Re: A word on Hope and recovery.

[Guest guest]

thank you for sharing!..seeing other parents find the way out of the tunnel is what we all need...I think it is so important for parents who are lucky enuff to find methods that work to share the success with others, I wish you an your child continued blessings:) channa

To: mb12valtrex Sent: Wednesday, April 4, 2012 7:44 AMSubject: A word on Hope and recovery.

Dear Other Parents out there who walk in my shoes...I wanted to let you know that my daughter, who was diagnosed as PDD-NOS, has been helped tremendously by the different methods I tried, and some I learned on this group site. I remember one letter here early on in my struggle that gave me hope about a boy whose mother wrote to say that today, her son is almost free of his afflictions. It gave me the sort of inspiration that kept me fighting.Today, even though I notice the signs, no one else, including her school, believe she could have ever been autistic. I am a single mother without outside support, and yet I was able to change my daughter's life, and so I believe that you can too. Like other parents, it was a matter of finding things that worked for her, and that took searching and pursuing, and continued effort, and tears, and time and resources I didn't have, but it was worth the struggle. Being in the land area, we

used the DIR facility in Bethesda run by Jake Greenspan, the son of Stanley, at jake@..., . They were wonderful for her, but they were not a resource for finding other methods that might help. Trial and error, and luck, as I had no friends for word of mouth, placed us with these other wonderful people.The other two most useful therapies for us were found with M. for Brain Gym at wrenxx@..., , and nutricianist Dorfmann at kellydorfman.com, . If I mention someone here it is because they were kind and helpful, unlike many people I met who did not have a clue.My daughter was diagnosed, tested, and helped by Dr. Taruna Ahluvalia

at ta@..., . We tested for allergies and asthma with Dr. Vaghi at , who had the sweetest bedside manner. She went for therapy at Kentland Kids with loving Dr. New at michellenew@..., , and she had vision therapy with Dr. Sandy Cohen at reidcohen@..., .There are other therapies and things that really help and make a difference. These were the ones that worked for us. I am hoping my post will help those parents who are suffering, by giving them hope, by offering additional ideas to those who feel they have run out of things to

try. and were both wonderful resources for new and additional treatments. Like many parents, we had some horrible experiences out there, but the good folks are worth the headaches. Good luck, and some day I hope you are writing a post here about how your son or daughter now has friends and a relatively normal life... All my hope and love, another mother.

[Guest guest]

Thank u, this is the kind of mail that keeps hopefully and working for our kidsSent from my iPod

Dear Other Parents out there who walk in my shoes...

I wanted to let you know that my daughter, who was diagnosed as PDD-NOS, has been helped tremendously by the different methods I tried, and some I learned on this group site. I remember one letter here early on in my struggle that gave me hope about a boy whose mother wrote to say that today, her son is almost free of his afflictions. It gave me the sort of inspiration that kept me fighting.

Today, even though I notice the signs, no one else, including her school, believe she could have ever been autistic. I am a single mother without outside support, and yet I was able to change my daughter's life, and so I believe that you can too. Like other parents, it was a matter of finding things that worked for her, and that took searching and pursuing, and continued effort, and tears, and time and resources I didn't have, but it was worth the struggle.

Being in the land area, we used the DIR facility in Bethesda run by Jake Greenspan, the son of Stanley, at jake@..., . They were wonderful for her, but they were not a resource for finding other methods that might help. Trial and error, and luck, as I had no friends for word of mouth, placed us with these other wonderful people.

The other two most useful therapies for us were found with M. for Brain Gym at wrenxx@..., , and nutricianist Dorfmann at kellydorfman.com, . If I mention someone here it is because they were kind and helpful, unlike many people I met who did not have a clue.

My daughter was diagnosed, tested, and helped by Dr. Taruna Ahluvalia at ta@..., . We tested for allergies and asthma with Dr. Vaghi at , who had the sweetest bedside manner. She went for therapy at Kentland Kids with loving Dr. New at michellenew@..., , and she had vision therapy with Dr. Sandy Cohen at reidcohen@..., .

There are other therapies and things that really help and make a difference. These were the ones that worked for us. I am hoping my post will help those parents who are suffering, by giving them hope, by offering additional ideas to those who feel they have run out of things to try. and were both wonderful resources for new and additional treatments.

Like many parents, we had some horrible experiences out there, but the good folks are worth the headaches. Good luck, and some day I hope you are writing a post here about how your son or daughter now has friends and a relatively normal life...

All my hope and love, another mother.

=

[Guest guest]

Thanks so very much for sharing! I just joined this sight and have been feeling overwhelmed as we are discovering our 2 year old son is displaying symptoms of ASD. So much to learn and being new to the Dallas area, we are unsure as to resources and which direction to go! I wanted to take the time to thank you for sharing your story and I hope and believe I will be sharing such joy with others! I have been reflecting on your words all day - thanks again for sharing hope and touching my heart.... I needed it today!!! Subject: A word on Hope and recovery.To: mb12valtrex Date:

Wednesday, April 4, 2012, 6:44 AM

Dear Other Parents out there who walk in my shoes...

I wanted to let you know that my daughter, who was diagnosed as PDD-NOS, has been helped tremendously by the different methods I tried, and some I learned on this group site. I remember one letter here early on in my struggle that gave me hope about a boy whose mother wrote to say that today, her son is almost free of his afflictions. It gave me the sort of inspiration that kept me fighting.

Today, even though I notice the signs, no one else, including her school, believe she could have ever been autistic. I am a single mother without outside support, and yet I was able to change my daughter's life, and so I believe that you can too. Like other parents, it was a matter of finding things that worked for her, and that took searching and pursuing, and continued effort, and tears, and time and resources I didn't have, but it was worth the struggle.

Being in the land area, we used the DIR facility in Bethesda run by Jake Greenspan, the son of Stanley, at jake@..., . They were wonderful for her, but they were not a resource for finding other methods that might help. Trial and error, and luck, as I had no friends for word of mouth, placed us with these other wonderful people.

The other two most useful therapies for us were found with M. for Brain Gym at wrenxx@..., , and nutricianist Dorfmann at kellydorfman.com, . If I mention someone here it is because they were kind and helpful, unlike many people I met who did not have a clue.

My daughter was diagnosed, tested, and helped by Dr. Taruna Ahluvalia at ta@..., . We tested for allergies and asthma with Dr. Vaghi at , who had the sweetest bedside manner. She went for therapy at Kentland Kids with loving Dr. New at michellenew@..., , and she had vision therapy with Dr. Sandy Cohen at reidcohen@..., .

There are other therapies and things that really help and make a difference. These were the ones that worked for us. I am hoping my post will help those parents who are suffering, by giving them hope, by offering additional ideas to those who feel they have run out of things to try. and were both wonderful resources for new and additional treatments.

Like many parents, we had some horrible experiences out there, but the good folks are worth the headaches. Good luck, and some day I hope you are writing a post here about how your son or daughter now has friends and a relatively normal life...

All my hope and love, another mother.

[Guest guest]

Would you like me to send you some info about Dr. ? He is in Texas on South Padre Island and a gem. He does the NIDS approach. Please email if you would like me to forward some info.Best,Marcia Re: A word on Hope and recovery. Posted by: " Jill Moeller " jillymoe@... jillymoe Wed Apr 4, 2012 6:19 pm (PDT) Thanks so very much for sharing! I just joined this sight and have been feeling overwhelmed as we are discovering our 2 year old son is displaying symptoms of ASD. So much to learn and being new to the Dallas area, we are unsure as to resources and which direction to go! I wanted to take the time to thank you for sharing your story and I hope and believe I will be sharing such joy with others! I have been reflecting on your words all day - thanks again for sharing hope and touching my heart.... I needed it today!!!