| # | Name | Comments |
|---|
| 801 | Sigrid Auslander | Maybe now something will be done to treat people with chronic Lyme disease the way they should be treated and the arrogant doctors will educate themselves and not be afraid to go against the "New Guidelines". |
| 802 | Cheryl Jankura | I have been battling lyme for over 10 years. Five years undiagnosed with negative lyme tests from Quest labs. A combination of Eastern and Western meds have improved my health to a functional level. I can not work but I can do daily tasks, physical and mental. I can care for myself and pay my bills. I lost my dream house that was paid in full to doctors bills not covered by insurance but that was only a thing and I have most of my health back to be functional. I found out the hard way about the old saying-----You have everything when you have your health. |
| 803 | jeff wilson | |
| 804 | Jackie Hawley | I've really angry.
Jackie |
| 805 | Kris Carpenter | I have fought Lyme disease for well over a year. Never tested positive and I believe taking samento for the last year and a half has saved my life and I am on the path of beating this crummy disease. |
| 806 | anne ellerbusch | |
| 807 | Gabriel Paavola | |
| 808 | Anonymous | |
| 809 | Teya Reyna | |
| 810 | Brian Reynolds | |
| 811 | gul shujah | A Movie named Fitna is on the air these days,,,,The dutch showing the sign of their cowardness has made this film...Its against human values ..this cant be called freedom of expression,,its totally unethical,... |
| 812 | Donna | |
| 813 | Sandra Lawson | |
| 814 | Anonymous | A Multitude of Misdiagnoises, Information is refracted or withheld, Insurance companies dictating treatment while people suffer and die! Let us live! Give us a chance! |
| 815 | Linda Hooper | I have suffered from Lyme disease and co-infections for more than 30 years. I was diagnosed 2 years ago. Prior to this time, I was diagnosed with chronic fatigue. I'm lucky I'm not in a wheelchair. |
| 816 | Rita | Stop the political medicine of Lyme Disease and expose the truth about how epidemic and dangerous it is. |
| 817 | Sandra Carr | |
| 818 | Karen Stillwell | |
| 819 | Anonymous | |
| 820 | Therese Larsson | I think Lyme disease should be considered as the global health problem as it is, making lots and lots of people losing their health, hope, lives and families. There really is need for lots of serious research of the disease, testing and treatments, which also should be brought to light and attention of people everywhere. It is difficult and tragic enough to be ill, without being misdiagnosed or ill treated. I am signing this petition in hope of making a difference! |
| 821 | Luigi Saracino | |
| 822 | Anonymous | |
| 823 | Roxann Contrenchis | |
| 824 | Anonymous | |
| 825 | Chad M. Halsey | |
| 826 | Anonymous | |
| 827 | Fran Rosencrans | I have Lyme Disease, Cat Scratch Fever and Babesia from a tick bite that was not properly diagnosed by my local doctors, infectious disease doctors, arthritis doctors and many more. It all started in 2001 when I went from a healthy working girl to one that couldn't even walk. It took me 3 years of fighting with my doctors to no avail, the help of a Lyme doctor in New York and the IGENEX Lab in California to prove I had Lyme & other tick born diseases. It's too late for me to be healthy ever again. I have to live in a hurtful depressing body for the rest of my life because of the POOR TESTING NEPA has for LYME. DO something before it's too late for the rest of the world. You know you have the power (United States House of Congress) to change things. JUST DO IT for our children. I can't bear the thought of my children & grandchildren growing up in a Medicall world that is IGNORANT TO LYME DISEASE. It's about time the People of the world know how dangerous & cripling this disease really is.
Fran Rosencrans |
| 828 | carol marshall | Proper testing and treatment needs to be done |
| 829 | Terrie C. Williams | |
| 830 | Judy Krawczyk | |
| 831 | Leslie Benvenuto | |
| 832 | Bonita Hager | |
| 833 | Janet Bradford | Lyme disease and all of it's deadly co-infections has ruined my life as well as my 14 year old sons. This is to no fault of mine, as I have pushed and pushed for help for 18 years!! I was just diagnosed 2 years ago. I was happy, thinking "finally there is hope to have my life back!" WRONG!!!! I am still, even with + tests in hand, running into "It's all in your head!" Running into Dr.s that still don't believe in Chronic Lyme, some that don't believe in Lyme at all! Referrals denied by insurance companies. LLMD's that have had to opt out of excepting many insurances due to non-payment. Their consults and treatment so expensive that most cannot afford it! So.....the disease slowly takes away your mobility, independence, pride, cognitive abilities, and eventually your spirit!!
WHEN IS THE GOVERMENT, MEDICAL SPECIALISTS, INSURANCE COMPANIES, AND DOWN TO THE GENERAL PRACTITIONERS THAT WE WERE TAUGHT TO TRUST GOING TO WAKE UP!!!!!!!
WHY ARE THE MANY DOCTORS, NOT ALL BUT SO MANY, NOT FOLLOWING THE OATH THAT THEY TOOK WHEN THEY RECIEVED THEIR LICENSE; TO CARE AND LISTEN TO EACH AND EVERY PATIENT!!!
YOU PUT ALL OF THIS TOGETHER AND WHAT DO YOU HAVE--------A LYME CRIME!!!
IT IS ALL THESE WALLS THAT WE BANG OUR HEAD AGAINST THAT HAS TAKEN OUR LIVES!! |
| 834 | Anonymous | |
| 835 | Anonymous | |
| 836 | Terri Campbell, PhD | |
| 837 | teresa minett | |
| 838 | Pam R. | |
| 839 | Anonymous | |
| 840 | Mitch Clements | |
| 841 | Christy Nelson | Please stop the Lyme Crime and help this epidemic be known for what it really is so we, those suffering, can be helped and for those not suffering, to be protected.
Thank you. |
| 842 | melissa kerins | |
| 843 | Janis Krause | I have had lyme disease for nearly 20 yrs. All this time the only thing that has kept me funtional is using antibiotics off and on. It's either the lyme or other co-infections that must make it resistant. We need all studies be heard. We must take action! |
| 844 | Thomas Robey | Ask around, I'm sure you will find someone who has this disease or knows someone who has. Check further, and you will find people who are chronically ill and have lost many things in their life. It's time to bring this to light! |
| 845 | Anonymous | 2000 Virgina- Tick bite, over 48 hours attached. I am so sick, I have seen so many doctors and specialists, I am so discouraged, I cannot even say anymore. |
| 846 | Anonymous | |
| 847 | Tracey Rainey | Please, please, please allocate research funds for this devastating disease that I have suffered with for over 22 years. I was originally misdiganosed with Fibromyalgia therefore my treatment didn't start until much time had passed. Now I have a long, hard and depressing road ahead of me. This illness not only devastates the person that suffers from it, but their family, friends, employer and the list goes on and on. |
| 848 | Clayton Wright | I contracted Lyme disease in 1984 and have been misdiagnosed until this year. This disease is all over the state of Texas as well as the rest of the country. Doctor's are not acknowledging the disease at all.
Please, please investigate this disease further. We are long time sufferers and deserve a right to a healthy life. |
| 849 | Linn Vaught | It's time the IDSA (directly related to the ALDF that pretends to know something about borreliosis infections) is stopped from being the sole influence of insurance companies and the AMA for approved ways of treating borreliosis. The research is out there that BB exists in the host post antibiotics, and that lyme tests show false negative results which leave patients untreated for an infection that can be spread by blood and sexually to other humans. The scientific and medical communities need to look outside their tiny box and get a clue. |
| 850 | brittany Moore | |