'Spinal Muscular Atrophy' - FREE Treatment for LIFE for Eligible Patients.
HTML-код
- Опубликовано: 21 июл 2019
- A rare genetic disorder affecting children and young adults.
A condition that costs Rs 14 crore for treatment, now to be treated free of cost for select 30.
Thanks to the efforts of Dr. Ann Agnes, a Pediatric Neurologist and neuromuscular disorder specialist from Sagar Hospitals, Bengaluru and a US-based NGO, Direct Relief. We are happy to support for their better health. Together we can make a difference.
Healthcare for Everyone.
![Jordan Adetunji - KEHLANI REMIX (feat. Kehlani) [Official Video]](http://i.ytimg.com/vi/EeJ8n5PxFGE/mqdefault.jpg)
Great job, keep researching for mankind.
I am ayyappa from raichur,Karnataka.now I am working as grade1 secretary in govt. But my life too much hard. No standing, no walking because of spinal muscular atrophy type 3...pls help me God Father's..
My child is 6 years old and he has SMA.
Plz advice what I can do for my child.
Thanks
My son is also patient of sma plz help us
Can a SMA patient become a doctor?
I have a friend who is suffering from SMA and 80%+ locomotory disability..
Please do let me know wether he is eligible for NEET?
I have bilateral lumbar atrophy,left leg weak also for 6years .Iam 38 year old women l have 2 children.many treatment took.no result .any solution ?please reply
I have a hypothesis for the mechanism that causes the truncated proteins in many neurodegenerative diseases where a number of the triplet CAG exceeds a threshold: the methylation of the citosines, followed by spontaneous deamination, could transform citosines into thymines, producing as a consequence, one or more stop codons TAG. An inadvertent STOP codon would explain truncated proteins in neuron cells. If this is indeeed the mechanism, then maybe inhibitors of methyltransferase ( for example, Decitabine ) could be useful to retard the onset of the symptoms; if it is possible to expand the production of DNA glycosilases ( in target cells ), it might also be possible to enhance the ability of cells to fix ( remove ) the wrong thymine bases.
Who are you man 😂😂 I mean like what you do
Tell me how can I get this benefit
I AM 30 yaar old muscular dystrophy patient sir is there a cure for it
Kya SMS and DMD muscular dystrophy ak jaishs bimari hai
How please is this worldwide? I know.someone who needs this.kind of help
Dear Mam..We are from odisha.. My brother 's daughter is in this type of same condition. She is now Only 6 months baby..She couldn't move her two legs..In odisha Cuttack, Shishubhawan they tell us ,this disease couldn't be curable.. I get a new hope to see your sugar hospital video..But gene therapy is much more cost for us..We can't afford this..Is there any another process for treatment???
Hi
My son is suffering from dmd he is 20years now please any cure for this prblm
Sir aapa se contact kaise kare
How i contect u sir
My daughter is also suffering from sma type 1 ,she is 7 years old. Please help me
my baby is effetct with smard 1 plz suggest me....
Please help my daughter,she is now only 52 days old sma type 1 .I am from west bengal
My cousin also patient of sma Disease please help us😔😞
Hello mam, my brother's daughter recently diagnosed with sma , she is only 6month old , plz help us for saving her , pls help us, we are so poor , we can't afford costly treatment, is thr any other way to raise the amount of injection of 16 cr
Also kindly get help from dr shanmugan Varma asaan running a research centre at coimbatore for treating sma children
How to know its SMA or down syndrome please explain how to know...
My baby 18 months old Doctor told he is suffering from down syndrome...
my baby 2 yers age SMA career. plz help
Ma babuku 6monthd type 1genetic tho bada padithunnaru plz help cheyandi mam
Sir/Maam, I am from Philippines and our daughter is diagnosed with SMA. She has undergo a tracheostomy operation. Hopefully you can help us🙏
@@user-dg5fm7wv8i sir, I have been suffering from spinal muscular atrophy since 1997 when I was 15. Can I be cured by using cow ghee ? Plz guide
@@user-dg5fm7wv8i what the fuck🤣🤣🤣🤣🤣🤣🤣
Mam please help my sis has some genetic problem please help
Sir me bhot pareshan hu plz help me sir mere son ko sma type 2 he
DMD muscular dystopian patient treatment age 24 please help me treatment
Sir ky 35 ki age wale ka bhi tratment hota h
My daughter is also patient of sma. Please help us she is 10 years old.
Please help us. My child is suffering from sma1 disease. He is in ventilation. Please save my child.
I am from bangladesh my child is 5 years old all-time he is suffering this disease and now he is spinal muscular atrophy type 1 then type 2 can you treatment type 2 please tell me sir as soon as possible because many many times he is supper with life support and resent i lost my second child he's also spinal muscular type 1. Please sir please help me.
Did u married to your relative ??
Save my daughter sivaranjani she is musucle week need genitic text and treatment please help me
Hii, my friend's son are also suffering SMA. Can u explain what is free treatment eligible for patient? And what is cost paying treatment?? हमको आपसे बहोत उमीद है.
Go for Ayurvedic treatment.
@@Kornsk please explain
@@Kornsk pls explain...
@@Kornsk where sir pls give address l
I'm suffering from spino cerebellar ataxia... Is there any permanent treatment available for SCA
I am Farhana Tabassum ABDUL Majid I live in Akola Maharashtra I am lgmd patient I ask lgmd treatment have provided there
Dear sir my daughter is two year old and not walking properly in her report use likely word with sma what it means
Sir plz share your what's ap number or social account so that we can guide or help you
namaskar Ami Bangladeshi my baby Anuradha spinal muscular sma type 1 place place help 🙏🙏🙏🙏😭😭
Hii sir.... Meri beti ko SMA hua hai koi madat ho sakti hai kya please sir
Am 24year old girl am suffering from 6year in the disease of the limb girdle muscular dystrophy 2I treatment plz help me sir plz cureable treatment sir plz
DM.
I'm suffering from the same dystrophy and feel kind of alone and lost. We can connect and share our experiences and try to look together for treatments.
I wish someone would do the same for me
How to contact your Hospital
Sir madam my 3 baccha sma pesent plz help me
Sir/Ma'am
Is there any chance for treatment of stage 1 disorder of SMA...please response....time is running out as my niece is already 6 months old
Yes but cost 2 million doller
My sister is suffering from SMA type 3.She is 29 years old.She's on wheelchair now.plz tell me how to contact.
M also suffering from sma type 3
@@hardik471hi mera baby ko type to hai humko Kuch samjh nhi aa raha hai Kya Kare 😭😭
@@Zoya-Ray humare sma k group me jud jaye to aap ko pata chalega kese care karna he aur kya kya karna he
@@hardik471Aapka group Mai Kaise Jundna hai pls tell me
Sir maam pls help my daughter , she is Sma type 2 pls help us to reach there we r from Kerala . She is intelligent and has good sense of humour .. pls pls
Hello from Brazil, I hope I can help; if my hypothesis is right, an existing drug ( decitabine, used to treat a form of cancer ) could stop of slow down the disease. But it's only a theory, feel free to share the idea with doctors for discussion. Here some information about drugs that inhibit the enzyme methyltranferase ( you may want to talk to doctors about it ): www.sciencedirect.com/topics/medicine-and-dentistry/dna-methyltransferase-inhibitor
Mam My Disease Also Sma Type 2
I Will Talk to You My Whatsapp No.7205454320 You Will Whatsapp Me
Sir I'm having claw hand ,, footdrop,, atrophy.. I can't fist my hand please treatment suggestions
How r you now
@@vigneshadc8157 still footdrop is there, clawhand also, but I'm walking little bit with support, but I'm suffering with severe footdrop
We are from Punjab, and our son daignosed SMA type 3 in the age of 3 ,and now he is 4year old , he is sitting with support but can't crawl nor stand we are find for treatment if U can help us please reply please , please, please .I'll wait for it answer
Hello from Brazil, I hope I can help; if my hypothesis is right, an existing drug ( decitabine, used to treat a form of cancer ) could stop of slow down the disease. But it's only a theory, feel free to share the idea with doctors for discussion. Here some information about drugs that inhibit the enzyme methyltranferase ( you may want to talk to doctors about it ): www.sciencedirect.com/topics/medicine-and-dentistry/dna-methyltransferase-inhibitor
I am from Bangladesh I have a child of sma
Please help me, my boy is very intelligent
@@salvadorhirth1641 please help me
@@meshkatreza7700 Don't worry stay positive. If you are from India, try contacting this organization. curesmaindia.org/
Hello sir please help me
My baby 4 month sufaring sma pls suport
My son is also present S M A plz help
Sir
My daughter is suffering SMA and she is four year old. Please help me
Sir how can I contact you plz share your social account or what's ap number
Sir muje Spain macular atrophy hai Mai Punjab se hu Meri age 39 hai kuy Punjab Mai koi center hai is bimari ka
I am also suffering from SMA since 1997 when I was 15. I cannot stand from sitting position without using my hand. Also can't run and cycling is not possible. Bibhu from Odisha
Plezz sir help me babe spinal muscular ples help me 5 matu
Good Morning Sir
Kindly save the child of kapil baisoya. His son is very critical suffering from Spinal Muscular Atropy. Kindly see the video shared. Plz help Dr sir🙏🙏🙏
Plz roly
How can I contact you Sir🙏
#save_mithra
#Savemithra
Plz help the sma children
Hello mem
Sir my child is 8 years old she can't control
Head and she can't lift hands legs she can't sit please help me or any contact no
Plz help me madam
Sis. Teera fights sma pls help her pls
Sir started the treatment of mascular dystrophy treatment
Please can I contact you if you know
Pls any updates 00971559190693
🙏🙏🙏🙏🙏please Jaldi btaiye
Sir, I am from Bangladesh I have a child ofsma please help me
Are u married to your relative ?
Sir my Frnd relative baby 2 month old and she have SMA type 1 disease how can the saviour Help ?
No much idea. But, this organization might help you. If not reachable, try reaching through Twitter or something curesmaindia.org/
Hi sir I need your nmbr.. can I gt??
Please help me
Hello from Brazil, I hope I can help; if my hypothesis is right, an existing drug ( decitabine, used to treat a form of cancer ) could stop of slow down the disease. But it's only a theory, feel free to share the idea with doctors for discussion. Here some information about drugs that inhibit the enzyme methyltranferase ( you may want to talk to doctors about it ): www.sciencedirect.com/topics/medicine-and-dentistry/dna-methyltransferase-inhibitor
Sir please mascular dystrophy patient
Am also limb-girdle muscular dystrophy 2i patient,,,, plz curable Treatment plz help me
I lost my niece of 2 year old on 26 may 2021
Sad To Hear and Hard To digest
Hello sir my brother suffering from DMD..he is 8 years old..can this be cure able..?
Sie my baby sapin muscler astrophy
kesa ha apka baby
Sir me khud spinal cord problem pe hoon me kuc nahi karpata hoon
Please help me sir
Agar aapse kuc hosake to
Mera pariwar hai sir
Mein bad pe hi sab time rehta hoon
From INDIA KOLKATA ph 9339777811
I am not afford to this cost so if you can help to my child,
So plz help me.
Thanks
Impact Guru can help you
Plzzzz madam
Hirayama dieses h
My baby 10 month SMA please help me
My baby ko sma h ,koi titament ho batana
Hello from Brazil, I hope I can help; if my hypothesis is right, an existing drug ( decitabine, used to treat a form of cancer ) could stop of slow down the disease. But it's only a theory, feel free to share the idea with doctors for discussion. Here some information about drugs that inhibit the enzyme methyltranferase ( you may want to talk to doctors about it ): www.sciencedirect.com/topics/medicine-and-dentistry/dna-methyltransferase-inhibitor
Sample showing and copy
Mara nam mursidu Madisin to bolo dubara jonom lenge to cancar mangugi gut gut se morna acha he 1,2sal me moru😭😭😭😭😭😭😭😭9304071103
Plz help the sma children