To start I’ve found out the local children’s hospital is a research hospital and is notorious for medical kidnap. Many parents have kids with special needs, I fortunately have an otherwise extremely healthy child but developmentally delayed with an unknown genetic disorder. For the first 5 years of his life we searched for answers. Over covid his pediatrician gave me concern so I moved him, this new doctor we saw once before I was concerned about how her practice bullied her into supporting things she didn’t believe. She then came out in support of the covid shots, which she was against before the bullying. I haven’t been back to her. My son was cleared from the neurologist, cardiologist, orthopedic, genetics clinics in our previous state. They had no answers so we do therapies and help him the best we can but haven’t reached out to any specialists in our new state. He is in a great school and is doing well but again we don’t know what’s causes his delays. I met someone today who told me about a program we could participate in that would draw his blood and enter him in a database to find “genomic” answers. He is healthy, he is happy, I have accepted he may never speak, I have accepted he will never live on his own. The last three years I’ve come to distrust most in the medical field, my son is amazing just the way he is. I know there is no fixing his issues but would you still look for answers? I’m torn between protecting him and helping him. I don’t know any doctors here to ask advice, any doctors I knew are from my previous state.
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We have a regular doctor, I don’t have a regular pediatrician I trust so we are sticking with just a regular doctor. He is not a baby, he is 9 y and we have been dealing with doctors and clinics since he was 15 month old. The geneticist said technology will have to catch up, he went as far as tech would take us- he was released from the neurologist, he was released from the cardiologist, he was released from the ortho clinic, he was told he doesn’t need Pt anymore. We are in Ot and speech. there is no treatment available from a developmental Ped because he has no behavior problems, they medicate and he doesn’t need that. We did ABA until moving states but he doesn’t really need it because he is in school full time and doesn’t have behavioral problems, he is potty trained. He is sweet, loving, happy and physically healthy. There are no medications to help his delays, he is developmentally delayed not physically ill. I could take him for a blood draw to enter him into a database not knowing what they would use it for and hope to someday get an answer. I don’t trust this children’s hospital, that is my dilemma. He is my youngest of 6 kids, I’m not new to this. We searched for answers for years, he has been put under general anesthesia for MRI’s, we have done blood tests, over 5 years of searching, Ultrasounds, many many hospital visits till we ran out of places to go. He can only do what he can do and like I said previously I absolutely love him for who he is and accept the amazing spirit God has granted me the the privilege to raise. I just don’t know that it’s worth it to enter him into the database.
I think that you have eliminated all the possibilities, and OT and speech therapy may help. But not entering into some database, that puts a target on your back. I am just thinking of what happened in Austria in the late 1930s, when they targeted disabled children. Now is not a good time.
Yeah that is my concern. I ran into a nurse practitioner during covid who actually works for this hospital. One of her concerns was the jab, she told me the list of kids considered “high priority “ for the jab were kids like my son but my son is extremely healthy and not at risk. She said red flags went off because it was a list of kids eugenicst would want to take care of first.
God bless that nurse, hope she collects evidence where she can and sneaks it out to PV or somewhere. Brave.
Lots of good suggestions here. I don't know if he ever had any shots, but mercury and other adjuvants can cause neurological injury. Colloidal silver is supposed to help the body clear that sort of thing, good for all ages, us parents too. Good luck in your search, it seems like you're doing all the right things. Prayers sent your way.
I wish I would have gotten her info! It was the peak of covid, husband and I went into grocery store maskless. She stopped us in the parking lot and thanked us for being two of the few who wouldn’t comply. She said she had been a NP for however many years and she says “look I’m a nurse practitioner, I know vaccines don’t cause autism…but I don’t know if vaccines cause autism”. I had trusted everything up till the start of covid for the most part…it’s what got me to question everything and actually led me here. Now I just want to protect my kids and especially my son most vulnerable in the world.