2nd CCSVI treatment

Well, my 2nd CCSVI treatment was with Dr. Arata at Pacific Interventionalists. Since I am on Medicare for my disability, I asked them to bill Medicare. Dr. Arata says in Calif. Medicare is managed by Blue Cross and they won't pay. I told them Medicare already paid almost half for my 1st CCSVI procedure which was done at DelMar Vein Clinic, thru Hubbard in San Diego, 6 months ago. Dr. Arata was surprised and said maybe it is because I am from Arizona. So in order to bill Medicare, I had to be admitted as an outpatient to Fountain Valley Hosp.,a few miles away. I'm sorry to say that Dr. Arata could Not reach my left IJV with the wire, so no work done there. But he worked on my right IJV and did something in my Azygos. I am still waiting to get Dr. Arata's report. Overall, my Brain Fog is gone, but I Do NOT have the physical improvements I had after the 1st CCSVI treatment. So I am disappointed, but looking forward to my next treatment. I think this is the Way to Go for me because of the multiple symptom improvements I experienced the 1st time.

CCSVI - I got an E-mail from Dr. Siskin

I feel so IMPORTANT -! I got an e-mail from Dr. Gary Siskin in Albany, N.Y. --WOW--!! If you are reading this & don't know how important he is and all the work he is doing with CCSVI, then you need to Google him & find out. I feel so Blessed & Honored that he took the time from his busy schedule to look at my records from my 1st CCSVI treatment and give his opinion if I should do another treatment. And he said "it's worth a second look", esp. since I had NOTHING done to the azygos vein, due to my scoliosis. I am So Happy-! I don't care that I have to wait until November, because I'm already booked to do my next/second CCSVI in March in Costa Mesa with the Pacific IRs. So N.Y. would be a 3rd time, if necessary. I have to keep all the irons in the fire, as MS continues to Progress & I have 30 years of destruction to undo...

GET BETTER WITH CCSVI TREATMENT-!

There is an Important Event in Seattle coming up, the last weekend in January. Doctors will consult with you ONE on ONE about your Status, so bring any tests you've had done with you & Good Luck!! For More Info. see Kathleen Lynch on FACEBOOK...

Happy Holidays

Happy Holidays and CCSVI Treatment to ALL that Need it -- this will FREE YOU from Many of your MS symptoms. Do you realize you've had this CCSVI condition since your Birth? The Neurologists don't know about this except Dr. Hubbard of San Diego -- ask an Interventional Radiologist who specials in Veins...

CCSVI - Do Ya Wanna Know What it is?

This is a lenghty, but informative interview with a neuro for ALL people with MS: http://www.komonews.com/home/video/106175483.html