My Lyme Disease Story (Part 2)
thane17 asked:
My story of how I have struggled with Lyme disease for over twenty years. lyme rife disease coil doug machine treatment blog depression fatigue anxiety story pain suffering supplements health herx economy collapse chronic unknown illness cfs cfids me ms als marshall protocol under our skin
Carlo
July 25th, 2009 at 5:46 pm
Susy
Yes I am looking forward to more videos from you. There is so much I would like to say as well but my mind is so foggy its hard for me to articulate it well so I am always happy to see a video where somebody is speaking for me.
July 28th, 2009 at 4:09 am
Bethany
Thane, I’m so sorry you’ve gone through so much. It’s awesome that you’ve posted so many vlogs about your illness. I hope to do the same because there is always so much to say.
July 29th, 2009 at 8:56 pm
Janet
I know what you mean, when I was at my best I worked as a salesman, now I can’t hardly look someone in the eye and social norms just escape me. I hope you are feeling better soon.
July 30th, 2009 at 5:35 am
Nancy
i used to be an extreme extrovert – i can’t connect with people at all now. part of it is i’m too sick to do the things i used to do, and part of it is my mind is gone.
August 1st, 2009 at 1:34 am
Susy
Thanks for watching my video. Sorry to hear you are having worse neurological symptoms. I hope you are now improving. I have been using the Melatonin and i seems to help quite a bit, sometimes I sleep like a baby after taking it. I’m using a rife machine now and it seems to be helping. I hope you are feeling better.
August 4th, 2009 at 1:25 am
Marilynne
Thanks for telling your story. My heart goes out to you. I have had Lyme Disease since 2003 and have tried all the thinks you mentioned. I was able to go back to work for a few years, but have started having more serious neurological problems recently. There is a good Dr. in my area, but he rarely accepts new patients. I found that Benedryl with Melatonin allows me to sleep after months of insomnia. My best to you.
August 7th, 2009 at 10:06 am
Louise
Hey Thane, thanks for posting your lyme story. Im sorry to hear about waht u have been through. Glad to hear that your on treatment and getting better. Hang in there man. let me know if u ever wana talk
August 7th, 2009 at 9:52 pm
Michelle
Thane- I am so sorry you’ve had to go through all of this. Just know you are not alone there are many of us out there. You have much courage and strength for dealing with so much. Take care of yourself and hope to maybe speak with you soon;-)
August 8th, 2009 at 4:29 am
Cam
I´ve had similar symptoms as you for 15 years. Vitamin d seems to have cured me, maybe you should check it out. It´s really important when fighting infections, also mental health. I´m not sure living in a basement is healthy. Good luck.
August 8th, 2009 at 1:08 pm
Vichelle
thanks for doing the vids, I have been wanting to do one for over a year now, and you make me want to do one. I am also ordering the doug coil you just bought, so it is great to see how things go with it for you, so keep us posted. I will do a vid soon hopefully, I to have watched so many stories and they have really got me through. Where do you get your meso silver???? You take care of yourself…..
August 11th, 2009 at 9:06 am
Marilynne
Hey Thanks for watching the vids! No, never had a rash that i recall, seems like most people never got a rash. I haven’t tried the herbal antibiotics much, used gse some and some other mild ones but have been using mostly seasalt and vitamin c and colloidal silver. Best get check out bro! Or, if you use one of these antibiotics and it knocks you on your ass then you really should get it check out. I wish you the best!
August 11th, 2009 at 10:23 am
Janet
Keep up the good work mate enjoyed them, ive been meaning to get tested for lyme for years, did you have the typical bullseye rash?
Have you tried catsclaw/samento?
August 11th, 2009 at 11:58 pm
Marilynne
Hi Sue, Thanks for the Silver info. I’ve actually had a couple requests for a chinese medicine spin on things so i am hoping to make another video about that when my brain is feeling up to it. I just ordered Dr. Zhangs book on treating lyme with TCM so i am going to read that also. I hope you health is progressing well! Thane
August 14th, 2009 at 10:38 am
Chris
Hey There….yes, i am still kicking ass. I just got back from a week in the hospital. Two days in I.C.U. Apparently, someone botched up my liver biopsy procedure on Tuesday and i ended up almost bleeding to death, requiring a blood transfusion, and a bunch of other emergency procedures. I’m just glad to be alive. I was surprised at how quickly one could bleed to death and was grateful to be in the hospital at the time.
August 15th, 2009 at 5:34 am
Susanna
Thank-you for sharing your story. It is nice to know we are not alone!
August 18th, 2009 at 10:27 am
lewis
Wow. I understand your pain my friend. We are in this together. I am on a mission to educate the world about our “invisible” diseases trough my own videos and a documentary I am making. It is so important for us all to tell our true stories. You really are not alone; we are in this together!
Sending love,
Dr Franky Dolan
August 20th, 2009 at 1:49 pm
Violet
Hi Thane, Thanks for your response! I take about 4 tablespoons a day (1 part mesoplatinum, 9 parts mesosilver). Although, my Dr. wants me to be taking 2 tablespoons more…just so hard with all the supplements. I actually don’t know if I’ve herxed on it or not. The Chinese herbs sound really interesting. If you are up to it, I’d love to see a video on that. What you found out in China, etc. I’ve been wanting to learn more about Chinese medicine and Lyme, having heard success stories. Thanks! Sue
August 22nd, 2009 at 11:30 pm
lewis
Hi Thane! Your story is amazing…much more difficult than I realized. I’ll be praying for you.
August 25th, 2009 at 4:18 pm
Louanne
Hi Thane, I’m happy you are doing better! I was wondering how much Mesosilver you are on and what you know about it. I’ve been on for maybe 6 months. A couple months ago I added Mesoplatinum to create a “Germslayer” effect. I’m not sure if it’s helping. But I did run out a few months ago and felt worse when I didn’t have it. Anyway, would love to hear how much you are taking and if it’s helping. Sue
August 27th, 2009 at 5:48 pm
Scott
Hang in LymeLies, you are probably flaring.
August 28th, 2009 at 7:35 am
Butch
I have derealization as well. It’s really scary. I remember the first time I had derealization was when I was probably 16 years old and was at work when it happened. All of a sudden wondered where I was, who I was, what I was doing, etc… it lasted a short while, but afterwards it leaves you feeling out of it for a while. Very scary!
August 29th, 2009 at 6:53 pm
A few days ago I felt like a new person, and now I feel like I’m dying. I guess I expected a miracle. Hope your doing better.
August 29th, 2009 at 8:14 pm
Franny
Hey Thane. That’s quite a story you got there man. Sorry for all of the years of suffering but I’m glad that you seem to be on your way to putting things back together. The folks on here have really been a great help to me. In fact, I only realized that what I had might be lyme by watching YouTube blogs. Searched “chronic illness” and found one person, then another and another. I’d love it if we all met in real life after all of our symptoms are gone and then talked about anything except Lyme.
August 31st, 2009 at 8:35 pm
Samantha
isn’t it amazing to realize you’re not alone? after all this time.. and the fact that many of us ARE alone, essentially, in our everyday lives. anyway, thanks for posting your videos, and much luck with your healing.
August 31st, 2009 at 9:10 pm
Emery
you are NOT alone…It does feel good to know that you are not alone when you here others with similar stories…makes you feel less crazy…since that i what most people have assumed we were or are. keep up with the blogs and keep us posted. hang in there!
October 6th, 2009 at 5:27 pm
Hi Shane,
I am in MN too. I really could relate to everything you said about brain fog.. I am in severe pain most days but i would rather have the pain then this crap in my brain.. i too have had lyme since i was a little girl and was just dxd in 1989 i have had this for a long time.. you need to just keep up the fight and keep your brain active..we CAN do it.. we are strong.. we are brave.. and WE CAN DO THIS especially when we all have each other..Not everyone is the same with this horrid disease that’s why it is comforting when you meet someone that has similiar symptoms.. it helps you “go on”.. it gives you a purpose for living.. because someone ” out there” is suffering like you are..it gives you *HOPE*