Happy Birthday Ayshy 

Dearest Ayshy..

Every year on your birthday I write to you with a secret hope that maybe one day you will be able to read my letters.My heart swells with sheer pride when I look at you. You have come so far and just like any mum, I am ever so proud of just how much you have achieved. I remember clearly that awful day when were given your diagnosis. You were sat on my lap staring in to space holding Winnie the Pooh, totally unaware of what was going on. The news I had just received, shattered my world. I remember holding on to you so tight. I had no idea what it meant for us or how I could help you! I didn’t have a clue how I was going to fix this? After all that’s what mums do isn’t it? They fix it, make it better but how was I going to fix this for you? My precious baby. My heart was breaking. No matter what I did I couldn’t make this go away, no matter how much I just wanted to make it disappear. That was just the beginning of the endless nights of tears, fear of the unknown and anguish, which would soon become a normal part of my life. 

How would this thing they called, “Autism” affect you? I had no idea! No matter how many leaflets I read, no matter how many books I looked at, I couldn’t predict which way this was going to go but I knew one thing for sure! No matter what we were in this together and I would do whatever I could somehow to make this right! I just needed to figure a way out. I made a promise to you and myself that very day, that no matter how bad this got, I would never give up on you. I promised you that I would never ever leave. I vowed never to let you believe that I didn’t want you or wish that you weren’t there. I would not allow myself to get angry. I would not let Autism take over our life. Today I say the same thing to you my darling daughter Ayshy! I won’t give in and I won’t EVER give up on you! I won’t let autism take you from me. 

Ayshy, if I have made mistakes along the way, I’m sorry. I didn’t always get it right. I had to try different ways because you couldn’t tell me which way worked, I had to guess. I Cried when I was wrong, I cried when I was right. So many times I wanted you just to give me a nod or the look to say, “yes mummy, this is working!” So many times I willed for a reaction from you. If I’m brutally honest the desperation to know what you was thinking drove me to the edge many times. Some days you wouldn’t even make eye contact. You wouldn’t let me hug or comfort you. Those moments literally broke my heart. I felt as though I had failed you. I felt as though my promises were falling apart. I felt I was failing you as a mother. I would pick myself up after these days, with a stronger resolve! I was determined that at some point we would make progress. Some day I know you will give me that nod and that reaction that my heart & soul needs so much!

It’s been such a long road, extremely painful, utterly heartbreaking and days were I believed that world would be a better place without us. If I couldn’t get it right for you who else would? But I truly believe God got us through it, after all, I only had faith on my side everything was against us. Slowly extremely slowly we started making progress. It wasn’t huge or life changing. It was slow but I could see a difference. The day you started school you looked so grown up in your uniform. We should have been talking about how great this was going to be, how you would make new friends & learn new things and how lovely the teachers would be that would look after you when I wasn’t there. Instead I was there with visual inputs, hoping you would understand. I wasn’t wrong about school though. Alexandar taught you many things, in fact they taught me many things too. 

We learnt together and it’s be an incredible journey! I’m so blessed to have have walked this journey with my very own little tour guide, the most beautiful little girl that I ever laid eyes on, that was you Ayshy. So we have had good days, we’ve had bad days and let’s be honest we’ve had dreadful days. The reality that you wasn’t going to do all the things little girls dream off hit home. The first meltdown scared me more than it probably did you! I didn’t know how to react or what to do but we learnt how to deal with them too. In fact Ayshy we learnt to deal with everything that came our way. No matter how small or how big it was we dealt with it. We’ve had the same conversations that consist with a few words over & over again. We’ve learnt the same words for years at a time to make sure you fully understand it. We’ve repeated numbers, colours, shapes and anything else that would help you almost every day over the last 19 odd years! 

Ayshy, you learnt words, you even learnt to tell me wether you like things or not. You learnt yes and no in the right context. You learnt to recognise your name and best of all you learnt to say “Mum”. You knew I was mum, I was your mum! I cried all day the first time you said it, you were nearly 6!! I’ve shed many a tear over the years but I don’t cry because I’m sad anymore. I cry because I’m so proud of you and everything you have achieved. Ayshy I know you’ll never know life like your siblings will. I know you’ll always need a carer. I know my dreams for you when I had you will never happen but guess what? What you have achieved is more than I dared to hope for, dared to dream about. 

Ayshy, we haven’t finished yet, we will make more progress, we will achieve more, I will make sure we do. I promise to guide you, support you, push you & do whatever I need to do. I will make sure you get to experience as much as possible. I will make sure you never feel alone or sad. Baby, if at times I annoy you, nag you, push you into counting or repeating words, please don’t hate me. You see one day mummy won’t be here and before that day comes mummy wants to help you understand & learn as much as possible.


Ayshy, you have brought nothing but immense joy to our life. Ayshy, you have shown us the real value of life. Ayshy, you have taught us humanity & compassion that maybe we would have never understood. Ayshy, you have taught us patience & tolerance. Ayshy, through you we have experienced faith like you wouldn’t believe. Ayshy, you taught us the real meaning of unconditional love. 

So you see Ayshy, just how amazing you truly are! It doesn’t matter how many birthdays you have. I know you don’t understand age & to me you will always be my baby, but Ayshy don’t ever forget how far you’ve come, how much you have achieved, how amazing your journey has been. Thank you for letting me ride this journey with you! 

Mummy loves you very much, much more than you’ll ever understand & mummy will do everything she can to give you every experience possible. That my promise to you, today, tomorrow and every day, I will do all that I can simply because I won’t let autism take everything from us. It chose the wrong mummy! We’ve got you Ayshy and you’ve got us, together will see it through. 

Happy Birthday Babygirl!! ❤️

She may never.. 

 So after 18 years in the education system school is officially over and off to college we go!

So what has 18 years taught her? She started school completely non-verbal, no words could she utter. She didn’t know her name or even how old she was. She didn’t know colours, shapes, numbers or even sizes. Truth be told she didn’t understand much. 

18 years at school have taught her a great many things. Today she can recognise her name. She may not be able to spell it out or even write it but she’s knows her name. She can count to 10 most days. She knows at least 10 popular colours. She recognises shapes and she’s learnt some words! Of course my favourite word from her mouth is “Mum”. I was never certain my ears would hear those wonderful words from my first borns mouth, but it happened! It was one of the most wonderful moments of my life.

What will college teach her? My hope is much needed life skills for her to be as independent as possible. I’m not expecting miracles. I’m fully aware the progress we have made so far is huge for her & I understand anymore is a bonus and a blessing.

She’s almost 20 years old now! I still have my what if moments. I desperately try not to let them surface too often but I’m a mother after all! What if she didn’t have autism. I often wonder but I’ll never know! I don’t know what tomorrow holds never mind next week. 

The truth is.. I’ll never see her take a driving lesson. I’ll never hear about the first day of college. I’ll never hear about the new friends she has made. I’ll never hear about the teachers she may not like. I’ll never see her change her outfit a 100 times for a night out with her college friends. I’ll never see her date anyone or tell me she’s found the one. I’ll never see her graduate. I’ll never see her say “I do”. I’ll never see her experience the wonderful joy of parenthood. I’ll never see her take her first holiday with her friends or her first all night rave. I’ll never text her and ask her where she is or say to her “wait till you get home”. She’ll never drag me to shops for new clothes or a new phone. She’ll never brush her own teeth properly. She has never been able to wash her hair or even pull out an outfit she wants to wear. I’ve never shared a secret with her and we’ve never had a pact. I’ve never even been given the chance to argue with her. We’ve never had a real conversation, we’ve never laughed at the same joke, we’ve never shared a bit gossip but we share many things that are priceless. We have an unbreakable bond of unconditional love. She can read my face and I can read her eyes. This our connection that I know she understands. So the list of I’ll never see her, will go on and on and on… But the one thing I know she’ll never feel is unloved. You see I may not have got what I was expecting but we soon learned to adapt & adjust the sail of our ship to the winds that were blowing our way. We wasn’t prepared to sink, even though life threw numerous sink or swim situations at us.

This is my daughter, Aaisha! She is the most affectionate person you’ll meet. She’s quite funny and loves joking around. She has compassion and doesn’t like seeing others upset. She’s just the most amazing young lady I know. Despite having autism, which lets be honest she probably doesn’t even know she has let alone understand it, she doesn’t moan and she doesn’t complain. She doesn’t ask for anything, she never demands. Meltdowns, bad days and days from hell, well that’s the autism not her, not who she really is. You see beyond the diagnosis she’s human just like you and me. She has feelings, she just can’t express them. She has emotions, she just can’t show them. She wants to understand us but often she finds this difficult and frustrating.

Autism doesn’t go away and you don’t grown out of it. It doesn’t get easier as they get older, in fact it gets harder, but no body tells you that. Yes as a parent it is utterly heart breaking. To most people she looks like a “normal young adult”. In reality my young adult is still my baby, still a toddler who needs constant supervision, still needs guidance, still needs her hand holding, still can’t let her out of our sight. 

So when I’m writing these blogs, I’m not asking for pity! I’m hoping that you’ll understand more about the impact of living with autism. I hope my blogs can help educate others. There are many parents like me out there. They have the same thoughts as me, the same heart break, the same pride for their child. All parents of autistic children have the basic right not to feel isolated. To feel that they can take the child where they want without fear, just like every other parent. We just want you to understand our children better and tell your children why our children are the way they are. It’s not them, its autism. You can control or tame naughty children but we can’t cure our children. Oh I wish we could but we can’t! If you can understand autism for us that’s all we ask. 

Miss Pam Malhi

Aaisha’s Hope  


School Is Over 

So my Angel has now completed school. It’s been an extremely emotional time for us all. It’s a bitter sweet moment, 18 years of education and my baby still can’t write her name. Will she ever be able to? I simply don’t have the answer to that, Just like a huge range of other unanswered questions. Does she understand she’s going to college? If I’m totally honest, the answer is, No, she probably doesn’t. Will she get to grips with the the new 3 day a week routine? Only time will tell. 
I’d like to think she will understand it’s a new era and it’s not school. I hope she settles in well and enjoys her time at college. I remember her being placed in specialist nursery at just over 2 years old and here we are at nearly 20 saying goodbye to that chapter of schooling. 

I’m actually beginning to think how this will affect her. The routine won’t be the same. The people won’t be the same. Starting college is daunting for anyone let alone Aaisha. She will never be able to tell me what she really thinks of this new place or how her day was. Oh how I would do anything to have those simple conversations with her. Even though I’ve know her future would be different and she’ll never be independent, it’s still so very hard. Some times I catch myself watching her playing with Lego or the uno cards and can’t help wonder if autism wasn’t apart of her, what career path would she have chosen? Or she could be driving by now and seeing whatever she wanted in the world. Would she be dating? As her Mum it’s only natural I guess that I think and feel these things. How will I feel when others her age are getting married and starting a new life? Knowing I’ll never see her as a bride.. 

Autism truly is cruel twist of fate but I can’t change any of it and I simply don’t know her any other way. It might mentally exhaust us some days but we will never let it take over her life or ours! There may be many things she may never do but through us she will live her life to the fullest. We will give her every opportunity to experience the things we do and along the way we will continue to raise awareness & acceptance of autism.  

 Pam Malhi

Aaisha’s Hope 

College Is Here 

Aaisha was 2 years old when she entered the education system. She was placed in a full time specialist nursery in the hope it would bring on her development. A year later, aged 3, she was diagnosed with autism. Now, at nearly 20 she’s leaving school. 

She still can’t write or read. Some days we can count up to ten others days we can’t. Some days we get the colours right other days we don’t.

Searching for a college placement has been hard. It was imperative that I could find her a placement that would fully meet her needs and provide 1:1 support where she could continue to learn & shine.

I always knew this was a decision I had to make for her. For the past 18 months however, I couldn’t help thinking over and over again, “I shouldn’t have to chose her college, this should be her choice.”

Then the answer hits me bluntly again. The stark reality that she can’t make those decisions about her life, just like many other decisions she’ll never be able to make. When she was younger I used to think it would get easier as she got older but who was I kidding? It gets harder. 

Words alone can not express just how difficult some days can be. She is now a grown adult, 5ft 7in tall. Looking at her just sitting there you would never guess there was anything different about her but it’s important to remember that autism isn’t just a physical disbility. As her parent I’m solely responsible for every decision I make for her and I pray I always make the right ones. From difficult ones such as college to simple ones to what she’s wearing every day. Even buying shoes can be difficult. Are they comfortable? Are they rubbing against her toes? Will she be able to walk in them properly? The tasks & decisions are endless. 

The thought of college does scare me if I’m totally honest. How will she makes friends when she has such limited speech? How will she react seeing so many new faces?  

 How will she understand this is college and not school? College for young adults with special needs is 3 days a week. For the past 18 years she has had a routine of 5 days a week of school. We now need to establish a 3 day week routine. This will be hard. We begin transition next week with me taking her in. I’m allowed to stay for a few hours and then hand over her care to teachers. It’s a huge change for her & us. I truly hope she settles in well and is happy in this new phase. 

What happens in 3 years when college comes to an end? I don’t know! What I do know is, that for me personally, residential care away from home is not an option. I don’t know how autism will impact her time at college. I know it’s never going to go away, I also know it could be a lot worse. Children with autism eventually become adults with autism, they don’t simply just out grown it. They become Adults but with child like minds. These young adults deserve the chance to experience life as we know it even if they never fully understand it. Please continue to support autism awareness, together we can make the world a better place for those living with autism. 

Pam Malhi

Aaisha’s Hope 

A New Month 

So April has come to an end just like every month eventually does, but oh what a special month it was. As many of you know April was Autism Awareness Month. For families living with autism however,  it simply doesn’t end in April. We live with this each & every day of our live’s. We don’t take anything for granted as we never know what the new day with bring. Living with autism is a life changing journey and no two days are ever the same. We simply just don’t what each day holds for us but what we do know is that this is forever our world. We have no cure but we do have hope, faith & love and that alone carries most of us through each day. 

No one can tell you exactly what this journey is, simply because no one truly knows. Everyone’s journey with autism is different. No one on this journey has it easier than anyone else. We all deal with emotions. We all think about things that no parent should have to.We are all just doing the best we can. You see the smile but look deep in to our eyes and you will see our pain. 

It’s vital that we are all fully aware of autism. It’s important to us and our children that you understand not only our journey but our children. Just because April has ended don’t forgot about those that are living with this each day. Please continue to support and learn about autism. Together we can make such a difference. I personally would like to thank each and everyone who has supported autism awareness. We are truly grateful to you all! X 

Pam Malhi 



Autism Awareness World Week 2015

Each year we have Autism awareness world week, and it’s here and it starts today, perfect timing as we head into April for autism awareness month. As the name suggests, we aim to raise more awareness and acceptance of autism. 

Autism is the fastest growing disability in modern Britain. 1 in every 68 children are diagnosed with autism. Autism is a life long disability and it has no cure. It’s an invisible disability, you can’t tell just by looking at someone that they have autism. The spectrum is huge and no two autistic people are the same. They may have similar tracts and comforting movements but they all lack skills in their development and understanding the world as we know it. 

I’m a huge autism advocate and I’m extremely proud of my daughter. She is my world along with her two siblings. Autism is a journey that nobody can ever truly prepare you for. There are many positives, many negatives and some life changing milestones on this journey. It’s always going to be filled with bitter & sweet moments. I share all the inspiring moments in our life as well as the bad days. It never gets easy! You get good days, bad days, amazing days and complete horrid days. 

I want to raise as much as awareness & acceptance as I can for everyone on this journey. I’m almost 20 years in on this journey. I’ve been told “I’m brave”, “I’m inspiring”, “I’m amazing”. The truth is, I’m not any of those things. I’m simply a mother. A mother who is trying to do the best she can. A mother who’s heart breaks on a daily basis. A mother who knows her daughter will never grown up. A mother who’s scared for the future of her daughter. A mother who still cries to sleep some days. A mother who at times feels completely useless. A mother who watches her grown adult daughter still behaving like a 2 year old. A mother for who time stands still for her daughter. A mother who has never experienced a real conversation with her daughter. A mother who will never get to see her daughter say I do or have her own children. A mother who knows her daughter will never have a independent life. A mother who so wishes their was a cure! 

So you see it’s not really inspiring at all! In all  honestly it’s cruel, it hurts, it’s tough but she’s my daughter, she’s inspiring!!  I will never  give up on her.  Autism effects everyone living with it. Her siblings have had to grow up before their time, they’ve had to make many scarifies, they’ve missed out on a “normal” childhood. They know more about autism than they probably do anything else. Autism chips away at you each day, as parent it slowly kills you, that’s the harsh reality of living with autism!! 

No matter how tough it really is I wouldn’t be without her. I wouldn’t know what to do with myself, this has become our life and it’s our “normal”. No one truly understands what it’s really like unless you too are living with it. I know it’s because of my daughter I am who I am. Its because of her I have more compassion, more understanding, more humanity. She has made me this way. Without her, I too probably would be wrapped in my own world, where my little problems would seem huge and I wouldn’t understand what real difficulties are, that’s the truth! So you see I owe her so much because of her we as a family unit are better people. As a family we take nothing for granted. As a family we have a amazing bond and unconditional love. As a family we share others joys & sorrows like they are own. We are not bitter at how it is for us. 

We don’t know what the future holds,  but what we do know is that we will continue to be her life line. We will continue to support her no matter how hard or tough it’s gets. We will get through the bad days together, we will laugh together through the good days. We will never give up on her or lose faith. We will love her unconditionally and we will be her eyes, her ears, her voice, her rock and anything else we need to be. Whether she’s 20 or 40 she will always be the baby of our family. She will always come first, her needs are placed above the rest of us. So maybe now you can understand why raising awareness and acceptance is vital & so important to those living with it. I want my daughter to experience as much of the world as she can with out stares or rude remarks. I want her to experience all the things we take for granted, above all else I want her to be acceptanced for the beautiful young lady she is. She didn’t ask for autism but as her family we ask for awareness & acceptance. 

Aaisha, we love you so much and we promise never to let go of your hand. We will do whatever we need to ensure your safe & happy always. #AaishasHope 

Pam Malhi

Our Sister

Autism.. It matters to us it’s matters that no one treats her any different, it’s important you understand autism. She may be our big sister but actually we’re her older siblings we will look after her, we want her to be happy, to be given every chance to do everything she wants like everybody else! She may never do the things in the way we do them but she has her own unique way and we wouldn’t ever change that.

We don’t want you to stare at her, she has no control over her movements or the sounds she makes, You see when you do stare she smiles back at you because she doesn’t understand hate she only knows love. She’s flaps when she happy she cries when she sad she feel the emotions like we do but just can’t express them like we do. We live with autism and some days it’s hard and some days it’s easy. We’ve never had a proper conversation with her, never shared a secret, never had a pact that we won’t tell mum that secret, we’ve never experienced getting told off by our big sister, we’ve never argued, we haven’t done much as her younger siblings simple because we have to be the older one’s but we love her so very much and wouldn’t change her, Because we live with autism we are better people because that’s what she’s taught us, to have compassion, to have humanity, to have patience and above all to have acceptance of everyone.

To her the little things matter to us seeing her smile matters we hope you too will learn how important autism is to the families who live with it. We hope everyone one day soon we will have autism acceptance & awareness. Our sister is a very special, she’s a gift and we love her very much and autism won’t ever take away our unconditional love that we has siblings share. We will always protect her and guide her. We just want other siblings like us to not have fight for awareness & acceptance. We alone can’t change this but with your help, together we can.

Aneesa & Cameron Malhi