Sylviane Schwarz - My new personalized car license plate, Thankful for my healthcare provider that was professionally trained by The International Lyme And Associated Diseases Society (ILADS).
Amber - Great idea to use the Jumbotron to educate the public! It would be great if the message could scroll continuously on the Jumbotron instead of every 20 minutes.
Jamie Kane - Wonderful Idea! Thanks for being our voice.
zonia peraita garcia - En Miami, los medicos niegan que hay casos de Lyme, tengo 2 anos con test positivo y sin tratamiento. ACTUALMENTE MI RANGO ES 1.84 WESTWERN BLOT. Me siento muriendo poco a poco, tengo 69 anos. QUE HACER??, EN QUE PUEDEN AYUDARME, TENGO MEDICAID."
Angel Spell - went undiagnosed for almost twenty years and now faced with the possiblity of having infected my whole family, I thank all of you for campaigning for Awareness, it means alot to us lymies and our loved ones.
Sonya Hill - Brilliant way to spread the awareness... :) Thank you
Patty Williams - Thank God for the JumboTron, there needs to be much more Lyme awareness. I pray each day that the system that is allowing all this suffering will come to their senses......but they may never unless someone they love gets Lyme but I pray they don't. Nobody should be allowed to suffer like this. This is my wife Patty. She was told for years there was nothing wrong with her even after telling the Dr's about her odd rash that looked like a bulls eye. She has been bedridden for years, we simply can't afford to travel to a LLMD or pay for IV treatments. This disease is killing people including my wife. She has always been a strong lady but there is only so much we can endure. She has lost hope. My prayer is for a cure before it's too late.
Sharon Lee - I contracted Lyme Disease in Northern California in 1978! I was misdiagnosed and totally disabled for 13 years. Since getting the right diagnosis from an ILADS MD, I began treatment in 2003. Soon after, I returned to work. I am now 90%-95% well. ILADS saved my life! Getting the word out in a big way using the jumbotrons is a wonderful idea!
Crissy LaBruzza - I'm in LOUISIANA. Lyme is everywhere! Thanks so much for getting the word out, especially in areas where people think it doesn't exist!
sharon gallagher - please give us a chance to be heard.
Andi Robinson -
Bernice Lavallee - Bernice Lavallee passed away because of her exposure to Lyme-illiterate doctors. Doctors refused to believe Lyme Disease existed in Canada. They ignored the Bulls-Eye like Rash on her neck.
Beth Nelson - Thank you ILADS and CBS for the Lyme Awareness Campaign. I hope it can save many others from being diagnosed so late in the game. Public awareness is key!
Kelly Vranes - Thank you for bringing this disease to light. I have only had it for 5 years now and am amazed how those who have had it for many more years have continued to survive daily life. Thank you again for all you are doing for all of us.
Mason Kuhn
June Cormer - Thank you! More people need to know about ILADS as the primary resource for accurate and progressive information about tickborne diseases. This epidemic is not going away and sick people deserve access to the very best research and treatment protocols available. Keep up the good work!
Jennifer Navara - Thank you for this Lyme Awareness Campaign. I hope it will help save many others from misdiagnosis or being diagnosed so late in the game. Awareness is key!!
Trish - Thank you ILADS for this incredible opportunity to educate the public and bring awareness to our cause.
Amie Levasseur
Monica - I am very pleased that more awareness is being made, there is no support group in Tennessee, I have been sick for 4 years, my children and spouse are being tested too. Thank you.
J B F Sparenberg - I think if the Lyme disease is taken seriously a lot of other well known diseases will be taken by their roots.
Lisa Botto - Thank you for this ray of hope!
Marcia Jarosz - Thanks for getting the word out. All physicians need to be trained in identifying and treating Lyme Disease.
Andi Robinson - I am 32 years old and have been living with Chronic Lyme for about 7 years. Everyday is a battle.
Mary Seals - Thank you ILADS..... Misdiagnosed and treated poorly by the medical doctors for many years until finally being diagnosed in 2007.
Missy Jacobs - Great Awareness about this explosive epidemic with the Jumbo Tron, AWARENESS! BEWARE! Lyme Disease is everywhere!
Karen Boucher - Brilliant!
Silvia England - let's bring attention to this debilitating and so often misdiagnosed.
Pamela Ward - It's so great to get the word out about this debilitating disease that so many people suffer from. Finally after 4 yrs. of being misdiagnosed, I have recently been clinically diagnosed with Lyme and two co - infections in Oct. 2011. After going through a timelime of symptoms, I have been suffering from this disease for 22 undiagnosed years. Thank you ILADS !!
Michele Brown - Photo of myself and husband. I have had lyme for a minimum of 30 years. I have only been diagnosed as of 3 years ago and have had two treatments and still the bacteria returns. We hope to make a difference in the lives of others.And the Jumbotron! is fabulous... Hope that more event's can sponsor this effort.
Amber Halmon - I am 16. I have had Lyme since I was 3yrs old. My mom cannot afford to get me treated. Some days I cannot make it to school. Thank you for the opportunity to help show the world Lyme disease is real.
kevin macisaac - chronic lyme disease
Amie Levasseur - It is so exciting to get the word out about the danger and prevalence of lyme disease on such a large scale, and have visuals showing just how many people Lyme Disease affects. Thank you!
Lisa DeBartolo-Martin - I am so grateful! Thank you for placing this JumboTron, in the middle of Times Sqaure. I am a Lyme disease patient, and I pray this will start bringing more awareness of how devastating this disease is. AIDS has so much awareness now, and I hope that Lyme will get the same attention, awareness, coverage, and medical assistance. Thank you again...Lisa - Idaho
