Greetings everyone,

I received the written report from my first follow-up scan.  It said I have reflux in my deep left jugular.  Ok what is reflux? Is this bad?  Do I need venoplasty again?

I started LDN last Sunday night.  The taste is awful.  I figure since CCSVI treatment isn't accepted or covered why not start another not accepted for MS medication, LDN.   The accepted medications didn't do a thing to slow down my MS.  I was literally steps away from using a walker, perhaps a wheel chair before I had my CCSVI treatment.

My energy level is still wowing me.  My fatigue is gone to take a nap somewhere besides in me.  My  muscle spasms are another story.  I find around 10 pm they start but are not as severe as before and settle down quicker.

If you live in Ottawa or near enough to drive to it come to my CCSVI get togther.  April 2nd, noon - 3pm

100 Malvern Rd. ( Walter Baker Centre) room 202.

Please r.s.v.p with me .

Stay strong, be brave, never loose faith.

Love

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