Sunday, January 10, 2016

therapy centers!!!!

A parent called up a couple of days ago. Her son has ADHD, and is undergoing therapies since last 2 and half years. Actually the follow up from home front began late and behaviour with regards to disciplining also took a while more for the child. However now he has almost caught up with peers baring motor issues in both physical and speech areas.
  The mother was however flustered and in order to know where her son stood development wise she decided to take an opinion from a development pediatrician.... different from whom she had been seeing last couple of years. This child was not writing in class but was doing it well with his remedial teacher.

This developmental padiatrician runs rehabilitation centers across the city and is a big name!
He told the mother to do some blood test, genetic testing (i dont understand the point since this is the second child and the parents have no intention to go for another kid. Also the tests are very expensive)
Next he told her that they would take a month to assess this child and give a detailed analysis (really????) So she had to pay the entire charges at one go (now i got it!!!)
He apparently told her he would tell "his" therapists what program to be taken up (oh yes this is a superman who plays multi roles!!!!) When the ,mother who happens to be well read met the therapists she turned up knowing more than them!!!!
Next he told her to start medication as he felt the child wasnt focussing on what the teacher spoke in class and so he was not writing. He said the meds would help him focus!! (he failed to realise that this is a child in Jr KG, and the kind of focus he was insisting this kiddo with ADHD  have was difficult. He didnt bother that the child could recall what was being done in class albeit not in continuity....... I want to know if all children in Jr KG level are able to totally focus in class!!! What about anxity element for not able to write???/)

The mother who was terribly upset and had few sleepless nights asked me why did he tell all the above??

My take:
I dont want to play a blame game here. Every professional has a right to put forth an opinion.  The mother too had a right to visit any professional of her choice for an opinion. Unfortunately the experience was very bad and emotionally draining for her. I often tell parents to take opinions with a pinch of salt.
As a mother i can say that no one knows our children as well as we do!

So dear parents, do not take professional opinions to heart. Be alert when you visit centers run by one professional and when there are other professionals "employed" there. Usually attrition rates are high here!!!
However great and renowned the professional may be every center has overhead expenses and loads of other kinds of top up expenses that have to be recovered from the consumer!
So please don't blame any professional for opinions and the high charges....... even though they were meant to soothe you. It was /is your decision to visit them!!

Enjoy the time with your child as much as possible. You are going to miss this time when they grow up.


Its a child first and the diagnoses come later!!!!
       

Sunday, December 27, 2015

speech-language therapy........

Dear readers,
            i wonder if its a coincidence.... but in this month of December itself i saw 4 children between the ages 4 yrs to 10 yrs, provisionally diagnosed with Autism. The major fact that caught my attention was all these children were trying to "speak ENGLISH". In fact when they reported for assessment too the parents insisted on English!!!!

While most of us have seen and noticed the need for being able to "talk" in English considering the global benefits!!!
But I personally have my reservations and not just for the specially abled but also children in general.
However i restrict this writeup here to children with needs.
My take"

  1. there is evidence that the child begins to hear from the time he is in the womb. So obviously he is exposed to the mother tongue right then!!!
  2. English in typical Indian homes is usually a learnt language, The mother tongue is 'acquired'.
  3. the child, till he gets diagnosed is exposed to the mother tongue. all of a sudden he is thrust into a world of imposed English. Now imagine us doing that!!!!
  4. In almost all cases i have seen that other family members like grandparents who are yet to accept the diagnosis are struggling to change their communication methods overnight! 
  5. the most important fact is in India,  which is a multi lingual country with varied cultures, a child is exposed to a variety of languages and their dialects. Home, pre school, day care at times, the park etc. 
  6. So personally i feel  (in case of parents speaking the same language) the mother tongue should take priority, especially since these days the diagnoses are early. Initial days the focus should be more on Occupational therapy which will help the child settle and get arousal levels under control, which will help him in speech-language development too.
  7. Once the child is familiar with communication in mother tongue then other language/s can be introduced, considering social communication. 
However Language development is an ongoing process and at every step there should be a  consensus reached between the parents and the therapist. The goals should be  clear and try being as close to natural as possible.

DO NOT MAKE YOUR CHILD BY HEART STATEMENTS. 
QUALITY IS MORE IMPORTANT THAN QUANTITY.  










Thursday, December 24, 2015

Dear readers,
Don't want to give excuses but was caught up with work and personal commitment. I had almost given up. However, many people who have called me in past six months have been insisting on continuation of the blog.
It is only the love and trust of my clients that I am able to go ahead.
Thanks all. I assure you of sharing more experiences with you as often as possible.

You can contact me on priyagole@gmail.com.


A merry Christmas and a happy and prosperous New year to all of you!!!!

Sunday, October 26, 2014

Cochlear Implant!!!!

Call this a co-incidence, i have been facing a lot of little children last 3-4 months who have been diagnosed with hearing losses (severe to profound). ALL yes ALL of them have been recommended Cochlear implants. Parents are worried but want the BEST for the child. But most dont know the ground realities.

First of all, what is a cochlear implant?
according to Wikipedia, 
 A cochlear implant (CI) is a surgically implanted electronic device that provides a sense of sound to a person who is profoundly deaf or severely hard of hearing. Cochlear implants may help provide hearing in patients who are deaf because of damage to sensory hair cells in their cochleas.

read more here http://en.wikipedia.org/wiki/Cochlear_implant#Candidates
Here its important to note: 
  • not benefiting enough from other kinds of hearing aids, including latest models of high power hearing instruments and FM systems
The reason i pointed out to this point was that all these children were given basic models of analog hearing aids and were declared unfit for use of Aids and hence implant candidates!!!!!
The parents are running pillar to post to arrange for the lakhs needed to fit the implant. (atleast 9L). 

Another point i want to draw attention is:
The brain develops after birth and adapts its function to the sensory input; absence of this has functional consequences for the brain, and consequently congenitally deaf children who receive cochlear implants at a young age (less than 2 years) have better success with them than congenitally deaf children who first receive the implants at a later age,[46] though the critical period for utilizing auditory information does not close completely until adolescence. One doctor has said "There is a time window during which they can get an implant and learn to speak. From the ages of two to four, that ability diminishes a little bit. And by age nine, there is zero chance that they will learn to speak properly.

Most of these children were 4 yrs and above!! The parents in their counseling were told, the child would "talk" once the implant was fitted. Not many were aware of the importance of intensive post operative therapies. parents were not aware that Implants are not magic wands out there set to make things right. The age of the child was very very important too.

Now, i am not undermining the benefits of Cochlear implant. I am opposed to rampant exploitation of technology and indirect forcing it down the throats of unsuspected non-candidates!

Here are a few points to draw home for parents:
  • the decision to implant your child should not be based on emotions. Its a team work. Do check if your child is tried with a very good quality hearing aid (it takes at least a month for you to know the effect). There are wonderful products available which you can ask your therapist about.
  • Do NOT decide only on basis of the BERA reports. Cross check if your child is indeed having hearing loss by observation and alternate methods (please read my article on BERA in this blog). 2 out of 3 children i saw last week were "normal hearing" children with faulty BERAs. They were recommended Implants.
  • If the child is multiply handicapped then you need to think twice. Commonly seen in this case are children with Cerebral Palsy (birth related i.e. Neonatal jaundice). BERAs in these cases may indicate Hearing losses but many a times close observation indicates normal hearing. I have even seen these children fitted with power hearing aids and parents dint know why the poor child kept wailing when wearing the aids. Picture yourself with loudspeakers on your ears and blaring a loud speech!!!!
  • Children with other disorders like Autistic Spectrum and mental retardation are not candidates for an implant. Very often toddlers with Sensory Processing deficits (read my article on APD) are confused with their symptoms pointing towards hearing loss. But most of the times they are not.
Though, as parents we aspire for the best for our children we also need to keep their best interests in mind before we rush to a particular solution.  Please take things with a pinch of salt.
Awaiting your comments/suggestions here or email me on priyagole@gmail.com

My apologies for not keeping up...........
I have been caught up with clinical and personal commitments which made it difficult to find time to blog, for 2 yrs now!!!!

However, off late I have been requested by unknown clients (who happened to read my earlier blogs) to reactivate this and here i am. 

I hope to be more regular and also waiting to hear from readers.

YOu can also email me on priyagole@gmail.com

Monday, February 25, 2013

Hi,
 there have been few comments in the last few days, which i ve been unable to publish due to technical issues with the account.
Pls email your comments to priyagole@gmail.com

Sunday, February 24, 2013

Back again!

Hello readers,
                       Sorry....... i havent been regular. But no i wasnt away, i was busy with my practise, so cudnt find time to hit the keys!!!
  a lot of clients and friends wanted me to resume the activity (that was great encouragement....) and so here i am.
Keep reading and mailing your valuable inputs!
Regards,
 Priya