Gluten free diet blog

i have a friend who wold like to take her daughter to a DAN doctor. Shelives in the Scranton, PA area.. Anyone help with a name of a good Doc? thankyou in advance

My 2 year old had been diagnosed with autistic spectrum recently. Heis in Speech & Occupational therapy; and we see progress. We alsostarted the diet, but not very strict just yet; trying to expand hisfood choices before we take some of them away. He’s not on anysupplements, and I don’t feel comfortable trying stuff without medicaladvice. Our pediatrician said that he doesn’t advocate alternativemedicine, thus we can’t get any help from him. I need to find a DANdoctor in the area - we live in Detroit metro/Northwest suburbs.

My son has an appointment to see a gastroenterologist. I have questionand things prepare for him, but I would like to know what kind of labshould I request for my son and what expect at this visit.

I have a wonderful friend with a very sweet 8 yr old boy. He just lost hisprivate school placement and needs a high quality ABA based, special day class. My friend will gladly move to live in the best area for this class. My boys aremuch older and I would be so grateful for any feedback you could give me thatwould help her.

Can anyone offer good or bad feedback on any classes for this special 8 yr oldboy? Which district would provide the best class?

Ex: Campbell, Cambrian, Los Gatos, Saratoga, Santa Clara, Los Altos, San JoseUnified.

Please email me privately or you can email me and I’ll give you my cell phonenumber to remain anonymous.

I see a lot of you have posted about the mB12 shots with Dr.Neubrander. It has been recommended for us by the nutritionist, asour son’s b levels are pretty low, and Dr. Neubrander is fairly closeto us. I have looked at the website, but have not yet made anappointment.

Can you give me your feedback on how it has helped your child, and ifis is hard to do? I’m not much of a needle person, so I’m a littlenervous. My husband is skeptical - it is fairly pricey and seems togo on for several months / years, so I would greatly appreciate havingsome feedback from all of you who have gone with this treatment.

What does DAN stand for. I have been trying to do the a gfcfsf, lowphenol diet and enzymes and etc myself with no change. I think I needto see the type of doctor you are all seeing. What are they and wherecan I find on in the Bay Area in Ca?

I just discover this forum and I hope that someone will be able tohelp me.

My daugther, who turned 1 at the end of October, has a globaldevelopment delay due to a disgenetic corpus calosum (brainmalformation). I work a lot everyday with her and she progresses buta friend just talked to me about special diets and complements(Taurine, Coromega, DMG). I talked to the neuro-paedetricians aboutit but they do not know much about this and anyway, they only seemto be concerned about diagnostic while my husband and I are lookingfor “solutions” to help her.

I am looking for a doctor that could help me to settle a good dietfor my daughter and that could also advise me about her development.I live in London (Wimbledon) but I am French so I go to Paris on aregular basis.

The GI dr. ordered the fallowing test on my son: IgA, IgG, IgM, Am,CBC, CMP, RAS testing for food allergies, PH & Reducingsubstance/stool/ stool wright stain/WB and culture difficult toxin.This am I got a call; he said everything came back normal. He wants todo more testing, so they will call me today. I asked by test comingback normal, what it can be wrong with my baby. For example if he eatsoranges he gets diarrhea within 2 hours. If he eats almond milk, hewake up screaming in pain, rolling in the floor and does not want tobe touch. What is next? What other test can be done?

Has anyone been to a DAN doctor in Central Mass? Anyone heard of Dr.LaCava in West Boyelston??

We have an appointment with a DAN! Doctor, but not until February 1st.Currently we are not using any specific supplements (well other thanGummi Vitamins) - should we wait until we see her to start anythingspecific?

Guidance from BTDT appreciated.

FYI: My daughter is 4.5 and has a language delay but I suspect mild PDDand my son will be 3 in 2 weeks and has been tentatively diagnosed ASD(will know more at a multidisciplinary eval in June (aack the waiting)if that helps.