Special Children of punjab

by DR. Preet
(faridkot , New harindra nagar , +919888914655)

Baba Farid center for Special Children

Baba Farid center for Special Children

Baba Farid Center For Special Children

Harindra Nagar Faridkot (Punjab)


Some years ago I met a mother of a profoundly autistic boy, called Ankit Sharma in Gaberone, Botswana, where she and her husband lived and worked. At the time we provided a unique therapy intervention to Ankit, then 8 years old, called Auditory Integration Training. The treatment is an electronically modulated music intervention, which stimulated the entire auditory system, but also provides a strong impact on the brainstem, midbrain and cerebral cortices, providing overall sensory integration and it also changes the neuro-immunological status of the brain.
Ankit was greatly helped at the time, but because no other metabolic interventions followed his first exposure to AIT (Auditory Integration Training), he again deteriorated and his autism became more and more entrenched.
Savita heard about Dr. Pritpal Singh in Faridkot, Punjab in G-News whilst she was still in Botswana. Her father lives in Himachal, one of the other states of India. She brought her now teenage son to Punjab for treatment. He attended therapy in Batinda and in Faridkot and it was during her stay here in Punjab that she wrote to me and told me that Ankit had improved greatly under the Neuro-Therapy treatment of Dr. Singh.
She asked me if I would be interested in sharing some of my work with this doctor and his staff and upon my positive reply I received a phone call early in January 2008 from Dr. Pritpal Singh to come over and visit his Center and assist with the special children they serve.
Many months of collaboration followed. Over the months I became more and more convinced that this community of therapists is very poor and that they serve families who are not able to provide for their children according to Western standards.


The Center’s director is a young man, called Dr. Pritpal Singh. He is energetic, a visionary and a deeply committed therapist of young children. Dr. Pritpal Singh is a Doctor of Naturopathy and Yogic Sciences. He started this work about 6 years ago and has worked for 12 hours per day for the past 6 years, 7 days a week training up young men who have since qualified as Neuro-therapists in 4 Centers in which there are currently more than 300 children receiving daily Neuro-Therapy.

Therapists to work with them at this time. Just this morning parents again arrived at the Center hoping to receive help for their children, but had to be turned away, as the waiting list needs to be supplied with therapists, before any new families can be enrolled – this means that there is an urgent need to train up more therapists, but limited resources prohibit training of a new intake of intern Neuro-Therapists. These young men aren’t trained up over-night – the full training to certification takes up to three years to complete.

I was in awe from day one about the constant stream of children who arrive here from early morning (7am) till late evening (some as late as 9pm), who come for help. The Center offers this unique kind of yogic intervention, based on a combination of neuro-stimulation which is the result of stimulation of internal body organs through direct and indirect pressure. The pressure provides better blood flow to organs, thus the metabolism of these organs increases and more hormones, enzymes, chemicals are secreted/produced, which supply the body with better nutrition. Better nutrition for the entire body, results in better nutrition for the brain. Direct stimulation of the spinal cord, peripheral and central nervous system, also brings about better enervation and yielding astounding results.

To date more than 62 children are fully recovered - the majority of these came to the center severely spastic, blind, deaf, with contracted limbs, crossed legs, unable to speak, feed themselves, with no bowel or bladder control and some profoundly autistic. Yet now, after a relatively short time in therapy (15 minutes every 2nd day), they have gained normal bodily functions, are able to walk, talk, can see, hear, feed themselves and are integrated in mainstream schooling!


It is scientifically unacceptable to hear someone make a statement that a happening has been a miracle in the making, but the recovery rates in these children bespeaks super-natural intervention. It is not the norm that severely disabled children, especially those damaged by severe hypoxia at birth or have sustained damage from neuro-toxins, show such recoveries. I have personally seen the MRI’s of the children and the damage is real. Occipital, parietal, deep white matter damage, mid-brain and cerebellar damage abound in these children. Yet, within a relatively short period of time, Dr. Pritpal Singh and his team of Neuro-Therapists apply their therapy and within days the parents start seeing a lessening of spasticity, normalization of squints, correction of severe bowel issues, and improvement in eye contact. Before long, the children start making their first struggling attempts at muscular movements with their hands and then attempts to sit and stand follow.

At last, the first giddy attempts at walking emerge and then they start straightening out. As these processes emerge from deeply injured brains, the children start communicating. At first there are just glances that meet your eyes, then they fix their stare and soon they smile and attempt to babble or the first poorly formed words are uttered. For a parent who was told that his or her son or daughter would never sit, stand, walk, talk or be independent, no-one can dismiss the miracle of the first “Mama” or “Baba” and then the speech-mechanisms start stream-lining, to produce clearer and more complete sentences.

The autistic child who is hyperactive, aggressive to self and others, and the Down’s Syndrome boy or girl who cannot communicate because he or she has a tongue too large for his / her oral cavity or who has huge motor planning problems and who sits or lies locked away, begin to crack smiles and open themselves up to touch and communication; the frenetic behaviours that so often characterize autistics, start diminishing. We met a little girl here with Down Syndrome. She was said to be completely autistic and unable to communicate with people. The day we arrived she still clung to her granny in shy withdrawal, but as the days passed we saw this little girl as active, normal and communicative. Noor has become totally normal and she is well-able to mainstream with regards to schooling. Neuro-Therapy has changed her little life!

In desperation, before seeing his MRI results, I went ahead and ordered a set of supplements from Marion Ellison in SA for him, but the cost of sending these here plus the purchase costs came to R6000.00 (almost $1000!/ Euros 500!) and for this Center, and the family, whose monthly income is a mere Rs8000 ($200), this was a devastating amount!
The situation on the ground here is dire due to poverty with resulting mal-nutrition. The average parental income is less than $150.00 per month and the very poor ones may earn as little as $15 per month, which is hardly enough to keep body and soul together, not to speak of keeping these little ones healthy and kept in a live-changing therapy service!

The net result is that many die or will die. I can’t believe that there is an affluent “West” out there where people have cars, homes and comforts, fast-food outlets and ample medicine, opulence and high quality medical services, and here in India, in places like Punjab, the children have to die, because parents can’t even access incubators for the prematurely born babies or where talking about nutritional supplementation is like talking about life on Mars! For these families such help is “out of this world”, out of reach and beyond hope. Just today we struggled for over 5 hours just to find a courier company which would transport two serum and a few hair samples to Germany for analysis. The outcome was, after contacting the Post Office, several local courier companies and even DHL India’s National Customer Care services, that sending the biological samples internationally is an IMPOSSIBILITY! When I told the operators of the DHL service that it was a life-and-death matter for these children, I was told it would take up to 21 days just to open an international export account for biological samples and the cost of sending these samples will then be so astronomical, that it will put the entire project in jeopardy.

OTHER OBSTACLES
The ones who are fortunate enough to have heard about the Baba Farid Center for Special Children, and can manage to find transport to come over the miles to obtain help, may need ongoing financial support from Dr. Singh to pay for ricksaw and taxi services (nothing like what we know in the West!), to commute over the many miles to and from their towns and villages for the 15 minute treatment session per day. And yet, remarkably, these children, when treated, become better and better and the spasticity leaves their little wracked bodies and they manage to start healing up.
However, offering free lab services to us means nothing if we can’t get the samples to the lab in Germany and even if we could get someone willing to transport the urine for us, the project will still not be viable if the cost of sending these samples becomes exorbitant.
I trust this little vignette of the work and scope of the Baba Farid Center for Special Children will aid potential donors or individuals in power to make a meaningful contribution to the lives of children who can't speak for themselves and for parents who are not able to advocate for their children because their station in life discriminates against them.
With kind regards
Carin Smit – C/CMT
SYNAPSE AFRICA NEURO-NUTRITIONAL CLINIC

Comments for Special Children of punjab

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mently retired & cp & seisures
by: Anonymous

sir,
my child has 14 years. at child hood about 3 years old he have mind fever & seizure till then I treated by various docters by dr bharati bansal neurphisician and pscho dr hp singh at agra during this my child progess but not releve in mental progress pl advice us how to progess his mental progresss.

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epilepsy
by: Anonymous

Sir my son 7 years old two years ago he have ago seizure then his mind not work and his eyes not visibility . That is why he is on the bed . Son please ask me The treatment of my son.

thank you

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blessings
by: Terry

I am glad to see Baba Farid Center for Special Children Harindra Nagar Faridkot. Such place is really a blessing for the kids who do not have parents. They also make sure about the education of kids.

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My Harvi
by: Kiran Baria

My daughter harvi 7 yrs. is downs syndrome baby is not able to speech. She can utter only few words. Childhood teeth has also not been removed. Moreover, four teeth has grow up behind lower row of teeth. Please advise me what I have to do. thanks in anticipation.

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hearing problem
by: Anonymous

helo,can anybody help.m having a problem wid my right ear.i lost my hearing on 1st march.i ot treatment from my ENT specialist.it reduced the problem n i regained my hearing upto 40-50%.but i need complete treatment.so dat i can live my life securely.pls help if there is anybdy who can help!!!!!!!!

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All the best
by: Anonymous

Dear sandeep Kaur,
your love for your child will definetly strengthen the baby to face the life. kindly do not lose hope, there are many children like your baby. Approach the centre and make use of the services. All the best.

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my dowmsyndrom 21 trysome kid
by: sandeep kaur

i have a boy baby 7 months old.when he was 47 days old i heared a news that he is downsyndrom 21 trysome baby.i was shocked.i can never think in my dreams that i heared that news in my life.its very hard time.still i am not accept it that he is ill.i am not very strong internally but i try to make me.i need a power to strong my self because it helps to make my child strong.i never want that my baby feel that he is lesser from the others.i want to make him internally strong,fit,self-confident.god is power house,i hope he will supply a power to make my child fit confidentaly on his foot.one day i will see that in my life and its not far its close.life depend on hope which is very helpfull in our life.i think i can get a full support from faridkot center which is special for these kids.i want to meet a whole team from that center thanks

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