Positive for Lyme how can she diagnose me with MS

[rena1791]

Positive ELISA and western Blot and my infectious disease doc sais forget about the lyme the MRI show damage caused from Multiple Sclerosis.  meanwhile I am out of antibiotics and feeling miserable.  I just want to live again.  This is so overwhelming wish I could find a doc that knows about lyme disease.  I need help please send any info you might have about a LLMD in Texas or anywhere else for that matter I just want my life back.  

[frustratedexchronicfatiguevictum310]

I am mearly telling people of something that worked for me. Just like anyone else when they talk about anti-biotics or any specific herb they are using.

[JackieCalifornia]

The poster above, 'frustratedexchronic etc.', has been reported to the moderators for trying to sell or promote products on this website, which is against the rules.

[frustratedexchronicfatiguevictum310]

If you would more info on the Resonant Silver. Email them at ***@****. They will be able to help you. This stuff can really help you. It helped me after suffering for many..many years. Good luck.

[rena1791]

Thanks for the help guys and your right no more ID docs for me.  Lesson learned and i am so not believing the MS crap.  

[frustratedexchronicfatiguevictum310]

You do not have MS. Doctors charge big money for patients with MS. So please ignore the MS diagnosis. As far as lyme. Getting tested to me is a really joke. The lyme bacteria (Borrelia burgdorferi) can change their surface protein in a couple hours so they can go undetected from any test and it will be negative most of the time. I do know of a colloidal silver that will turn you around right away. I have had lyme my whole life and I feel better now then ever. I stopped going to my LLMD becasue any "dr" can't really help.

[JackieCalifornia]

Oh my, you are having a rough time.  

I understand that there are not a ton of Lyme docs in Texas, and they don't advertise their existence to avoid problems with the medical authorities, but that doesn't mean there is not anyone ... it just means looking a little harder and quietly.

The best sources are websites and online searches, which will take you to forums like these and to groups of patients.  The following websites change over time, and I haven't checked them all lately, but they may have referral functions where you can search for a local doc.  The last two links below are to Texas groups, if the links are still good.  

ilads [dot] org
lymediseaseassociation [dot] org
truthaboutlymedisease [dot] com
lymenet [dot] org
chroniclymedisease [dot] com
lymedisease [dot] org (California Lyme Disease Assn -- CALDA)
standupforlyme [dot] org (I think this is a Texas-oriented website)
txlda [dot] org  (txlda I think is short for Texas lyme disease association)

Also, I would just search online for "LLMD Dallas" or whatever you are near.  Digging around is sometimes the best way, as tedious as it can be.  

fwiw, infectious disease MDs have drunk the koolaid when it comes to not believing in Lyme.  One of the US docs who first identified Lyme some decades ago is a bigwig in the IDSA (Infectious Disease Society of America), and what he says becomes the official policy of the group, and nonID docs look to groups like IDSA to set standards.

Above all, don't give up!  Let us know how you do, okay?  Take copies of your test results with you when you see a new doc, and always keep a copy of your own of everything.  A good, documented medical history is worth a lot in pursuing a diagnosis.