stage 3 lyme

I found out I have demylination in my brain and my MRI indicates MS or lymes disease. I have memory issues, cognitive thinking issues, nerve pain, brain fog, speech delays. I had a positive test last July but was told it was negative and didn't find out otherwise until I switched doctors. When will something be done to create more awareness with the medical profession... ?

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People & Blogs

Tags:

• Stage 3 lyme
• lyme disease
• herxing lyme

[cleric1104]

Hi Nancy. Thank you for your video. It is indeed a very frustrating disease. So much to deal with in our own bodies and then dealing with the realization that the mass of the medical community is not on our side. It is a struggle. I wish you luck in your journey and my hope for you is that you have many more good days than bad days. I look forward to your updates.

[cleric1104]

Hey Nancy. It sure is a tough hand of cards that we have been dealt. I hope that your treatment will be very successful. It is so hard to stay positive when there is so much going on in the body and when you realize that the great majority of the medical community is not on your side. I wish you many more good days than bad days and a speedy recovery.

[calihipchick]

I was dx'd in 99 .. Lyme can and does get worse. It varies of course, most do get worse tho. One thing most even LLMD dont address is thick blood our bodies life source, its no wonder there are so many symptoms. Other causes as well. Ck out Hemex Labs on line, call ask to send you or doc test kit for hyprercoagulation panel for Lyme. More info on Pain Regimen I found that anyone can use, just not market, in my FB notes Cynthia Rhiner Chase.

[shmero444]

i've been sick for about a year and a half with these exact same symptoms, I've been diagnosed with CFS and depression but now ill be seeing a lyme specialist soon.  This sucks, i used to play D1 bball now i can barely get out of my house. I feel for you lady. I want my life back too!

[Amos1010]

How are you doing? I totally understand! I have been dealing with it for like 2 years and I can really really really relate to what you are saying. Gosh, I know, people don't understand what we are going through. Check out my Lyme Disease Defense Days on YouTube, hope to encourage you.

[bpyjktgiuk]

Brain chip - CHECK MY SITE.

[TruthAboutLD]

Lyme causes brain lesions & many other sympt similar to MS. I am very serious neuro-lyme w/lesions . I am SURE mainstream Md's would say I hve MS. I would not treat for MS since the treatments r corticosteroids & they will weaken you if you have LD a bacterial infection. The most cautious treatment is LD treatement. Stage 3 means little, we all are stage 3 = having 1 year or more. Hang in there keep vlogging. IV helps many - if it has been offered, it can't hurt. Take care.

Prayers,

Dana

[mitchbguitars]

Hi Nancy, Thank you for sharing your story . Please hang in there . my name is Mitch ive came a long way and still fighting (it has bin for me over 12 years)I hope this helps you it helps me. incase you did not know. Have your PH level checked if you can keep it on the alkaline side it will help you feel a little better. ;).oo

[DaveCares54]

Hi Nancy, Thanks for sharing your story. I'm in a similiar situation, long term lyme and just try to accept each day and whatever I need to fight off as a challenge. You are on your way because you are in treatment, that's great. Please keep us posted.

[oldrn73]

Same here, misdiagnosed for about 20 years, found the right doc Oct 08.

Medical doctors remain ignorant by choice. Too hard to treat so tell a patient they aren't sick, it's in their heads.

As in your case, and mine, it really is in your head and everywhere else in your body, the Lyme that is!