Michelle On Lyme - part 1

My story on Lyme Disease - part 1

Category:

People & Blogs

Tags:

• Judd
• Sather
• Studio
• Michelle
• Lyme
• Lymes
• Lime
• Disease
• Borrelia
• Numb
• Tingling
• MS
• Multiple
• Sclerosis
• infection
• tick
• ticks

[michelle6823]

3 months ago I was diagnosed with Lyme disease after loosing my mobility. I live in Canada and have been antibiotics for three months now. I'm slowly regaining my mobility, but suffer with severe fatigue, muscle and joint pain. The health care system here in Canada is in denial of Lyme and many medical professionals don't believe in chronic Lyme.

[venold1969]

@venold1969 I am afraid to get the results because one part of me wants to say I told you so but the realistic side of me knows that even if I prove that I have Lyme, Canada will not treat it. Your story will help to drive me to be tested and I thank you for that because sometimes I begin to think that the doctors are right and I am just crazy.

[venold1969]

I live in Canada and I will be having to get my Lyme testing done in the US at Igenex, I, like you, have been diagnosed with MS but I have a feeling I have Lyme disease. I had the rash but I thought at the time it was ringworm, now my doctor in Canada and all the professional people I have encountered just think I am losing my mind and I never had the rash.

[JasminePeteLee]

I'd highly suggest you pursue it. I'd be curious to see how you responded to antibiotics.

[pris72]

The more and more I read up on Lyme, the more and more I am wondering if this is what I have? I am going through the ringer right now getting test after test after test. I went to Different Dr's Mon-Thur of this past week, and I am still not done. My husband pulled a tick off of my left side going towards my back over a year ago. I live on 5 heavily wooded acres of land in Ga. Now they are testing me for MS, Lupus, MD or multiple myeloma. I have HORRIBLE vertigo. Can't drive not due to it.

[peroxide85]

@JasminePete hey ive been fighting the disease for almost a year now. what kind of treatment did you pursue that seemed to be most effective? iv been doin vit c drips and herbal supplements

[dllmissingerror]

@JasminePete Thanks for the Advise.... yea my D was low too I am on 5000 iU D3 per day.

[JasminePete]

@dllmissingerror Glad you are resonding well. A word of advice if I may...be a patient first AND THEN go advocate ; ) Hard to do but your story will even be more effective. It is 11/10 and I'm still symptom free...did find out though about 1 year ago that my Vit D was THREE!!!! Crazy low - I know it is a 'hot' topic now but get yours checked : )

[dllmissingerror]

Hey Michelle , Great video... I had Symptoms for 5 years

I finally went to a Naturalpathic physician who suspected lyme and ordered the Western Blot

I also cam back Band 23... and after finding out this Band is lyme specific I found a LLMD.

curently going into 4th month of treatment and responding well..

glad to here you are doing well and I will also be putting out a video like yours soon.

Paul

[ilovetrim]

@twinglebaby1 what part of florida do you live in. I also have lyme I live in palm coast. that is just above

daytona beach just in case you don't know.