by Teresa ConrickTwo years ago, I wrote about my beautiful, vaccine-injured child, Megan, turning 16.  March 2nd marks her 18th birthday and boy, has she gotten some horrible gifts!   the Supreme Court of our United States declared on February 22nd,   (HERE),  that she would be unable – EVER – to receive compensation for her childhood vaccine injuries that have detoured her from a healthy, and pain-free life.  Her vaccine injuries happened 16 years ago, yet we were never told by any of the professionals back then that autism symptoms can be medically related to brain, gut or mitochondrial injury from vaccines.  we are unable to go to those companies who made her vaccines and prove, to a judge and jury, that they were dangerous to her and injured her into "autism."now some false autism advocates will try to convince you that autism "just happens", that it's "just genetic", that "we are better at diagnosing it", or that it's such an intense diagnosis that "parents WANT to get their child labeled" for all of the perks and benefits. PERKS & BENEFITS?  What a crock!  how about this perk- severe medical issues, many of which continue to be ignored or dismissed by the US Medical Establishment. So back to Megan — innocent, injured, nonverbal, and now ….. seizures.  in August, Megan had a seizure, first in 2 years.  She had an initial one back after her 16th birthday and we tested, consulted and waited as her EEG showed no seizure activity. two years, nothing, thankfully, until this past August of her 17th year.  now like many of the symptoms of autism and many of Megan's medical symptoms, nothing is NORMAL and there always seems to be a puzzle piece begging to be solved.  She had that seizure on August 22nd, then the next on September 27th, then October 24th, November 23rd, December 25th, January 27th and now yesterday, February 28th.  Do you see the pattern?  First, I have to say how thankful that these are a monthly experience as SO many children have numerous, daily and even hourly seizures.  they are though of the grand mal/tonic clonic type and so we did initially have her neurologist recommend and start her on anti-seizure medication.  She was on this for much of this time while the monthly seizures were not stopped and instead she began to have erratic and concerning behaviors AND also develop a BAD RASH.  That was a huge concern and we had to stop the medication, which had unfortunately shown no benefit for her anyway.So as the trees to the forest showed a picture, hormones became the culprit.  Megan is completing hormone testing for a full month to help determine how her hormones might be causing these catamenial seizures. Initial blood testing showed abnormal estrogen and progesterone but could not tell us when or how. I came upon that word, catamenial, as I have been doing a lot of reading on hormones and seizures: (HERE)"Catamenial (from the Greek kata, by; men, month) epilepsy refers to seizure exacerbation in relation to the menstrual cycle. Traditionally, the term has been used to refer to seizure exacerbation at the time of menstruation. in its purest form, a woman with catamenial epilepsy may have seizures only at the time of menstruation, but this form is not very common". …… So again, my daughter's medical symptoms exhibit the "not very common."   "Menstrually related hormonal fluctuations in estrogen and progesterone underlie the patterns of catamenial seizure exacerbation. Estrogens facilitate seizures, whereas progesterone protects against seizures. During the menstrual cycle, serum levels of estradiol and progesterone fluctuate Estrogens (in particular estradiol, the most important of the different estrogen forms) have potent proconvulsant properties. they exert an excitatory effect on neurons by stimulating the N-methyl-D-aspartate (NMDA)- type glutamate receptor. in women with epilepsy, intravenous administration of conjugated estrogens activates epileptiform discharges and may result in seizures."Well that seems to be what we are seeing but why?  now it is interesting that words like NMDA and glutamate are at work here as those are also involved in research on autism, like here.."Neuronal glutamate receptor immunoreactivity patterns are abnormal in the hippocampi of thimerosal treated SJL mice" (HERE)

Dr. Nemes, who had duplicated some of the work of Rife, was killed in a mysterious fire which destroyed all his research papers. A similar fire also destroyed the Burnett Lab, which was validating Rife’s work. Royal Rife himself was killed in 1971 by an “accidental” lethal dose of Valium and alcohol at Grossmont Hospital.

Participating in the original 1934 USC study were the following people: Director of the Northwestern Medical School Arthur Kendall, president of USC Rufus Klein-Schmidt, Milbank Johnson, Edward Kopps of the Metabolic Clinic in La Jolla, George Fischer of the NY Childrens Hospital, Kurt Meyer of the Hooper Foundation in San Francisco, and the Chief Surgeon of Santa Fe Railway Whalen Morrison. Dr Milbank Johnson, who was the professor of Physiology and Clinical Medicine at USC, and chairman of the Special Medical Research Committee, operated his own cancer clinic utilizing the Rife therapy for 10 years. He was able to document many cases of cancer reversal there.

The United States medical establishment has not been particularly receptive to Dr. Rife’s research since then, in spite of the numerous anecdotal cases of complete cancer remission, as well as full remission from hundreds of other symptoms, from auto-immune disorders to tuberculosis.

Mark Rigney has been an entrepeneur and health professional for over two decades.electronic cigaretts