My Lyme Story & Why it Matters // Lyme Disease // Chronic Illness

[@HealingWithRachael]

Thank you for sharing your story and your faith. I am years into my own chronic illness journey and my doctors are suspecting lyme. It is so tough, but you're right, God is always there for us during the most difficult and scary moments!

[@Uvas83]

I cried. I cried hard. everything you described IS me NOW!! I've been to the ER about 15 times I the past 2 years with the same symptoms. I have been diagnosed with Depression and severe anxiety! My Doctor is more concern about me making an appointment with a psychiatrist then listen to me. When you said "my organs are failing" that is exactly me. I can't take it anymore.

[@johncgibson4720]

Good for you. Being your own good doctor is one of the very important things that modern society over looks. Don't trust doctors more than you trust yourself.

[@marcialavelle8327]

noooo. you probably have undiagnosed lyme disease. Please find d a lyme Dr. I went to a primary Dr who found what,was,wrong with me Dr. Stuart Orsher in ny. Good luck. This ladys story is also very,very similar to mine

[@marcialavelle8327]

Please see Dr Stuart Orsher in Ny. He found what was wrong with me. Good luck. I have been miss diagnosed for 6 years. I have lyme disease.

[@carlbernngl]

Marcia Lavelle hi, did you’re Lyme test come up negative when you were misdiagnosed?

[@derekeccles7612]

carlbernngl mine did,I didn’t trust the test results so I sent mine to armin labs in Germany and it came back positive in 13 different categories

[@TheDoveChronicles]

God bless you, Claudia. I am newly on the path of chronic lyme, a believer of Jesus Christ and I'm really having a hard time. I'm so grateful for your story - of how you give all glory and gratitude for our Lord. I don't know how anyone can get through this without faith in God. What a blessing, you are right. So far, I am grateful to have gone through what I have, too. When you said you are willing to put yourself out there and share your experiences, I feel the same way. I feel called to share my ups and downs and to also give glory to God in all circumstances - to show that it IS possible (even though it IS hard sometimes!) I've begun a lyme blog and am finding my faith is weaving into it even more than I thought. I have a lot of non-believer friends and family so I'm a bit worried about hearing backlash from them, but for the most part I've not found that. I, too, have been blessed by God in many areas of treatment - to affording my first appointment with a lyme literate dr. to finding Christian friends in town when I came for treatment. It's a remarkable journey and I'm so grateful you are sharing yours. I stand beside you in health as we claim our boldness and love in Jesus Christ and share that with the world.

[@HealthyPreparedness]

TheDoveChronicles Thanks for sharing yout story as well! There are far too many people suffering with Lyme - it gives those who are suffering much needed support and encouragement to hear from others who have been through the same thing and understand their suffering. Thanks again for commenting!!

[@rebekahguillotte7778]

Thank you for sharing your story! It's such a comfort to know I'm not alone in my journey, and to know what I'm feeling and experience isn't all in my head. Thank you!!!

[@jesussaves8549]

Thank you for sharing. I completely understand I am now and went through similar situation. I don't wish it on my worst enemy. I was single mom pregnant, working, and sometimes I would lay in bed thinking I wasn't going to wake up the next day having to go to work. You go to the Dr and "it's all in your head". I felt like no one believed me they thought I was lazy or needed psychiatric care. God bless!

[@ambereastman6176]

Thank you so much for sharing your story. I have tears in my eyes hearing you articulate so clearly your own experience as though it were my own. I feel comforted knowing that I am not alone. No matter how many people love & have concern for you, it is an exceptionally lonely illness where you feel so trapped in your body with all the pain & exceptionally worrying symptoms. I felt such a burden and so lost that often times I prayed to slip away in the night & never wake up. My heart goes out to all of you suffering right now and to those who have been misdiagnosed, neglected or abandoned by the medical system . It is so very difficult to feel terrible & to then have no one take your symptoms seriously. I can't tell you how many times I lay awake at night crying- unable to sleep because of headaches, extreme anxiety, sense of a lack of air, racing heart & this internal feeling of shaking nerves. This illness is so debilitating! Thank you for sharing in such detail, it has been a great comfort to me. I hope you are doing better these days.

[@tammygonzalez9313]

Amber Eastman I’ve felt exactly everything you wrote. How are you now? I have CIRS which is a bio toxin illness and Lyme (just found out last week).

[@CarolJamieson]

AMEN. Thank you for sharing this story. I can relate to that feeling of slipping away, like just hanging on to life by a thread. The Lord blessed me also. I'm on ASEA now because the Lord brought me to it. I'm getting my life back. Praise the Lord.

[@jasonaustin1038]

Everything you have said is SPOT ON! I know exactly how you feel. It is such a terrible disease. Faith in God!

[@KMason-zn3sc]

Thank you so much for opening up and sharing your story with the world. I will be sure to keep you and your family in my prayers. May God bless you in all that you do.

[@creativesolutionsart-h3o]

As I declined further into this disease, my family support unraveled. They actually called me insane and tried to take my son away from me. I knew I had something wrong with my health and I spent the last two years seeking answers and looking for better support. I never treated my son bad other than being tired I still fulfilled my parental responsibilities and was there for him as much as I can possibly be. I'm estranged from my family now and they still do not know I was experiencing chronic lyme illness. I was just officially diagnosed yesterday, but I know what I've been going through for the last 40 years. Your story resonates with me God bless you.

[@iamlaurayournot]

I had the horrible neck pain and back pain and then started going numb on my left side. Next thing you know I am in the hospital. I was diagnosed with a rare spinal cord disease called Transverse Myelitis similar to MS. Ever since..I have been going down hill. Especially with my brain fog and joint pain.....turns out I have Lymes.....trying to fight it..You are so lucky to have such a great husband that was able to support you hile going th this. I am the bread winner and I support the family. I have a 20 month old daughter. I force myself to get out of bed everyday.

[@rubencastillo8305]

+Laura Lake I would like to prove to you or anyone with Lyme disease either in its early stages or advance stages that it can be treated succesfully and fast but accross the border south of San Diego California. I do this because I have seen very effective and possitive results and testimonials but they are in Spanish they might not be that credible because they are in a foreingn language so my idea is to collect some testimonials in the English language so that they can be credible to those who only dominate the English language. Apitherapy in Mexico is far much more superior than any country in the world I know because i have seen with my own eyes.Youll be surprised how much most people DON'T KNOW and because of that people with Lyme and othaer illneses must continue to suffer. try me rubenberthaud 2001 at hot mail dot com

[@EasyFold007]

I take my hat of for you and your family and for sharing this Lyme Disease experience with all of us...

[@HealthyPreparedness]

Wonder Around Thank you!!

[@MKing-je2xu]

Thanks for sharing your story! It has given me some hope that I really needed right now. I have been very sick for over 3 years now, and no one has known how to help me, but just over a month ago I was finally officially diagnosed with Lyme. Now at least I know what is wrong so I have a direction. I can't wait to see your protocol. Maybe I can add it to the ozone IV's that I have started. Heavenly Father seems to be giving little pieces at a time to help me get better, and I think learning from you will add to those pieces! :)

[@rubencastillo8305]

+M. King I would like to prove to you or anyone with Lyme disease either in its early stages or advance stages that it can be treated succesfully and fast but accross the border south of San Diego California. I do this because I have seen very effective and possitive results and testimonials but they are in Spanish they might not be that credible because they are in a foreingn language so my idea is to collect some testimonials in the English language so that they can be credible to those who only dominate the English language. Apitherapy in Mexico is far much more superior than any country in the world I know because i have seen with my own eyes.Youll be surprised how much most people DON'T KNOW and because of that people with Lyme and othaer illneses must continue to suffer. try me rubenberthaud 2001 at hot mail dot com

[@laurapopp7976]

Thank you for sharing. I've gone through a similar case of Lyme and co infections. Can't believe I made it this far .. 4 years and counting. May God bless you!!!!

[@HealthyPreparedness]

+Laura Popp Thank you Laura! Way to fight your way through the disease! I hope you are feeling better and will continue to get better as you go.

[@nataliearcher]

Wow. What an incredible story. Such strength. I am an endometriosis sufferer and your story resonates with me deeply. I sent you a message about my story. Sending all my love. Natalie x

[@Warrior-In-the-Garden]

I love your sincerity and love for our Father. His work is timeless and although it is almost 3 years from this video, it has encouraged me today. I am just beginning on my Lyme journey. I have textbook case saw the tick, rash 2 months later, saw my Dr. treated for 21 days but not getting better, getting worse actually. He is the only thing keeping me together. Hope all is well with you and your family.

[@planetdog1641]

Long term treatments work. It can take up to 4 years of heavy doses. Most doctors give up, but my doctor had me stay on the program for 4 years and I got out of it.

[@HealthyPreparedness]

Edward Middlecamp I'm so glad you recovered! Thanks for sharing your story - I'm sorry it took so long!

[@DominateDepression]

Still doing good? What was your protocol?

[@erinc.6941]

Thanks for your story! I started getting sick with Lyme at the age of 12 and now I am almost 19 and got diagnosed about 5 months ago. Ive been on oral antibiotics for about 4 months now and was getting better but am now going back down hill. I know I just have to have faith that God will get me through! :)

[@HealthyPreparedness]

+Erin Bywater Yes, having faith will be such a strength to you as you go through the good and bad with Lyme. I know it was for me. That and continually fighting my way through it. *I* wanted to be the warrior and not let the Lyme win the battle. I know you can win in the end as well.

[@e.cahill9594]

I found your channel by watching Momma O, she mentioned you in her video in what she eats, and mentioned you had Lyme Disease. My daughter is 28, and has chronic Lyme Disease. She never knew she was bitten by a tick, we live in Massachusetts, she never had the classic bullseye rash. One day, it was Easter Sunday 4 years ago, she woke up and her knee was huge. She was tested, and came back positive for Lyme Disease. The first doctor said in the emergency room, she was wearing her high heels too much! I had her seen that next day by an ortho doctor, positive for Lyme Disease. She has been on a ton of oral antibiotics on and off, different doctor's... She has gotten better, but she still suffers from it. She is now looking at a homeopathic route.I am so glad you are doing better! I first started watching April and Dave's KZbin channel a year and a half ago. You have wonderful extended family!! Can't wait to watch your videos!!

[@MrSpookysnipes]

really great video everything you said coincided with how I've felt for the past year I have found out I have Lyme disease a week ago and like you have had to do everything on my own to this point. this was really helpful you are a beacon of hope. thank you

[@MLF-gg6fv]

I could find the protocol video you stated that you would post. I am very interested in it. Even though I have not had the incredible journey you have had, b/c I just found out, but it answers a lot of questions. I would really like to know your protocols b/c there is so much out there and you just don't know who to trust. But something in my heart trusts you, and I believe its the Lord! I am so glad that you are doing better and living life again. I have lost hope, but with your story, some of that hope has been restored! Thank you for your courage!!

[@dawndawnadams5446]

I couldn't find it either :(

[@curturweider9473]

I watched this six months ago . I think about her every day because EVERY DAY I say the same thing she said in this video " It's Unbelievable " , it really is. There is a reason why it is the MOST deabilitating out of all the Chronic Diseases

[@christinebuelow6616]

This is such a lonely disease. I must have contracted Lyme somewhere in my early 40's (about 20 years ago- I am in my early 60's now) and while had crazy symptoms for a long time, that doctors told me were all in my head, the bomb hit in my life at a time of intense sustained stress. Every part of my body and my life has been affected. even devastated. There were many days I was sure I was going to die, and so much time spent suffering and unable to function. Now, even though I am doing better, I am not better. The past 14 years have been beyond hard, and I am still looking for treatments to help me even though along the way God has brought help. It has also been expensive, which is also devastating on families. I wonder what life would have been like had I been diagnosed early, and I worry about the future. Thank you for your video.

[@rubencastillo8305]

+Christine Buelow Dont believe a lot of things you hear about Lyme Disease OTHERWISE YOU WILL NEVER SEE THE END , if you like to know what is like to live a normal life without Lyme it will have to be done with apitherapy but 20 minutes south of the San Diego California border in Mexico. Ill be glad to walk you through the process. rubenbertha 2001 at hot mail dot com

[@rubencastillo8305]

+Christine Buelow I would like to prove to you or anyone with Lyme disease either in its early stages or advance stages that it can be treated succesfully and fast but accross the border south of San Diego California. I do this because I have seen very effective and possitive results and testimonials but they are in Spanish they might not be that credible because they are in a foreingn language so my idea is to collect some testimonials in the English language so that they can be credible to those who only dominate the English language. Apitherapy in Mexico is far much more superior than any country in the world I know because i have seen with my own eyes.Youll be surprised how much most people DON'T KNOW and because of that people with Lyme and othaer illneses must continue to suffer. try me rubenberthaud 2001 at hot mail dot com

[@curturweider9473]

I wish everybody with chronic Lyme the best. I can only say hang in there keep moving your body call. Once your body stops it's over. Positive thinking to all

[@seekinglight1111]

Thank you so much for sharing. Just diagnosed and have no idea what is ahead of me.

[@stewiegriffin9801]

Kelly Hale how did you get diagnosed

[@NcScbeach1]

Thank you so much for posting this video! I've had Lyme disease for 12 years now and suffer most from neck pain/migraines, fatigue and memory loss. When diagnosed, I started the antibiotics but couldn't take them due to side effects. Long story short, here I am 11-12 years later and fighting this without anything because I don't make enough to pay for alternative treatment. I've taken it to God who has definitely sustained me, and am now thinking of doing a "Go Fund Me" so that I can get more help. God Bless you and once again, thanks for sharing!

[@HealthyPreparedness]

+NcScbeach1 I'm sorry to hear you're dealing with Lyme disease. Do the "Go Fund Me" campaign! In order to get through this illness we have to fight! We fight for our lives every day and fighting is what will get us to be the conquerors in the end. Do whatever you need to to get the help you need. Good luck with everything - you can get through it and be the conqueror in the end.

[@NcScbeach1]

+Healthy Preparedness I've been praying about the "Go Fund Me" to help me with the cost for treatments. Thanks for the suggestion, and it's one I've thought about.

[@marcialavelle8327]

please get help soon. Go fund me is a good idea. long term antibiotics will kill this bacteria. 6 months or a year. Find the right Dr that will help you.

[@pollyannarocks]

wow l didn't even know you were going through all of that! How thank ful l am that Johnny was there to help you out and that God was there to get you through and the knowledge that you have gained! wow and wow and you are simply amazing! Just know we love you and wish l could have helped you more!

[@forestque1531]

Wow, your story is so similar. The legs giving out and just not working at all has happened to me. I hope I can get treatment soon as well!!

[@HealthyPreparedness]

+Forest Que I hope you can find solutions that work for you as well. It's unnerving - especially when losing the ability to walk - but the body wants to heal and as long as we keep trying and continue finding answers healing and health will come, even if it takes some time. Good luck with everything!

[@jaclynmoylan1905]

Glory be to GOD!!!! I am so thankful to have stumbled upon this video. Every single thing you said hit home. I was diagnosed with Lyme and co in 2015 and the antibiotic protocols are what got me well enough to at least function a little bit. After a year of almost 30 pills a day (antibiotics, supplements, nystatin for candida) i started to work on detoxing more and became very ill to where I had to stop all medication because i couldn’t even keep water down. I slowly improved for a little while, and now I’m back to square one and just recently saw my LLMD and was put back on an antibiotic protocol (this time I’m doing injections twice a day). I cannot tell you how much I can relate to the neck and head issues you talked about. Every time I get sick it starts with my neck stiffening, then the blurry vision, then the migraines. I have been on antibiotics again for 4 days and today is the first day without a headache and my neck is starting to loosen up. It’s like the pressure is being released. I have to MAKE myself to continue through the highs and lows of this terrible chronic illness. I will pray that you continue to heal. Thank you so very much for sharing your story. It really helps to know we are not alone.

[@nikifox2445]

I'm so close with my higher power in my heart. During this experience I've cried and begged. Now today I'm seeing this video. After scheduling with my infections disease Dr. God is working thru you for sure because you just gave me hope 😟 I also have kids and I've been laying in bed with my life flashing before my eyes, I feel like I'm going to die. Like I'm loosing control. Like this is something I can't beat. I can't miss work because my kids depend on me, so at work I have to run to the bathroom and cry. I always been very high engery I can't take anymore of this. It's killing me. I'm Shakey, I feel like I have a calcium problem, I was thinking I had bone cancer, all kinds of horrible stuff! This attacked my heart, I've never been so scared in my life. I whole heartedly leaned on God and he brought me here tonight 🙏

[@tammygonzalez9313]

niki fox so sorry. Blessings for healing. How are you now? I understand because I have CIRS and Lyme. I’ve prayed for God to take me home. I’m on the protocol for this bio toxin illness first then I will have to start on a Lyme protocol.

[@2emeraldeyes]

Thank You for sharing this, it helps to know that your not alone ya know? And you are my sister in Christ which is a huge plus! My tests came back inconclusive as yours did. Yes the fatigue is horrible. I'll barely do anything and I'm back in bed for a nap. My symptoms started with severe joint pain that never went away, it only gets worse and has spread all over my body, and now I have all manner of things going on so similar to what you've described down to not shaving my legs! (ha) The headaches are stabbing pains in my head which can become a bit frightening. Some days I think it might be my last. I have no insurance (same reason you couldn't afford treatment at first, just don't have the funds) so the Dr.'s say their hands are tied for lack of the tests they think i need. My story is so similar to yours. It gets so hard to walk sometimes, the dizziness, yes the neck pain part of the stabbing head pain, on and on. Was that nasty medicine Oregano oil? That stuff is disgusting but yes we will do anything to get better! I have to say, I'm so happy to have Jesus and His word, He gives me peace through all of it. He's with us through the harder days and I'm assured that if I die I'll be with Jesus and that is much better! Still I'm tired of suffering here and pray to be cured some day cause I know if he chooses to heal me He will. I am so glad for you, and thank you so much for sharing! I so look forward to your protocol! You look wonderful and God bless your family for being so supportive especially your dear husband - Praise Jesus!

[@zolushka4823]

I too had severe headaches. Always on left side of my brain with neck pain severe. You know what one "doctor" told me when I complained about my terrible headaches? She told me to drink "coca-cola" since it has caffeine in it...... Thank you for sharing your story. Glad you are recovered and better now. I too, have days when I have to just lay down and sometimes I get spikes of fever out of blue to 104.7..... frasturating. Wish youtube had more videos like yours.

[@johncgibson4720]

Don't trust the doctor more than trusting yourself.

[@morgan4474]

Has....past tense. What healed you??? The headache is my worst symptom.

[@zolushka4823]

Traci Morgan I still have them. I was tested and told "no lyme disease" but my headaches are now horrible and go on every single day and all day. My doctor can't help me ...... I just feel like I waste thousands of dollars do useless tests and everything comes back negative....

[@morgan4474]

I am the same. My lyme test at my doctor's office was negative (that was the ELISA test). There are not accurate so I paid to test through IGENEX and that one showed positive for lyme. My head has also hurt 24 hours a day for about six years now. I know how horrible it is. I haven't found my cure yet but am doing bee venom therapy right now. Are you on facebook?

[@zolushka4823]

I think my doctor told me the other test you are talking about IGENEX cost a few thousand $$$$. I have terrible health insurance and can't afford that test. I paid for the Lyme test $360 and that was still too much for us. It it will so bad that I'd be screaming I guess then we'll ask for IGENEX test right now I still tolerate them but they became a lot worse and always on one side of my body (left). :(

[@cread9103]

Thank you for sharing your story. I was bitten by a tick in the UK 27 years ago, developed the bullseye rash within a week or so. Went to doctors and they sent off a standard Lyme Disease antibody test which came back negative. So I wasn't treated at all but my symptoms just kept coming, mainly pain and fatigue. Had fibromyalgia diagnosis in around 2000 and tested positive for Lyme antibodies in 2002. I am stuck though. Even though I have tested positive for Lyme disease, the doctors in the UK do not seem to understand Lyme very well at all and will still not treat me in any way for Lyme. They say that testing positive only proves that I had it once. It's tough, I am a single working mum but with a very low income, so not many choices at all. Does anyone know of any Lyme Literate Doctors here in the UK who are available on the NHS?

[@sammhammiam]

+C Read Can this help? www.wadhurst.demon.co.uk/lyme/

[@cread9103]

+Samantha Hanson Thank you, I will take a look.

[@rubencastillo8305]

+C Read I would like to prove to you or anyone with Lyme disease either in its early stages or advance stages that it can be treated succesfully and fast but accross the border south of San Diego California. I do this because I have seen very effective and possitive results and testimonials but they are in Spanish they might not be that credible because they are in a foreingn language so my idea is to collect some testimonials in the English language so that they can be credible to those who only dominate the English language. Apitherapy in Mexico is far much more superior than any country in the world I know because i have seen with my own eyes.Youll be surprised how much most people DON'T KNOW and because of that people with Lyme and othaer illneses must continue to suffer. try me rubenberthaud 2001 at hot mail dot com

[@NYROCKERCHICK1]

C Read look up cowden protectol on Amazon burbur pasely samatro bandroyl pinellia brain cleanse

[@panoramicLight]

Many thanks for sharing your experiences of this highly complex illness. Well done.....

[@HealthyTreasures]

Thank you!

[@ttilles]

Thank you for this :) I am in fear of dying and unknown stuff from Lyme and other coinfectitons. I was ill all year last year. Then I got real sick last fall. I was lucky to have found a dr who could test me for Lyme. It was positive. While I was waiting on the test results to come back, I continued to be worse. By the time i found the dr who could help me, my digestive system pretty much quit working. The Lyme bacterias are attacking me in the gut, as well as fatigue, foggy head, crashing after meal, and all the GI symptoms you could think of. I am one month into treatment. So far my GI is still not working as it should. I am scared. I pray that I can go back to being a mom to my two girls. They need me!

[@michiejewel5989]

Tommie Happie Stamps I hope u are now feeling better

[@patrickremillard2745]

Wow just stumbled upon this and your story is very similar to mine! Got bit by a tick when I was younger and never thought anything about it. Never really had any problems except anxiety until after the birth of my 3rd child. My health went downhill fast and the doctors thought I had post partum. I told my husband I was gonna die if we didn't seek alternative medicine. Sure enough I had Lyme, Co-infections, Ebstein Barr Virus, and much much more. Got much better from 9 months of treatment and die off was horrific!!! Still dealing with something (thinking it's candida), but can't seem to get better! On a strict diet (no gluten, diary, soy, rice, hemp, oats, sugar, sesame) been eating that way for 2 years. 18 months ago moved out of a moldy house and started feeling a lot better but still not 100%. Lots of heart palpitations when I eat anything antifungal, workout, am in the heat / sunlight, in a moldy environment, or eat anything sugary. Thank you for sharing your story!

[@tammygonzalez9313]

Patrick Remillard get tested for CIRS. This is “mold illness”/BIO TOXIN illness. It is believed that one in four people are born with a predisposed gene inherited from parents that make a person highly susceptible to mold illness after activation at some point in their lives. I have been so very ill for so many years! I am still on the long journey of protocols for the bio toxin illness and now my doctor tells me I will also need to be treated for Lyme afterwards. They often go together! Blessings

[@lilypoppy1962]

this is so touching im almost teary eyed watching this. im not saying i know what you went thru but i def been hitting my rock bottom. the biggest treatment i got from a doctor was telling me to take iron becuase i had severe anemia. i was so angry. words just cannot describe. she never even checked my heart iv had fainting issues for almost a year... when she was diagnosing me all those days and days after i thought i was going to die my heart would barely beat on some days i thought i had heart failure the doctor didnt even give me a blood transfusion nor did she prescribe me iron i bought my own at walgreens. she didnt even explain to me that it would take 3 months of taking iron till my body would start producing enough blood. the really shitty part is that i do not feel well im may not be anemic anymore but i do remember what being healthy feels like years prior my health started decling. and i know how i feel right now is not normal. yet when i see a doctor they just shrug everything off like its okay to be sick and tired. you know your own body you know something isnt right.. it pains me that doctors will not help or run tests. so lazy. i try all the time homopathich stuff but nothing works. my friend even suggested maybe i should try to get stds test just to be safe and i thought you know who knows she could be right you know so i went to a gyno and asked to get std checked and she only ended up doing a pap smear on me.... i swear this stuff happens to me all the time no one helps me and i feel like im just supposed to deal with it the worst part is i know there is treatment out there there are tests and medicine and transplants you name it... its out there but a doctor cant give me enough time of day to be empathatic and go out of her way to help a human being isnt it there job? it just sucks so much especially since im only 24 and everyday is a struggle. i know im not lazy... becuase i do wish to do everything... but doing anything is so tough. and knowing i tried seeing a doctor and that there is no help out there just really sucks sometimes..... im supposed to be trying to get my life togehter going thru college making friends trying to get married maybe have kids but instead this is going to be it and i just have to deal with it and suck it up becuase it is what it is. doctors make me so angry. on another short story my mothers been sick too she just got diagnosed with kidney issues and other stuff yet they just caught it recently if doctors wouldve been doing there job she wouldnt have kidney issues since she sees a doctor regularly they shouldve caught it long time ago.. shes eats healthy and no alcohol or smoking. they werent paying attention and no one is ever responsible for this stuff. if i went to work and fucked up i wouldve gotten fired just saying and these lives we are talking about doctors to cheap and lazy to go out of there way and be empathetic to help others. it makes me so angry that everyone deals with this it literally hurts. im sorry to hear of your struggle but i do believe it empowered you to be that much more stronger and empathetic in life.

[@marcialavelle8327]

OMG please call Dr Stuart Orsher 2125357763 in Ny. He will do all kinds of test from lyme disease to sexual transmitted diseases. He will find what is wrong with you. He doesn't take insurance. You only need the diagnosis of wathever is going on with you. He will find it. You may need about a $1000 or so. He took at least 20 tubes of blood from me and found lyme disease, H pylori bacteria, herpes simplex, and low very low vitamins. After that you may not be able to go back to him. He is too expensive but at least you will get your diagnosis. Good luck. Please send me a message to see where you are with your health.

[@lilypoppy1962]

Marcia Lavelle im not in ny nor do have that much cash laying around but maybe one day. does doctor with no insurance even prescribe things like antibiotics?

[@marcialavelle8327]

He doesn't take insurance. Yes, they can prescribe.

[@tammygonzalez9313]

Lily Poppy aw! I’m so sorry! How are you doing now? Regular doctors don’t have answers for many things. They’re trained in medicine in med school to take care of symptoms. Often only Functional Medicine doctors can help diagnose. Unfortunately They are not covered under insurance. I have CIRS and Lyme. I’ve just been diagnosed after more than 20 years 😢. Unfortunately it is very expensive and draining. I have some Hope now though since I’ve started my long journey. It’s scary still though.

[@Godsdetox]

Thank you so much for sharing your story with us. It's a great encouragement to know I'm not alone and there is hope. :')

[@luannking5594]

I am so sorry to hear all about your are suffering! I would love to be able to talk with you! I am suffering with so many of the same symptoms!

[@rubencastillo8305]

+LuAnn King I would like to prove to you or anyone with Lyme disease either in its early stages or advance stages that it can be treated succesfully and fast but accross the border south of San Diego California. I do this because I have seen very effective and possitive results and testimonials but they are in Spanish they might not be that credible because they are in a foreingn language so my idea is to collect some testimonials in the English language so that they can be credible to those who only dominate the English language. Apitherapy in Mexico is far much more superior than any country in the world I know because i have seen with my own eyes.Youll be surprised how much most people DON'T KNOW and because of that people with Lyme and othaer illneses must continue to suffer. try me rubenberthaud 2001 at hot mail dot com

[@JanaKay]

Thank you so much for sharing! This video definitely helped me become more aware when I was trying to get my diagnosis.

[@awinkie12]

Thanks for your video! Love it. I have lyme disease that caused several chronic illnesses and just started a vlog as well!

[@ThrifterPickerShipper]

Oh thank you Jesus. What a good good father you are. Your story is my story. Exactly. I am so excited to go watch your protocol video right this minute and I pray it works. I love the Lord as well, but I gotta tell you I am in the depths of despair with this illness. I'm just tired so tired. I have the official Lyme with Bb diagnosis as well from Western Blot. I've tried everything for 3 years now and I just keep getting worse. I can hardly take another day whew! God bless you for sharing this.

[@tammygonzalez9313]

Debbie Wilson I’ been so very sick myself for many years! Have you looked into Bio Toxin Illness as well? I have recently been diagnosed with CIRS (chronic inflammatory response syndrome) from mycotoxins in my body from this “mold illness “. My doctor (functional medicine doctor) told me just last week that I would need to do a Lyme protocol after I do my this mold protocol I’m on. These two often go together. Are you working or living in a home that’s had water damage? There could be mold that you don’t see. I was tested for the gene that predisposes the susceptibility to high sensitivity to mold (inherited from parents). It came back yes, I have the gene; but it also showed high susceptibility to Lyme...higher than mold Toxicity actually. Guess what, we had our home checked and sure enough they found the deadly black mold on the plenum in our ductwork, under our hardwood floors and on the wall behind our double ovens (caused by a slow water leak from a cracked water hose from our refrigerator). Ive had seizures and so MANY scary symptoms. By the way, CIRS is a multi symptom multi symptom illness. I’ve thought I was going to die and even started praying for God to take me home. I’ve been so lonely for so many years because of having no support. People don’t understand the “invisible” things. 😢 Blessings to you!

[@wanitahansen]

thank you so much for sharing this with us. I am learning more from you than the doctors I have been to. Love your courage and stamina. Thank you thank you thank you

[@HealthyPreparedness]

+Wanita Hansen You're welcome Wanita. Thank you for your comment.

[@katilda2726]

Looking for the second video on the actual protocol! Can you share?

[@lymelightjourney2564]

Thank you for sharing this!

[@yosimt]

Thank you for sharing this. I believe God is definitely using you to help others. Thank you for helping me.😊

[@diannereynaert9729]

Oh my gosh!! I think that all the time…need to stay clean in case of hospital……so much fear😩

[@coconut7812]

thank you for sharing your battle with Lyme disease just so you know because of YOUR videos I learned Bentonite clay, diatomeceous (sorry cannot spell), and activated charcoal. I have both the first two still ordering the activated charcoal. so, thank you so much. May God bless you always along with your kids and husband. Don't worry God is there with you. Trust God always. 😇

[@colettem1974]

Thank you for sharing your story. I don't see a video regarding your protocol. Is there a way I could get that? My 12 year old was just diagnosed with Lyme.

[@purrview]

Thank you for sharing your story mine is very similar but the cause is mold and mycotoxins illness that cause the inflamatory response and it affects my body and my brain i can totally relate to the brain issues

[@karlhans6678]

why you remove your protocol video?

[@Thundersnowy]

I don't know where to even start. Your story is exactly like mine. But now my daughter has it. I have to work full time in agony. I just don't know how I can possibly get through this every day and now find a way to help my daughter. Undiagnosed for years. I couldn't walk for years, felt it in back of my head. You're the first person I've ever heard who has my symptoms. I've been bit by many ticks in Oklahoma. And pulled about 100 off a friend's dog that died the next day. I've never found help. my Lyme tests were negative and I only started wondering since my daughter started getting so sick she had to quit school and had two positive antigens for Lyme on western blot. Could she have it?? infectious disease doc said no? Could I have it tho Negative? I had 3 c sections and that was so easy next to this pain and other symptoms. I know what you've been through! Thought I was dying too. Please give me just one thing, one step I can take for me and now my daughter. If we even have Lyme.

[@bakerkiddx3]

Yeah this here...... sigh. I haven’t been to an actual doctor in years bc I couldn’t afford insurance and my family was going through a lot and I was just being irresponsible. I tore my MCL while serving 8 weeks ago, went through MRIS and they diagnosed me w chondromalacia (runners knee) from overworking and being off balance plus the tear so I wasn’t able to walk for a while and am off both jobs still . Started doing physical therapy and finally got state insurance, went to doc for a normal check up and they wanted to do blood work to check my sugars bc I had been real fatigue and I have a history of type 2 diabetes. The doctor called me this morning and said one test was positive for Lyme and there’s a second part of testing that was done but It was 60/50 but they started me on antibiotics for 21 days. I’m weak. Fatigue. Awful swelling and joint pains in both knees and elbows. Even now as I text this. Headaches, and I’m pretty scared. I am concerned bc the physical therapy is like the opposite of what I should be doing w Lyme disease I feel, a lot of times I’m a zombie .. makes sense. It’s nice to know I’m not alone though thanks for sharing your story!

[@specialk5589]

Ash theArtist OMG! Thank you for sharing so recent. I had a meniscus tear in one knee, finished up therapy but now both knees hurt. Head ache every day. I went to the ER last week because my lymph nodes were so swollen on the back of my neck. It hurt to lay on a pillow. My eyes feel heavy and somewhat burn. They gave me something called Doxycycline and some thing for head ache and sent me on my way. My dermatologist told me that med. was for Lyme disease 🤔🤔🤔. I don't even know what to do now!! My knees hurt soooooo bad trying to stand. What do I do, where do I go???? Sorry so late.

[@exsleepyink]

I couldn't read all the comments, so forgive me if this is repetitive. I was just wondering what procedures you went out of state for (I saw you had an iv in). I was living in a mold filled basement with no ventilation for 5 years. I gradually deteriorated within six months in every bodily system. Right now the scariest to me is that my chest rib and back muscles have tightened and paralyzed so much that I've only taken tiny breaths for the last few months (they get smaller every day and it's unexplainably painful). Digestive, neurological etc are horrendous, but that scares me the most that it's permanent. Like my body is tightening and tightening around me. The doctors treat the symptoms like they are diseases or say I'm fine or depressed or stressed, meanwhile I was climbing mountains, traveling, playing music and teaching people with disabilities, acting and living my life, now I can barely walk up the stairs, lift a pot or walk down the street (and hot days just aren't liveable). Why would I want this? Most days I feel it gutted me and took my soul away. I was (sort of) diagnosed with CiRS, so I've been tying to get to a safe apartment for months to no avail, but a few alternative docs think I also have chronic Lyme (I've pulled hundreds of ticks from under my skin being a hiker and camper who travels and lives of Long Island). Do you have any advice for me? I'm at the point where I've spent all my savings, might lose my job and insurance in coming weeks (due to lack of strength and concentration and the histamine/cytokine affect the building also has on me). Your story and family life seem very hopeful and mine seems to be falling apart. I could use it rubbing off on me. Thank you for the video

[@tammygonzalez9313]

chris schafer oh gosh!!! So sorry!!! I feel for you! After being sick for over 25 years, I’ve finally been diagnosed with CIRS and I KNOW the multi system multi symptom illness all too well. I’ve had seizures and my body began to deteriorate on a downward spiral the last three years... all tests came back positive and my doctor said “Tammy, you’re living in a water damaged home!” Sure enough we found black mold under hardwood flooring and in the wall behind our double ovens...also inside our ductwork in our attic and basement. I also tested positive for MARCONS in my nasal cavity that came back positive (colonization of mycotoxins from mold spores derp in the nasal cavity). The inflammation in my brain caused seizures. 2 weeks ago my doctor told me I will need to do a Lyme protocol after I get farther along 😭. I’ve researched and these two illnesses often go together!

[@ashlee8408]

Is your video of the steps you took now not free?

[@Gorlami90]

I just found out I’m positive for Lyme, it’s been getting so bad I can barely function and feel like I’m stuck in a black hole. I took time off work and I hate the fact my family thinks I should go back to work cause they know someone who has had it before. I wish there were better information on Lyme out there

[@tammygonzalez9313]

Free living it’s so difficult when our own family and even the close ones at that don’t support... I have CIRS and Lyme...I feel like I’m dying some times.

[@nikifox2445]

I'm just being diagnosed 😟 I had nuero and cardiac effects. Also muscles and nerves.

[@nikifox2445]

It's horrible

[@mommiesfrugalfinds7318]

I 'm going through this. How did you get better. I was diagnosed with fibromyalgia and cfs but I am convinced it is lyme. I have have had the same results from western blot. I am now having ms type symptoms numbness in legs and arms, major headaches, sinus pain pressure so many symptoms. So glad to hear your are better. I wonder how many others are dealing with this.

[@marcialavelle8327]

Hello dear. I have lyme disease. I put up a video about the meds I am taking. I am currently doing antibiotics IV. Ceftriaxone antibiotic, azythromycin IV, tinidazole antimalarial, ursodiol to help the liver process the antibiotics and avoid gallbladder stones. Long term antibiotics will help kill the bacteria. Find a Dr that will do that for you. Usually Drs will prescribe doxycycline but there is more out there. I am myself again. Listening to this lady story is like listening to mine.

[@quantumeseboy]

They all tell you it's depression... inadequacy of medical professionals gives me depression. It took me nearly two years to diagnose Lyme in NY and even then they just give you a basic 30-day course of antibiotic that is useless. Personally I've suffered more from doctors(and hc system) then from illnesses. The best therapy for Lyme management that I found is IV ozone.

[@joshteel3226]

God bless you! Keep on keeping on!

[@corbinmcmillen1985]

ASEA helped me and has helped thousands with illness.

[@KingKong-zq6so]

I have chronic Lyme disease I do take antibiotics but they didn't ever help on the second month started researching more about it. I'm taking antibiotics, shiitake mushrooms pills and monolaurin symptoms are going away

[@mituche3633]

Ben how long u take the antibiotics &what? they are?please

[@HealthyPreparedness]

+Benjamin White I'm so glad to hear your taking something that's helping you! I hope you're still making progress!

[@KingKong-zq6so]

+mituche36 sorry it took so long. I took doxycycline monohydrate 150mg for 3 months I also took lots of silver shield liquid at 20 ppm I made my own machine and I'm totally healed hope this helps others I know its very powerful disease please hang in there it won't last forever

[@Laura-ze4dp]

In the page of ASEA they dont explain what is inside, the ingrefients. Where can i check what is this ASEA? Thabks so much ❤️

[@chelseatomlin7951]

There was a girl with Lyme disease and she had it since she was 10 now she's 21 still fighting it and she's had some problems with her brain and she barged into my house and I couldn't t believe that she has had Lyme disease but it's true her name is Maria and she is a true Lyme disease warrior she has survived for 11 years now and her family is trying very hard to raise some money so she can go to Germany to get a treatment I don't know if they went yet tho but every one who reads this should go check out her story on the Internet it's very touching and I hope she gets better soon

[@HealthyPreparedness]

+Samantha Tomlin There are so many heart wrenching stories out there - I sure hope Maria gets the help she needs. There are far too many people suffering with this deep and complicated disease. Thanks for leaving a comment.

[@LookUpp-2024]

Why does your story sound like mine? Mild issues in teens, worse after pregnancy around age 30, first thought i presented to dr was candida ( or my ex was poisoning me lol). Over time more symptoms manifested. Between mold and possible lyme….ive been sick with 40+ issues. I also tried to explain to family to stay away from me cuz if they get me sick things happen to me in my brain that are much worse than their cold symptoms. No one understood or took that seriously. My brain/neck inflammation was out of control…still is.

[@mylymejourney579]

IV antibiotics did not cure my Lyme. It simply gave me short term relief. Give Teasel Root Organic a shot. It gave me huge relief. People need help and there is not one channel with this that addresses practical approaches to this complicated illness. More importantly don't give up! I've seen my low point in life and I know what it is like to be there where you cannot seem to get out.

[@HealthyPreparedness]

My Lyme journey Exactly! We can't give up! There are always answers. And there is always hope! Thanks for commenting.

[@broscottgaming3743]

I want to understand something. Have you fully recovered from this. I suffer as well and I'm waiting to be diagnosed the 5th of december. I hope you see this and reply back

[@ashleyhavoc1940]

I just found this video and I have to ask, Did any of your children have it? My doc told me it can pass to your fetus during pregnancy. I wanted to have another child but I'm afraid.

[@Stardust-q9o]

How is it going for you? Are you fully healed, or made improvements?

[@AyyRalphy]

My mom is going through something so strange and I fear it may be Lyme Disease. She works in an area where there is a lot of forest/wood/water. On February 25th, she experienced her jaw locking with shortness of breath, neck tightening and this pressure on her chest. We took her to the ER and they said ohh it's just a "mini stroke" days later she felt fine but then again these symptoms would come and again off to the ER. She has had an array of tests done and nobody can find anything. She experiences strange symptoms like loss of coordination, ear sensations (left side) and one night she said she felt numb on her left side of arm and leg and she couldnt feel them. At night a sudden jerk would wake her up and just like you, she paces in her room to make sure she's in her cognitive state. I am so sick and tired of seeing my mom suffering and I am at the verge of taking her to Mexico. she has had spinal tap, mris, they found lesions but the stupid neurologist wont give her medicine.

[@AyyRalphy]

She also feels fatigue

[@empowerunu6564]

I am just told probably I too have bromelia infection and probably chronic one...and all i hear is, it is mental... because I have the same symptoms for more than 5 years and have been to many many doctors it is scary. what are your tips?

[@jackieschling6305]

Wonderful video thank you!

[@HealthyPreparedness]

You're welcome!

[@user-jq1oi6ur2x]

are you cured or improved? sound not working on my phone at the moment. my pain is horrible. .. also, I don't meet cdc criteria for Lyme. I took as test from Igenix (sp?) and they said I have Lyme. I test positive for three Lyme bands.

[@chelseatomlin7951]

And you are amazing having to go tho that your are also a true fighter

[@HealthyPreparedness]

+Samantha Tomlin Thank you Samantha!

[@merebearbelieve1852]

Would you know of any funding source to get someones treatment off to decent start ? My Babesia seems to getting worse And Doctor that originally tested me lost original testing records when he moved I think I have been in some type of denial however the Lyme disease seems to me accelerating They think I contracted when I was 17 years old at Deer Isle Mine but it was dormant to just before I turned 27 years old after a mild brain injury . Major problems are brain fog and getting more anemic . Shortened leg muscles and neck Thank you

[@ILoveMyBunny100]

Hi, I require Doug Coil Rife Machine for delivery in Singapore in order to treat Lyme disease. Would anybody have any recommendations which Co/model to use? Thank you in advance Regards Anna

[@jeannac4]

I know people who have had good results with TrueRife and the Resonant Perl (but it's much pricier). I am saving up for one, however I personally have found a couple supplements and drinking structured water (to alleviate die-off symptoms) that have turned my life around with Lyme, Babesia and Mycoplasma. I am finally feeling normal after 3 years of being sick AND without spending thousands on treatment or using traditional antibiotics. I still have Lyme but I'm functioning at 95% again.

[@urthesmile4me990]

The herb “Teasel” for Lyme disease

[@creimom2536]

Thank you so much for sharing.

[@yoya9193]

I'm researching Lyme disease because I have all the symptoms. I got bit by a tick in 2011 and was diagnosed with hyperthyroid in 2012 .my immune system is deteriorating

[@hellshade2]

i have recently been bitten in the leg by some unknown bug.it is a red raised area on my left calf but does not show the bullseye hallmark of lyme. my doctor has me on antibiotics and steroids atm. as of today there has been no change in the bite area though i still have another 5 days of meds to take.hoping it is not lymes because i already have diabetes and nerve damage and kidney issues.so if i now have lymes it's not going to end well. peace.

[@Reikihandsoflove]

Which essential oils helped you?

[@7digitalSunday]

some of your symptoms also sound like my gluten sensitivity. when i finally stopped eating grains, especially wheat, i felt much better. the anziety attacks stopped. but the brain fog didnt. .. been on an autoimmune paleo diet for a few months now and it helps with symptoms. diagnosed with lyme a couple years ago. still doing banderol and cat's claw when i need it. staying off sugar is important. OZone is one of the best things to combat lyme and other infections that i have seen people talk about. Hi, What was in the IV cocktail the doctor in Idaho gave you ?

[@HealthyPreparedness]

It was called the Chronic Illness protocol. It was a mixture of high doses of vitamin C and some B's. There's might have been more in it but I don't remember what it was. I've also done ozone therapies at home and ozone IV treatments at the clinic. Good luck with all your'e doing to combat the Lyme. I hope you find something that truly works for you.

[@7digitalSunday]

thanks for your reply. are you still on the product ASEA.? i have a friend who is always trying to me to join the business.. do you feel a sustained benefit from it ?

[@claudiaorgill1113]

7digitalSunday It definitely is the staple of the protocol - it's the remedy that is fixing my cellular health and eliminating pathogens from my body. So, yes, I'm definitely benefiting from it.

[@claudiaorgill1113]

The IV cocktail was called the ?Mylar? cocktail aka "Chronic Illness Cocktail".

[@broncobrian2620]

Claudia Orgill Meyer"s Cocktail

[@evelyninoaart4430]

Thank You! So much...I was diagnosed with Lyme disease , I'm so fatigued ...I feel like I'm dying . You are an inspiration. Blessings

[@seomastersdegree]

What are the most effective remedies? How do i find the information? Thanks!

[@HealthyPreparedness]

Tina Rawlins Hi Tina. I talk all about that in my Lyme Protocol video. I hope that helps!

[@7digitalSunday]

check out ozone sauna and lyme. i seen testimony of people who made great recovery using ozone sauna, as well as other forms of ozone. also, look at the work of andy cutler and mercury poisoning.

[@Star5dg]

did you take antibiotics?

[@nikifox2445]

I have like a restless feeling. I feel like I'm going to be permanently disabled it's so scary

[@mariolimonciello5286]

What were the iv of that saved your life?

[@zolushka4823]

Don't be so sure about "I would've been diagnosed with MS". I've read stories when people have had MS for 5-8 years and doctors weren't able to diagnose them. I suffer from similar symptoms and $30,000 even more in medical bills/debt and not a single doctor can diagnose me. My Neurologist ran MRI/Spine fluid tests they both came back negative he said I am like a 20 year old only my body tells me different. I feel that my disease is advancing rapidly I can eat now tiny small portions because my stomach began to hurt. Soooo frasturated so much money wasted - not a single diagnosis

[@HealthyPreparedness]

+dev ochka It sounds like you might just be right. I'm so sorry you've been down the same complicated journey - MS is another one of those complicated and horrible journey's far to many go through. I hope you find your health again.

[@joannab8763]

+dev ochka +Healthy Preparedness When I first began to have weird symptom five,six years ago, my doctors have been suspecting MS right away but told me they needed time to see if I develop more symptoms. Of course I did and they were 100% convinced it was MS and diagnosed despite my complaints of having bizarre, unexplainable sensations. They said I JUST have anxiety.They tried to put me on MS meds which I refused to take. So yes I was easily misdiagnosed with MS. It wasn't until a few weeks ago that I ran a blood test at a German lab and it came back positive, for Lyme and other co infections. I'm seeing a naturopath and will be starting treatment soon. So yes, most doctors rush so fast into a diagnosis without exploring other possibilities. Had I not taken matters into my own hands, I now would've been injecting expensive MS meds into my body, while the Lyme bacteria would be lingering and getting progressively worse...

[@rubencastillo8305]

+Joanna Bennett I think I can really help you because there is this treatment in Tijuana Mexico very efective and inexpensive and if you are familiar with apitherapy and want to get back on your feet and have you illness become a thig of the past ill be glad to give you more information. You wount regret it.rubenbertha2001@ hot mail dot com

[@ksuter200]

It would have been more helpful had you actually mentioned what treatments you had specifically and how useful they were or were not. Your story mirrors mine and just seeing you in a suffering state you do not have to convince me many of us watching have been there to some degree or more.. I hope you add some notes under your video to explain the treatments. Thank you for sharing at least your story.

[@dezertraider]

Blank mind-NO! You got to be mistaken? Did you trip yet??LOL

[@Kiirree325]

My son just got diagnosed with lyme disease... hes only 7. :(

[@HealthyPreparedness]

+Best Crafts by Keri I'm so sorry to hear that Keri. Children respond really well to homeopathic remedies - even for Lyme. I'd find a good Lyme doctor who knows how to use Lyme homeopathic remedies for your son. If you don't go that route though - there are always other options that will work as well - children, fortunately, recover much more quickly than adults. I hope your son recovers quickly and fully.

[@TheCondor300]

You should try Lowdosenaltrexone....

[@DonWesley]

Did you try MMS?

[@HealthyPreparedness]

Don Wesley Yes, I did. It helped some but wasn't the answer to everything. I was hoping it would be - but it wasn't.

[@Cybelle2006]

Healthy Preparedness Did you try it by IV? Jim Humble describes it a bit in his book. Search for it on Google (or whatever search engine); as well as search for more into on KZbin. I may start it soon as well. You can also try the Gerson Therapy. Good Luck in all your endeavours to get well.

[@kathyhirsch379]

how u doing with your treatment ,have u seen this Dr video// Finally a Cure for Lyme Disease

[@erich5091]

You left out the most important part of lyme disease discussion..... the testing. You say you were diagnosed with 8 strains of lyme among other things, but you don't even say anything about the type of testing you received to get to this diagnosis. This is important because the western blot test that you first did is rather unreliable and 50% of people with lyme will test false negative. Only a few of the labs in the U.S. have advanced testing for lyme disease. Would you care to elaborate on your testing that showed you were positive for lyme?

[@claudiaorgill1113]

Hi Eric. The western blot came back with multiple "indeterminate" marks - which caused all the doctors I brought the test to telling me that I "may or may not" have Lyme disease. One doctor (finally!) told me that yes - based on those indeterminate marks - I did have yet. The other tests I did were dark field blood microscope testing and bio-meridian testing both of which found Lyme in my system.

[@MrFumeCinema]

I'm so sick and I feel like giving up. It's been 4 years. I don't know what to do and I'm so scared

[@tammygonzalez9313]

MrFumeCinema how are you? I hope you didn’t give up! 🙏🤗

[@dezertraider]

Walking LOLLOLLOL OMG I dont drink but Hay ????? have been drunk before ,How do you like the Baby step shuffle???LOL OMG

[@ValiantfortheTruthManuela]

God bless you... I too have suffered with chronic illness similar to Lyme ( CFS) Jesus Is my strength and comfort. He loves you and died for you and for all our sins. I tried to link a bible passage ( book of John, but you tube wouldn't let me!) I hope anyone reading this knows the Truth and real Hope

[@janinacoats2849]

I just had a tick on me now I am scared

[@dezertraider]

NO Shit! ON cant get out of bed.I get out of bed cuz I cant sleep! WEEKS of improper sleep 4-5 h on a good night