What Alternative Therapies Are Working for You?

Yesterday I received a phone call from a mom on a mission. She wants to gather information about alternative therapies which are used in the DS community. Here is her subsequent email to the ES email list:

Attention All Trailblazing Parents: Here is an opportunity to impact
cutting edge research!

Intro
My name is Edie Howard, and I am conducting a survey for Dr. Mobley,
Founder and Director of The Center for Research and Treatment of Down
Syndrome at Stanford University, to learn what therapies and supplements
are working to overcome the challenges presented by Down syndrome. The
question is simple - “What is working?” We will be looking for clusters
of similar initiatives resulting in similar outcomes. If those clusters
do form, then further analysis will be done. If we see trends which
could be helpful, we will also make a report available to parents.

Request
We need your HELP please. We need to compile a list of every single
therapy and supplement parents have used. Please email me what you have
done or are doing with your child in terms of therapies, treatments,
supplements, you name it - we want to know about it. I owe Dr. Mobley
this information by April 14th, so I would appreciate your input by
April 9th. Even if you cannot remember everything, that is OK - please
just email me that which you do remember.

Next Steps
The next steps will be as follows: 1) Design initial survey instrument,
2) Test the survey via phone interviews on 5 individuals then 10 then
50, 3) After 50 surveys are completed the final survey instrument will
be written, 4) Conduct 2,000+ surveys. The final survey may or may not
be phone based. We will also explore an Internet based information
gathering system as well. If you would be willing to be a guinea pig
for a phone survey, please indicate so in your email and provide me your
phone number. Your input and time would be very helpful and
appreciated!

Background - FYI
I proposed to Dr. Mobley in August at the NDSC convention a
complementary therapy research project. The research I proposed was too
broad. He, instead, came up with the idea to simply survey parents to
learn what is working. Pharmaceutical companies go through a similar
process when researching chemical compounds to find breakthrough
products. Surveying patient groups, however, breaks new ground in the
research world. Usually scientists do not communicate with the
“end-user”. (Isn’t that amazing? I did not realize this until visiting
with him. From my non-researcher’s perspective, it appears the
scientists have made a tremendous error in oversight to ignore such a
rich source of leads.)

I sure hope you will take a few minutes to email me your input. I
cannot compile this list without the help of hundreds of trailblazing
parents. Let’s be heard!!

Thanks,
Edie Howard

As we talked, Edie spoke about the children with DS who enter school at appropriate age with no cognitive delays. They aren’t common, but they are out there. No one has ever done the research to learn what those parents did differently, if anything, in order to find out what is working.

No, I need to rewrite that… No prestigious scientist has published research about what those parents did differently. I would say that the neurodevelopmentalists at NACD and ICAN have plenty of research that they hold within their groups, and they have data from hundreds of families about what is working. There are probably other therapists and educators who have gathered data. But no one with research clout has gathered it and processed it in a statistically significant manner.

That is where you can help. The comments on this post are a place to list the therapies which you use that you believe are successful. It will help Edie if you give a brief description of that therapy, or a link to more information about it.

If you are on a DS email list, it would be helpful if you would send a post to the list with a link to this post, and ask people to comment about which therapies should be included in the survey.

I think Edie is on to something.

4 Responses to “What Alternative Therapies Are Working for You?”

  1. Eli DS aged 6 no health issues just colds had Tonsils and Ads out aged 4
    I started taking Eli to a natropath aged 4 when he was sick after his tonsils out he would not take anything (in any form ) for the pain and was quite a mess it took so long for him to recover she gave him a tintiture for his cough and immune system
    Eli it works really quickly within a week
    Eli stopped going to pre school activities with other children with disabilities, for 2 years he attended a local preschool with his peers with no aid, this year he started prep at the local state school and he is booming.
    his speech is amazing he is toileting himself at school he walks to his class without me, actually running so he can get there himself and does everything and more that some of his peers in the same class.
    He only has one big sister and she is not like that at all
    I believe his independence is from being with typically developing children in a role model inclusive setting.
    good luck
    d

  2. Hi
    just seen this post. My son is 14 has mosaic DS. no medical issues except common cold. had tonsils n adenoid around 3/4 yrs. try to give him TNI a few years back but he did not like it. he seems to have some sort of PDD mainly on behaviour type. has started to give him Equazen oil. seems to have help him improve a lot in term of development. nowadays good speech understanding coming up. he attend main stream school. enjoy music sports etc. My only sadness is that he not always do them when we want.
    please would like to be kept posted about this research. at present taking part in another research by DSRF in London.

  3. My son Joey is 21/2 years old, I have been doing several Movement based learning activites with him as well as visual and tactile stimulation. he is doing very well. When he was about 9 months old he held up a large card with huge red letters and said CAT .These were cards i made up for him to teach him words while stimulating his vision. I have lots more.

    CM

  4. I hope you will continue seeking research, i have lots of info i’ve pulled up over the last 21/2 years. i just now found this site. please let me know.
    CM

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