been charged by the Medical Board of Maryland with serious violations.
The last investigation was initiated by a complaint from a major insurance company with which I previously participated with, 3 years ago.
A number of patient charts were reviewed and sent to "peer review." My reviewers were IDSA infectious disease doctors. One of the reviewers is a well known Johns Hopkins faculty member -- well known to be on a mission to stamp out doctors such as myself.
I am charged with violating the standard of care for each of 6 patient charts evaluated. In the charges ILADS' views are entirely nullified; the standard of care is solely based on IDSA guidelines.
The charges against me are serious. I face prosecution by the Attorney General's office of the State of Maryland at the behest of the Medical Board. The Board has informed me that the charges are public; the details are available for anyone to read.
The penalties may be wide ranging and may include suspension of my license to practice medicine.
I am asking that current patients and former patients of mine to write me a letter of support describing their experiences with the medical system and their experiences with care I provided for them. For now only send these letters to me, by email or snail mail.
Thank you for your support.
Daniel Jaller, M.D.
15245 Shady Grove Road
Suite 315
Rockville, MD 20850
Paradigmmedicine@ gmail.com
Daniel Jaller, aka Lymemd.
Posted by Lyme report: Montgomery County, MD at 9:07 AM 15 comments:
Forum Moderator
Date Joined May 2014
Total Posts : 4894
Posted 5/12/2015 5:07 PM (GMT -6)
Oh no, is right!
I can't believe this is still going on! It's ridiculous.
How about they start investigating the Doctors that leave people getting sicker and sicker...and telling them there is nothing wrong with them...or sending them to psychiatrists....Symptoms started Sept, 2013 (maybe sooner?)
Buhner's protocol May 15/14 to July24/14
Igenex positive July 3, 2014; Doxy: July 4-Aug.24/14
Zithro July26-Aug.24/14
Amox 1000mg x3 + Probencid started Aug. 29/14; added biaxin 500X2 Sept. 26/14
Disc. amox and added Ceftin Nov. 20th. End of Jan/15 pulsing Tindamax ; disc biaxin
Buhners bart herbs started Dec/14
Forum Moderator
Date Joined May 2007
Total Posts : 19605
Posted 5/12/2015 5:10 PM (GMT -6)
Thanks for posting this Utahgal. I wish I could speak up - I've been reading his blog on and off for several years and have learned quite a bit for my own healing - but I've never been one of his patients.
Such a shame how we loose doctors. I'd really like to get those IDSA docs that reviewed Dr. J into a back room that was sound proof .... only for an hour or two and I wouldn't hurt anything but their pride - I promise!!!
Herb only treatment for Lyme & Bart ended 12/11 - no active symptoms for 2 yrs -Herb only treatment for Babesia ended 12/12
www.healingwell.com/community/default.aspx?f=30&m=2977364
Had Lyme, Bart, Babs, RMSF, Ehrlichia, Myco, Anaplasmosis, EBV
Back in treatment for new Lyme case 8/2014
*I can usually post a link to any info that I post. Wish to see a link? Please just ask!
Veteran Member
Date Joined Jan 2015
Total Posts : 972
Posted 5/12/2015 5:16 PM (GMT -6)
It is really sad! I can't believe an insurance company he contracted with over 3 years ago is going after him.
I wish they would leave our doctors alone. It's disgusting.
Forum Moderator
Date Joined May 2014
Total Posts : 2613
Posted 5/12/2015 6:38 PM (GMT -6)
Shame on them.
" I'd really like to get those IDSA docs that reviewed Dr. J into a back room that was sound proof .... only for an hour or two and I wouldn't hurt anything but their pride - I promise!!! devil"
Go, Trav, Go! ;)Moderator Lyme Forum.
Symptoms 2010; CDC Positive Lyme April 2014; Clinical dx Lyme & Bart May; Dx Aspergillus, MARCoNS, Mycoplasma, C. Pneu, EBV, HHV6. Aug 25 stopped abx.
Current treatment as of Apr 27, 2015: Chronic Tonic, Morinda, Tick Pathogen Nosode, Spigelia, Vit B Complex, Vit C, Curcumin, Magnesium Glycinate, Pekana Detox, Nystatin, Diflucan, Probiotics, Multi-vitamin, CoQ
Regular Member
Date Joined Dec 2014
Total Posts : 151
Posted 5/12/2015 9:36 PM (GMT -6)
The politics of this disease are truly amazing to me. Medicine in general in the United States is just in a terrible place. So many kickbacks to doctors and politicians from insurance companies. I would never wish this disease on anyone, thats just inhumane, but if I had to it'd be the IDSA docs first. Live a month in my shoes and I guarantee they'd be convinced of chronic lyme.
Veteran Member
Date Joined Dec 2014
Total Posts : 1096
Posted 5/13/2015 12:43 AM (GMT -6)
They are trying to scare all the LLMDs to look in their closets for skeletons that may be up to 3 years old :( Is there a limit the insurance companies have to sue doctors? How long does a patient have to sue an incompetent doctor for malpractice? No time limit?
I hope he will win the battle. This isn't right! It is cruel! It's all aboutthe money!Me: At 99.9% symptom free--no abx for the past 5 years for Lyme and Bartonella;
Son: Bull's eye rash and Bartonella Igenex+
Both Daughters have symptoms of Lyme and/or Bartonella
Love God, trust Him, and He will heal you. He is the best doctor.
I felt I was slipping down fast, and He caught me by my hand.
"I can't do it... I must do it... I will do it"
Veteran Member
Date Joined Feb 2014
Total Posts : 895
Posted 5/13/2015 7:33 AM (GMT -6)
Ugh, so awful. It makes me so mad.Sarah
-positive IGM Western Blot- 39, 41 in January 2014// Igenex & CDC positive 11/14
-positive ANA and very low CD57
Chronic daily headaches since 2005
Veteran Member
Date Joined May 2012
Total Posts : 894
Posted 5/13/2015 8:03 AM (GMT -6)
This very thing almost happened to my LLMD. After I got a prior approval for Mepron 3 months in a row, the insurance company called my LLMD and basically threatened him. I was dropped as a patient.
Veteran Member
Date Joined Jun 2006
Total Posts : 844
Posted 5/13/2015 8:31 AM (GMT -6)
This is my LLMD. :(
I've only seen him once so far, and see him for my second visit soon.
I don't have a strong opinion about him yet, but his blog is amazing.30s F. Crohn's ileocolitis dx2/06. Proctitis dx 10/12. Arthritis dx9/09. GERD dx1/13. Asthma dx4/13. Raynaud's. Chronic headaches/migraines. Chronic chest pain.
Lyme: ER 7/14, confirmed 4/15 (IgM+ bands 23, 37, 41, 93).
Meds: Remicade 75mg Nuvigil, 75mg Trazodone, 50mg Zoloft, Klonopin, Zyrtec, Maxalt/Botox (migraines). 30B probiotics, Vitamineral Green, turmeric, Vit D, B, Mag, Charcoa
Veteran Member
Date Joined Jun 2006
Total Posts : 844
Posted 5/13/2015 8:42 AM (GMT -6)
Also, here's the full complaint: /www.mbp.state.md.us/bpqapp/Charges/D3313804.225.PDF30s F. Crohn's ileocolitis dx2/06. Proctitis dx 10/12. Arthritis dx9/09. GERD dx1/13. Asthma dx4/13. Raynaud's. Chronic headaches/migraines. Chronic chest pain.
Lyme: ER 7/14, confirmed 4/15 (IgM+ bands 23, 37, 41, 93).
Meds: Remicade 75mg Nuvigil, 75mg Trazodone, 50mg Zoloft, Klonopin, Zyrtec, Maxalt/Botox (migraines). 30B probiotics, Vitamineral Green, turmeric, Vit D, B, Mag, Charcoa
New Member
Date Joined May 2015
Total Posts : 13
Posted 5/13/2015 8:43 AM (GMT -6)
This breaks my heart! I wish there was something I could do to help. The whole system makes me SICK!! A few months ago I watch “Under Our Skin” and last night I watched “Under Our Skin 2”. It all really makes me angry!!! How is it OK for Drs to prescribe long term ABX for acne but NOT OK for Lyme? AND how is it OK for my Rheumatologist to DX me with non sero rheumatoid arthritis and try to put me on multiple medications?!?!?! He laughed in my face when I mentioned Lyme but he had NO problem giving me a diagnosis based on my history and symptoms, even though my labs said I was negative. How is that any different than diagnosing someone with Lyme based on history and symptoms?!Symptoms started in March 2012 ( maybe sooner)
IGenex Results May 2015 IgM WB 39 IND, 41+/ IgG WB 39 IND, 41++, 58+/ B. microti, IgM 80/ Babesia FISH Positive
Life is not a matter of holding good cards, but of playing a poor hand well.
Regular Member
Date Joined Apr 2015
Total Posts : 231
Posted 5/13/2015 9:03 AM (GMT -6)
this shows everything thats wrong with health care in our country this would never happen in Europe, its so sickening
Regular Member
Date Joined Sep 2014
Total Posts : 95
Posted 5/13/2015 9:50 AM (GMT -6)
myeezy24 - I'm afraid it's even worse in the UK. Those few doctors who were trying to help patients with Lyme were prevented from practising years ago. There is denial that Chronic Lyme exists at all. There is inadequate NHS testing, a refusal to accept overseas test results and completely inadequate treatment (just weeks of doxy for the very lucky ones).
There has been a Lyme protest in London today, representing the thousands too ill to attend. So many lives devastated by this, but the denials continue.
So sorry to read about LymeMD - I love his blogs! It all makes me very sad and angry.
Veteran Member
Date Joined Sep 2014
Total Posts : 890
Posted 5/13/2015 10:43 AM (GMT -6)
It is TOO discouraging that so MANY ailing patients & docs have fought the LD battle for YEARS!
On the doc's blog, he states that "science is catching up," but is it really, when politics & greed continue to rule?!
Re the 2001 NYTs article, "Stalking Dr. Steere Over Lyme Disease, By DAVID GRANN, the doc's revealing comments:
"Although this piece was written 14 years ago, nothing, or very little has changed. Dr. Steere, a once virtuoso violinist whose career was cut short by a finger injury turned his focus to medicine. By serendipity Lyme fell into his lap and he has been a Moses of the field for the last 40 years. Contemporary medicine has no experience with a multisystem disease such as Lyme disease. The specialization of American medicine makes it more difficult for physicians to see recurring patterns of the disease.
Patients instead are diagnosed with psychosomatic disease, fibromyalgia or chronic fatigue syndrome. It is fascinating that Dr. Steere says that chronic Lyme has become a garbage can diagnosis and that fibromyalgia is frequently the real answer. Dr Steere tells the reporter: “there is no controversy amongst scientists.”
"[They] live in a bubble, have lunch with each other and validate their beliefs: Lyme is easily treated with short courses of antibiotics. Their influence continues to have far reaching consequences leading to devastation for so many Lyme patients.
Personal attacks, such as in the case of Dr. Steere, have an effect opposite of that desired. The besieged only become defensive, clinging more tenaciously than before to their flawed system of belief.
Science is the best weapon we have. It is finally catching up.
Fourteen years later after this interview, when nothing seems to have changed, a study published a few days ago in PLOS one by Auwaerter, (Feng, Zhang) a stalwart “Steerite” leading the charge in the Lyme war against the Burrasconites, firmly contradicts the basis of the Steere hypothesis.
In this study the Hopkins’ group admits the cause of ‘Post-Lyme” is uncertain. The idea that Lyme bacteria persist after 2-4 weeks of amoxicillin is “controversial” according to the authors of the study, who then proceed to provide clear, concise and convincing evidence that Borrelia burgdorferi, the Lyme agent,cannot in any world, possibly be killed by this recommended therapy.
The evidence is clear, there is no single drug is capable of eliminating Lyme persisters in mice, dogs, primates and humans -- or in a test tube. There is no known combination of two drugs that can eliminate Lyme persisters. The authors have discovered a single combination of three drugs: daptomycin + cefoperazone + doxycycline processing the unique ability to eliminate Lyme persisters in a test tube. This is a huge step forward.
We may not be able to readily adopt this study for clinical purposes. Daptomycin is an extremely expensive drug and is currently reserved for the sickest hospitalized patients. Infectious disease physician's "stewardship" over antibiotics will likely be a roadblock against the use of this potent drug, and, third party payers, hiding behind the banner of FDA approval will likely not pay for it. Cefoperazone I have tried to prescribe; pharmacists have told me it is not available.
Only a veritable nuclear bomb of antibiotics could kill all the Lyme in a test tube. Still, Dr. Auewater (at his other job), along with the coterie of Steerites will continue to tell us the pea shooter therapy is all our patients should ever need...
New research at the test tube level with drugs such as Claritin and the "nuclear option" may prove to be helpful. Test tube science does not always translate into clinical cures but may certainly provide key, new evidence.
The study gives us another rock to throw at the edifice of the Steere - IDSA - CDC dogma. It remains a David vs Goliath battle. For now, Lyme remains a political disease. We know the science, which are adversaries claim to hide behind, will prevail in the end."
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Date Joined May 2007
Total Posts : 19605
Posted 5/13/2015 11:12 AM (GMT -6)
myeezy24 said...
this shows everything thats wrong with health care in our country this would never happen in Europe, its so sickening
This does happen in Europe as well - it's happening all over the world. That's why we get members from all over the world asking what they can do because they don't have access to a LLMD in their area.
But, that's because almost every other country has it's eyes on the US on how to deal with these infections. So while the IDSA sticks to their statements, it hurts people world wide.
But trying to get things changed in my own state have proven very difficult. I can't even get the elected officials to answer my emails, so it's time to change tactics.Herb only treatment for Lyme & Bart ended 12/11 - no active symptoms for 2 yrs -Herb only treatment for Babesia ended 12/12
www.healingwell.com/community/default.aspx?f=30&m=2977364
Had Lyme, Bart, Babs, RMSF, Ehrlichia, Myco, Anaplasmosis, EBV
Back in treatment for new Lyme case 8/2014
*I can usually post a link to any info that I post. Wish to see a link? Please just ask!
Veteran Member
Date Joined Jun 2011
Total Posts : 1107
Posted 5/13/2015 12:23 PM (GMT -6)
This is awful, his website is full of wonderful info. God help him battle these
ba$tards .Started anaplasma and mycoplasma treatment 03/2014. Tens years sick. Hoping to see consistent improvement this year.
IGENEX results 2013
IgM Negative **31 - IND **34 - IND **41 - IND **83-93 - +
IgG Negative **41 - +
Veteran Member
Date Joined Sep 2014
Total Posts : 890
Posted 5/13/2015 8:53 PM (GMT -6)
Go get 'em, Traveler! All the zombies here need to brainstorm!
Regular Member
Date Joined Oct 2014
Total Posts : 275
Veteran Member
Date Joined Jul 2014
Total Posts : 678
Posted 5/14/2015 2:22 PM (GMT -6)
This is awful - the Lyme community can't afford to lose doctors. I recently recommended you to a person in Md. that I'm SURE NEEDS a good dr. like you. Must say, I'm a bit abashed that I sent you flowers thinking you are a gal from Utah, to cheer you up! Well, I would send more, but I think you would need the "man flowers" I have also sent.
I wish I could write a letter for you as a patient in support. You have been awesome on this site.
I did just write and send letters to the psychiatrists that misdiagnosed my son, the critical care response man who handled our case and to the intake specialist at our hospital. I informed them of my son's REAL problem and begged them to consider lyme in the future, not so easily label someone as Bipolar with ocd, odd and ticks and heavily drug them with psych meds. ESPECIALLY when the patient has POSITIVE lyme blood work from the past with them at a visit or hospital stay!!!!!!!!!! I also recommended Dr. B's training on line for psychiatrists across the country. Only 600 have participated in the training, but that is a start.
Prayers are with you Utahgal, your patients and those in the future NEED you!!! Many grateful to you for saving their lives, I'm sure.
Veteran Member
Date Joined Jul 2012
Total Posts : 592
Posted 5/14/2015 8:33 PM (GMT -6)
It is a travesty. Not only so because it affects thousands and thousands of people with pain and other debilitating symptoms, but also the many who die because they aren't treated properly. I truly believe my husband's ALS is at least partly due to Lyme/coinfections. He is currently on 4 treatments that appear to keep him stable, but it is scary to say the least. It is also wrong of course for these courageous doctors to be condemned for trying to help people. I hope many of his patients come forward to support him. I would if my husband or I was treated by him."Facts do not cease to exist because they are ignored" Aldous Huxley
Husband, Toby, diagnosed with ALS summer of 2012. Tested positive for Lyme Spring 2013 - Igenex Lab. Treatments used: Rife, Erchonia Laser, Acupuncture, Antibiotic - Doxyclycline, Herbal Remedies - Japanese Knotweed (powder form), Cat's Claw, Detoxifying - Ionic Foot Baths, Quantum Neurology, coconut oil.
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Date Joined May 2013
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Posted 5/16/2015 7:06 PM (GMT -6)
What the heck is wrong with Maryland????
Considering how close it is to DC, one would think that it would be more open minded.
I live in NC of all places (rural no less), and a lot more docs are now accepting Chronic Lyme. Granted, they know diddly-sh-- about it, but still!!
My cardiologist's NP said more (regular) docs are now open to it.l
Maybe being in a rural area actually helps.
I think the ID department at John Hopkins needs an avalanche of mail, phone calls, etc.
Also, have you talked to ILADS and Calda's new website?
I imagine you have.
How many patients do you have?
MargaretHELLO!! :) :)
Margaret, 53, Lyme, relapsing remitting c. diff., complete thyroidectomy, remote breast cancer, Interstitial Cystitis, Babs, Bart, Fibromylagia, Immuneglobulin Deficiency, depression, asthma and allergies, migraines, myoclonous and remote seizures, orthostatic hypotension and dysautonomia
Medication, herbs, vitamins, probiotics.
Veteran Member
Date Joined Mar 2014
Total Posts : 2111
Posted 5/16/2015 7:11 PM (GMT -6)
Wow. I am shocked. I naively thought this trend had been curbed, given the legislation developments to more appropriately protect alternative treatments. Have you considered contacting MDs previously raked through the same coals for support?
I am grateful you posted his plea. Wondering what ways we can help. Perhaps posting messages on his blog?
pChronic late-stage lyme—likely infected in 2000; Clinically dx 3/2014 w/ Babesia, tested positive for Bartonella, CDC-positive for Borellia. Multiple viruses and GI/immune treated first; started AL-Complex in May; started A-Bart and A-Bab in July; have IV port installed and started on Rosephin.
Detox: Pinella, Burbur, Parsley, Milk thistle seed, Burdock root tinctures; japanese knotwee
Veteran Member
Date Joined May 2013
Total Posts : 3761
Posted 5/16/2015 9:23 PM (GMT -6)
p
I like that idea.
MHELLO!! :) :)
Margaret, 53, Lyme, relapsing remitting c. diff., complete thyroidectomy, remote breast cancer, Interstitial Cystitis, Babs, Bart, Fibromylagia, Immuneglobulin Deficiency, depression, asthma and allergies, migraines, myoclonous and remote seizures, orthostatic hypotension and dysautonomia
Medication, herbs, vitamins, probiotics.
Link here- http://www.healingwell.com/community/default.aspx?f=30&m=3405157
Veteran Member
Date Joined Mar 2014
Total Posts : 2111
Posted 5/17/2015 11:05 AM (GMT -6)
Hi blog has only 29 comments… please contribute!
pChronic late-stage lyme—likely infected in 2000; Clinically dx 3/2014 w/ Babesia, tested positive for Bartonella, CDC-positive for Borellia. Multiple viruses and GI/immune treated first; started AL-Complex in May; started A-Bart and A-Bab in July; have IV port installed and started on Rosephin.
Detox: Pinella, Burbur, Parsley, Milk thistle seed, Burdock root tinctures; japanese knotwee
Veteran Member
Date Joined Jul 2014
Total Posts : 678
Posted 5/28/2015 8:15 AM (GMT -6)
I found this today on facebook... wow.....
14 hrs
I am sure many of you have hear that Dr Jaller – LLMD is being actually charged with crimes for treating Lyme patients in Maryland. He is my Dr and literally saved my life. He is a terrific Dr and treat Lyme patients with respect and dignity. I know he has treated and helped literally hundreds of people with great success. I went to pick up a prescription the other day and he was in between appts so we had a time to speak. I wanted to share some things with you that you all may not know about his situation.
1. I have seen Dr Jaller for 5+ years. The first 3 he took insurance and if he hadn’t I probably wouldn’t have gone to see him or any other LLMD since I just couldn’t believe that the situation with Lyme patients was so totally insane and criminal in my opinion. Because he cares so much about treating people with Lyme he continued to take insurance, as payment when I know they paid him less than a manicurist would make for the 40-50 minutes he always spent with me.
2. When he had no choice but to stop accepting insurance his rates have always been very fair and I am more than happy to pay him out of pocket. Additionally, it is because he took insurance so long that he is in this legal mess. I will explain;
3. United Healthcare? filed complaints on him. The medical board then had a phony peer review group review cases that United Healthcare paid for. This phony group included the ****Infectious Disease Dr of all time – Dr Auwaeter from Hopkins. Naturally out of hundreds of cases they found six that they found to be out of what Dr Auwaeter considered normal treatment methods. Rather than only file complaints with the medical board Auwaeter had them file criminal charges with the States Atty of MD!
4. The six patients from these out of “normal and proper treatment” cases all will testify in affidavits that Dr Jaller saved their life. None have any problems with the way he treated them. None got sicker or had bad results. All six actually got much better!
5. So far Dr Jaller has spent tens of thousands of dollars on legal and clerical fees just to comply with their requests for patient records.
6. This kind man Dr Jaller who has treated and helped Lyme patients from all over the world may easily serve jail time for doing what he does – save peoples lives.
So what can we do? Here are a few sites where we can go and post our opinion about Auwaeter – go bash him – I did. This idiot is useless and is responsible for as many deaths as Bin Laden
http://www.healthgrades.com/physici…/dr-paul-auwaerter-xkp56
http://www.vitals.com/doctors/Dr_Paul_Auwaerter.html
https://www.facebook.com/Johns.Hopkins.Medicine
Dr Jaller told me that the States Atty kind of threatened him against going to the media with this. I told him BS – we should stage a press conference and go right after the States Atty. I mean here he is going to charge him criminally while the patients whose treatment they question all say that he saved their life. If it comes to this I will let you all know and I hope people locally will show up. If you have other ideas please post them.
This is such an injustice that I want to grab this idiot Auwaeter by the throat and…… but I wont. But I will do whatever I can to get him straightened out for this. That I promise
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Date Joined Jan 2015
Total Posts : 972
Posted 5/28/2015 11:20 AM (GMT -6)
Thanks for the update LMCM! It's incredibly appalling.
Do you mind sharing the link (if you have time to post it)? I looked for it and could not find it. I would like to follow what is going on. My doctor has been fighting as well. I'm curious what we can do to help.
Obviously, the best thing is for them to avoid getting in the situation in the first place. It seems so far out there. It does not seem like he could have anticipated this though. The witch hunts need to stop.
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Date Joined Mar 2014
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Posted 5/28/2015 12:25 PM (GMT -6)
Yes, thanks LMCM for the update. I checked his blog yesterday and there were a couple of posts from a few of us (hugs) but not enough!!
And I embrace the Facebook post's charged up energy, and yours too, Chris. We have to do something. For now, the petition and posting and sharing the stories are the best and easiest places to start. Once we're well, hopefully we can be more impactful.
Keep up the momentum. Chris, funnel that fantastically intense energy into your treatment. Nothing is more important than healing right now… We will have our moment with the enemy.
pChronic late-stage lyme—likely infected in 2000; Clinically dx 3/2014 w/ Babesia, tested positive for Bartonella, CDC-positive for Borellia. Multiple viruses and GI/immune treated first; started AL-Complex in May; started A-Bart and A-Bab in July; have IV port installed and started on Rosephin.
Detox: Pinella, Burbur, Parsley, Milk thistle seed, Burdock root tinctures; japanese knotwee
Veteran Member
Date Joined Jul 2014
Total Posts : 678
Posted 5/28/2015 12:32 PM (GMT -6)
I'm taking it from FB and so can't post a link or anything. I'll post when I see things added and let you know Lymie girl. I plan to follow it. The post is on a friend of mine who's son is very very ill. At the moment, I think Lyme is the least of the problems, though the cause of the problems.... so young, my son's age, and so sick... :(
Want to respect everyone's privacy though....
A couple of responses...
there is a protest at the US DOJ coming up June 1st. .............'s group is going and they have filled criminal charges against the US DOJ. So, maybe something will come out of it This group has filed so much legal paperwork against the US and its crimes against humanity…. its a shame that United Healthcare are jerks……. Dr Jaller is a good man. I can't figure out for the life of me…. why they (US) doesn't want CLD treated! It has to be the bio warfare stuff…. but why against American's? We all stand behind our doctors who are good to their patients. there are many LLMD's who are not good to their patients and neither are their charges……
Reply
Dr Jaller is an intelligent and caring MD. This persecution of our doctors has got to stop. He is the second of our 10 LLMDs that's under persecution. Meanwhile, every R. arthritis MD in America is giving abx to their patients "off label" and every pscyhe doc in America is giving their patients pscyhe meds "off label". My dermatologist told me, "if I hadn't given off label meds in the past, ppl would have died." This is a Lyme specific attack on our access to medical care.
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Date Joined Jul 2014
Total Posts : 678
Posted 5/28/2015 1:24 PM (GMT -6)
Oh, I FOUND IT!
Join Us!
/www.facebook.com/events/804422736243381/
#OccupyTheUSDOJ #June2015
The complete, 100+ page Charge Sheet document is available here, as well for everyone to read!
badlymeattitude.com/2015/05/25/occupy/
Go here on Facebook (you actually have to go to it on facebook, can't make the link work here, have tried for an hour!) and you can click on the link to read the 116 page document with all of the charges...
Lyme Disease Support in Iowa
May 26 at 11:37am ·
The complete, 100+ page Charge Sheet document is available here, as well for everyone to read!
https://badlymeattitude.files.wordpress.com/…/chargescomple…
badlymeattitude.files.wordpress.com
badlymeattitude.files.wordpress.com
Post Edited (Lovemychildren Mom) : 5/28/2015 1:32:03 PM (GMT-6)
Veteran Member
Date Joined Jan 2015
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Posted 5/28/2015 5:15 PM (GMT -6)
Thanks LMCM! I never meant to ask you for a link to a private page. I thought it was on Dr. J's page. It's so sad.
Sending you and your son my very best!
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Date Joined May 2013
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Posted 5/28/2015 8:25 PM (GMT -6)
I think this was asked before, but can the DC Dr. J., who went through the same thing in NC before moving to DC, can he help Dr. Jaller?
MHELLO!! :) :)
Margaret, 53, Lyme, relapsing remitting c. diff., complete thyroidectomy, remote breast cancer, Interstitial Cystitis, Babs, Bart, Fibromylagia, Immuneglobulin Deficiency, depression, asthma and allergies, migraines, myoclonous and remote seizures, orthostatic hypotension and dysautonomia
Medication, herbs, vitamins, probiotics.
Veteran Member
Date Joined Jul 2014
Total Posts : 678
Posted 5/29/2015 5:31 AM (GMT -6)
That would be really great, not sure if it's wise for him to get involved though - he's off doing great work quietly and many need him to continue....
Regular Member
Date Joined Oct 2014
Total Posts : 275
Posted 5/29/2015 5:35 AM (GMT -6)
So sorry i will try and find the link and read up on it hugs and prayers
Veteran Member
Date Joined Sep 2014
Total Posts : 890
Posted 5/29/2015 8:25 AM (GMT -6)
LMCM~Thank you for updating & continuing the righteous fight. Being in the DC metro area makes it that much more of a reason to ignore this travesty.
Perhaps a slam dunk type lawyer should take on the compromise that these courageous LD treating docs will NOT be penalized, & that insurance made to pay for ailing patients. Even though crimes against humanity is the phrase, in my estimation, our powers that be are not going to ass-ume culpability for all of these bioweapon years, Gulf War, vaccines, etc.
But as it unfolds, please keep us aware. And please give all info as to lawyers fighting this & what they need in terms of people in numbers or testimonies to support.
Post Edited (happyjo) : 5/29/2015 11:01:59 AM (GMT-6)
Veteran Member
Date Joined Jun 2006
Total Posts : 844
Posted 5/29/2015 8:53 AM (GMT -6)
I can also speak to this as I'm also a patient, albeit just for a few months. Auwater has had it out for Dr. J for many years and has tried to bring charges against him on at least two other occasions but they were dismissed. When I first met him earlier this year he said he had no fear of charges because they were baseless but this time it is different. He seems genuinely concerned about the case.
Dr. J is a wonderful man whose No. 1 goal is to help patients get better no matter what they're suffering from. In my two appointments with him, I've spend over three hours talking with him and him giving me very detailed explanations of the science (which I appreciate) and going through all the options, ordering relevant tests (like a sleep study) that no one had thought to do before, and only then beginning my treatment.
From one perspective, I can understand why Auwater does this, but his reasons have nothing to do with patient safety. It truly is political and scientific advancements seem to be pushed to the side.
As a patient, I'm frustrated. I can't imagine what these doctors are going through.30s F. Crohn's ileocolitis dx2/06. Proctitis dx 10/12. Arthritis dx9/09. GERD dx1/13. Asthma dx4/13. Raynaud's. Chronic headaches/migraines. Chronic chest pain.
Lyme: ER 7/14, confirmed 4/15 (IgM+ bands 23, 37, 41, 93).
Meds: Remicade 75mg Nuvigil, 75mg Trazodone, 50mg Zoloft, Klonopin, Zyrtec, Maxalt/Botox (migraines). 30B probiotics, Vitamineral Green, turmeric, Vit D, B, Mag, Charcoa
Link Here- http://www.healingwell.com/community/default.aspx?f=30&m=3405157&p=2
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