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

CCSVI - Liberation and MORE

Hi EVERYONE - ! Sorry I have Not Posted Here for 3 months -- WOW-!! The World has Changed for me since I went to San Diego to get my CCSVI treatment...I came back with a UTI because I have to travel long distances with a catheter. This may have impacted the results of my treatment. I had Good Things Happen but they slowly faded after several weeks. I now have minimal improvements come & go that I did NOT have before. I was told that this has happened to othewrs. Since I've had MS for so long, I'm looking forward to my next CCSVI treatment. Dr. Hubbard had an interview with the Seattle news. Two MS patients from Seattle came to San Diego for CCSVI testing, then treatment at the Del Mar clinic. Because of this, a Seattle newsman gave Dr. Hubbard a lengthy interview on what CCSVI is and how it shows that some of our MS symptoms can be Improved and/or "fixed" because the symptoms are VASCULAR. This is a Breakthru and I believe ALL people with MS should be TESTED for CCSVI. If tests show they have this condition, the treatment is a selection of existing procedures that are Already Being Used for Other People with Other Problems in their veins.