Lyme Disease
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19 Forum posts tagged with "Lyme Disease":
Betty Gs CHRONIC LYME Story
by roy
In Lyme Disease Support Forums > General & Support
"Hello friends,
we've published a new article by Betty G, her personal story.
Betty Gs CHRONIC LYME Story
I think its a great article for anyone who has an interest in Lyme Disease, I hope others would want to share their story as well.
thanks Betty G !!!"
In Lyme Disease Support Forums > General & Support
"Hello friends,
we've published a new article by Betty G, her personal story.
Betty Gs CHRONIC LYME Story
I think its a great article for anyone who has an interest in Lyme Disease, I hope others would want to share their story as well.
thanks Betty G !!!"
Related Discussions:
Lyme
by Sherri
In Lyme Disease Support Forums > General & Support
"Last year my husband and I were exposed to Rabies. We had to go for the immunoglobin shot and a series of Rabies vacines. Can the immunoglobin shot cause any problems with the acuracy of the lyme blood test results?"
In Lyme Disease Support Forums > General & Support
"Last year my husband and I were exposed to Rabies. We had to go for the immunoglobin shot and a series of Rabies vacines. Can the immunoglobin shot cause any problems with the acuracy of the lyme blood test results?"
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new to this
by suazojones
In Lyme Disease Support Forums > Introductions & Personal Stories
"had a positive test in aug 2006. The westren bl. came back neg. so I wasen't getting treated for lymes for 6 months. I was getting worse and worse. finally i went to a doctor that started me on antibiodics for lymes. I was on it for a little over a month. I was felling good. Now I have been off it for about three weeks and i'm starting to feel real bad. I'm scared that it wasn't agressive enou"
In Lyme Disease Support Forums > Introductions & Personal Stories
"had a positive test in aug 2006. The westren bl. came back neg. so I wasen't getting treated for lymes for 6 months. I was getting worse and worse. finally i went to a doctor that started me on antibiodics for lymes. I was on it for a little over a month. I was felling good. Now I have been off it for about three weeks and i'm starting to feel real bad. I'm scared that it wasn't agressive enou"
Related Discussions:
Penis Rash ..
by Vaughan
In Lyme Disease Support Forums > General & Support
"Well I've had this mysterious rash for about 1-2 years now. Ever since I've started treating my lyme disease (which is 1-2 years ago), this rash has remained in the place that I should be proud of. But I can't with this disgusting rash.. There are little white bumps, red on the head, everywhere (even on the ball sack).. Is the rash the spirochetes coming out of my skin? or whats up? Can you pl"
In Lyme Disease Support Forums > General & Support
"Well I've had this mysterious rash for about 1-2 years now. Ever since I've started treating my lyme disease (which is 1-2 years ago), this rash has remained in the place that I should be proud of. But I can't with this disgusting rash.. There are little white bumps, red on the head, everywhere (even on the ball sack).. Is the rash the spirochetes coming out of my skin? or whats up? Can you pl"
Related Discussions:
Is Lyme sexually transmitted?
by Bland
In Lyme Disease Support Forums > Tips
"I heard something like that, but never got into it deeper, and I can't find many resources.
I'd like to know if it's possible for my father to have gotten lyme from my mother, before he left.
Also, my mother could never have a serious relationship, since people tended to believe it's a STD, like syphilis. Well, is it? I mean, can it be?"
In Lyme Disease Support Forums > Tips
"I heard something like that, but never got into it deeper, and I can't find many resources.
I'd like to know if it's possible for my father to have gotten lyme from my mother, before he left.
Also, my mother could never have a serious relationship, since people tended to believe it's a STD, like syphilis. Well, is it? I mean, can it be?"
Co-infections
by caregiver
In Lyme Disease Support Forums > Introductions & Personal Stories
"My husband was diagnosed last June with lyme. Was already stage two. Then in December he was also diagnosed with ehlichious or human anaplasmosis. This co infection attacks the muscular system and also the neurological, which has already taken a beating from the lyme. Any one else with co-infections"
In Lyme Disease Support Forums > Introductions & Personal Stories
"My husband was diagnosed last June with lyme. Was already stage two. Then in December he was also diagnosed with ehlichious or human anaplasmosis. This co infection attacks the muscular system and also the neurological, which has already taken a beating from the lyme. Any one else with co-infections"
Related Discussions:
Mental problems in lyme?
by Largerthanlife
In Lyme Disease Support Forums > General & Support
"Can lyme cause psychological problems? My grandma's been living with Lyme half of her life, and was diagnosed about 15 years ago. She was always more or less a wreck, and since she started the treatment she's started to also have better days.
Lately she started to behave very oddly, her, that was always calm and pleasant, now she became aggressive, firstly in language, then even physically, she"
In Lyme Disease Support Forums > General & Support
"Can lyme cause psychological problems? My grandma's been living with Lyme half of her life, and was diagnosed about 15 years ago. She was always more or less a wreck, and since she started the treatment she's started to also have better days.
Lately she started to behave very oddly, her, that was always calm and pleasant, now she became aggressive, firstly in language, then even physically, she"
Related Discussions:
son with lyme disease
by estor12
In Lyme Disease Support Forums > General & Support
"Hi everybody,
We just came back from the doc who said he thinks my son has lyme disease (thinks ?!?!).
He needs to do a couple of tests which I didn’t really understand.
It was so confusing. So many things fall on you at once.
I would also like to get a second opinion on this, can anyone recommend a good doctor for us?
Also I would very much like to hear from other who were in this spot.
Wha"
In Lyme Disease Support Forums > General & Support
"Hi everybody,
We just came back from the doc who said he thinks my son has lyme disease (thinks ?!?!).
He needs to do a couple of tests which I didn’t really understand.
It was so confusing. So many things fall on you at once.
I would also like to get a second opinion on this, can anyone recommend a good doctor for us?
Also I would very much like to hear from other who were in this spot.
Wha"
Related Discussions:
'Happiness depends upon ourselves' -Aristotle
by musicandl0ve
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hey everyone!
Well, I honestly feel like Scarlet819 with starting this. I also don't really know when I got this, my parents and I think it was about 6 years ago when I thought I some how managed to get ring worm. We didn't really think much of it so I kept going on with everything I did without a second thought. I was involved with band, basketball, cheerleading, soccer, judo, and tr"
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hey everyone!
Well, I honestly feel like Scarlet819 with starting this. I also don't really know when I got this, my parents and I think it was about 6 years ago when I thought I some how managed to get ring worm. We didn't really think much of it so I kept going on with everything I did without a second thought. I was involved with band, basketball, cheerleading, soccer, judo, and tr"
Related Discussions:
I think it's Lyme
by erleichda
In Lyme Disease Support Forums > General & Support
"Hi everyone. I have some questions. Several years ago, I had a large red ring on my arm. It looked just like the ones you see from people who have Lyme disease. The doctor said it looked like Lyme but that I couldn't get it here. I didn't get sick so I didn't take it further. With time, it faded.
A few years later, I developed severe fibromyalgia symptoms with full-body pain, fatigue"
In Lyme Disease Support Forums > General & Support
"Hi everyone. I have some questions. Several years ago, I had a large red ring on my arm. It looked just like the ones you see from people who have Lyme disease. The doctor said it looked like Lyme but that I couldn't get it here. I didn't get sick so I didn't take it further. With time, it faded.
A few years later, I developed severe fibromyalgia symptoms with full-body pain, fatigue"
Related Discussions:
feels like a first date...
by Scarlet819
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hi all,
I'm nervous to "tell my story," and I don't really know where to start. I don't know when I got it, so I don't know where the story begins.
My senior year of college I got severely depressed. I ended up writing a suicide note, not with the intention of ending my life, but because I wanted to know what it would say (and I wanted it on hand should I decide to take that cou"
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hi all,
I'm nervous to "tell my story," and I don't really know where to start. I don't know when I got it, so I don't know where the story begins.
My senior year of college I got severely depressed. I ended up writing a suicide note, not with the intention of ending my life, but because I wanted to know what it would say (and I wanted it on hand should I decide to take that cou"
Related Discussions:
New TEEN/KIDS column in PUBLIC HEALTH ALERT pape
by Bettyg
In Lyme Disease Support Forums > General & Support
"[color=#0000FF]from BettyG:
go and check out for yourself the online newsletter they publish monthly! You can a bulk box for $10 for shipping handling; papers are FREE!
I ordered 1 box and took my medical clinic/hospital/red cross/blood banks/ER .. the drs. who treat us. Plus sent copies to my federal senators/house rep and state senator/house rep, plus our govenor, health dept. directo"
In Lyme Disease Support Forums > General & Support
"[color=#0000FF]from BettyG:
go and check out for yourself the online newsletter they publish monthly! You can a bulk box for $10 for shipping handling; papers are FREE!
I ordered 1 box and took my medical clinic/hospital/red cross/blood banks/ER .. the drs. who treat us. Plus sent copies to my federal senators/house rep and state senator/house rep, plus our govenor, health dept. directo"
Related Discussions:
Lyme Literate Doctors
by Linnie
In General Health Forums > Open to All Health Related
"How come Lyme Disease is not listed in your list of doctors? Did I miss it some how? There isn't even a catagory for L. Why?"
In General Health Forums > Open to All Health Related
"How come Lyme Disease is not listed in your list of doctors? Did I miss it some how? There isn't even a catagory for L. Why?"
Related Discussions:
Almost 18 and still have lyme disease
by lizwood17
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hello all! I am going to be 18 in May and hopefully graduating soon. I have had Lyme Disease all my life since I was born... my mother was really sick with lyme disease when she was pregnant with me. The doctors did not treat it soon enough and now it is long term. Since I was 6 or 7 I can't remember too well, I have been getting a injection once a week of bicillin. When I didn't get these shots"
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hello all! I am going to be 18 in May and hopefully graduating soon. I have had Lyme Disease all my life since I was born... my mother was really sick with lyme disease when she was pregnant with me. The doctors did not treat it soon enough and now it is long term. Since I was 6 or 7 I can't remember too well, I have been getting a injection once a week of bicillin. When I didn't get these shots"
Related Discussions:
Vasculitis or MS
by sweedy
In Community Forums > Introductions
"I am new to your on-line community and I had a question I was hoping someone here my be able to answer. I have been ill for a number of years with confusing sytoms that come and go in bad flares. In the begining it was thought to be MS, then with all tests normal, I was given the run around by neurologists. Now many years down the road the flare-ups are getting worse and my MRI shows patterns of d"
In Community Forums > Introductions
"I am new to your on-line community and I had a question I was hoping someone here my be able to answer. I have been ill for a number of years with confusing sytoms that come and go in bad flares. In the begining it was thought to be MS, then with all tests normal, I was given the run around by neurologists. Now many years down the road the flare-ups are getting worse and my MRI shows patterns of d"
Related Discussions:
Stopped taking medicine – what should I do?
by dina34
In Lyme Disease Support Forums > Medicine & Treatments
"Hi,
I’m new here, hope you can help.
My friend has Lyme Disease. He was diagnosed about six months ago.
Yesterday he told me, he was not going to take his medicine anymore.
I’m terrified. What should I do?
Please help.
Dina"
In Lyme Disease Support Forums > Medicine & Treatments
"Hi,
I’m new here, hope you can help.
My friend has Lyme Disease. He was diagnosed about six months ago.
Yesterday he told me, he was not going to take his medicine anymore.
I’m terrified. What should I do?
Please help.
Dina"
Related Discussions:
Life with a twist of Lyme
by Pat
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hello,
You can read my "Bio" at this site. I don't want to type it all over again!
I was 50 when I originally made this site. Luckily, I'm still here to update
my age, 60.
http://www.angelfire.com/ny/lymedisease/
Also, I was a coeditor of Lyme Matters Newsletters which we do not publish anymore but you can read the past issues here.
http://www.angelfire.com/ny/lymedise"
In Lyme Disease Support Forums > Introductions & Personal Stories
"Hello,
You can read my "Bio" at this site. I don't want to type it all over again!
I was 50 when I originally made this site. Luckily, I'm still here to update
my age, 60.
http://www.angelfire.com/ny/lymedisease/
Also, I was a coeditor of Lyme Matters Newsletters which we do not publish anymore but you can read the past issues here.
http://www.angelfire.com/ny/lymedise"
Related Discussions:
My name is Mike and I have Lyme Disease
by mikescetz
In Lyme Disease Support Forums > Introductions & Personal Stories
"My name is Mike and I have Lyme Disease. I found out I had it October 2006. I think that I got the disease in July 2005. I was misdiagnosed an uncountable amount of times. I found out I had Lyme after I honestly thought I was dying. The way I found out I had Lyme was when one of my friends at work told me he had it and it sounds like I have it. And then my mothers friend said the same thing. The d"
In Lyme Disease Support Forums > Introductions & Personal Stories
"My name is Mike and I have Lyme Disease. I found out I had it October 2006. I think that I got the disease in July 2005. I was misdiagnosed an uncountable amount of times. I found out I had Lyme after I honestly thought I was dying. The way I found out I had Lyme was when one of my friends at work told me he had it and it sounds like I have it. And then my mothers friend said the same thing. The d"
Related Discussions:
Great to be here!
by CindY
In Lyme Disease Support Forums > Introductions & Personal Stories
"I’m not too good at presenting myself. I always stutter at job interviews when I’m asked to say a little about me… So I’m gonna keep it simple. My name is Cindy and, during a Safari trip in Panama with my family, I became infected with the Lyme disease bacterium. After a long and painful series of misdiagnosis, the disease was discovered when it already was too late and I became chronic. Still cop"
In Lyme Disease Support Forums > Introductions & Personal Stories
"I’m not too good at presenting myself. I always stutter at job interviews when I’m asked to say a little about me… So I’m gonna keep it simple. My name is Cindy and, during a Safari trip in Panama with my family, I became infected with the Lyme disease bacterium. After a long and painful series of misdiagnosis, the disease was discovered when it already was too late and I became chronic. Still cop"
Related Discussions: