Yolanda Foster's Experience With Lyme: LRA Gala

[@cornelisverhoef9282]

She was in my class in high school in Papendrecht in the Netherlands. What an incredibly strong and intelligent woman she has become..

[@serahnock6025]

This speech hits home and speaks the heart and minds of everyone who suffers from Lyme disease. Thank you.

[@CharlisCraftyKitchen]

Great to hear more awareness being spread about Lyme disease.

[@basque727]

Thank you so very much Yolanda. I have had Lyme for 21 yrs. I have seen 30 drs in 16 yrs. I hope that you kick Lyme's butt. You are an awesome Lyme warrior!

[@janeeiseman]

I cried with you during this very eloquent speech. English may not be your first language but you summed up what we go through perfectly. It's funny how an illness makes us all more human. You're no longer just "the woman with all the money", you're a Lymie just like the rest of us. I'm no longer jealous of your cars and homes and clothing...I'm just jealous of your lemon trees! I hope your recovery continues as mine has just begun :(. Be well.

[@infowazz]

my mom's good friend up in the Albany area got diagnosed over a year ago and now she is super weak and depressed. she is not married and her 2 kids stop by to help. it breaks my heart because she is one of those special sweet people that are rare in this world. she retired and has a little barn with a horse and assorted animals. she used to make stained glass. really amazing person. i am now going to devote my extra time to see what i can dig up to help her. i am very good with doing this sort of thing. for instance, i believe Lyme Disease is manmade. a byproduct of bioweapon testing on Plum Island in Connecticut.

[@norbertsmom]

YOLANDA IM SUFFERING FROM BREAST CANCER STAGE 3. YOUR SPEECH WAS INSPIRATIONAL. WE BOTH HAVE A TOUGH JOURNEY. I WILL KEEP YOU IN MY PRAYERS IF YOU KEEP ME IN YOURS. WISHING YOU MANY BLESSINGS

[@elitetone]

Thank you so much for describing what it is like to have lyme disease. I could not have said it better than myself.

[@amandaf6390]

Yolanda, you couldn't have expressed what we all go through any better. You did great!!!!! We love you!

[@Robertitoseminario]

Bravo Yolanda! blessings to you and your family

[@floratoadfoot]

Thank you for having the courage to stand up and speak on behalf of all the Lyme sufferers around the world. You said it as it is... !!

[@mrs.jillsansouci702]

Having had Lyme disease and suffering with all I went through, we need more support on this disease and research. Maybe a ice bucket challenge or something to raise money for this would be good.If you have had this you would be interested in starting such a fund raiser

[@jd749]

How about a Tea-Bagging challenge?

[@angelerice3819]

Thank you for being a Lyme Disease Advocate! In a day and age when even saying you have Late Stage Lyme Disease is a politically charged topic. We have needed more people with influence to speak our stories. I pray your Lyme journey is smooth with recovery in your sites. I hope in the future you continue to help us. And by the way we speak Lymie and we understand fog brain :) We are more than glad to support a fellow Lymie Warrior!

[@annettekramek2917]

Thank you so much for speaking out, I have just come to the deep realization of how complex this disease is and how all of us healing need each other. I will look to see how you are doing now. Blessings.

[@ellelon]

Wow Amazing! Exactly what I went through. I'm so thankful she is using her fame and influence to speak up and be an advocate. It is sad that with all the controversy surrounding lyme disease I almost feel like I'm not even allowed to mention what I've been through to people. Having to hide it from mainstream doctors, the general public having absolutely no idea how incredibly sick you get from this disease. Being scared, with no support system and raising two kids alone all while being so sick and feeling like I was losing my mind has taken every last bit of strength I had. It has been a nightmare, a 5 year long nightmare. All my savings are gone, I cannot work, I get no child support. I just hope I am well enough to work again some day. I've never been so scared in my life. What a great video. I'm so glad someone is speaking out for all of us.

[@anaa7836]

ellelon how are you ?did treatment help with your symptoms ?

[@CathyRadkecureistolaugh]

I can relate to your story Yolanda. My daughter has suffered from seizures undiagnosed since 2012, our struggles are so similar. I was the caregiver and my daughter is 24. Now I too am a caregiver advocate and am so excited to have some one with your power speaking out. Could you continue to mention the struggle and effects it has on families. So sorry your hurting but together we will smile again with your help.

[@terriworthington2663]

Thank you yolanda!!!!!!!!!!!!!! we MUST get the word out, save our lives and the lives of others.

[@ronunger5212]

Thank you Thank you Thank you Thank you !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!Sooooo much !!!

[@onemelissa2003]

Thank you for creating awareness. From a fellow Lymie!

[@marciephalen9443]

Thank you, thank you, thank you. My brother battles Lyme and it breaks my heart. Well articulated and it really hit home. My biggest prayer is that he gets better one day. This was amazing yet difficult to watch because I feel the pain and know the struggle is very real.

[@susanpatton6477]

Hi Yolanda Thank you so much my daughter has just turned 17 and has chronic lyme disease luckily we are getting treatment in Connecticut, hopefully she will make a full recovery please continue to fight for us it is just ridiculous that people are not being helped. I cryed when I saw your video it is a nightmare for the caregivers as much for the sick person the worry. I only hope there will be help one day for everyone, if only the doctors would wake up. Love to you

[@lymemom7914]

Thank you for sharing your story! It helps bring awareness to the rest of us still fighting this horrendous disease. Thank you for being a light for all us lymies!

[@joannahudson2005]

Thank you for your courage! I saw you segment on GMA this week. I have been suffering with Lyme for three years so I can relate to your nightmare

[@chriso.8806]

You are 1 of my biggest influences and thanks to you I still have strength and hope. I have a bunch of autoimmune diseases and recently found out I have Lyme w 3 co infections. Not much hope for ever recovering completely but honestly trying my best. My bf of 10 yrs just dumped me too. It's made my struggle so much harder. I really did depend on him. Its not his problem. He's got it to and is progressing beautifully. I cannot keep up. Yolanda, you keep me going and hearing you actually brought a smile to my face. That's a lot of work. ☺ Thank you for being so relateable. I wish I could afford to give. Someday soon I hope. God bless you.

[@TheInvisiGyrl]

Thank you, Yolanda, for highlighting the struggles and changes that happen with undiagnosed Lyme Disease in US. You ARE lucky to be and have a wealthy and most importantly, supportive, husband and family. I can see you wobble on stage ( I too cannot stand in one place for more than a minute) I can see fatigue and how much you want your life back. You ARE lucky Yolanda, and an inspiration to us who do not have the resources you have had, to feel even a little bit better.

[@HouseOfAqua]

I have had many extensive workups and our system is frustrating. Many doctors rely solely on labs, fail to look outside of the box when diagnosing and treating, almost always drugs to treat symptoms. Thank you for sharing!

[@barbarabarney2317]

This story is such an inspiration, and each of us should take up the challenge and spread the word far and wide. I have had Lyme and co's since I was about 10 and I am now in my 60's was diagnosed with CFS almost 30 years ago, I was one of the pioneers. Only 2 1/2 years ago was I confirmed with testing, 2010 it was only a clinical diagnosis. It has been an extremely horrible and devastating experience. One LLMD recently said to me, that I don't know what it is like to feel normal. What a pity!!!! But I will give it my best shot to help others!! Thanks, Yolanda, sorry for your experience, but making this national spotlight, I know others will be helped. We must work together, hope is eternal!!!

[@neidinallen8241]

Thank you Yolanda! Thank you for spreading awareness!💚💚💚

[@TheIanlandry]

You are such a good woman!!! What an inspiration .. Love you

[@susanpainopraseuth2097]

Thank you, thank you, thank you for taking the time and energy to share our real struggles!

[@lisettetrela4934]

God bless Yolanda!

[@Up2Late2]

Wow! If she is still sick, I love to see her when she is fully recovered, because she looks great!

[@gregschneider4081]

Cannot thank you enough for voicing the nightmare that we live through - hope has finally been restored in my family's life, after 9 years of hell, thanks to finally finding the right doctor...thank you thank you thank you for voicing this to the large audience.

[@Pumpkin_The_Morkie]

What doctor?

[@debbie7526]

How awful & agonizing to not know why a person is so sick. To be told the person is just overworked and in some cases, crazy & lying about their symptoms. Glad there's more awareness now of Lyme disease.

[@merlodge]

Thank you so much for saying what many can't

[@Afura33]

Thank you for speaking about that

[@cesare-ferrari]

Thank you for spreading awareness.

[@Duzerma]

Thanks Yolanda, please keep telling your story to educate others about Lyme Disease.

[@rachelmcdonald1]

Tears running down my eyes listening as you speak after I, myself, living the feeling of having lost the woman that I once was too-an intelligent educator and mother. We have spent so much money on treatments and I still am not where I once was. I pray that the medical field will listen and respond to help diagnose and treat so many who are suffering, and find a true cure-so that we may take our lives back once again! Thank you Yolanda and to all the LRA and LDA supporters.

[@martineschoup310]

Thank you so much Yolanda ! I am so surprised you came to Belgium for treatment....:) After being undiagnosed for many years I finally tested positive for lyme when I changed from family doc. After months of oral abx I felt almost without symptoms...right now I am as sick as before.....it's like you say...it's a struggle to get from the bed to the bathroom....Thanks again for sharing what we all going trough.x

[@anaa7836]

Martine Schoup how are you doing ? hope your feeling better ? did you have any neuro symptoms ?did you find anything that helped ?

[@kristenlewek3594]

True of what she's saying. And with hospitals and government that can't push forward of using the word HELP!

[@mayamithraca]

Thank you for speaking so eloquently, Yolanda. We are a sick and tired community (my daughter has suffered over fourteen years so far) but the truth is our mantra and we will be heard. Love to the community!

[@JawbonesintheDust]

Bless Yolanda xxxxxx

[@Levi4980]

Thank you. Thank you. Thank you.

[@MsAldousSnow]

thank you for this upload, and thank you, yolanda, for using your resources, status, & experience to raise awareness for all of us!

[@theonlynikkijo]

Thank you thank you thank you a million times over. You put into words so eloquently the reality of this dreadful disease. I do not know if I have Lyme, so far I have been diagnosed with M.E (CFS) but have not got the money for Lyme testing. I have been sick since I was 17, am I now 32. We have long needed someone like you to speak out for us, I am only sorry you have had to suffer this awful disease as well. I'm so glad you have your wonderful husband and children for support

[@MustangsTrainsMowers]

I’m one of the first people in Minnesota to get Lyme disease which happened between 1982 and 1984 with a bullseye rash on my right upper arm. The first Lyme disease diagnosis in Minnesota was 1980,,, the 4th Lyme disease diagnosis in Minnesota was 1985. I wasn’t diagnosed until 2013. I have posted several Lyme videos in the last 5 years.

[@nourao8482]

i truly believe that very soon we ganna find a cure for this disease. prayers for you Yolanda and everyone suffering from Lyme disease.

[@annlanders978]

+Roadside Stew I don't think she got antibiotics fast enough. You need to catch this disease in the first few weeks.

[@soonermimi53]

ann landers so true.

[@Toril64]

There are a cure in US and Polen. S. O. T. I have done that treatment, and I feel so must bether now. Remember S. O. T.

[@sonyafly]

I love you Yolanda.

[@monikkohnke2757]

Thanks God my Doctor caught in time my Lyme disease i am fine now but the migrane are horrible yes i always was very very tired :(

[@amandalynne9314]

Thank you so much. Thank you

[@HudsonValleyHandymom]

There's hardly a family I know who has escaped Lyme where I live...in New York and on the border of Connecticut. Fortunately, it's one of the first things doctor's look for here due to it being prevalent. Unfortunately, only one member of my family of six escaped it. It really is worse than people know.

[@tinagoldman9335]

Thank you Yolanda for such a wonderful speech, i my self have gone through many doctors and given the same answers as you.After doing a lot of research i found Igenex in California and they are sending me my kit to get tested. I have all the symptoms, I quit my job in January and been progressively getting worst each day. I live alone and i have never been so scared for my life. I live in florida and theres no one that will help me. Ive applied for disability and was told it could take up to year. I know once i get the medical attention i desperately need, i will let my voice heard to prevent people to suffer like my self. God Bless you, Tina Goldman

[@carolynhamilton9728]

Tina Goldman hi, I hope you have found a lyme literate doctor in your area. Wait out the one year for disability, they will back pay you from the day you requested it, so if it takes one year, you will be paid for that. can you get general assistance and a food card ? you can always contact lymedisease.org for help finding a llmd. "be kind for Lyme" has a lot of help along with "ILADS" and many other groups. go on your local lyme disease groups for help. Google llmd in - your area , and contact only ILADS supported groups, approved groups. blessings.

[@soonermimi53]

Tina Goldman I got my positive diagnosis there about 10 years ago through a doctor in TX who started treating me for my "fibromyalgia." That's the first test he ran. I have been sick now for 30 years. Most people don't even believe there is a place to get a blood based diagnosis. They think the only way is clinical.

[@StandUpAndThrift]

Thank you!

[@TheInvisiGyrl]

Me - 45+ years infected and counting, no help, no treatment, not even a car to get to the Dr. in. Family does not recognize and prefers to judge, incorrectly, that I am lazy. My childbearing years - gone. Too sick to date and marry, I am alone, poor, struggling to stay alive - I ask you what should -I- live for? AWARENESS I guess. You do give people like me some hope, Yolanda, thanks for speaking out - not for ourselves, but those that follow.

[@geguessman6441]

49years

[@ritaj7080]

I have a chronic disease , I relate so much , it is indeed a lonely battle your body doesn’t belong to you

[@lelamoore7178]

awareness and a cure. thank you.

[@teresadixon2559]

Living as a nurse in England I had heard of Lyme disease but never come across it, or in even looked into it. I did not realise what a dreadful thing it was, how it could affect people mentally. I was even more shocked find out how widespread it was, yet so little research has been carried out into finding either a cure for it or at least a drug to stabilise it. Is there a reason for this?

[@Cazanu417]

there is a cure but for lyme disease the cure is basically 14 to 28 days of antibiotics sometimes intravenous if there is severe damage,what she thinks she has is chronic lyme disease wich is not scientific proven by any study that was done is more of a fake disease created by some quack doctors called llmd to make some money and have a pretty big cult like following that believes they have it most of them are white females in their 40s,

[@2000balumba]

This is seriously offensive. Just because there is no diagnostic test doesn't mean that it doesn't exist. It hides in tissues and not blood. Why would someone make this up even if there are white females in their 40's. I wouldn't wish this disease on anyone but i wish it on you-maybe it'll teach you compassion.

[@soonermimi53]

Joanne Roberts actually there is a place to get a REAL BLOOD TEST for Lyme disease. The "gentleman" you spoke to did not realize that at Igenex Labs in CA I tested positive for the disease. It is really strange that dogs can have chronic Lyme and they can test them for it, but there is only one place in the US That I know of that does. I imagine Dr. HOrowitz in NY can get it done somewhere there, but I do not know. There are several good doctors in that area who treat this terrible disease and they are very well respected men practicing out of some of the most prestigious hospitals. Thank you for sticking up for the several hundred thousand victims of this disease as even recognized by the CDC. What an ignorant man

[@soonermimi53]

JaCk MeOff I got my diagnosis from Igenex Labs in CA. Even the CDC acknowledges that "at least 300,000 people, and maybe up to twice that many, have chronic Lyme disease. If you don't believe US, men, women and children that are victims of this disease, the families of the victims, the GOVERNMENT agencies, then who do you believe? From your attitude, it's obvious you don't really have to have any basis, just whatever you choose to believe.

[@Cazanu417]

LeAnn Cottman oh please with the conspiracy bullshit,the lab you have been tested on wasnt an infectious disease hospital lab go to your local hospital and get an ELISA igg if afther this much time its negative you do not have lyme disease,that igenex it is not regulated and used by quacks giving lots of positive results and is to be avoided.unless you want to get scammed,horowits is the biggest scammer of all,why with 12000 pacients not one single trial of his treatments actually working or his pacients actually being sick with lyme disease,compared to 2 gold standard studies that says otherwise, its all a scam but hey if you dont have anything to spend money on and destroy your health with pointless antibiotics for months and months so be it,but you should trust real infectious disease doctors they are there for a reason not some scammers that sell books and wicthcraft treatments for disease that dont even exist .

[@indirapersaud5328]

I LOVE YOU BEYOND WORDS. I am praying for you my dear.I would like to contact you personally....... You have thought lots of us about positive thinking. Love seeing you in your own atmosphere Amersterdam. God blessings to you for beating this horrible disease.

[@sweenykim]

Good for you and many thanks Yo! Your efforts help elucidate our cause on a broad scale. When and if the time is right, would be nice to see you, your husband, Daryl Hall, and other affected notable individuals to speak out publicly, perhaps via a state, NIH and/or Congressional Health Subcommittee hearings on our chronic Lyme dilemma. Perhaps a David Foster & Daryl Hall presents: "Lyme Aid" Concert to benefit the LRA, Columbia, TBDA etc is also be a thought.

[@liesh705]

Yolanda, je bent een Power woman! Keep fighting the ignorance to save lives.

[@2385437]

my 31srt year lymes this april 2015,took 5 years 1989 first treatment.GETTING LYMES 12 TIMES HERE CENTER OF MINN,MY RANCH.BABEISIA AND BART TOO.I KNOW LYMES BRAIN ALL TO WELL OVER YEARS..NOW THIS MY 25TH YEAR LYMES ADVOCATE HELPING OTHERS, geof steiner cushing minnesota.pop 65.

[@normajeanmonroe4404]

I'm fighting illness like this same symptoms and all my tests came back normal accept my blood count shown my white blood cells are not building up as fast as they should.

[@hiphopboy711]

Wow...

[@aceman1969nlb]

👍❤️👍❤️. Total truth.

[@dtandoc]

Maybe you can try ACT- Advanced Cell Training. I am still on it. If you have Facebook...try to go and visit and see the testimonies of those especially have graduated.I hope it will help you.

[@Emotionalenlightment]

I teach Lymies EFT emotional freedom to get rid of fears, panic & other negative emotions from past & presence. They seem to be correlated to what is happening to brain & body. My clients are healing with rife machine, salt treatment, aroma therapeutic oils, homoeopathy, & some herbs. Until medical treatments are in place, this substitute/combination of few things together seems to bring good results. Thinking of all of you out there. Dana Ritchie

[@thewhittlingwood6985]

I carry this/i understand this ...my nightmare started 3yrs ago.i thought being autistic was hard enough.u knw the way ppl can treat you..i was a very happy mum wife..a self taught woodcarver/desp wanting to be a chainsaw carver...best time of my life.till the bite. Like a fresh coloured painting an someone throwing water down it.best describes things.within mnths i ended up in a wheelchair/bedbound for most..i agree with yolander.easier to hear anther speake.out i carnt get my words out.i.e neuro probs.last year i had 3 events like strokes.total loss of feeling always leftside .and lost my speech.we are jst into 2018 ive already had 2 events loosing my speech or asphasia..as a family it crushed us.because i spoke out.i never got the help we should of had.i am grateful for my family.and for every breath ..i carve relief bits n bobs when my body permitts..so i dnt lose who i am totaly.i had to reteach myself how to move.eat.talk..i struggle with so many things.i try hard each day.if i push to hard i get sick.i dnt take anything for granted.my husband is my carerxx Lastyear

[@Hk78666]

So sorry it's horrible dieseas how r u now in2022?

[@thewhittlingwood6985]

@@Hk78666 ill most days .some worse than others.

[@Hk78666]

@@thewhittlingwood6985 any tinny recover is it possible that lyne come immediately with severe disabilities with Neuro symptoms after c vax?

[@thewhittlingwood6985]

I've not had vaccs so I can't answer.i use lots of herbal stuff.i have good an bad days.but better than I was

[@Melanie_Rijkers]

Wish we had Yolanda here ... 'Zo Niet Saar' (Facebook page of young mother of 2, suffering from neuro borreliose stage 3) is also suffering the same symptoms... I reckognize every word of her story in Saar... yes, we need money, heaps! to cure this new danger to public health

[@lelamoore7178]

yes mam.

[@ionaworld7034]

Love you yoyo. Am going through hell. Got diagnostic finally in germany.but treatments long.can hardly walk. Cough. Vomitting. No appetite .insomnia.pains pains....its shit. C est la vie ma cherie. Ruined me and my family and kids. Xxx

[@who9and10]

Very powerful. However, one issue with what she said. There IS an established treatment protocol, written by Joseph Burrascano.

[@Miss_M85]

💚💚💚💚💚

[@jaymcquhae]

finally..she is being treated with the best ..RHP ozone therapy

[@Securityinc1]

I had Lyme. After a year on antibiotics I was getting worse. I was cured in under two months using a Rife machine. Have a great day.

[@soonermimi53]

Securityinc1 I have one but it is not working for me. Tell me how you used it please.

[@jb-fp2vs]

I was wondering what the indigenous people did when they got lyme eons ago????? I have been on a pic line with 2 bags of meds for one of which was stopped when my blood work showed me losing health. I was going to an infectious disease doctor whom could really not help me. I finally found a Lyme disease doctor whom said I had been on those meds long enough and I had her take out the pic line. I can not say whether I am rid of lyme as she told me there is no test to tell me if it is out of my body only a test to tell me it is in my body I hear people talk as if having lyme is nothing......but I can only hope that they do not get it western New York state is now getting more and more cases. but no one is taking it seriously and no one is doing research to find a cure so I live with it in me

[@tarnsand]

Yolanda once mentioned that she and David bought the piece of land in Malibu where she says she 'had a hand in building every inch of from the design to dealing with 100 workers every day for months to every detail of the decorating. I don't know how I did it'. There are literally hundreds of neurological diseases. When she describes her symptoms it sounds a lot like Adrenoleukodystrophy-middle age onset for which there are no medications or cures. You look healthy but suffer from exhaustion and you can do everything until you cannot do anything. But in between suffer from numerous infections some moderate frontal lobe deterioration.

[@carolynhamilton9728]

Tarn Sand She has "lyme disease" and has gone through all the same things that all lyme infected people go through, including myself. I was in perfect health when I went camping for 3 days. I came home and found a tick that had fallen off my back shoulder blade, and some blood from when it was attached to me, there was a picture perfect erythema migrans - bulls-eye rash on my back shoulder blade. I was diagnosed with lyme disease at an emergency room. The lyme literate M.D I started seeing ran all the appropriate lab work, done at Igenix lab in California. the results showed up that I also had 2 co infections, Babesia and Rocky Mountain Rickettsia along with the high lyme levels as well. Yolanda and her two youngest kids all have lyme disease. they lived on a horse farm and we're avid riders. horses, just as deer, carry ticks. it's obvious they were bit by a tick or ticks, you no longer only get tick bites in the mountains or forests, there are more ticks in your backyard and garden that people are getting bit by and never feel them because they are the size of a poppy seed about this size > • She has been tested positive for Lyme Disease and co infections, she has lyme disease. She even mentioned that in her speech, which is now very out of date. some places that say they treat lyme are not approved by ILADS or regognized by the lymedisease.org such as a place in Florida. ... true LLMD 's do know how to help you.

[@carolynhamilton9728]

Tarn Sand She has "lyme disease" and has gone through all the same things that all lyme infected people go through, including myself. I was in perfect health when I went camping for 3 days. I came home and found a tick that had fallen off my back shoulder blade, and some blood from when it was attached to me, there was a picture perfect erythema migrans - bulls-eye rash on my back shoulder blade. I was diagnosed with lyme disease at an emergency room. The lyme literate M.D I started seeing ran all the appropriate lab work, done at Igenix lab in California. the results showed up that I also had 2 co infections, Babesia and Rocky Mountain Rickettsia along with the high lyme levels as well. Yolanda and her two youngest kids all have lyme disease. they lived on a horse farm and we're avid riders. horses, just as deer, carry ticks. it's obvious they were bit by a tick or ticks, you no longer only get tick bites in the mountains or forests, there are more ticks in your backyard and garden that people are getting bit by and never feel them because they are the size of a poppy seed about this size > • She has been tested positive for Lyme Disease and co infections, she has lyme disease. She even mentioned that in her speech, which is now very out of date. some places that say they treat lyme are not approved by ILADS or regognized by the lymedisease.org such as a place in Florida. ... true LLMD 's do know how to help you.

[@michellecoronado4608]

Help me please I am in Texas !!!

[@MRAIDANGWALSH]

I want you completely 100% well do not get me wrong but at the same time do not settle for a full lyme diagnosis because tesearch is pointing to more than lyme infections...Also lyme tests as you are fully aware not reliable plus these tests also indicate 'antibodies' turn on the same for ebv, cmv, hhv6 etc. Some top molecular biologists believe this is actually 'internal ionization radiation injuries', I do not mean to worry or scare you Yolanda want you to be fully aware ok 'get well princess'

[@dacek5804]

💔

[@HouseOfAqua]

I had many extensive workups,

[@tinaneaderhiser9127]

🔥💥😍👍🤗👏🥰💥🔥

[@drinkallthesunshine]

"I finished filming my season of Beverly Hills Housewives".... Bitch please.... Take a damn seat.

[@annlanders978]

Exceptional woman. What is she doing with the likes of David Foster?????

[@soonermimi53]

ann landers I do not think they are together anymore. You need to check me on that to be sure. To this day, she is still sick.

[@elaineclementsfinn1872]

Wrote a Lyme disease brochure with the help of two Lyme specialists. Will email a copy to anyone interested.

[@elaineclementsfinn1872]

+Beth Shatara NOT SPAM.....spreading good information !!

[@dayamix13]

[e-mail]

[@rhondamyers4277]

Its not privilege its called hard work

[@annlanders978]

I don't understand this. Back in the 80's they knew how to test for Lyme Disease. Two main simply tests. Why didn't she get them?

[@lymestats3855]

+ann landers Hi Ann, the ELISA test is only meant for general field studies and has a 49% success rate. Lyme is a clinical diagnosis. This is all on the CDC website... People have different symptomology at different times and there are multiple ways of contracting Lyme and co-infections. More info can be found at ilads.org

[@Cazanu417]

she got them they were probably negative so she found a llmd who diagnosed her with chronic lyme,lime literate dr is bassicly a quack who profits off people with unspecific symptoms and believes in a version of lyme disease with no rash,no positive tests, just other 300 symptoms that the human body can feel even farts i think is a symptom

[@soonermimi53]

JaCk MeOff you are an uninformed jackass. You can go to Igenex Labs in California and get a PROPER and EFFECTIVE Lyme test any day of the week. It's just that Doctors don't want to lose their liscences in some states by making a positive diagnosis. It is getting a little better, now, in spite of idiots like you! With citizens like you, we will never get cured! If I were an evil person, I would wish it upon you, but I cannot be that cruel. I suppose you believe everything the gov't and its agencies say. Well, you don't have to take my word for it, just read a few of Oliver Stone's books and you will find out how loyal this or any other gov't is to its subjects along with the hundreds of thousands of Lymies like me who the CDC is finally recognizing as having chronic Lyme.

[@Cazanu417]

LeAnn Cottman ok then,go get scammed "lymie" lol,you people have problems and its not a disease,but sure government doesn want to give you a diagnosis and you need to find one,good luck and obviously go wish your fake disease on everyone you want.

[@sararao8429]

Thanks yolanda , no one cares in my life

[@daliasaul]

dr Douwes terapie on youtube.helpt

[@jackiedoocey8798]

Has she really lime desesee

[@lelamoore7178]

know the neurological effects of lymes.

[@emeraldzell]

I cant support this. The government has already botched Lyme disease research to the abysmal state that the CDC/IDSA have left it in. We need a new source of research, and a new source of funding that is not poisoned by politics. Give to ILADS, give to CALDA , but don't waste your time waiting for the government to solve this epidemic.

[@MsJoniJones]

It takes a really good actor to be able to cry on cue. I almost believed it. She's feeling pretty sorry for herself. She amuses herself. She thinks she's pretty clever and cute. She needs other people to think that, too, and she believes she's gotten people to buy into her cutesy act as a "little Dutch girl." She believes being Dutch makes her more special than the rest of us.

[@chriso.8806]

You are 1 of my biggest influences and thanks to you I still have strength and hope. I have a bunch of autoimmune diseases and recently found out I have Lyme w 3 co infections. Not much hope for ever recovering completely but honestly trying my best. My bf of 10 yrs just dumped me too. It's made my struggle so much harder. I really did depend on him. Its not his problem. He's got it to and is progressing beautifully. I cannot keep up. Yolanda, you keep me going and hearing you actually brought a smile to my face. That's a lot of work. ☺ Thank you for being so relateable. I wish I could afford to give. Someday soon I hope. God bless you.