Saturday, June 17, 2017

HR985 MDL THEORY V. MDL REALITY: POWER TO THE PLAINTIFF

This event was light on facts, long on theory and in the best interest of attorneys who do not want HR985 FAIRNESS IN CLASS ACTION LITIGATION ACT OF 2017

The question you have to ask yourself is:
Why does J. Maria Glover, law professor at George Washington University, completely agree with Stephen Harburg, an attorney who represents pharmaceutical companies?

These 2 together should tell you everything you need to know about HR985:
WHEN IT PASSES THE SENATE AND IS SIGNED INTO LAW BY PRESIDENT TRUMP IT WILL BE POWER TO THE PLAINTIFF!!

EVENT:
THE GROWTH OF MULTIDISTRICT LITIGATION:
EMERGING ISSUES and POSSIBLE SOLUTIONS


LEC_CongressionalCivil_CMYK











2:07 minute video of J. Maria Glover speech:    https://goo.gl/photos/4ELwv9Fr1HEP99xVA

More videos were made and will be published!



Tuesday, May 30, 2017

BUST MULTIDISTRICT LITIGATION CORRUPTION BY ENTRENCHED REPEAT PLAYERS AND THEIR ENTRENCHED LAW FIRMS...MAKE LITIGATION FAIR FOR PLAINTIFFS!

PLEASE WRITE SENATE LETTERS SUPPORTING 
HR 985 HOUSE BILL

“Fairness in Class Action Litigation &
Furthering Asbestos,Transparency Act of 2017”

MAY 30, 2017

E-MAIL YOUR LETTERS TO LanaKeeton@MedDeviceExpertLLC.com

COPIES OF ALL WILL BE PRESENTED TO EACH OF THE SENATORS
WE VISIT ON
"VISIT YOUR SENATOR DAY",
MONDAY, JUNE 12, 2017!

YOUR 7TH AMENDMENT RIGHT TO A TRIAL BEFORE A JURY HAS BEEN DENIED TO MANY, MANY OF YOU BECAUSE YOUR ATTORNEY DID NOT TAKE YOUR CASE TO TRIAL!

Please include the following info:

1    1. Your name, state and e-mail.
2    2.  Your Senators.
3    3. The Mesh Product and Company Name implanted in you.
      4.  Short list of Complications and the impact on your life. (2 short paragraphs at most)

Next describe your feelings about your lawyers treatment as follows. This does not violate your confidentiality agreements but merely describes your treatment by your lawyers related to getting you to sign the settlement agreement:

1.      Can you please describe if you were pressured by your lawyers to sign legal documents without a full understanding of how much of the money is going to the lawyers, and how potentially little in comparison is going to you?

2.      Why don’t you feel that your lawyers have been responsive to your questions or kept you fully informed about where the settlement money is going?

3.      Have your lawyers fully explained why you are being offered the specific amount of money they are pressuring you to settle for, and not some other amount?

4.      And could you describe any other ways in which you think your lawyers have not adequately represented you or kept you fully informed, or left you frustrated by their conduct in your case?

5.      Did you feel intimidated or bullied or disrespected by your attorneys? If so, in what way?

LINK TO LIST OF ALL SENATORS 115TH CONGRESS & CONTACT INFO 2017

COMMITTEE ON THE JUDICIARY

SUBCOMMITTEE ON THE CONSTITUTION

Majority Members:
5
Total Members:
9
Minority Members:
4

Members:
Members:
Cruz, Ted (TX), Chairman
Cornyn, John (TX)
Crapo, Mike (ID)
Sasse, Ben (NE)
Graham, Lindsey (SC)
Blumenthal, Richard (CT), Ranking Member
Durbin, Richard J. (IL)
Franken, Al (MN)
Coons, Christopher A. (DE)

DEAR MESH INJURED PATIENTS, BOTH PELVIC AND HERNIA,

I am, and have been, working in D.C. to expose the fraud and corruption at the FDA to get ALL MESH off the market through the House Government and Oversight and Reform Committee since I arrived in the D.C. area at the end of March. 

I am working with the House Judiciary Committee on their Bill, HR985“Fairness in Class Action Litigation & Furthering Asbestos Transparency Act of 2017” to get the Senate to take up their version of HR 985 to bust the corruption and fraud in the MDL's. There is language being added for transparency in the settlements in pelvic mesh litigation and other benefits to the mesh injured. Our goal is to rename it the “Fairness in Class Action Litigation & Furthering Asbestos, Pelvic Mesh and Hernia Mesh Claim Transparency Act of 2017” No one is protected by these lawsuits except for the pocketbooks of attorneys who are already extremely wealthy. Now Jane Akre is going to tell you this is bad because she makes a living from attorneys. No your civil rights will not be lost and there will not be an end to mass torts.

Your rights are CURRENTLY BEING VIOLATED in the Multidistrict Litigation in West Virginia.

Hard to explain my strategy in Congress. Guess it's like a salesman who keeps calling on a customer to get them to buy a product. Except I want the Senate and the House of Representatives to take action which will lead to taking mesh off the market. Johnson & Johnson, Boston Scientific, American Medical Systems and C.R. Bard all have millions and millions to pay lobbyists to go to Congress to keep their products on the market. Since I don't have millions, I use my knowledge and experience from being a medical device expert and legal consultant to present irrefutable facts to our elected representatives of the harm caused by mesh to get them to take real action to remove it from the market.

HR985 will never be signed into law as it is currently written. The Senate will pass it's version and it will go back to the House. And so on and so on like any bill going through the legislative process.

Elizabeth Burch who writes in opposition to the bill wrote a 64 page doc in 2014 "Judging Multidistrict Litigation" explaining how a handful of Attorneys "Repeat Entrenched Players" and "Repeat Entrenched Law Firms" have controlled ALL the MDL's for years now. I know those guys personally and they are cheating the hell out of you guys just like they cheated me. In fact Jane Akre works for some of them. I have worked within the MDL system for 7 years now hoping to influence plaintiff's attorneys. The MDL's are ugly for the injured plaintiffs. Just as ugly as the FDA. Just as ugly as mesh companies. A handful of attorneys in the U.S. make literally billions of dollars while hundreds of thousands suffer the consequences of the injuries from the corrupt manufacturer's products.


Support the legislation. Take charge of your own destiny. Stop the rampant hidden fraud and corruption in the legal system. Always find out who is behind the articles against the legislation that you read before you decide to accept it as fact. It is very complex. Look at the mission statements of the group's and their websites and their actions over a long period of time. Be your own judge!

© 2005 - 2017 Lana C. Keeton All rights reserved. Peace be with You.
This material may not be published, broadcast, rewritten or redistributed.
Med Device Expert LLC
Device Expert . Legal Consultant . Expert Witness . Patient Advocate
1602 Alton Road, #423, Miami Beach, FL 33139

305-671-9331 phone . 800-509-9917 fax
786-566-7780 . 305-342-8002 cell phones






Tuesday, May 23, 2017

WESTIE LOVE....SIR ALEXANDER ANGEL BOY BUTTER BEAN....MY FOREVER ANGEL! BUY ADORABLE POSTER OF B.B.!


Hey Guys, 

I created this amazing, adorable poster to finance my work in D.C., $20.00 plus shipping. It's fun to have and great to give...

Guaranteed to make you smile every time you look at it!


Lana Keeton (C) All rights reserved 05-23-2017

11" x 17" on heavy matte card stock. 
Great for the kitchen, family room, your office or the kids room. 

Go to my personal website, www.LanaKeeton.com, bottom of home page to order!

Or go direct to paypal to my paypal account: Lana@LanaKeetoncom 

Saturday, May 20, 2017

ALL MESHED UP! MEDICINE AND LAW SERVE CORPORATIONS, DOCTORS AND ATTORNEYS. PATIENT BE DAMNED!

In our Meshed Up World, the total insanity of implanting polypropylene into humans is ignored.

You're harmed by synthetic mesh? Ha, ha, ha, ha, ha.

You filed a lawsuit against Johnson & Johnson, American Medical Systems, C.R. Bard, Boston Scientific, Caldera Medical, Cook Medical, Coloplast with the expectation of being compensated for your harm?

Ha, ha, ha, ha, ha.

You signed a contract with an attorney to represent your rights and your interest against one of the companies?

Ha, ha, ha, ha, ha.

Very, very sadly, the joke is on us.

Patient be damned. :(



You know what, I guess I will just continue calling on

the House Judiciary Committee and

the House Government Oversight and Reform Committee and

the Senate Judiciary Committee.

Let's see who's laughing at 

the end of the legislative session.


Sunday, May 14, 2017

WRITE YOUR SENATOR SUPPORTING HR985 "FAIRNESS IN CLASS ACTION LITIGATION; FURTHERING ASBESTOS, PELVIC MESH AND HERNIA MESH CLAIM TRANSPARENCY ACT OF 2017" ...BUST A MOVE....STOP THE ABUSE OF INJURED PLAINTIFFS IN MULTIDISTRICT LITIGATION!

PLEASE WRITE SENATE LETTERS SUPPORTING HR 985 HOUSE BILL
to be renamed &
 language added specific to all mesh plaintiffs

“Fairness in Class Action Litigation & Furthering Asbestos,
Pelvic Mesh and Hernia Mesh Claim Transparency Act of 2017”

MAY 14, 2017

E-MAIL YOUR LETTERS TO LanaKeeton@MedDeviceExpertLLC.com 
COPIES OF ALL WILL BE PRESENTED TO EACH OF THE SENATORS WE VISIT ON
"VISIT YOUR SENATOR DAY", MONDAY, JUNE 12, 2017!

YOUR 7TH AMENDMENT RIGHT TO A TRIAL BEFORE A JURY HAS BEEN DENIED TO MANY, MANY OF YOU.

Please include the following info:

1)      Your name, state and e-mail.
2)      Your Senators.
3)      The Mesh Product and Company Name implanted in you.
4)      Short list of Complications and the impact on your life. (2 short paragraphs at most)

Next describe your feelings about your lawyers treatment as follows. This does not violate your confidentiality agreements but merely describes your treatment by your lawyers related to getting you to sign the settlement agreement:

1.      Can you please describe if you were pressured by your lawyers to sign legal documents without a full understanding of how much of the money is going to the lawyers, and how potentially little in comparison is going to you?

2.      Why don’t you feel that your lawyers have been responsive to your questions or kept you fully informed about where the settlement money is going?

3.      Have your lawyers fully explained why you are being offered the specific amount of money they are pressuring you to settle for, and not some other amount?

4.      And could you describe any other ways in which you think your lawyers have not adequately represented you or kept you fully informed, or left you frustrated by their conduct in your case?

5.      Did you feel intimidated or bullied or disrespected by your attorneys? If so, in what way?



LINK TO LIST OF ALL SENATORS 115TH CONGRESS & CONTACT INFO 2017

COMMITTEE ON THE JUDICIARY

SUBCOMMITTEE ON THE CONSTITUTION

Majority Members:
5
Total Members:
9
Minority Members:
4

Members:
Members:
Cruz, Ted (TX), Chairman
Cornyn, John (TX)
Crapo, Mike (ID)
Sasse, Ben (NE)
Graham, Lindsey (SC)
Blumenthal, Richard (CT), Ranking Member
Durbin, Richard J. (IL)
Franken, Al (MN)
Coons, Christopher A. (DE)

DEAR MESH INJURED PATIENTS, BOTH PELVIC AND HERNIA,

I am, and have been, working in D.C. to expose the fraud and corruption at the FDA to get ALL MESH off the market through the House Government and Oversight and Reform Committee since I arrived in the D.C. area at the end of March. 

I am working with the House Judiciary Committee on their Bill, HR985“Fairness in Class Action Litigation & Furthering Asbestos Transparency Act of 2017” to get the Senate to take up their version of HR 985 to bust the corruption and fraud in the MDL's. There is language being added for transparency in the settlements in pelvic mesh litigation and other benefits to the mesh injured. Our goal is to rename it the “Fairness in Class Action Litigation & Furthering Asbestos, Pelvic Mesh and Hernia Mesh Claim Transparency Act of 2017” No one is protected by these lawsuits except for the pocketbooks of attorneys who are already extremely wealthy. Now Jane Akre is going to tell you this is bad because she makes a living from attorneys. No your civil rights will not be lost and there will not be an end to mass torts.

Your rights are CURRENTLY BEING VIOLATED in the Multidistrict Litigation in West Virginia.

Hard to explain my strategy in Congress. Guess it's like a salesman who keeps calling on a customer to get them to buy a product. Except I want the Senate and the House of Representatives to take action which will lead to taking mesh off the market. Johnson & Johnson, Boston Scientific, American Medical Systems and C.R. Bard all have millions and millions to pay lobbyists to go to Congress to keep their products on the market. Since I don't have millions, I use my knowledge and experience from being a medical device expert and legal consultant to present irrefutable facts to our elected representatives of the harm caused by mesh to get them to take real action to remove it from the market.

HR985 will never be signed into law as it is currently written. The Senate will pass it's version and it will go back to the House. And so on and so on like any bill going through the legislative process.

Elizabeth Burch who writes in opposition to the bill wrote a 64 page doc in 2014 "Judging Multidistrict Litigation" explaining how a handful of Attorneys "Repeat Entrenched Players" and "Repeat Entrenched Law Firms" have controlled ALL the MDL's for years now. I know those guys personally and they are cheating the hell out of you guys just like they cheated me. In fact Jane Akre works for some of them. I have worked within the MDL system for 7 years now hoping to influence plaintiff's attorneys. The MDL's are ugly for the injured plaintiffs. Just as ugly as the FDA. Just as ugly as mesh companies. A handful of attorneys in the U.S. make literally billions of dollars while hundreds of thousands suffer the consequences of the injuries from the corrupt manufacturer's products.


Support the legislation. Take charge of your own destiny. Stop the rampant hidden fraud and corruption in the legal system. Always find out who is behind the articles against the legislation that you read before you decide to accept it as fact. It is very complex. Look at the mission statements of the group's and their websites and their actions over a long period of time. Be your own judge!

© 2005 - 2017 Lana C. Keeton All rights reserved. Peace be with You.
This material may not be published, broadcast, rewritten or redistributed.
Med Device Expert LLC
Device Expert . Legal Consultant . Expert Witness . Patient Advocate
1602 Alton Road, #423, Miami Beach, FL 33139

305-671-9331 phone . 800-509-9917 fax
786-566-7780 . 305-342-8002 cell phones



Friday, April 21, 2017

SURGICAL MESH STILL ON THE MARKET. WHY? @ETHICON - @$JNJ MDL02327 PROTECTED BY PLAINTIFF ATTORNEYS? COLLUSION OR COINCIDENCE? MESH INJURED PATIENT....YOU DECIDE!


1.       Plaintiff Attorneys used an anemic trial strategy despite significant scientific expert evidence and knowledge to the contrary. Ambiguity remains. Hundreds of thousands of women are at risk from unsafe surgical procedures using synthetic surgical mesh in the female pelvis and reproductive system for serious permanent disabling injuries.

2.       Plaintiff Attorneys did not integrate all the causes of the harm from transvaginal mesh procedures in their strategy. The procedure, synthetic surgical mesh and trocar combined in the female pelvis and reproductive system are catastrophic along with comorbidities, age, concomitant procedures, again catastrophic.

3.       The Trial Strategy used was a limited concept of pore size which is difficult to prove and does not integrate the myriad physical and chemical properties of polypropylene synthetic surgical mesh and wound healing, critical to the understanding of mesh injury. Most important physical property: the polypropylene synthetic surgical mesh shrinks itself due to inherent manufacturing defects.


Synthetic Surgical Mesh remains on the market. Why?


1.       Plaintiff Attorneys,

2.       the American Urogynecological Society (AUGS)

3.       the American College of Obstetrics and Gynecology         (ACOG)

4.       Doctors such as Dr. John Miklos and Dr. G. Willy Davila

5.       Hospitals such as Cleveland Clinic and the Mayo Clinic

6.       the United States Food and Drug Administration’s   Center for Devices and Radiological Health (FDA’s CDRH)

7.       the director of the CDRH, Dr. Jeffrey Shuren, and David Krause, and other top officials at the FDA and

8.       Johnson & Johnson’s Ethicon

Kept mesh on the market by a series of events.


The events listed below culminated in plaintiff’s attorneys proving abdominal sacral colpopexy was a better, safer alternative procedure to Pleivc Organ Prolapse repair through the vagina in bellwether trials in the U.S. District Court for the Southern District of West Virginia.


January 2012: The FDA’s CDRH issues 522 orders to 33 companies for 99 products they must begin clinical trials testing their synthetic surgical mesh products for safety and efficacy.

April 2012: Dr. John Miklos and Dr. Robert Moore hold doctor conference in Atlanta. Henry Garrard III is only attorney speaker on the agenda. Topic of speech, how doctors can avoid legal liability when implanting mesh
April 12, 2012 Mass Torts Made Perfect Panel         
Abdominal Sacral Colpopexy recommended
Pelvic Mesh: How to Represent the Victims
Robert Price, Levin Papantonio Thomas Mitchell Rafferty & Proctor
Amy Eskin, Hersh & Hersh
Henry Garrard, Blasingame Burch Garrard Ashley
Lana Keeton, Truth in Medicine
April 27, 2012 Lana Keeton sends letter to all Plaintiff’s Attorneys in the MultiDistrict Litigation warning of the significant dangers of Abdominal Sacral Colpopexy including clinical trials
May 2012 Johnson and Johnson’s Ethicon will stop selling 5 of their transvaginal mesh products. Only the TVT Secur was removed and the rest of the TVT bladder sling meshes remained on the market.
GYNECARE ProliftTM Pelvic Floor Repair System
GYNECARE Prolift +MTM Pelvic Floor Repair System
GYNECARE ProsimaTM Pelvic Floor Repair System
GYNECARE GYNEMESH MTM Partially Absorbable Mesh
GYNECARE TVT SecurTM System (not all TVT products)
Ethicon also notified FDA's Office of Surveillance and Biometrics of their intention to make a labeling change to the Indication for Use for GYNECARE GYNEMESH PS Nonabsorbable PROLENE Soft Mesh indicating it for abdominal (open or laparoscopic) use only.
(ABDOMINAL SACRAL COLPOPEXY!)
With approval of the labeling change by the FDA, the 522 orders for their products were placed on hold and eventually  terminated since the orders were applicable to vaginally placed POP mesh products only. Sales continued in the US and globally under the then current indication until regulatory approval of the labeling change was obtained in each country.
June 2012: Johnson and Johnson’s Ethicon send letter to Judge Joseph Goodwin they are removing 5 products from market
September 2012: The applied for approval of label changes for indication for use to Abdominal Sacral Colpopexy was eventually signed by Dr. Ben Fisher at the FDA’s CDRH
This Very neat package NEVER publicized Kept Mesh on the Market for use in the Female Pelvis and Reproductive System. This, in my opinion, is a crime against women. It PRESERVES:
a.       Use of mesh for abdominal sacral colpopexy by doctors
b.      The mesh profits for Johnson & Johnson’s Ethicon         Gynemesh
c.        Injury to hundreds of thousands of women patients
There is NO LEVEL ONE (1) EVIDENCE of success
of abdominal sacral colpopexy despite decades of use.

COLLUSION OR COINCIDENCE?

Tuesday, April 18, 2017

WHITEHOUSE.GOV WE THE PEOPLE PETITION SENT TO WEST VIRGINIA MDL PLAINTIFF'S ATTORNEYS TO HELP MESH INJURED WOMEN GET MESH OFF THE MARKET!

Dear MDL Litigators,
Over 100,000 lawsuits have not gotten pelvic mesh off the market.
SO I HAVE CREATED A PETITION…..and the injured patients and the friends and families of the dead worldwide are going to do just that. GET MESH OFF THE MARKET!
Please join us by signing the Petition at WhiteHouse.gov. There will still be thousands and thousands of lawsuits as mesh is phased out of medical practice…so please, please sign.
WE'RE LIVE!! 324 SIGNATURES so far on www.WHITEHOUSE.gov.
GOD is GOOD!
LET'S DO THIS!! EVERYBODY "SIGN ONE...GET ONE"... We have 24 days to get another 99,676 signatures to reach 100,000!
PROTECT PATIENTS from DANGEROUS MEDICAL DEVICES, INVESTIGATE and END FDA CORRUPTION, FIRE FDA/CDRH DIRECTOR JEFF SHUREN.
Truth in Medicine Incorporated calls for an end to fraud and corruption at the FDA, the root of International Medical Carnage. In the U.S. alone, over 100,000 women are internally mutilated by pelvic mesh devices, over 33,067 women horribly injured by the essure sterilization device and hundreds of women dead from occult cancer set free in their bodies by a morcellator device used to remove fibroid tumors. Other countries follow the lead of the US FDA.
Hundreds of thousands more are injured worldwide. None of these women knew a surgery performed by their doctor would permanently disable, injure or kill them.
Under FDA/CDRH Director Jeff Shuren, ALL REMAIN ON THE MARKET. Remove these dangerous devices from the market now. Investigate and end FDA corruption.
Director Shuren "You're Fired!"
Lana C. Keeton
© 2005 - 2017 Lana C. Keeton All rights reserved. Peace be with You.
This material may not be published, broadcast, rewritten or redistributed.
Med Device Expert LLC
Device Expert . Legal Consultant . Patient Advocate
1602 Alton Road, #423, Miami Beach, FL 33139

305-671-9331 phone . 800-509-9917 fax

786-566-7780 . 305-342-8002 cell phones

Monday, April 10, 2017

PRESIDENT TRUMP, WHITE HOUSE PETITION ASKS PLEASE PROTECT PATIENTS from DANGEROUS MEDICAL DEVICES, INVESTIGATE and END FDA CORRUPTION, FIRE FDA/CDRH DIRECTOR JEFF SHUREN.


I just started a petition on the White House petitions site, We the People.

Please sign it now!

We the people ask the federal government to Propose a new Administration policy:

PROTECT PATIENTS from DANGEROUS MEDICAL DEVICES, INVESTIGATE and END FDA CORRUPTION,
FIRE FDA/CDRH DIRECTOR JEFF SHUREN.

Created by L.K. on April 10, 2017

LET'S DO THIS! WORLDWIDE! 

SIGN WHITE HOUSE PETITION!

SEND THE MESSAGE...WOMEN RULE!

GET MESH, ESSURE AND MORCELLATORS OFF THE MARKET.

FIRE FDA/CDRH DIRECTOR JEFF SHUREN.


HERE'S THE LINK TO SIGN THE PETITION:

https://petitions.whitehouse.gov/petition/protect-patients-dangerous-medical-devices-investigate-and-end-fda-corruption-fire-fdacdrh-director-jeff-shuren


Truth in Medicine Incorporated calls for an end to fraud and corruption at the FDA, the root of International Medical Carnage. 

In the U.S. alone, over 100,000 women are internally mutilated by pelvic mesh devices, over 33,067 women horribly injured by the essure sterilization device and hundreds of women dead from occult cancer set free in their bodies by a morcellator device used to remove fibroid tumors. 

Other countries follow the lead of the US FDA. Hundreds of thousands more are injured worldwide.

None of these women knew a surgery performed by their doctor would permanently disable, injure or kill them. 

Under FDA/CDRH Director Jeff Shuren, ALL REMAIN ON THE MARKET. 

Remove these dangerous devices from the market now. Investigate and end FDA corruption. 

Director Shuren "You're Fired!"

Thursday, March 30, 2017

LANA KEETON ON CAPITOL HILL...JEFF SHUREN, MD, JD, DIRECTOR OF THE CDRH...YOU'RE FIRED!




LANA KEETON AT WORK ON CAPITOL HILL

JEFF SHUREN....YOU'RE FIRED!

JEFF SHUREN, MD, JD, DIRECTOR OF THE FDA'S CENTER FOR DEVICES & RADIOLOGICAL (CDRH) HEALTH, OBAMA APPOINTEE IN 2009

SHUREN PROTECTS UNSAFE MEDICAL DEVICES, 
NOT PATIENTS!

NO. 1
GE HEALTHCARE'S UNSAFE MRI  
(JEFFREY IMELT, CEO OF GE, WAS OBAMA'S JOBS CZAR)

NO. 2
SYNTHETIC SURGICAL MESHES FOR HERNIA REPAIR, BLADDER SUSPENSION & 
PELVIC ORGAN PROLAPSE
ETHICON/J&J
BOSTON SCIENTIFIC
C.R. BARD
AMERICAN MEDICAL SYSTEMS
COOK MEDICAL
CALDERA
COLOPLAST

NO. 3
ESSURE STERILIZATION DEVICE
MANUFACTURED BY BAYER

NO. 4 
MORCELLATOR DEVICES FOR FIBROID TUMORS
WOMEN DIE WITHIN MONTHS FROM OCCULT CANCER IN THE FIBROIDS JOHNSON & JOHNSON & OTHER MANUFACTURERS

PRESIDENT DONALD J. TRUMP  

HUNDREDS OF THOUSANDS OF INJURED PATIENTS ARE ASKING YOU
TO TELL JEFF SHUREN, MD, JD, DIRECTOR OF THE CDRH...YOU'RE FIRED!

FDA CLEARED (NOT CLINICALLY TESTED FOR SAFETY AND EFFECTIVENESS) MEDICAL DEVICES ARE KILLING AND INJURING HUNDREDS OF THOUSANDS EVERY YEAR, EXPONENTIALLY INCREASING THE COST OF HEALTH CARE AND BURDENING THE COURT SYSTEM, MAKING PLAINTIFF'S ATTORNEYS MULTI MILLIONAIRES WHILE COMPLETELY DESTROYING THE LIVES OF UNSUSPECTING PATIENTS!

PLEASE, PLEASE HELP US!






Tuesday, March 28, 2017

LANA KEETON, WEEK TWO ON CAPITOL HILL!

Great meeting yesterday at Judicial Watch with a lead investigative counsel on the issue of fraud and corruption at the FDA/CDRH. He gave me direction and I will be meeting with him again very soon. He was an amazing source of information and I am very grateful to him for the 2 hours he spent with me. I want to expose the fraud in clearing mesh at the FDA.CDRH in hopes President Trump will look at it and make HUUUGGGEE CHANGES THERE! PRAY!!

Pics below


Thursday, March 23, 2017

LANA KEETON, A DAY ON CAPITOL HILL MARCH 22, 2017

A DAY ON CAPITOL HILL....

Yesterday I met with the House Judiciary Committee, headed by Representative Bob Goodlatte, who is currently seeking information from RELION, a lead generator for Plaintiff Attorneys for Mass Torts. Having worked with Mass Tort Plaintiffs Attorneys as a Legal Consultant, Medical Device Expert and having been a Patient Advocate through the patient advocacy organization I founded, Truth in Medicine since 2007, I have very valuable input to the House Judiciary Committee to protect Mesh Injured Patient Plaintiffs.

I also met with the House Oversight and Government Reform headed by Representative Jason Chaffetz and had the good fortune to actually meet and introduce myself to Representative Chaffetz. It was quite an honor.

MESH INJURED PATIENTS ARE FIRST INJURED BY SYNTHETIC SURGICAL MESH, POLYPROPYLENE, AND A MYRIAD OF OTHERS.....

THEN THEY ARE FURTHER INJURED BY THE COURT SYSTEM,  A TRAVESTY BEYOND WORDS FOR THOSE WHO HAVE LOST NOT ONLY THEIR HEALTH, BUT THEIR FAMILIES, THEIR HOMES, THEIR JOBS, THEIR INCOME AND THE RESPECT AND DIGNITY NORMALLY AFFORDED US.

THE SYSTEM WINS!

TIME FOR THIS TO STOP. TIME FOR LEGISLATORS TO PROTECT US FROM THE MEDICAL HARMCARE SYSTEM DESTROYING SO MANY LIVES!