About

I created this blog to help us all find better ways to manage complex illnesses, like Autism, Arthritis, Allergies, Chronic Gastrointestinal problems like Crohn’s and Ulcerative Colitis, Parkinsonism and Alzheimer’s Disorder.  So many diseases have a common thread of environmental toxicity and damage to the internal ecosystem.  This was so apparent that when I observed changes related to autism in a child, I knew I might see autoimmune diseases in the parents and/or Parkinsonism in the grandparents.  We will discuss how these all tie together and how we find better solutions.

DISCLAIMER:  Nothing in this blog is specific advice for any patient.  This blog does not establish a doctor – patient relationship.  The reader is solely responsible for taking any of the general information provided and determining how best to use it. Many of the discussion may involve off-label application if medications or novel treatments.  This is for the purposes of assisting discussions.

38 Responses to About

  1. Tara says:

    Hi Dr. Bradstreet, I am a mom of a vaccine injured child who now has autism. I recently had the opportunity to go to the chamber of hope and get 40 dives for my son. I was looking into stem cell therapy for my son, and I wanted to know how to go about getting this for my son. I haven’t seen any literature on it except for your studies. Do I have to go to you? or can I just have this ordered from my son’s MD?
    Thanks
    Tara McMillan.

    • I will be writing a lot more about stem cells in ASD in the future. There is one hypothetical article about stem cells in ASD but no controlled studies. yet. One in in the final stages and we will see if it was successful in the study soon.

  2. maria says:

    Buongiorno sono una mamma con un bambino di 10 anni affetto da autismo. Dall’età di 3 anni e mezzo è in terapia prima omotossicologica e poi da circa un anno e mezzo il Dan, vorrei sapere se è possibile incontrarla se per caso viene in Europa o riceve solo in america.
    Grazie.

  3. nanaymiriam says:

    hi Dr. Bradstreet.
    glad to have found your site, I will link your site to my blogrol

  4. Jagruti Patel says:

    I attended your Sept.17 lecture and I signed in for stem cell treatment information. Can you please send it to me?
    Thank you.

    • In essence this blog is that information. But I will be updating more about this as the trip to Kiev unfolds. Look at the stem cell related posts on this blog. Use the buttons on the top of the face page to guide you. The blog is also word searchable. Enjoy.

  5. Steven Smith says:

    hi,

    im a bit lost on how to contact you but just wondered what you thought the best treatment available right now in medicines or natural products would be to help normalize the nagalese levels. Also, would that trigger your body to kill the virus or is there also a viral medicine which would be good to use? my autism is getting worse and i totally believe that the viral path could be key and am eager to find out more about which path of treatment to try. They keep me on ssri medication which has no effect and even makes things worse, i really think they miss the mark by such a long way.

  6. Traci A says:

    Oh, wow, the 1st paragraph in your “About” section really hit home for me! My son is on the spectrum, I have autoimmune issues, and my mother has Parkinsons disease. I cannot wait to read more of your blog posts.

    • I have seen a dramatic increase in autoimmune disease over the past 30 years. I hope the information on this blog can help you communicate with your health care providers.

      • There’s been a dramatic increase in a whole load of things over the past 30 yrs. Due to the introduction of non-gamma-2 amalgams from 1976 onwards, which emit 30-50 times more mercury vapour. Promptly following this most reckless experiment in history on uniformed victims, there began a huge exponential upcurve of autism, and exactly concurrently a manyfold increase of adult disability claims in the uk. Disability now consists mainly of the mental/metabolic problems that are characteristic of merc poisoning. This isn’t rocket science folks, it’s straightforward criminality being covered up by lies such as you can see the proof of at http://www.bit.ly/foihg
        Cheers.

      • Mercury is clearly a serious neurotoxin. However the amalgams and autism is not easily established. The Geiers claimed an increase in autism for mothers with more then 6 amalgams. Regardless mercury in any level is not safe for anyone. It is a bad toxin and as Prof Haley has said all along – one mercury molecule is one protein that is denatured in the body. Amalgams make no sense to anyone who thinks about mercury toxicity for more then a second. Its stupid for the FDA to allow its use in dentistry or medicine.

  7. Gina says:

    I recently found out that my 6 year old has high levels of arsenic which may be contributing to the following symptoms: chalky taste, licking walls, eating paper, and focus/attention/cognitive/behavior challenges………and I think it’s more than this. A colleague, and naturopath, recommended oral chelation products that he’s been taking for a month now, with no improvement. This same doctor suggested I look at your products, and I would like your input as to your recommendations.

    • Hi Gina, I would like to know what the arsenic level is and what the source of the sample is (hair, urine, or blood). If urine are we talking about pre or post chelation provocation? Once I have this data I would be happy to speak directly to your doctor about therapy.

      • Gina says:

        I forgot to mention that his once excellent memory has changed. His birthday is in April, and prior to Christmas he was excitedly planning a sleepover, putting together his guest list, wanting to make invitations, and this weekend when I was talking to him about what he wanted to do for his birthday, he could not remember this. I am very concerned.

  8. Gina says:

    His arsenic level is 0.047 taken from a hair sample, analyzed by Trace Elements Inc. He is presently taking Chelex by Xymogen 1 qd, ACZ nano by Results DNA 5 sprays qd, Chlorella 3 bid, Super ZeaXanthin by Life Extension 1 qd, Vitamin D3 (liquid) 1000 IU qd, Yummi Bears by Hero 3 qd, and Rhino Gummy Omega-3 2 qd.

  9. Tracy says:

    I am wondering if you are aware if anyone has tried GcMAF for Melanoma? It’s a tricky one but highly affected by the immune system. Loved to know your thoughts.

  10. Joshua20 says:

    Well that’s superb work! I would like to thank you for the efforts you have made in writing this article.

    Carl Balog MD

  11. ella says:

    Hi Dr. bradstreet,

    I have a question about GC maf treatment. Is this only helpfull when your nagalase level is high?
    Or can you have benefits of it while your nagalse is ok?
    kind regards ella

  12. Jill says:

    Hi Dr. Bradstreet – I am heading to AutismOne, my first autism conference, to meet you specifically and hear more about GcMAF. We have two boys on the spectrum, 7 and 3; my youngest is non-verbal, but it’s so obvious that he’s alert and aware and understands more than even we give him credit for. He babbled, then stopped. We tried SPEAK, saw some babbling, and then again it stopped. We tried MB12 with Dr. Neubrander and saw no results (whereas our oldest is responding well to that and HBOT). My oldest speaks, but was delayed and isn’t very spontaneous or conversational. Hearing all the successes with this, it’s giving me renewed hope. Beyond meeting you in passing at AutismOne and attending your presentation(s), how do we make an appointment to see you?

  13. Ann says:

    Hi Dr, my son will be 7 next month. he mimics a little and understands a few commands. i have tried so many therapies including stem cells with no results. i am now currently seeing a homeopathic for the past 6 weeks but no changes. He is quite aggressive. he has dark circles under his eyes, wants to eat certain foods only. Do you thin McGAF would help him?

  14. Yael Ben-Elkana. says:

    Dr Bradstreet, my son is 22 with autism. A lot of problems with the guts.and deficiency and problems with the b12. Tried to reach your office with the telephone but it’s not working. It’s written that you accept new patients. Are you still accepting? Thank you. Yael.

  15. mandalamama3 says:

    Dr. Bradstreet,

    What are your thoughts on using stem cells to treat Post Concussive Syndrome? Do you know anyone in the US who is currently treating this? Thank you in advance!

    • Unfortunately there is an absence of data on this. However perhaps there is a place for combined HBOT and stem cells. I would be happy to talk to you. contact my office if desired

  16. Mohammed albawab says:

    Hi Dr.Bradstreet
    The daughter of a friend of mine who lives in Saudi Arabia had a car accident about two years ago . and as a result she had loss of vision . the MRI taken 4 moths ago showed bilateral encephalomalacia in the occipital lobes . What I’m asking for is do you have a treatment for encephalomalacia ? please if you have contact me . Coming to US is not a problem if there is a treatment . Thank you reading this …………

  17. Autism Mom says:

    Dr. Bradstreet,

    Thank you for your research. My son is 29-months-old and developed Autism after having a bad Roseola infection (HHV-6) at 15 months. We got the MMR two months later and he was socially “gone” after that. He developed Roseola a second time 7 days after the MMR. He’s had Roseola a total of 3 times along with random fevers and rashes spanning the last 14 months. He has constant loose stools, his toenails and fingernails have white spots and his hair is brittle from not absorbing nutrients. He is jaundiced, and his bowel movements are undigested. We are currently having Nagalase testing done by our DAN! practioner and are cautiously optimistic waiting for the results and hope that this will give us many answers. Our regular Pediatrician suggested Ritalin for his stimming behaviors and hyperactivity and we said no. Hoping we are on the road to recovery soon!

  18. Samantha says:

    Dr. Bradstreet,
    Do you have any experience with alopecia areata in children? My 14yo DD had AA since 10. We have tried literally everything, nothing has worked. All her blood work, thyroid, etc. tests are normal. The only abnormal tests are high ASO titer – she had strep at 5 yo. She seems to have very high inflammation although her CRP, sed rate are normal. Thanks.

  19. As with any support group – I try to do my best to help them gain control of their children’s care, quality of life and recovery efforts. We will do our best to help. Sent you an email.

  20. maria says:

    I have to send an email? I understand you co
    rrectly? Thanks

  21. rrrr says:

    Ooops. I think I posted this at the wrong spot. I am not sure how this blog comments section works. Sorry!

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