Hi. My name is Candice Accola and I am so grateful to lend my voice to spread Lyme Awareness through Lymenaide.
Almost four years ago I was home in Orlando, Florida, visiting my family, and had the opportunity to catch up with one of my dearest friends, Teri Raser, whom I had grown up with.
In elementary school we performed together in our girl group, Girlzone. In middle school we were going to overnight camps. By high school we were double dating to homecoming.
We found ourselves on a friends porch, a year after graduating, and it felt like our lives were just starting. Teri, enjoying her new life as a student at University of Miami. Me, working to start my career as an entertainer in Los Angeles. We had a blast catching up and looked forward to whatever was next.
When, months later, she told me she was sick, I felt it was unfortunate, but I saw (and still see) my friend as the invincible woman. “It’ll pass”, I thought. With a continent between us and busy schedules, we didn’t keep in touch too often. Texts of “Hello’s” here and there.
Little did I know, while I was going on auditions, Teri was touring the top doctor circuit, reaching all the way to Columbia, trying to find out what was making her sick. What was causing her blackouts, seizers, blinding headaches, heat intolerance, and severe Autonomic Nervous System Dysfunction (can’t stand or sit up without blacking out after a few minutes).
Months turned to years. And years turned into a diagnosis of Late Stage Lyme disease. I could not believe it had been years and, not only was she still sick, but that she had Lyme.
All I had ever heard about Lyme was that you got it from a little tick bite. I never knew this disease was not so little. It has the ability to take over your life. I was shocked to hear about all of her symptoms and what this disease had put such a beautiful young woman and her family through. This disease had taken over my friend’s life.
I was even more shocked to learn of the politics revolving around the disease in the medical community. Doctors who’ve saved the lives of patients with Lyme getting their licenses revoked. Which made it difficult for my friend and her family to find a doctor to treat her. (Difficult is an understatement)
For such a complex disease, for all of those who have it, and for all of those working to find a cure, why do most people only know Lyme comes from a tick bite and NOTHING of what it can grow to become?
Why is almost every personal account of Lyme littered with a list of misdiagnosis’ by doctor after doctor?
Why was I not already aware of the seriousness of this disease when my friend told me she had it?
I admire the strength and solidarity of the Lyme community more than I can say with words. I’m ready to learn. I’m ready stand. I’m ready to lend my voice. Let’s Paint May LYME GREEN!
Please help by DONATING TO PAINT MAY LYME GREEN and participating in awareness activities this May!
Candice Accola plays Caroline Forbes on the CW’s hit series, The Vampire Diaries. Click here to see her CELEBRITY BIO

April 27, 2010 at 4:37 am
Thank you, well spoken. I also can’t understand all the controversies involved in diagnosing and treating Lyme disease. I had the tick, ALL the symptoms, but only 3/5 bands were positive. Yes, I got the 10 days of antibiotic treatment; I began feeling better. Two weeks later, BAM! Within the month, I was completely incapacitated. Told no, it wasn’t the Lyme, the antibiotics cured me. What else could it be? I became this ill after I found the tick. It was just a coincidence, think NOT. I just don’t understand. How much more clear cut could my diagnosis have been?
April 27, 2010 at 6:23 am
Candice, thank you so much for bringing awareness to this disease. I, of course, happen to be a fan of you and the show, but I think what you are doing here is commendable. Also, so glad you have now decided to join Twitter, what a perfect way to get your message out about the awareness of Lyme, and also connecting with fans that absolutely adore you! In us, you will find a group of genuinely caring people all over the world that will join you in spreading the word about Lyme.
I personally did not know much about the disease or the controversies involved. I’m so glad I stumbled across this blog post, I plan on reading as much as I can about it. Thank you so much for sharing your story. And my thoughts and prayers are with your friend and her family, and I plan on posting about this on the blog if that’s ok. I will even add a banner to our sidebar. What ever I can do to help spread the message.
May 14, 2010 at 2:09 am
hi Ruthie. i am the friend Candice is speaking about. it is so great to read your words-they so such genuine and honest intrigue into such a messy and devastating world. your desire to look further into it is really heartwarming and is exactly what a blog from Candice can do. she’s got a heart the size of the universe. sounds like youre a big fan…and rightly so!!
so, i clicked on your website’s link and saw that on your “Vampire Diaries Spoilers and News” site that you have put up a LYME green ribbon. thank you so much for that exposure, it means the world to us. i hope youve seen the PSA’s that Candice,Katerina Graham, and Kayla Ewell (all your vampire diary faves) each filmed for lyme disease. if not, the link to the main page is
http://www.youtube.com/user/lymenaide
there are PSA’s from other young hollywooders too as well as some lyme victims.
check it out. good luck with your website too, girl.
lots of love
teri
May 14, 2010 at 2:13 pm
Hi Teri!
Wow…Thank you so much for your wonderful words! You are right, I am a huge fan of Candice. And yes, I have seen the PSA’s and posted them on the site! I think it’s a wonderful thing they are all doing.
I’ve been reading stories of people affected by this disease, and it just amazes me what some have had to go through to get a diagnosis. Years and years of not knowing what was wrong or knowing and no one believing them.
So I am so glad that I am able to help spread the word about it!
Thank you again, for taking your time to respond to me. I’m so honored and I appreciate the encouraging words on the website. It’s been one amazing year, The Vampire Diaries is extremely successful and I bet you guys are so proud for Candice!
Take care, lots of love!
Ruthie
May 26, 2010 at 2:56 pm
Thank you all, for all of this. I’m trying really hard not to tear up.
Social media, sadly- yet fortunately, is the new way to reach people. It’s hard enough having an invisible disease, but one with so much controversy, with so little actual coverage- is that much harder.
Thank you for everything- and Ruthie, you are so lucky to have a friend who has stood by you, and more so has the ability to spread word through public arenas.
April 27, 2010 at 6:50 am
[...] fans, she’s also spreading the message for awareness of Lyme Disease. Recently, Candice shared her friend’s story with Limeaide, a community blog of those “living in harmony with Lyme”. Please take your time to stop [...]
April 27, 2010 at 8:02 am
I’m so glad that you’re doing this for your friend!
April 27, 2010 at 8:38 am
[...] We also want to help promoting a cause she supports to increase awareness of Lyme Disease. You can read the story she shared about a friend who suffers this disease and how you can support the cause, HERE. [...]
April 27, 2010 at 9:39 am
Awesome!!! I’m thrilled that the Lyme community is getting much needed celebrity support.
I had a lot of the same questions that she posed when my dad was sent to dr. after dr. with no answers, only to be misdiagnosed with ALS. 6 months passed before he was clinically diagnosed with Lyme disease, but the disease had already taken hold…
I too knew about Lyme disease, but only knew about dogs getting it…and definitely didn’t know the severity or politics of it. Each case I heard about was eerily similar to my dads…got sick, misdiagnosed, late stage Lyme disease.
Thank you Candice & her fans for joining the movement to stop this debilitating disease that so many suffer terribly with. =)
April 27, 2010 at 9:59 am
Is there anything we can do besides donating money? I love helping with great causes but being a college student I lack the funds to contribute that way. I do however am capable of volunteering for organizations trying to raise awareness. Thanks
April 27, 2010 at 10:55 am
There are all kinds of suggestions for how to help on this website. Go to the Paint May Lyme Green Page.
Paint your facebook profile Lyme green and spread awareness with us this May.
Ask all your friends to join and encourage those who can to donate to the project- http://www.causes.com/causes/457717?recruiter_id=106882238 (this is the link to our cause page on facebook).
April 27, 2010 at 10:11 am
Just wanted to say that as a child my lil cuz Robert got bit by a tick and got LYme fever we thought he was going to die but thank god he pulled thru it I wish you the best and in your fight with lyme I wish I had the money to help but I don’t right now but as soon as I can I will keep up the fight
April 27, 2010 at 10:27 am
Wow, what a story! I’m from Brazil and I’ve never heard about this disease… I just searched it and there are cases here as well, so why haven’t I heard about how serious it is? What you are doing for your friend and her family and all the other cariers of this disease and their family is great!
Let’s pain may LYME GREEN!
April 27, 2010 at 10:45 am
WOW, Candice, what a sad story. Thank you so much for sharing. I really hope you can make a difference by using your voice! I truly hope your friend gets better and cured.
April 27, 2010 at 12:17 pm
Candace,
I watched you grow from an adorable little girl with a dream to a beautiful young woman whose dream is coming to life. You and Teri always shared a special bond since 5th grade, Girl Zone, and lots of special memories.
As you know, she always believed in you and encouraged you to follow your dream even when others doubted it was reachable … and because of your perseverance, now your dream is bigger than life.
I want the world to know that you are much, much more than a great actress. You are an incredible person and a loving, caring, and devoted friend.
Thank you so much from the bottom of my heart for standing by Teri when so many others did not … Thank you for caring, for sharing, and for lending your voice to this noble cause … Thank you for giving a voice to the MILLIONS who are forgotten and unheard … Thank you for being the special person you are!
I know very well why Teri loves you so much. The entire Raser family loves you and will always be your biggest cheerleaders and fans!
My love always,
Helen Raser
April 27, 2010 at 12:17 pm
Candace,
I watched you grow from an adorable little girl with a dream to a beautiful young woman whose dream is coming to life. You and Teri always shared a special bond since 5th grade, Girl Zone, and lots of special memories.
As you know, she always believed in you and encouraged you to follow your dream even when others doubted it was reachable … and because of your perseverance, now your dream is bigger than life.
I want the world to know that you are much, much more than a great actress. You are an incredible person and a loving, caring, and devoted friend.
Thank you so much from the bottom of my heart for standing by Teri when so many others did not … Thank you for caring, for sharing, and for lending your voice to this noble cause … Thank you for giving a voice to the MILLIONS who are forgotten and unheard … Thank you for being the special person you are!
I know very well why Teri loves you so much. The entire Raser family loves you and will always be your biggest cheerleaders and fans!
My love always,
Helen Raser
April 27, 2010 at 12:30 pm
I appreciate every and all efforts made by supporters of this disease. It is so complex and so hard to understand. My friends and family only see me on the “good” days. Good days are days I can get out of bed. So it’s hard to see the true picture of someone suffering from lyme disease. So thank you for putting it into perspective for all.
April 27, 2010 at 12:41 pm
Thank you Candice and thank you so much to everyone involved in painting May lyme green.
April 27, 2010 at 1:16 pm
My ex-fiancee and still very dear friend was also originally mis-diagnosed, and it took doctors a long time to figure out the real causes of her illness. I would just like to say thank you Candice for speaking out and sharing your touching story. Lets get as many people behind this as we can. Thank you.
April 27, 2010 at 1:35 pm
[...] Candice Accola on Lymenaide [...]
April 27, 2010 at 1:47 pm
Candice,
You are a true voice for the unimaginable suffering for those of with lyme disease. Whatever you can possibly do to help and gain awareness is so appreciated!! I thank God for you.
Blessings,
Holly
April 27, 2010 at 2:07 pm
Thank you so much Candice for sharing this with everyone and helping to Paint May Lyme Green. All of us in the Lyme community truly appreciate all the help those without Lyme give to us, and the support with which they join us in fighting this disease. Your words are truly appreciated.
April 27, 2010 at 4:30 pm
thanks Candice!! well spoken! i hope your great love.
<3 Jamie Pos.
April 27, 2010 at 4:31 pm
Thank you so much for being a true friend to a fellow lymie…and while writing about how you see her suffer you support MILLIONS of lymies.You have a big heart and i will start watch your show more and Alexander Skarsgård. Greatful! Eva Stockholm Sweden
April 27, 2010 at 4:46 pm
Thankyou from all of us Lymies We love you for doing this for us ..Bless you..my prayers are for your Friend, and the rest of us who are not being heard..again thankyou!!!
April 27, 2010 at 5:56 pm
TY Candace for helping us to educate and bring awareness to our neighbors and surrounding communities. Lending your voice gives a voice to hundreds of thousands of Lyme patients across the nation; countless, yet real people, young and seasoned, who are so very sick and unable to speak for themselves.
I hope and pray that your friend is getting the help that she needs now. What a beautiful woman you are to speak out for her. We will all benefit and so will the hundreds of thousand others who need to be equipped so that they can advocate for their health and well-being.
Blessings, ~diana
April 28, 2010 at 6:34 am
Thank you so very much – we need people like yourself, people who are visible in the media to not only understand those suffering but also to educate people about how fast this disease is spreading, I was told it is in pandemic proportions now. I went to a conference and the scientist explained why ticks are more prevalent and why it is spreading.
Because of man’s disturbing the balance of our ecosystems, destroying many areas where the animals have lived, many of them eiter die or run off to find places they can survive. Lyme is mostly spread by the white footed mouse is what I found out and, when the animals that prey on mice are no longer there, the mice are left to carry the ticks, each one has thousands per lifetime on them, and their larvae drop.
Thus, we have more and more tick infested areas. BE CAREFUL IN NATURE! IT CAN COME TO BITE YOU! HAVE FUN BUT WEAR DEET OR SOMETHING ELSE JUST PROTECT YOURSELVES, AND LOOK OUT FOR TICKS ON YOUR BODY YOU WON’T ALWAYS GET A RASH!
April 28, 2010 at 10:34 am
Candice,
You are such a doll for posting this for Teri and all those suffering with Lyme across the world. It’s mind-boggling that there is so much misinformation out there about this disease and the havoc it wreaks on people’s lives. The medical community should be ashamed for ignoring this and brushing it under the rug for so long.
Thank you from the bottom of my heart for using your voice to spread awareness, and even more important to me… thank you SO much for standing by Teri when so many others didn’t. You are a true friend and I can tell you as her big brother that you mean the world to her. She speaks so highly of you and values your friendship more than you’ll ever know. THANK YOU, THANK YOU, THANK YOU!
With Love,
John Raser
April 28, 2010 at 10:38 am
Hey Candice, I just wanted to say very well put. It really does break my heart to know that such a great human being like Teri is having to go through something so terrible. From what I remember from the LHPS days she was always such a sweet, kind, and giving person. My thoughts and prayers go out to her and her family.
-Nida Khan.
April 28, 2010 at 11:51 am
AAAH! I read this post and was so touched–I did not recognize your pic until I read the bottom — and I am a huge Vampire Diaries fan! I will blame it on Lyme brain.
I wish when Lymies got bit they could just put on a scarf until the symptoms go away like Caroline did when she got bit by Damon. (I also wish the getting bit part was by a hottie like Damon, instead of damn bug.)
Your story is sweet and touching, and we appreciate the exposure. Taking the time to post your and your friend’s story is more helpful than you probably realize.
Thanks,
Mimi
(recovering lymie, and fan)
http://www.iammimi.com
April 28, 2010 at 11:56 am
[...] In case you’re out of the Twitter loop, the lovely Candice Accola is now officially part of the Vampire Diaries Twitter Club. (Someone make sure she receives her super-cool membership card.) You can find her at @CandiceAccola. Accept no substitutes! While you’re clicking that follow button, make sure to read her guest post on Lymenaide.com: Candice Accola Lends Her Voice to Lyme Awareness. [...]
April 29, 2010 at 10:25 pm
Candice,
Its so great that your lending your voice to this cause. I too Have loved ones that are affected by this disease and would love to help as well. I live in the LA area now. But please let me know how i can get in touch.
Kimberly Leemans
Americas Next Top Model Cycle 9
April 30, 2010 at 7:12 pm
[...] on the subject of Ms Accola, Candice is helping to spread the awareness of Lyme disease. Helping her out with this are fellow castmates Katerina Graham and Kayla Ewell. The pair have [...]
May 2, 2010 at 4:57 am
Hey Candice!
I think it’s a very good thing, what you’re doing to spread the knowledge about Lyme disease.
I leave in Poland, and here and all across the Europe we have a lot of Lyme disease cases. We also have some gouvernment programs to spread the awareness of its symptoms through the society, so that we can notice it very soon, when it’s easily treatable. I myself had the Lyme disease, but it was just in a form of a specyfic rash called erythrema migrans. As I went to the doctor with this, there was no problem to recognise it and just a simple 3 week antibiotic therapy was enough to get rid of it. So you can tell, it’s very important to react quickly if anything worries you, if you notice any symptoms, and to know that a simple “bite” may not be such “simple” and “innocent”.
Good luck with spreading that knowledge, because you’re doing a very good thing here!
May 2, 2010 at 11:10 pm
[...] FONTE: Lymenade [...]
May 3, 2010 at 7:34 am
Hello Candice.
I think you acted correctly,tell about the disease your friend. Many people are hesitant to do so and,sometimes even don’t want to communicate with a patient. Stumbling on your message,I read about this disease. You know,I study English by myself and,maybe I don’t understood something….. BUT I HOPE that with your friend will be all right and She will soon feel better. I think you’re a good person and loyal friend. Stay well. Good luck.
May 4, 2010 at 2:22 am
[...] historię jej przyjaciółki która przez lata chorowała na boleriozę, przeczytać ją można tutaj. Coraz więcej gwiazd przyłacza się do akcji i nawołuje do wsparcia i dotacji. Powstał [...]
May 4, 2010 at 7:04 am
[...] Katerina Graham and Kayla Ewell have been helping to promote the awareness of Lyme disease, with Candice blogging about her friend contracting the disease, and Katerina and Kayla contributing by making public service announcements videos. We have [...]
May 4, 2010 at 10:42 am
yesterday I read these message about Lyme and today (right now) I heard from my brother that he found a tick in our dog. My brother took our dog to the vet and now we wait until a tick will come out. My dog feels bad,he don’t wants to eat. I Hope that tommorow he will be feel better and everything will be good.
I wish all people never get sick Lyme or other diseases…. We must be Healthy, always…
May 4, 2010 at 12:26 pm
[...] Paint May Lyme Green! Posted by: Maddie · Category: Site Updates If you are following Candice Accola on Twitter, it’s likely that you’ve seen her many mentions of Lyme disease. She and other individuals (including TVD’s Kayla Ewell and Katerina Graham) are participating in the fight to raise awareness for Lyme disease, a disease that many people suffer from and that many others are uneducated about. For more information, make sure to visit Lymenaide. There you can learn about how YOU can Paint May Lyme Green, make a donation if your funds allow it, and read up on Candice’s story. [...]
May 5, 2010 at 11:18 am
[...] aqui Tradução: Tatiana Mareto Silva _________________________________ – Publicado Por: Fransciane [...]
May 15, 2010 at 8:07 am
[...] I received a notification in my inbox. Someone had replied to my comment that I made on Candice Accola’s blog post on Lymenaide. A blog dedicated to the awareness of Lyme Disease and a platform for those affected with it to [...]
May 27, 2010 at 2:59 am
Super great writing. Honest!
May 29, 2010 at 1:17 pm
Very awesome post! Honestly!
May 29, 2010 at 9:52 pm
If only more people would read about this.
May 30, 2010 at 1:47 pm
If only more than 37 people could read this..
May 31, 2010 at 6:59 am
Hah I am honestly the first comment to your amazing read.
October 3, 2010 at 2:02 pm
Thank you Candice for your courage and for putting a face to an illness that no one wants to, and for giving lyme patients a public voice. Thank you also for understanding the complexities of the disease, from misdiagnosis to treatment, and the politics involved. I’m sorry your friend is ill. I understand too well. In solidarity. You go GIRL.
October 4, 2010 at 11:31 pm
Candice,
Kudos to you for raising awareness to this insiduous disease and standing by a friend when very few people can truly comprehend the depths of suffering people with Lyme disease experience.
Your voice will reach a segment of our population, our youth, who may not take heed to warnings about a preventable disease; as well as the warning signs of Lyme.
October 8, 2010 at 10:47 am
Candice, there r no words to express my gratitude. God bless you for all you do to bring awareness to such a misunderstood, monster disease. My son 25 and me have it. I do believe half the battle with lymes.or any chronic. Illness is support,and understanding. The deficiency. In this disease is mainly do to lack of knowledge. The patients suffer just as much from possible removed compassion as well as the sickness. Thank you for your dedication in setting a foundation on educating the public. Many best wishes to you in future endeavors. I know my son and are extremely positive. Hugs and prayers. Jeannine
April 22, 2011 at 9:35 pm
I didn’t know much about Lyme disease before. Thank you, Candice, for bringing awareness to this disease. You’ve started a ripple of change and I admire you so much for that! <3 You're an inspiration to me in many ways. God bless you, your friend Teri, and all those affected by Lyme disease.
April 24, 2011 at 2:13 pm
OH LYME DISEASE My girlfriend at the time diagnosed me with MUSH FOR BRAINS M.F.B Said I partied my brain away turns out was a 38 year battle with chronic Lyme disease contracted in Lyme CT 1973 visiting a school buddys home and 30 years of continious exsposure as a logging contractor in CT
August 14, 2011 at 5:48 pm
[...] that are important to them; Candice Accola (Caroline) has been looking to increase awareness for Lyme Disease sufferers and Katerina Graham (Bonnie) has been helping raise money for The Water Project to help [...]
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