Ask The Community About Lyme Disease
 
 

View General LymeTalk in All Categories

 
View questions by:
 

 
View My Profile
 
View Profile

Rife machine? Where to research, buy? How are you using yours?

  • Moto Lymie asks: I don't know anyone personally who is using or has used rife machine therapy. When I mentioned it to my doctor awhile back he shrugged it off, maybe because I wasn't at a place in my treatment to be ready for it, maybe because he doesn't advocate them, I'm not sure. But I'd like to understand more about them from people who have used them....read more
Asked on 2012-05-07 in Treatment
 
 
 

 
View My Profile
 
View Profile

Anyone using sauna therapy?

  • Moto Lymie asks: Wondering what types of sauna therapy people are using for detox/Lyme treatment....read more
Asked on 2012-05-02 in Treatment
 
 
 

 
View My Profile
 
View Profile

if you are treating babesia with mepron/azith, how long until you noticed improvement?

  • benniferobins asks: i am about 2.5 months into treating babesia with mepron and azith. i have a clear cycle of good days and bad days. the bad days i have extreme head pressure, dizziness, fog and then as head symptoms begin to lift, i have major flu like symptoms. how long until you noticed improvement on these meds?...read more
Asked on 2012-04-23 in Treatment
 
 
 

 
View My Profile
 
View Profile

Searching for LLMD South Florida

  • brekashil asks: Hello Fellow Lymies - I am new to the group and have been dealing with Lyme disease for 9 years. I was diagnosed 1 1/2 years ago by a wonderful LLMD in N. CA. My husband and I lived in Indiana our whole life which is where I was bitten. We are now both retired and trying to sell our home in Indiana. We spend several months of the year near Los Angeles and about 7 months in the Florida Keys. I am desperately trying to find a LLMD in Southeast Florida. If anyone can refer a good one to me I would be so grateful. ...read more
Asked on 2011-10-28 in Support Groups
 
 
 

 
View My Profile
 
View Profile

May is Lyme Awareness Month so I will stand with my friends, acquaintances & the other hundreds of thousands of Lyme patients who also are suffering from Lyme.

  • FuN FuNkY Art By Keri Joy Colestock asks: It was not \"in our heads\" it was under our skin. Because of this debilitating disease we feel each others pain as it will strip your life right out of you. The symptoms & damage is HORRENDOUS. Most of us went undiagnosed as cases were not being reported. We never got the bullseye rash that \'shows\' that one has Lyme. 80% never get it. Besides Fibromyalgia & Lyme Arthritis (which I can ignore) I was damaged very badly Neurologically. I also have chronic sinusitis which knocks me to my knees post Lyme symptoms like to reek havoc & make all of your other symptome act up worse. In 9+ years I have had 11 piklines-yes that is what you see in the picture, an IV threaded to my heart. I can get 1-3 infusions a day of antibiotics -I\'ve had them in for up to 3-4 months. 11 piklines in 9 years. My art was my saving grace as staying home in bed was not an option. I decide after I could stand up & focus (8 months) I would concentrate on my art. I sold 1400 \"Wall Dancers\" dolls each made 1 at a time on Ebay then I went to Etsy. So this \"Babe\" knows what one goes through. the reason for this ugly picture & story is because people tell me \"Keri if you can do it I can try... I always wanted to paint... I would like to sew ............so my heart & prayers are with you all & I will stand by your side. This is MY story. Last week i was written up in Artizen Magazine. I know everyone wants to ask questions but I do NOT do support groups or get all over Lyme websites. I KNOW what the disease is so please try & respect my right to not want to talk sick talk with anyone. Say \"hi\" if you like/dislike my work. I am blessed with a beautiful family & friends. I have met great people & learned many lessons on my journey. I cannot change the Lyme Disease but I can choose how I want to live my life & I do! To all of you that have gone through so much of this with me over the years-I love you to pieces! Hugs, Keri...read more
Asked on 2011-05-01 in Emotional Support