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.
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.
@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.
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.
@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
Thanks for this video. I have Lyme, and also the same confusion and frustration from the doctors. I have a lot of the same symptoms, and am sorry and sad that the peson I used to be seems to be gone now. Unfortunately I do not have religious faith and I am not about to get any....so I just feel alone, I have Lyme, that's it. ALL my blood tests showed positive for Lyme, I had the rash, I have all the symptoms.Five doctors told me I am only crazy. They say there is no reason to think I have Lyme
Michelle, this video is an Ace! Quite an attention getter. It should be viewed by politicians, med students, doctors and lay. This chronic infectious Disease is allowed to cause 'unnecessary' ruin and suffering. It should be an envy of any terrorist.
wow incredible........Drs. should really brush up on Lyme disease..........Maybe some new med. I have Lyme also...........in Fla. where the Drs. dont really know an awefule lot...........Im fighting this hell too. God love you.
Thanks so much for posting this. I sent this link to a friend who is being treated for MS. She has an appointment in June with the doctor in Mo. My son and I have Lyme but are to far (like in another country) away to go see him. Is there any way we could pm each other?
I was on a rotation of antibiotics for 14 mo.(nystatin the whole time too)(off for every Herx). My biggest gains happened when I was flat on my back for almost 2 weeks with an unrelated to Lyme ruptured disc. I learned quickly that REST is HUGE to one's recovery. I also cut the sugar and pushed the greens-alkanized. I got lots of exercise, sunshine, water to flush system, but believe my biggest "tool" was prayer. My faith/trust in Jesus sustained me throughout. God is the Great Physician !
What a blessing! thank you so much for making this video and for sharing about your faith. It is God and God alone who can heal and repare! God bless you!
You are definitely one of the lucky ones, there are so few it seems that get well. Same as destiny4 below, I have many more symptoms and have battled for years. You lucked out and hit the right combo of abx.
I know about what yr going threw. I was bit in 1992, then 1996, and now get to stay home 24-7, becouse I cant do anything without colasping. Google Dar's Toy Story, I wrote it 1 year ago, to let others know what we go threw every day. Been downloaded 6 Mil. times in 1 year. Its on Lyme-Net. Dont look back@what ya did, see what ya can do, it could be worse,like me. Prayers can only help. Were alone out here,and can,hoping anybody will hear us. Texas Dar !
Michelle, we have a Christian Lyme forum at truthaboutlymedisease (dot) com some of the people would love for you to visit us and post...we would love to talk with you.
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.
michelle6823 3 months ago
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.
venold1969 6 months ago
@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 6 months ago
I'd highly suggest you pursue it. I'd be curious to see how you responded to antibiotics.
JasminePeteLee 10 months ago
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.
pris72 10 months ago
@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
peroxide85 11 months ago
@JasminePete Thanks for the Advise.... yea my D was low too I am on 5000 iU D3 per day.
dllmissingerror 1 year ago
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
dllmissingerror 1 year ago
Thanks for this video. I have Lyme, and also the same confusion and frustration from the doctors. I have a lot of the same symptoms, and am sorry and sad that the peson I used to be seems to be gone now. Unfortunately I do not have religious faith and I am not about to get any....so I just feel alone, I have Lyme, that's it. ALL my blood tests showed positive for Lyme, I had the rash, I have all the symptoms.Five doctors told me I am only crazy. They say there is no reason to think I have Lyme
portnoysplace 2 years ago
Michelle, this video is an Ace! Quite an attention getter. It should be viewed by politicians, med students, doctors and lay. This chronic infectious Disease is allowed to cause 'unnecessary' ruin and suffering. It should be an envy of any terrorist.
andadorsag 2 years ago
wow incredible........Drs. should really brush up on Lyme disease..........Maybe some new med. I have Lyme also...........in Fla. where the Drs. dont really know an awefule lot...........Im fighting this hell too. God love you.
twinglebaby1 2 years ago
@twinglebaby1 - Olive leaf extract and beef lard, lamb fat is no.1
Catherine8raw 1 year ago
@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.
ilovetrim 1 year ago
Michelle,
Proud of your bravery, we need more like you.
Fight the fight.
There are many of us trying very hard, just published, proves chronic Lyme.
Thers lots of love and support out there.
LymeReality 2 years ago
Thanks so much for posting this. I sent this link to a friend who is being treated for MS. She has an appointment in June with the doctor in Mo. My son and I have Lyme but are to far (like in another country) away to go see him. Is there any way we could pm each other?
karged 2 years ago
You are an amazing person. Best of luck to you & God bless!
chiefer99 3 years ago
I was on a rotation of antibiotics for 14 mo.(nystatin the whole time too)(off for every Herx). My biggest gains happened when I was flat on my back for almost 2 weeks with an unrelated to Lyme ruptured disc. I learned quickly that REST is HUGE to one's recovery. I also cut the sugar and pushed the greens-alkanized. I got lots of exercise, sunshine, water to flush system, but believe my biggest "tool" was prayer. My faith/trust in Jesus sustained me throughout. God is the Great Physician !
JasminePeteLee 3 years ago
What a blessing! thank you so much for making this video and for sharing about your faith. It is God and God alone who can heal and repare! God bless you!
levierica2008 3 years ago
God and suffiicient funding for research.
bridude2001 3 years ago
Wrote an informative Lyme brochure with help of 2 Lyme specialists. Will email to anyone.
Elaine in VA
ecftube 3 years ago
Thank you Michelle:-)
alicat4377 3 years ago
You are definitely one of the lucky ones, there are so few it seems that get well. Same as destiny4 below, I have many more symptoms and have battled for years. You lucked out and hit the right combo of abx.
lymelights 3 years ago
I love the video. Very positive and informative.
RaiseCFSawareness 3 years ago
I know about what yr going threw. I was bit in 1992, then 1996, and now get to stay home 24-7, becouse I cant do anything without colasping. Google Dar's Toy Story, I wrote it 1 year ago, to let others know what we go threw every day. Been downloaded 6 Mil. times in 1 year. Its on Lyme-Net. Dont look back@what ya did, see what ya can do, it could be worse,like me. Prayers can only help. Were alone out here,and can,hoping anybody will hear us. Texas Dar !
texasdar 3 years ago
Michelle, we have a Christian Lyme forum at truthaboutlymedisease (dot) com some of the people would love for you to visit us and post...we would love to talk with you.
cotmh 3 years ago
Great video, I had a lot of the symptoms that you talk about. Im still battling.
destiny4mee 4 years ago