What Worked For Us : Conversations with Mothers and Rita Kara Robinson

This is the most important conversation I have recorded in the 12 years of working with non verbal and autistic children. It's not clickbait. This has impacted my work enormously in the last 2 years.If you have a child whose speech regressed I implore you to listen to this. It is going to change some children’s lives.Maybe yours?If this happens to your child , please do circle back to let me know - partly because this conversation is unedited and completely raw, I am nervous to publish it, and I want to know if my time spent on these things is having any impact at all? The reason I stopped recording the chats with my mothers is because editing and publishing took so long I could not find the extra time to do this. So please make allowances because this is real, messy, live, and uncut.There are three mothers in my community that I have been especially yearning to record a conversation with. They are all clients of mine, and every time we speak - I hear so many valuable stories which I know can impact more families.This is one of those mothers. We both happen to be ex-teachers, therefore, we see children in an extra dimension when observing them - we see them as patients with symptoms to heal but also as pupils, and we have a lot to discuss and problem solve together.This is a live discussion about how I have been observing a little girl who would lie on her bed and blow the hairdryer on herself for sensory comfort each homeopathic appointment. Since her mother started focussing hard on pointing, using a yes/no board and then spelling using a specific method - she is now talking to me during our consultations in detail. She tells me where her pain is and how she feels about school.Her mothers sends me videos of her doing maths questions, yet her school teachers think she in incapable of any of these things and treat her as an incapable infant. Jenny is one of the few children who have turned my working life upside down. She has taught me that language is in inside ( most, or nearly all? How will we know? I will say nearly all for now) non-verbal children who have regressed.The problem is not language. The problem is the mechanism of speech. They are hearing and understanding everything that is said.Jenny has told me herself via spelling that she feels a “disconnection” between the brain and body. When she tried to talk, she feels “apraxia“ and “scrambled” and “stuck”.I asked her what does she want us all to know?“Believe”.Barely anyone I work with is using Audrey’s methods. WHY? I don’t understand why??? It’s not discussed in schools, in fact it has been discouraged in some cases to my astonishment. I can’t fathom it. It’s accessible, its cheap and it just takes time and dedication and its going to be all on the parent to unlock this form of communication.I have only seen positivity, improvement in frustration, behaviour and connection.You are all capable. They are all capable given time and patience.Feel free to get in touch via my website if this affects you in a positive waywww.rita-kara-robinson.comRHere are the links from Audrey that accompany this conversation.Spellers MovieSpelling Providers RPMSpelling Providers : S2CSpelling Providers : SpellersUk Spelling organisationAmerican Spelling organisationSpelling it out PodcastThere will be a live discussion with Audrey about this conversation in my closed patient group soon.

I got teary eyed again listening to this emotional recount of Oakley's early days, and also so uplifted at hearing his amazing story of how he is slowly recovering against all the odds handed to him at 2 days old. Her energy is infectious and I am deeply humbled listening to their life story.Daryl is a powerhouse of a mother, forging his path with him. You can find her on Instagram at @acornupdatesOakley was born with an imperfect brain, and was on a NG tube, intubated and was having seizures. He isn't fully mobile, is registered blind and non-verbal.This is their wonderful story worth listening to. You don't have to have everything in common in order to gain so much from their experience.Timestamps:0.52 Birth story1.59 Painful diagnosis at 2 days old3.47 Taken to NICU ( ICN)4.25 What the MRI showed about Oakley's brain5.19 Seizures started7.05 NG tube placed8.32 What he can do today: Tube free, not blind anymore10.00 Attitude is key14.25 Hard days and mum guilt. What works, what doesn't.18.00 They pick everything up21.00 How he uses a whiteboard27.00 From NG tube to eating normally31.00 Typical day34.00 Improved sight38.00 Oakfest - see @teamoakleyeventsThe Cricketer's Pub, Hitchin, Herts, 12th July 2025 11-6 Please go and support and meet Daryl and Oakley if you're living in that area.

Disclaimer: during this recording, the internet cut out so I had to edit this conversation. The thing is, I was a bit overzealous with the editing, a bit like when you cut your own fringe for the first time and cut too much off, and now you can't go back. So I sound like I'm in a hurry at the start, but I promise I calm down.I have worked with Arjola and Steven for several years and seen tremendous progress. Working with a child for so long has helped me see what can really be achieved, how long it tales, and what it takes, so I can pass that information onto mothers, without relying on theories.They are both bilingual, living in the USA. He had severe eating issues, he could not chew and held food in his cheeks. When I observe him in calls now, he looks neurotypical, plays appropriately for his age and answers my questions by typing on a tablet.We both never knew this was going to happen at the start, and persevered.  This is Arjola's story:Timestamps:0.54: Symptoms at the start1.36: Using homeopathy and supplements3.56 Food issues, could not chew solids, limited diet10.00 Non-verbal11.00 Using play to measure progress17.26 School not helping18.56 What happens when the mother takes homeopathy and heals22.00 I thought I was fine28.00 I used to focus just on speech, because I want speech to come now29.00 He is now typing advice to his parents

This is Abigail's story describing all the things she has learned along the way, in 5 years of healing her son with autism issues. She talks about other therapies, how her own healing impacted her child, and how best to the play the long game.Josh came to my homeopathic team at 6 years old, because he regressed and lost his speech at 18 months old. He had a whole list of issues to be healed.  This is his story, as a child who has made tremendous gains, some came fast and some came slow and steady. At the centre of his recovery is his mother, with her calm and determined demeanour, who has a lot of advice and experience to share with you.Timestamps:3.31 Gains on the first prescription5.23 What she was doing before that first prescription9.24 Using a homeopathy kit herself for acutes and becoming more confident13.31 When the parents heal, the child heals. "Your child feeds off of what you're going through."21.19 "They are paying attention to everything around them."22.15 "Who's going to take care of my child?"30.23 What do you say to the mother who is looking for that one thing that's going to do it all?35.00 "I don't know if this is going to work because he won't take anything by mouth"38.00 He found changes hard40.00 One of the things in common, in all the children I work with, who are making the best progress43.00 Her thoughts on working with Siobhan ( on the team)

Carla gave birth to her son at only 24 weeks old.He had many issues but Carla has done amazing work with her son.Listen to her story about her experience in the NICU unit, how she dealt with overwhelm in this situation and how she made sure her son had a good diet.She also talks about tantrums, sleep and screens, and her journey with homeopathy.She has much to offer mums on a similar journey.Timestamps:2.14 NICU unit experience9.20 Dealing with overwhelm12.13 How the right attitude helps16.32 Diet23.00 Tantrums27.35 Sleep and screens35.00 Homeopathy and other therapies

Carly talks about how her son has gradually healed over the past few years, the things she has done and the choices she made at home to facilitate his development in play and speech. She discusses the changes in him over the years and shares her advice for mothers with infants on the spectrum.These chats are live and unedited. If you have any questions after listening to this episode, please send a message on this recording located on Substack.Work with me as a homeopath here.

This is Michelle Vahey's story of how she recovered her daughter Koa who was given an autism diagnosis at 23 months and is now recovered at 8 years old.Michelle explains what was important in their journey - and that "it isn't just that  one thing". She tells us what was key for them, and what might help you on your healing journey.Work with me as a homeopath at www.rita-kara-robinson.com

Today I am answering 2 questions I get asked a lot and they are"Can I do this other therapy with your homeopathy?""Can I take this supplement/spray/add-on with your homeopathy?"Finally I get the chance to answer these questions fully so you can make that decision.The information I give is solely based upon my own experience treating around 2000 patients with homeopathy.This is an episode from my old podcast series. It still gets listened to so I have added it to this series.If you have any questions after listening to this then get it touch via my contact page on my site here Thanks for dropping by, I appreciate your interest.R x