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i HAVE BEEN SICK FOR 9 YRS i HAVE HAD SO MUCH THAT HAS HAPPENED IM ON IV ANTIBOTICS RISPHEN PLEASE EMAIL ME AT plottlisa@yahoo,com and im on facebook too friend request me there are alot of support out there on facebook take care u are not alone
Hi I hope you get this. Well I sure u had lyme disease. Well recently I have seen a tick in my christmas tree my father squshed it. But I think I may have touched it. Any way. I don’t know if I have a tick on me but now I’m totally freaking out. How should or would I know if I have lyme disease. ? please reply I need help some one needs to explain it to me. How long did it take for u to figure it out.
Have to consider the use of medicines like Bactrim, Flagyl, Albendazole; Tindamax or Tinidazol, Plaquenil, Aralen, Ivermectin (Stomectol), Mephron, Atovaquone, even quinine and what ever is handy. It is a very tough fight, and then has to clean the house, meaning clean the body to get rid of those toxins. Hope you all get help and can recover!
This is not a regular disease that will go like a cold does; this is being invaded by bacteria and parasites and different types of bugs, so the way to recovery is by “killing the bugs”, not only with antibiotics and herbs for long periods of time, but also need treatments with anti-parasitics, anti-malaria; dewormers and more.
I was originally diagnosed with MS in Feb of ’08 and was put on Copaxone daily injections which made me worse. Did a lot of research and stumbled upon LDN (Low Dose Naltrexone) and joined the LDN Yahoo newsgroup. Through that group found many others who had been dx’d with MS only to find out, with the proper testing, they had Lyme. I had my Igenex Labs done last month and I am IgM positive for Lyme. Currently seeing an LLMD and on abx. Joe, I’m wishing you the best man. Get well! – KenC.
Hey guys. . . . PLEASE register at the Oprah Winfrey website and let her know how much you would like to see her do a show on Lyme disease. Dr. Oz thinks the “UNDER OUR SKIN” documentary is wonderful but a show about Lyme won’t be done unless she sees lots of interest. Request that LLMDS and patients be the guests so that we can be heard. Also, Daryl Hall would make a great guest. OPRAH needs to hear about YOUR experience with Lyme disease. WE ARE ALL IN THIS TOGETHER !
God Bless,
Elaine
Google. . . . . “Low Dose Naltrexone Homepage. ” And also here on You tube. . . “Controlling Lyme Disease,” and see the LDN videos by “TropicalDawg” here as well. I have been using LDN, for just over a week now, and feel the need to pass the buzz. This is a drug that helps with the immune system, inflammation and endorphins. Eat as if you had a yeast problem, because Lyme loves what yeast loves. And no sugars of any kind. . . “Including Fruit!”
Hi Joe.
I’m really glad to hear a real live story. I have the exact same symptoms like you , but here in Belgium , test aren’t really accurate, cause they don’t even know alot about this deseas.
Best of luck and get well!
Matt from Belgium (Europe)
What finally helped me after 2 years on antibiotics and Lyme always coming back was Stephen H Buhner’s core protocol. A must read is his book “Healing Lyme”. I am so thankful my infectious disease doctor told me to read it.
Keep the videos going, you’re doing great and make the rest of us realize that we are not alone. . . what a battle we are fighting and the more of us that let the world know, the better the chance that things will change!!
Thanks alot for watching my video and commenting Thane. Sorry to hear that your sick and going through the same problems. Hope that you see improevements soon. Good luck. Message me anytime u want to talk or my name on aim is jocus20 if you use that.
Hey Joe, Congrats on making the video! I just got diagnosed a few weeks ago. I’m about the same age as you. I’ve been sick since childhood and am relieved to finally attach a name to my ailment. I have nearly the exact same neurological problems as you. The derealization sux totally. Its completely handicapping. Its so hard to engage in this world when it doesn’t even seem real. I am also having a lot of trouble with relationships. I wish you the best of luck joe.
Hey Thanks Shandy. Sorry for the volume issues. I do remember many tickbites in my lifetime all throughout growing up. Also about 4 months before i got sick i found i tick on me not attached.
Hey Jocus. I got the LD and Co as well. WE’re about the same age, and it sucks. I got mine in junior year of college. The derealization sucks, i have that and its the worst symptom ever. Its terrible. I’m hoping it will go away when i go on Levaquin for Bart. But if this IV stuff doesn’t work i’m doing herbs and the Marshall protocol.
February 26th, 2010 at 7:31 am
will he ever get better ?
February 26th, 2010 at 8:21 am
i HAVE BEEN SICK FOR 9 YRS i HAVE HAD SO MUCH THAT HAS HAPPENED IM ON IV ANTIBOTICS RISPHEN PLEASE EMAIL ME AT plottlisa@yahoo,com and im on facebook too friend request me there are alot of support out there on facebook take care u are not alone
February 26th, 2010 at 8:57 am
Hi I hope you get this. Well I sure u had lyme disease. Well recently I have seen a tick in my christmas tree my father squshed it. But I think I may have touched it. Any way. I don’t know if I have a tick on me but now I’m totally freaking out. How should or would I know if I have lyme disease. ? please reply I need help some one needs to explain it to me. How long did it take for u to figure it out.
February 26th, 2010 at 9:55 am
Have to consider the use of medicines like Bactrim, Flagyl, Albendazole; Tindamax or Tinidazol, Plaquenil, Aralen, Ivermectin (Stomectol), Mephron, Atovaquone, even quinine and what ever is handy. It is a very tough fight, and then has to clean the house, meaning clean the body to get rid of those toxins. Hope you all get help and can recover!
February 26th, 2010 at 10:25 am
This is not a regular disease that will go like a cold does; this is being invaded by bacteria and parasites and different types of bugs, so the way to recovery is by “killing the bugs”, not only with antibiotics and herbs for long periods of time, but also need treatments with anti-parasitics, anti-malaria; dewormers and more.
February 26th, 2010 at 11:17 am
I was originally diagnosed with MS in Feb of ’08 and was put on Copaxone daily injections which made me worse. Did a lot of research and stumbled upon LDN (Low Dose Naltrexone) and joined the LDN Yahoo newsgroup. Through that group found many others who had been dx’d with MS only to find out, with the proper testing, they had Lyme. I had my Igenex Labs done last month and I am IgM positive for Lyme. Currently seeing an LLMD and on abx. Joe, I’m wishing you the best man. Get well! – KenC.
February 26th, 2010 at 11:35 am
I am in the same exact boat as you Joe =/ just stay strong because you can over come this, thats what I keep telling myself.
February 26th, 2010 at 12:07 pm
Hey guys. . . . PLEASE register at the Oprah Winfrey website and let her know how much you would like to see her do a show on Lyme disease. Dr. Oz thinks the “UNDER OUR SKIN” documentary is wonderful but a show about Lyme won’t be done unless she sees lots of interest. Request that LLMDS and patients be the guests so that we can be heard. Also, Daryl Hall would make a great guest. OPRAH needs to hear about YOUR experience with Lyme disease. WE ARE ALL IN THIS TOGETHER !
God Bless,
Elaine
February 26th, 2010 at 12:34 pm
Google. . . . . “Low Dose Naltrexone Homepage. ” And also here on You tube. . . “Controlling Lyme Disease,” and see the LDN videos by “TropicalDawg” here as well. I have been using LDN, for just over a week now, and feel the need to pass the buzz. This is a drug that helps with the immune system, inflammation and endorphins. Eat as if you had a yeast problem, because Lyme loves what yeast loves. And no sugars of any kind. . . “Including Fruit!”
February 26th, 2010 at 12:57 pm
Hi Joe.
I’m really glad to hear a real live story. I have the exact same symptoms like you , but here in Belgium , test aren’t really accurate, cause they don’t even know alot about this deseas.
Best of luck and get well!
Matt from Belgium (Europe)
February 26th, 2010 at 1:34 pm
What finally helped me after 2 years on antibiotics and Lyme always coming back was Stephen H Buhner’s core protocol. A must read is his book “Healing Lyme”. I am so thankful my infectious disease doctor told me to read it.
February 26th, 2010 at 2:30 pm
Thanks Addy, I appreciate it. I will be making a new video soon. Hope you are doing well.
February 26th, 2010 at 3:03 pm
Keep the videos going, you’re doing great and make the rest of us realize that we are not alone. . . what a battle we are fighting and the more of us that let the world know, the better the chance that things will change!!
February 26th, 2010 at 3:10 pm
Thanks alot for watching my video and commenting Thane. Sorry to hear that your sick and going through the same problems. Hope that you see improevements soon. Good luck. Message me anytime u want to talk or my name on aim is jocus20 if you use that.
February 26th, 2010 at 3:56 pm
Hey Joe, Congrats on making the video! I just got diagnosed a few weeks ago. I’m about the same age as you. I’ve been sick since childhood and am relieved to finally attach a name to my ailment. I have nearly the exact same neurological problems as you. The derealization sux totally. Its completely handicapping. Its so hard to engage in this world when it doesn’t even seem real. I am also having a lot of trouble with relationships. I wish you the best of luck joe.
February 26th, 2010 at 4:15 pm
Thanks for your comment Mrs mozart.
February 26th, 2010 at 4:18 pm
Joe, Thank you for giving those of us with Lyme a voice.
February 26th, 2010 at 4:44 pm
Hello everyone,
Wrote a Lyme brochure with the help of 2 Lyme specialists. Will email to anyone.
Elaine in VA
February 26th, 2010 at 5:02 pm
Hey Thanks Shandy. Sorry for the volume issues. I do remember many tickbites in my lifetime all throughout growing up. Also about 4 months before i got sick i found i tick on me not attached.
February 26th, 2010 at 5:55 pm
Joe, I could barely hear you
Did you say you remember a tick bite??? I am so happy you are making videos now, the more voices the better!! 
February 26th, 2010 at 6:27 pm
Hey Jocus. I got the LD and Co as well. WE’re about the same age, and it sucks. I got mine in junior year of college. The derealization sucks, i have that and its the worst symptom ever. Its terrible. I’m hoping it will go away when i go on Levaquin for Bart. But if this IV stuff doesn’t work i’m doing herbs and the Marshall protocol.
ps. conniekillbug is single.
February 26th, 2010 at 7:17 pm
Thanks so much JD. Ive seen your videos and they were some of my inspiration to do this.
The sound is really low on this so i was thinking i might have to redo it. Im not sure tho.
I appreciate all your kind words and support.
February 26th, 2010 at 7:20 pm
Thank you for having the courage to share your story. I have a lot of your symptoms, so thanks for going more in depth with ur neuro symptoms.
I feel for you, hang in there. Definitely make more vids, it is so healing meeting other lymies.
I will pray for you.
Best wishes ,
JD
