Could I have ms / lymes desiese or anxiety disorder

Hey James.   Anxiety is just one of many symptoms of Lyme.  Doctors in Canada are catching on now that it's running rampant.   It's really easy to cure tho.  Well it was for me and those that will listen.  I'm using a product called MMS. It's got a bad rap for being called bleach but it isn't.  Lots of doctors in Tijuana are treating with it now.  Best to actually call in water purification tablets in liquid form because that's what it is.  

This will take all your symptoms away if you start slow and get up to 20 drops per day.  It's sodium chlorite mixed with an acid.  Best is citric acid.   Or lemon juice/vinegar can be used as a substitute.    The drops cost 1 cent each so it's a whopping 20 cents to make u feel like a gazillion dollars again.    My motor skills and my clarity is now better than it ever was.  I'm beating everyone in golf and squash because my hand eye has improved a Tonne.   It's magic potion and just google it and read the testimonies.    Mmstestimonials.is I think.   Anyways it's saved me.  Hope u believe it cuz I suffered with Lyme to the point i thought I had less than a few weeks to live and then someone shared this product with me and I was working after being on it 3 days.   I would suggest going on a product called copper1 and Lyme ease and Lyme core as well.   And take turmeric.  It's magic as well.  Hope this helps.   Cheers 

To reply to your question and the above poster about Lyme, the fact is you don't really have a clear diagnosis in hand.  Could be Lyme, it could be MS, it could be a lot of things.

I would advise going to a doctor and getting tested for Lyme or seeing if they refer you to a neurologist to get an MRI and test.

Now I have to speak up regarding Lyme, and don't mistake I'm saying it's not real, because it is, but I was told I have Lyme by several well meaning friends and a "Lyme literate" doctor, and after chasing the Lyme thing for over a year with various treatments and antibiotics, etc, I never found any success or accuracy to it and none of these things worked for me.  They will tell you that you have to get tested by a specialty lab and 'normal' blood tests wont discover it, but I've found that to be a lot of hogwash.  My blood test came back positive for Lyme from a 'specialty' lab but none of the treatments ever amounted to anything.  I don't know about this MMS thing since I've never heard of it, but all I can share is that all the various supplements and theories proposed for me were a waste of time, money and energy.  I will however agree with the tumeric, I've been taking that and black seed oil and it really seems to help with inflammation, which lends itself to the fact that  I indeed have MS, not Lyme.

The bottom line is both Lyme and autoimmune diseases are rampant and a lot of our symptoms match these diseases.

In any event I will share what HAS been working for me, and really should help anyone and everyone which is diet and exercise.  I always thought I was a healthy eater until about 6 months ago I saw a doctor who advises a plant based diet (no meat, dairy, eggs, essentially vegan)  While I was skeptical, I recommend this to everyone because it really helps out with the fatigue and energy thing.  If you watch documentaries like forks over knives or what the health, you will see what and how we eat is really affecting our bodies and you can control a lot of medical conditions by your diet.  Let food by thy medicine.

Try it for a month and see how you feel while you research and look for a diagnosis of your actual medical condition(s).

I couldn't agree more with what jaredboy said!  Very solid advice.  I have MS confirmed by clinical as well as MRI and so far function pretty well.  My main symptoms are fatigue, weakness in my limbs that comes and goes, some leg spasms and of course numbness and tingling mainly in feet.  I have felt poorly for approximately 8 years but diagnosed 2 years ago.  I did go down the Lyme road because that was a more acceptable diagnoses to me than MS because there is potentially a cure for Lyme.  I did have my blood sent to a private lab in California and tested borderline positive for Lyme.  Fortunately, I am blessed to have a wonderful GP who was willing to put me on the standard Lyme treatment.  She knew I was having a hard time accepting a diagnoses of MS and has supported me fully as I've done the research and gone off on certain speculations as to what this could be.  I really liked the above poster's advice when he suggested diet and exercise to try for a month while seeking an actual diagnoses.  Well said!  I do believe that that along with proper rest is vital when dealing with MS or any autoimmune disease.  It's an excellent starting point and in the meantime, do the research to educate but please, please don't let it define your life.  It's easy and scary to get caught up in all the internet has to offer so maybe limit yourself to a small amount of time each day to dedicate to research.  Lyme is definitely out there but I fear that many Lyme labs and Specialists are taking advantage of scared and vulnerable people.  Good luck to you.