Autisticate Dalmayne

6.9.15

A twinkle in the night sky.

Tamara Wilcox -Curtis was quite simply blessed, she was delivered of a beautiful son on the 3rd of December, 2008 . He was a twin to his younger sister. She named her blessing Fuzani.

As Fuzani grew older the joy he brought was was enlightening, people often said it was as if he had been here before as he had a knowing look in his eyes coupled with a cheeky little smile.

He was always smiling.

“ Fuzani was always a happy baby”, recalls Tamara.

“ When he was 1 and half years old he started crying a lot. We did not know the reason.

He then started to get ear infections. Antibiotics didn’t work. He continued to have the infections. So at the age of 2 we got ear tubes in his ear.

The ear infections went away. Fuzani was doing fine”.

The relief Fuzani must have would have been immense, but then he faced another challenge, his verbal communication did not develop. This led to great frustration.

He began to have meltdowns, violent mood swings that lasted for a long time with no reason apparent to the family.

“ We then started to noticed that he wasn’t talking. His sister was talking and saying words that was aligned with her development.

We talked to his doctor about this and we were keeping an eye on this.

Then all of a sudden he would out of the blue get violent.

He would head butt you. He would throw hisself on the floor and he would hurt himself.

I was very concerned. He was doing these things and he was non verbal. I didn’t know what to do.

We continued to go to his doctor about his actions and development.”

Tamara’s motherly instinct clearly told her something was different about her little son, he had a sense of adventure that knew no bounds and recognised no danger.

More worryingly he did not outwardly react to pain either.

“ The last straw was when he chipped his 2 front teeth. He didn’t cry or anything. In fact when he would hurt himself he never cried. I just noticed he chipped his teeth.

Another thing that caused my concern was when he smashed a light bulb. He walked into my room and he had glass and blood coming from his feet. Again he wasn’t crying. He just stood there.

He was fixated on lightbulbs. So we took every lamp out our house….

Then his doctor gave us a referral to see a neurologist. At that same appointment they diagnosed him with mild to severe autism.

They gave us a lot of information that day. The neurologist also told us that it was good that he was diagnosed early because with lots of therapy and support he could become better.

It was a sad and hectic time for my family. We enrolled him is another school which had an autism classroom with only 8 students and 3 teachers.

We started physical and occupational therapy for him.

I researched and started to learn as much as I could. We even started learning sign language as a family. As a means to help Fuzani communicate with us.

Fuzani was diagnosed with autism at the age of 2.”

Finally the family had an answer as to what made their son so unique, looking after him was a rollercoaster of emotion, challenging yet loving with a inner light that could light up a cloudy day. From Tamara’s memories of day to day caring of Fuzani she told me as follows,

“ Caring for Fuzani was very hard. However we learned to adapt to it quickly.

Numerous doctors appointments, therapist appointments, school, trying to potty train.

Even having to make him his own special meals and grocery shopping specifically for him.

He was a very picky eater. His favourite foods were chicken nuggets, cheese pizza, dry cereal, and chocolate chip cookies(homemade).

He loved water and milk. Actually water was his favourite drink. He would drink a litre a day, he started to like grilled salmon, waffles, bagels with cream cheese and grilled chicken.

Through time and struggle, Fuzani was a lot more happier. He loved to kiss and hug people.

Life however wasn’t without its challenges, sensory issues, a mixture of frustration and shutdowns could make it hard for Fuzani, but he was a cheerful little boy who with a lust for life and a curiosity that amazed all around him.

“ I believe he was content. Fuzani loved the outdoors. He lives to play and run. He loved his wagon and his big wheel. He could stay outside for hours.

My best memories of him was the fact that he loved his brother and sister. He would always grab their hand and take them to where he was.

He would sit and watch his older brother play his video games, watch cartoons with his twin sister.

Fuzani loved Spider-Man, veggie tales, puzzles and his iPad. His favourite toys were his sensory castle and Thomas the Train.

He loved to laugh and smile. His laughter and smile would brighten up any room. He love to show love and be loved. He loved to kiss and hug.

He didn’t do well playing with other children, he always played beside them.

However he loved adults. Many adults loved him as well.

I was constantly told by other adults that you have a very special child. He is so precious.

Autism professionals will tell me that a lot of children with autism have very keen sensory issues. They don’t like to be touched, hugged or anything.”

Fuzani was truly unique and very caring remembers Tamara.

Tragically Fuzani passed away on Feb 27,2015.

Tamara now recounts Fuzani’s last days, the joy of him playing with his siblings then up to that fateful day when Fuzani passed away, leaving his family devastate with a hurt that will never leave them.

“ Fuzani was very healthy. In fact he had just had his annual physical a month prior.

Fuzani never spent a day in the hospital except when he was born and that day. Fuzani was gone within an hour.

He, along with his brother and sister were playing in the snow the day before.

Later about 5pm he started a fever. We gave him medicine and a bath.

He did fine. Around 11pm my husband him more medicine. He still had a low grade fever.

I went to work at 11pm. I got off at 7am

When I returned home. I asked my husband about him. He says that he was doing fine. He didn’t have a fever.

I checked his temp and it was 99.

So I gave him more medicine.

I have him another bath. I fed him oatmeal and apple juice. He ate it all and drank all of the juice.

Fuzani went downstairs and brought me a bottle of water to open for him. I opened it and he drank some and them he lay down.

I tried to make a doctors appointment but they couldn’t see him until 2pm.

So I told my husband “ Lets just take him to urgent care. I think he needs antibiotics”.

I showered. Then I lay down. I told my husband to get our other children dressed and get your self dressed because urgent care opens at 10.

He says “ Ok I’ll just go to work after”.

He woke me up around 9:30 and told me he was going to warm up the car.

“ Go ahead and get Fuzani dressed. Everyone is ready. “

I got up got myself together.

Then I went to get Fuzani up.

I turned him over and he took his last breath.

I instantly ran downstairs and told my husband to call 911 and tell them CPR is in process and it’s a 6 year old boy.

I started performing CPR on my precious son. My husband was on the phone with 911 and they were giving me a lot of support and instructions.

I work in the medical field. I had just re certified my CPR and first aid 2 weeks prior.

Then the paramedics arrived. It seemed like it only took 5 minutes. Then other EMTs arrived along with police officers.

Long story short. They transported him to the hospital. He passed away within 1 hour. He didn’t make it to ICU

My husband and I held him until the end. While his grandmother and grandfather were present.

We are still waiting on the autopsy report. Even to this day 6 months later…..

I can add a lot more.

That day when he passed.

Fuzani didn’t have a fever throughout the night.

Actually my husband checked his temp 1 hour prior to me coming home and throughout the night.

He had a low grade fever when I got home. It was 99.

His twin sister sat next to him with her iPad and played videos that he loved. She kissed him a lot.”

I can’t begin to imagine the pain.

Tamara has since raised awareness and promotes acceptance in the autistic community in Fuzani’s memory, she has a substantial Facebook support group and a heart warming tradition of Fuzani Friday. Each Friday a tribute post and a photo of her precious son appears in my newsfeed. I cherish it as many others I know do.

To Fuzani, P. I .P.

Play In Peace, a twinkle in the night sky.

Parasites, what do they actually look like?

Posted by: Emma Dalmayne

According to the “Angel” Kerri Rivera and her book ‘Healing the symptoms known as Autism’ parasites are the cause of autism, and using chlorine dioxide which is used to clean swimming pools can flush them out. How? By flushing CD otherwise touted as Patriot Water or Miracle Mineral Solution mixed with purified water straight up into the colon in an enema or given orally. This, she says will cure your child’s neurological make up thus ridding them of autism which many parents see as an inconvenience.

There’s no disputing that parasites exist as the following links show BUT what’s being lost, no taken from these children is bowel mucus and lining not parasites.

The tragedy being that as you can see in the attached screenshots from the closed group CD Autism, the things that are being photographed and put up are plainly not parasites.

They are the lining of the children’s bowel. Parents put these pictures up proclaiming that they are worms and boast over the size of their own children’s detached bowel lining

The admins, one being Rivera advise them on their worries which range from “My child’s lips are turning blue, my child can’t walk” and most memorably “ My child has turned yellow”.

They are advised not to seek medical help, not to give the children paracetamol and never to confide in a health professional or social worker what they are dong to their children.

If this can show at least one of these deluded souls that what they are reaping from their children after they held them down and flushed bleach up them is not parasites then I’ll have done my job here today.

Oh and me? I’m an autistic adult, with autistic children. I will show you what parasites, real parasites look like and you will see the difference.

I’ll show you look at the screenshots………..

http://www.afraidtoask.com/bm/

http://www.parasitecleanse.com/GALLERY.HTM

Bowel mucus

http://youtu.be/ePPu7l739xM

http://www.healthline.com/health/mucus-in-stool#Overview1

Tapeworms

http://youtu.be/wZcsGe3FYF4

Roundworms

http://youtu.be/0RQ4-Q7V5PM

http://youtu.be/kUsQO5hx3DQ

Guinea worm

http://youtu.be/T9uom0zhGYQ

http://youtu.be/O6nYlRhjQ3o

Pinworms

http://youtu.be/PrUlhufWlIA

Ascaris worms

http://youtu.be/N0hY4_MMxM4

Sorry so many but I want to blast these fuckers right out of the water!!

3.9.15

David Noakes and the GcMAF controversy – Exclusive

Posted by: Emma Dalmayne

After speaking with Doug Jewell, this reporter was keen to dig further into the people who are selling GcMAF and alleging it can cure/purge autism. I had seen David Noakes previously on The BBC One Show in May and have shared my opinion on his Immune Biotech in a previous article. The UK health watchdog branded GcMAF “a significant risk to health” back in February of this year when the product was identified as being contaminated. Importing the drug GcMAF into Guernsey was banned. So I reached out to Mr Noakes to get his side of the story.

The following article includes the opinions of David Noakes, Fiona Oleary and Catherine Hall, the head of The National Autistic Society for Guernsey.

Mr Noakes was very hesitant at first, asking assurances that Autism Daily Newscast would not twist, misrepresent and mislead people. He was very concerned that when BBC One Show came to Guernsey everything he said was fraudulently misrepresented. (Readers can watch for themselves part 1 of this of the BBC One Show below.)

I duly gave my assurance that Autism Daily Newscast would let his words speak for themselves. For fairness and transparency, all three interviews are verbatim emails sent to this reporter.

Fiona Oleary herself is an autism advocate and keen campaigner against autistic mistreatments and has two autistic sons. Catherine Hall has three sons on the autistic spectrum and has met Noakes face to face at their AGM for the NAS where he stood up and announced he could cure autism.

As follows is my correspondence from Noakes where he has given Autism Daily Newscast permission for this as long as it is printed without editing. Bear in mind this is an unlicensed unproven product and Noakes has been shut down by the MHRA. Noakes has no medical background.

“Dear Emma,

GcMAF is a human protein made by 5 billion healthy people. It is a human right. One billion unhealthy people can’t make it, because their disease (which includes cancer) blocks it.

200 scientists have written about 120 scientific research papers on it, so its a well understood protein.

At Immuno Biotech our four scientists wrote 32 research papers, peer reviewed and published in the world’s top scientific journals.

Our scientists, who have spent 22 years in GMP, extract our GcMAF to better than GMP quality, and test each batch 9 times. Our sterility is done internally, and externally by an independent laboratory. It has always been perfect.

We have supplied 9,000 people through 350 doctors and clinics in 80 nations.

Of those 9,000, 3,500 are autistic children.

In our clinics our seven doctors, with the scientists help, took the autism recovery rate from 15% when we started, to 60% today.

The last method we were using was for the child to breathe in the GcMAF through a nebuliser, and then hold an ultrasound probe on their temple, to open the blood brain barrier.

60% of autistic children would then recover inside 2 weeks.

The MHRA then closed us down. They protect the billion dollar profits of the big pharmaceutical corporations, have big pharma directors on their board. and deny the public access to safe, proven, effective remedies like GcMAF. See www.mhracorrupt.st for the 10 public bodies who have written reports stating the MHRA is corrupt.

The public petition to disband the MHRA has reached 8,000 signatures in 4 months.

We no longer supply GcMAF but our distributors still do. If you go to immunobiotech.eu and register, we will put you in touch with them or with their clinics.

A vial of GcMAF, often enough to eradicate autism, costs €450. It treats cancer successfully in 70% of cases. Chemotherapy costs £40,000 a round.

GcMAF:

Rebuilds the immune system

Improves human neuronal metabolic activity through cAMP signalling – autism, ME/CFS, MS, ALS

Counters toxic effects including cadmium – ME/CFS

It abolishes neuropathic pain due to neuro-oxidative stress (stress due to the anti-cancer drug oxaliplatin) in the lab. (neurodegenerative diseases and autism that have oxidative stress as a pathogenetic mechanism)

It increases neuronal connectivity by promoting differentiation and the formation of dendrites and neuritis (autism and ME/CFS, where there is a lack of connectivity between neurons).

We have written research papers on all of these. See “The science” on the gcmaf.eu website.

14 doctors have been clumsily assassinated. That is to scare off other “alternative” doctors – they can see it is not suicide, and can see it is murder. The clumsiness is deliberate. That still leaves 350 doctors using GcMAF in 80 other countries.

There are a number of autism Mums who are horrified when they learn autism can be eradicated. It is as though their status is being threatened. We’ve met quite a few. We think every child has the right to the best future possible, and their mums should not hold them back.

Emma, you have the right to use everything I’ve said here, providing you leave its meaning as it was when I wrote it.”

Noakes also sent further correspondence that he asked not be quoted, which is unfortunate, as it contained great insight into his views on autism and the parents who refuse to use this product.

Fiona Oleary has also had contact with David Noakes. In her email she shares some quotes on his views regarding Amanda Mary. This information can not be verified by Autism Daily Newscast.

“Dear Emma

I Fiona O’Leary of organisation ART Autistic Rights Together give permission to Emma Dalmayne to use my quotes for an article she is writing.

David Noakes is under investigation by the authorities for his involvement in the production, advocating and sale of GcMAF both as a ‘Treatment’ for serious diseases such as Cancer and shockingly as a ‘Treatment’ for Autism.

I am liaising with the MHRA regarding this matter.

I have spoken to David Noakes on the telephone where he accused me of being a bad Mother who is making the wrong moral choices for my Autistic children.

When I asked David Noakes about his ex colleague Amanda Mary Jewell and the claims she was making regarding her life being at risk from big Pharma, he replied he “would be pleased if she was murdered”.

The people selling and advocating these illegal and unregulated products to Autistic children are criminals and should be treated as such!

After that shocking disclosure in which he allegedly expresses the view of being “pleased if she was murdered” regarding Amanda Mary Jewell I shall say this,

In my opinion what Noakes and people like him are doing is wrong, from previous articles of mine, you will know my views and from my reading of his emails he views autism as a illness or disease that can be cured/purged from the body.

We know autism is a neurological difference due to the synapses in the brain not pruning back in the first years of life the same way a neurotypical brain would. A neurological condition is not something that can be altered regardless of medication and certainly not with unproven unlicensed products sold by a company who were closed down by the MHRA. This experimentation on autistics must end.”

Finally, the views of Catherine Hall can be read below.

“Hi Emma

See below for the statement I published in the Guernsey Branch newsletter. As you will see it is expressed in very moderate and neutral terms. I am only too aware of the polarised opinions that parents have about autism. I am in a very different place myself in terms of knowledge, understanding and personal perspective on autism to where I was 15 years ago when I was trying to cope with two small boys with autism and a new baby.
I can readily understand how parents are desperate to find solutions, how unsupported they can feel and how vulnerable they are to the idea that there might be a quick fix solution to the challenges they and their child face.

I am not against any appropriate intervention or treatment that might help people with autism. I am however against the exploitation of vulnerable children and the sale of untested and potentially dangerous experimental products.

GcMAF is, as David Noakes is at pains to point out, a naturally occurring part of the immune system. This is probably the only thing he has said that I could agree with. It is clear that the has no real understanding of the complexity and range of neuro developmental differences that occur within the umbrella diagnosis of autism. The rationale for the use of GcMAF to treat autism is based on the unsubstantiated opinion that autism is a disease caused by viruses and the unproven theory that giving additional GcMAF can stimulate the bodies own immune system to fight this supposed viral disease.

GcMAF is derived from human blood, it is administered via injection, nebuliser or suppository which means it has to be classified as a medicinal product. As is has not been fully tested for safety or efficiency it remains an experimental product and should only be used to treat people under full medical supervision as part of clinical trials.

The only published study I can find on the use of GcMAF in autism is a small scale is an open label study by Dr Bradstreet. It isn’t a very robust study, the subjects are self selected ( their parents already believed that their children were ill and were actively seeking treatment) many seemed to have additional gastrointestinal symptoms or seizures. Some were also receiving other biomedical intervention and/ or therapies and special education programs. Progress was monitored by an ‘in house’ checklist rather than by any standardised measure of autism symptoms. Even Dr Bradstreet admitted that the results were inconclusive. This study seems to be the main basis for Dr Bradstreet and Immuno Biotecs claims that GcMAF can cure autism.

I cannot find any research documents or clinical trial results that support the use of ultrasound/ GcMAF treatment for anything at all and certainly not autism. There are very few papers written on GcMAF and autism and all of them appear to have been written by people with vested interest (that is who are selling GcMAF treatment) and are there for subject to bias.

All other ‘evidence’ provided by Mr Noakes to support his claims seems to be anecdotal. Statistic he quotes are skewed as he is only basing them on a small percentage of patients treated. Mr Noakes himself has admitted in interviews that he doesn’t get feedback from most of the people who buy GcMAF.

I find it absurd and somewhat arrogant of Mr Noakes to question the morality of the mothers of children with autism who decline to use GcMAF. He is the one selling an unlicensed product that has not been thoroughly tested for safety or efficacy, based on an unproven theory as to the cause of autism. He has been promoting its use to treat vulnerable children without medical supervision or long term follow up.

Hope this clarifies my position. please feel free to quote any of this email or the attached newsletter statement.

Catherine

PS. My eldest doesn’t mind his case been used as an example of how people with autism can mature and develop. He had delayed and disordered language development and lots of challenges through his early years. At 7 he was assessed as having low IQ and Moderate Learning difficulties. By the time he was 12 he was coping in a mainstream school, he eventually passed his GCSEs and A Levels, D of E bronze, silver and gold, various school prizes including artist of the year ( twice). He is now an undergraduate, living independently in a flat in London. He is politically aware, has strong moral values, and is son any mother would be proud of – what’s to cure?”.

What’s to cure indeed?

I would like to thank all three who took the time to write, express their views and gave this reporter permission to use their quotes.

Disclosure: I am an autistic advocate and mother to autistic children seeking clarity of information and justice for autistic children. I reserve the right to do so.

By Emma Dalmayne – Originally published on Autism Daily Newscast

1.9.15

Doug Jewell speaks out on GcMAF and MMS and Dr. Brandstreet – Exclusive

Posted by: Emma Dalmayne

As Published in Autism Daily Newscast August 31, 2015 by Emma Dalmayne

On the 27th of August this reporter contacted Doug Jewell husband to Amanda Mary Jewell. Over the next few days we had numerous interactions.

I phoned and spoke to Doug Jewell. I told him my name and that I am a freelance journalist interested in hearing his side of the social media arguments between Fiona Oleary, well known autism activist and spokesperson of ART Autistic Rights Together organisation and his wife Amanda Mary Jewell self proclaimed cancer researcher and procurer of GcMAF and MMS.

Amanda Mary Jewell is well known to the British press particularly as being connected to the notorious Genesis 2 Church which she has vehemently denied. Amanda allegedly fell out of favour and was removed from her role after disagreeing with Kerri Rivera on the Andreas Kackler MMS parasite protocol. The Andreas protocol involves flushing chlorine dioxide bleach into the colon of autistic children and adults in a bid to rid them of so called parasitic rope worms which they proclaim causes autism.

He was more then happy to speak with me and we spoke four times in the phone with bad reception. He was at a hotel in Bulgaria which he and his wife own and which has been the subject of some controversy surrounding MMS treatments.

Doug agreed to send me a statement and permission to use his quotes which he duly did, and it explains very clearly his view on MMS, GcMAF and his opinion of Autism as being a terrible condition which he cannot understand why any parent would not wish to cure. He states that Autism is caused by vaccines and praises the work of Dr Bradstreet and Kerri Rivera.

The following email is printed in full and no editing has occurred. I will let you read for yourself the views of Doug Jewel and his opinions.

Dear Emma,

It was good to talk to you earlier even if it was for very short periods of time !! I hope that one day we can have a proper interview, but for now I will get straight to the points you want to know about and do my best to fill in the gaps.

I was sent a link today about yet another blog which I shall attach for you to see that Fiona O’leary had posted about Mary and myself, basically making comment about our Hotel in Bulgaria and continuing on her nearly worn out theme now that we are just doing this for money and selling people false hope. She commented that we used to sell MMS and made lots of money from this until it was basically shut down and then moved over to GcMAF for the same reason.

I thought to myself, this woman is clearly either a paid and programmed troll that has done no research at all, or is simply quite evil.

Why do I think this ?

If she truly cared about Autistic children and her own in particular, then how the hell would any decent parent or even human being give up hope that her child could be cured of such a terrible condition ?? Even if there was a tiny hope of a cure why would you simply say there was no cure and no hope !!?? She has publicly stated this on a number of shows including Richie Allen show. Also she has stated on a number of occasions that she believe’s that all vaccines are good and everyone should have them, despite the fact that over 250 top Doctors and scientist’s not even counting the inside whistle blowers have proven beyond any doubt that the vaccines cause brain damage and destroy your immune system so badly you are unable to survive without a host of patch up pharma drugs. This is no longer a myth this is a indisputable fact ! With Autistic children of her own how could she support vaccines when she would know very well that they cause major damage, and may have even contributed to her own children’s Autism !!?? There is something very, very wrong with this woman and she is reducing the chances of so many children getting help for Autism that works. I have personally seen with my own eyes the improvement of some children that have been taking GcMAF . But not let forget the positive effect that quality Cannabis oil can have as well, GcMAF is not the only thing and real specialist’s like Dr Bradstreet and Kerry Rivera pointed this out.

12 years ago my Mary was written off by the system and told to go home and die, but I refused to except this and even if there was a 1 % chance of a cure I would never give up and as a result she is still here. So what sort of woman is Fiona O’ Leary ??

Well first of all we never made any money from MMS and one of the reasons we used it at all was because it helped save my wife’s life over 12 years ago now and had seen first hand the wonderful things it can do, this brought us into becoming full time cancer researchers to try and give other people a second chance in life. While living in Bulgaria we helped many people to treat themselves with natural cures and I never charged anyone for anything, that was never my aim or goal, to see people get better was reward enough. I can also assure you that the people today that sell good quality MMS do not get rich from it and never will !! It has been demonised because it is simply to effective at curing many illnesses including malaria, is to cheap and cannot be patented and therefore cannot be controlled by Big Pharma, it really is that simple, but I can assure you after 15 years experience with it, it WORKS and is safe.

Now to Autism and GcMAF , I cannot claim to be an expert with Autism because I focused all of my energies on cancer, and also I was always not keen to give children’s parents advice on curing themselves because, they are more vulnerable than adults and I always felt I would to easily become personally involved and with many children of my own I did not ever want this extra responsibility.

However Dr Bradstreet and several other Doctors dedicated a good part of their life to the treatment of Autism and Dr Bradstreet published several reports that proved that Autistic children that were treated with GcMAF all showed significant improvements and a smaller number appeared to be cured completely or at least be able to return to a normal child’s life. Off the top of my head out of 10115 cases Dr Bradstreet reported that 85% showed significant improvements over a 3 month period and 15% were able to return to normal life. !! This is reported and recorded fact that has been brutally suppressed.

Why do we fight for GcMAF? First of all it works !! It’s that simple, it is not the golden bullet but it is the most effective defence against cancer and brain damage done by vaccines, and is probably the only know defence against an overload of nagalase which has a direct link proven by Dr Bradstreet to vaccines. Nothing else that I know can reverse the levels of nagalase in the body.

Several papers and Fiona O’Leary have highlighted that we have a Hotel in Bulgaria and live a luxury life style. Well we don’t and we did not own the house in the papers but we do own a Hotel in Bulgaria that we built over a ten year period. Also not mentioned is the fact that I was a professional Engineer for over 25 years working all over the world for companies like Guinness and Mary was a successful real estate developer for over the same period of time and we worked very hard for our money during this time, this was before we became full time cancer researchers, and have certainly never made any money from cancer research !! Has she got something against people who work hard to better themselves ? Is that a crime now as well.

I believe that we are being attacked so strongly because we are not only exposing the agenda to dumb down and depopulate humanity, but also have a counter offensive to fight back. Everyone who apposes the truth no matter where they are in the system are assisting in the euthanasia of humanity and I for one will not sit back and let this happen. I pray there are more good people out there that understand this really is about the end game and standing up against this is the only real hope for all of us.

I would be happy to talk to you in more depth any time Emma and I am on Facebook and twitter although I am IT useless !!

Thank you

Doug Jewell

Disclosure and Follow-up:

I advocate strongly against MMS and GcMAF as they are both harmful treatments with serious side affects which cause great harm to vulnerable children who’s misguided parents are sucked into the money making propaganda machine of being able to cure or purge autism as if it were an illness, sickness or disease. I’was sure Doug will be displeased to learn that I am an autistic rights advocate and a colleague of Fiona Oleary. However, when he discovered my views, Doug was most respectful, writing “I wanted to let you know that I completely understand why you did what you did, and have no problem with this at all.” I reconfirmed my position to him. “I do not believe vaccines cause autism and know there is not a cure for autism as its a neurological difference not a disease or illness. I do not believe vaccines cause autism and know there is not a cure for autism as its a neurological difference not a disease or illness. While I completely disagree vehemently with Doug Jewell’s statements, I wish to thank him for his candour and openness in discussing the issues with me.

Editor’s Note:

Opinions expressed by Autism Daily Newscast Contributors are their own. Autism Daily Newscast has made it a policy to present all sides of an issue but we are not without our opinion. We share Ms Dalmayne’s views that autism is not a disease, does not need curing and is a neurological difference. We oppose the use of MMS and GcMAF as it potentially very harmful, has no evidenced based and peer reviewed research and as such has not been approved by any viable medical agency for use. While everything has its risks, we support vaccination. The evidence is clear and even Autism Speaks finally had to admit, vaccines do not cause autism.