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Is anyone in here familiar with the similarities of RA and Lyme

Disease? I was dx with RA in June 04 and was just tested today for

Lyme, waiting on results now.

While I've been treated for RA I always seem to have these other odd

symptoms come up that just never fully fit with RA. I have always

felt it's just one thing after another. Mostly just weird little

symptoms that by themself dont seem too alarming. Id either ignore

them and they'd eventually go away or just seem too silly to mention

to the dr, and definetely not worth making an apt for. But after

stumbling upon an article about Lyme and a woman being misdiagnosed

with RA I did just a little looking into Lyme and got this sick

feeling inside, because I have almost all of the symptoms.

I went to my family dr today and he agreed the possibility is there

once I started talking to him about all the little odd things that

have come up over the last two years, and the fact that I've had the

bullseye rash only I thought it was ring worm, and when my arthritis

first started, we camped all the time during the summer that year and

the year before. He quickly agreed that I needed to be tested to see

if I was right and said he wished he'd have had all this info before

now.

Anyways, I'm anxious for results, and they might take up to a week to

get back but was just wondering if anyonelse in here has had any

experience like this. My husband said I should be a little happy

because hoping the Lyme we can get rid of, RA we know I can't.

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I’ve only read about Lyme disease

but from what I’ve seen the typical test for Lyme is often negative even

if a patient has Lyme disease. I think the more sensitive and accurate

treatment is called the Western Blot Test but I’m not sure. Just check

to make sure you are being tested by the more sensitive test. I hope the link

below helps. God bless.

http://www.lymenet.de/labtests/brenner.htm

From: Rheumatoid Arthritis [mailto:Rheumatoid Arthritis ] On Behalf Of i_live_in_slippers

Sent: Tuesday, December 12, 2006

7:14 PM

Rheumatoid Arthritis

Subject:

Lyme Disease

Is anyone in here familiar with the similarities of RA

and Lyme

Disease? I was dx with RA in June 04 and was just tested today for

Lyme, waiting on results now.

While I've been treated for RA I always seem to have these other odd

symptoms come up that just never fully fit with RA. I have always

felt it's just one thing after another. Mostly just weird little

symptoms that by themself dont seem too alarming. Id either ignore

them and they'd eventually go away or just seem too silly to mention

to the dr, and definetely not worth making an apt for. But after

stumbling upon an article about Lyme and a woman being misdiagnosed

with RA I did just a little looking into Lyme and got this sick

feeling inside, because I have almost all of the symptoms.

I went to my family dr today and he agreed the possibility is there

once I started talking to him about all the little odd things that

have come up over the last two years, and the fact that I've had the

bullseye rash only I thought it was ring worm, and when my arthritis

first started, we camped all the time during the summer that year and

the year before. He quickly agreed that I needed to be tested to see

if I was right and said he wished he'd have had all this info before

now.

Anyways, I'm anxious for results, and they might take up to a week to

get back but was just wondering if anyonelse in here has had any

experience like this. My husband said I should be a little happy

because hoping the Lyme we can get rid of, RA we know I can't.

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Don’t give up too quickly on Lyme

disease. I looked up Lyme disease diagnosis through Google and the first

couple I read say that blood work is never conclusive to either prove or

disprove Lyme disease. If your history has included the classic symptoms of Lyme

disease I suggest seeking another opinion with someone who is an expert in Lyme

disease. I’m from the Pacific Northwest

and I don’t think we have Lyme here at all, and I sure don’t have

it. All I know about it is what I read on the web.

http://www.niaid.nih.gov/dmid/lyme/diagnosis.htm

I hope you get an accurate diagnosis and

effective treatment. Not knowing what we have and not having a firm plan for

effective treatment is very stressful, and stress is not good for us. God

bless.

From: Rheumatoid Arthritis [mailto:Rheumatoid Arthritis ] On Behalf Of i_live_in_slippers

Sent: Wednesday, December 20, 2006

4:35 PM

Rheumatoid Arthritis

Subject:

Re: Lyme Disease

Thanks for info. I'm from Indiana. My bloodwork came back lastweek

negative. They did two different test, one being the Western Blot and

they said that you had to be over 1.2 to be considered postive and

below .9 to be negative and I was a .2 I was shocked. I was convinced

this was a forsure diagnosis.

I guess I kinda feel like I should let it go and not let myself be so

sure of it anymore because if I do, I may look like a crazy woman

trying to self-diagnose. I dont want to have to get a bunch of second

opinions by other doctors and such. I guess I feel for now I will

just have to keep searching for the reason I have all these odd

things going on all the time.

Thanks

> >

> > Is anyone in here familiar with the similarities of RA and Lyme

> > Disease? I was dx with RA in June 04 and was just tested today

for

> > Lyme, waiting on results now.

> >

> > While I've been treated for RA I always seem to have these other

> odd

> > symptoms come up that just never fully fit with RA. I have always

> > felt it's just one thing after another. Mostly just weird little

> > symptoms that by themself dont seem too alarming. Id either

ignore

> > them and they'd eventually go away or just seem too silly to

> mention

> > to the dr, and definetely not worth making an apt for. But after

> > stumbling upon an article about Lyme and a woman being

misdiagnosed

> > with RA I did just a little looking into Lyme and got this sick

> > feeling inside, because I have almost all of the symptoms.

> >

> > I went to my family dr today and he agreed the possibility is

there

> > once I started talking to him about all the little odd things

that

> > have come up over the last two years, and the fact that I've had

> the

> > bullseye rash only I thought it was ring worm, and when my

> arthritis

> > first started, we camped all the time during the summer that year

> and

> > the year before. He quickly agreed that I needed to be tested to

> see

> > if I was right and said he wished he'd have had all this info

> before

> > now.

> >

> > Anyways, I'm anxious for results, and they might take up to a

week

> to

> > get back but was just wondering if anyonelse in here has had any

> > experience like this. My husband said I should be a little happy

> > because hoping the Lyme we can get rid of, RA we know I can't.

> >

> >

> >

>

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