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Anyone know of a child diagnosed with leukaemia (ALL) and have a happy outcome? Some positive stories needed please.

57 replies

Myworldjusthim · 28/09/2023 07:58

My DS has been very unwell. Has had covid and a few other viruses for about 4-5 weeks. He was getting over the viruses but kept spiking temperatures. He was also sleeping a lot.
took him to the GP twice he said just viral. Took him A&E they said just viral but because his fever was high they would admit and start antibiotics.
Long story short, he had lots of blood tests that showed he had low wbc, low platelets and low red cells. So they admitted him. I asked several times about leukaemia and was told bit would show in his bloods especially the film. His fever kept stopping and starting. Sometime high, sometimes mild. They then said they wanted to look at his bone marrow as he wasn’t making any new cells at all. They suspected aplastic anaemia.
Last night we got the news he has ALL leukaemia. And they want to start treatment straight away.

Anyone know of anyone who has been in a similar situation? What is the outlook for leukaemia? What can I expect? Can he go into remission or recover?

OP posts:
MrsMitford3 · 28/09/2023 08:55

@Myworldjusthim what a lot to take in!

Is there someone you can have with you when you speak to the consultant so you are clear about what they have said after they leave?
Def take notes and write down all of your questions so when you do see consultant you are prepared.

There is no point fretting about what has happened re slow diagnosis-right now you need to put you focus in to support for your DS.

Make sure you have strong support. Do you have other children?
Accept all of the practical help you are offered.

And please don't google!! Good luck.

Sunandstorms · 28/09/2023 09:00

The most intense part of treatment was 6 months and during that time it did totally dominate all our lives. But we got through it. I sympathise also with the stress of slow diagnosis - we had a similar experience and I hated it

Myworldjusthim · 28/09/2023 09:04

Yes I have 2 more DC at home with me. My eldest doesn’t even know yet. Not sure how to break the news.

OP posts:

Interested in this thread?

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Stickytreacle · 28/09/2023 09:19

My daughter had ALL at two, she's now a wonderful 34 year old.
It isn't easy, but children are more resilient than we give them credit for. You get used to medical procedures as part of everyday life and you will find new friends in parents going through the same thing.
I think knowing that every day of treatment was a day closer to remission helped.
It will get easier when you get over the shock. I wish you and your son well. Xx

OhmygoshREALLY · 28/09/2023 09:42

Hi OP. Sending you loads of love and another positive story - my DD was diagnosed with ALL 2 years ago almost to the day when she was 3, she’s now 5 and coming up to the end of treatment and doing absolutely fabulously.
It totally turns your world upside down and I’m not going to lie, it’s very very hard in so many ways. But I promise you can and will get through it, and there is support out there from all kinds of unexpected places, both formal (charities etc) and informal - just the day to day kindness of people.
Don’t worry about not taking anything in right now - for weeks if not months I just lived a day or two at a time. Never knew what was happening beyond the next couple of days; the treatment is long and complicated and a HUGE amount to get your head round at the start so don’t worry, no one’s expecting you to remember it all!
The other posters are right when they say that ALL has excellent recovery rates and outcomes are very good. On the day my DD was diagnosed, one of the nurses said to me “if you’re going to have a childhood cancer, this is the one to get” and for some reason that stuck with me and was very reassuring, over and above all the statistics and whatnot.
Please please message me if you want to - I’m not on FB or anything but will happily give you my number if you’re on WhatsApp. At the start I used to look at the parents of kids in maintenance/remission and think it was a world away, couldn’t imagine ever being there, but we made it and we are here - but I remember being you so very well. It’s one of those things that no one really gets unless they’ve been there and I preferred talking to other cancer parents over and above anyone else for a while as it was the only time I didn’t feel so alone.
Best of luck OP, you’ve a long road ahead of you but you’ll get through it because you have no choice ❤️

Myworldjusthim · 28/09/2023 09:49

@Stickytreacle @OhmygoshREALLY
so sorry to hear your DDs had the same, but so pleased that they are doing well. This gives me so much hope.
@OhmygoshREALLY thank you so much for the generous offer of messaging you. If it’s ok with you I will take you up in that. I have another meeting with the consultant this evening and hopefully will know more 💐

OP posts:
User562377 · 28/09/2023 10:25

I hope you learn a bit more at the meeting tonight. Take a pen and paper, maybe even a less involved family member who can take notes for you?

It was my friend's child rather than mine who had leukaemia but I remember the information overload at the beginning. In no time at all my friend was sharing medical language like a pro. But it's tough going at first so write things down, write a list of questions. Ask everything and don't be rushed. Consultants do this every day and can forget sometimes that it's all new to the patient and their family.

They had intense chemo phases then a break where they could be quietly at home for a while. But their life was not normal for a very long time.

Their ds needed a stem cell transplant and had every complication going. But many people have a much easier time. Fingers crossed it's as smooth as possible for your boy.

CurlewKate · 28/09/2023 10:30

How terrifying for you. I am old enough to remember when Gary Linneker's son was diagnosed as a baby-and I will never forget the look on Linneker's face when he was papped. His son is now an obviously fit and healthy 30 year old. The recovery rate is even better these days.

OhmygoshREALLY · 28/09/2023 10:34

@Myworldjusthim yep definitely do message me as and when you’re ready, happy to listen, commiserate, discuss treatment, anything you need ❤️ xx

ElsaMars · 28/09/2023 10:37

Hello, I imagine you are in such shock. My brother had ALL at 16, I will never forget being told. He's now late 30s and all fine. It completely changed his outlook on life. Sending your son all my best wishes and you a hug it's such a bewildering time.

YouCantBeSadHoldingACupcake · 28/09/2023 10:54

A friends dd was diagnosed when she was 3. Her parents were repeatedly fobbed off by the gp before she finally got tested. She is now 11, and completely healthy, although she does have to have regular tests in case it comes back.

ThatbloodyRoblox · 28/09/2023 10:55

Hello
I am sorry to hear you are going through this. My son has ALL and had treatment over about 31/2 years. He is 5 years clear now. Due his annual check up next month.
I will be honest, it is a scary and difficult time for all of you.
I would say check if your local ward has a parents group- parents who are going through similar are very supportive and can also show you the ropes re the ward/ hospital where things are , little tips to make things easier.
We had a very good team and our consultant and clinical cal nurse specialist and community team ( once you get past initial treatment ) we're very good about informing us of what was going on.
Do you have friends and family nearby? Practical stuff like cooking decent meals, doing a wash etc are a Godsend when running between hospital stays and home. I was lucky that although I have no family close by, friends were very good to us.
I hope your sons treatment goes well Flowers

Orangebadger · 28/09/2023 10:55

@Myworldjusthim so sorry to hear about you DS diagnosis. You will all have a long difficult journey ahead for sure, as I am sure you know. But on a more positive note treatment for childhood leukaemia is fantastic now, it's very treatable.

onlyoneoftheregimentinstep · 28/09/2023 10:58

So scary for you, but lots of positive stories out there. Gary Lineker's oldest son for one. And personally, a friend's grandson was diagnosed age 6 and is now thriving in y11.
Really hope you get some better news soon. X

Mariposista · 28/09/2023 10:58

A girl in my mum's class had it (Reception). She is now at university.

HerculesTheBercules · 28/09/2023 10:59

My cousin had childhood leukaemia, he is now nearly 60 and well.

good luck to you all.

pimsts · 09/10/2023 17:19

I am very sorry to hear about you son and I know it is some weeks since you posted, I have only just joined Mumsnet. I picked up on two things, one that the blood counts and symptoms didn't quite fit leukaemia and the other that your son was 4-6 weeks after Covid and had spiking temperatures. Did they ever consider PIMS-TS also known as MIS-C, as the time frame and the symptoms and blood results would suggest this as a possibility, if you hadn't said they had diagnosed leukaemia? I am an admin of a support group for this condition. Our families created a website (I hope it is ok to post this admins?) which gives lots of information about PIMS-TS www.pims-hub.org.uk. I hope your son makes a good recovery x

PIMS-Hub Home Page

Information for families and medics on Paediatric Multi-inflammatory Syndrome - PIMS

http://www.pims-hub.org.uk

TidyQuail · 05/08/2024 20:18

My beautiful teenage daughter was diagnosed with leukemia on 22 September 2023, and it has been a nightmare 10 months.
For 10 months solid she was an inpatient at alder hey, and has only been living at home for the past 6 weeks. Even now, she has to return to the hospital everyday, 7 days a week for a 2 hour anti-fungal infusion, due to developing a rare fungal infection last October.
Lily turned 17 on 10th May, and has been so devastated by all this, as we all have. We had a family holiday to Majorca last August, and little did we know what was round the corner. It just came completely out of the blue. We returned from Majorca on 12th August, and she kept saying she had a really sore throat and was worried it was septic tonsilitis. On the bank holiday weekend, last weekend of August 2023, she came upstairs and said she felt like she couldn't breathe, and so I rang an ambulance and blue lighted her to the local A & E. She had done her GCSE's that summer and had got a place at the local FE college to study Hair and Beauty (bitter irony, as little did she know she was set to lose all her waist length blond hair). The A & E department ran some blood tests and couldn't understand why she had hardly any white blood cells and neutrophils of 0. something. During years 10 and 11 at school, she had frequent absences because she was always ill with a sore throat/chest infection/cough/cold, where nobody else in the household was ill. For 3 weeks, they continued blood tests and were clueless, coming up with things like "Aplastic Anemia". After 3 weeks of puzzlement, they decided to do a bone marrow biopsy, which I knew wasn't a good sign. A consultant rang me one night after 3 weeks and said they were transferring her to Alder Hey as they had more resource for children, and he still thought it was aplastic anemia. Then came the bombshell, on the day we were transferred to alder hey.
She was diagnosed with ALL (Acute Lymphoblastic Leukemia) on 22nd Sept last year, and my world collapsed. I honestly felt like I would die of a broken heart.
And I still feel this way.
She had 5 weeks of aggressive chemotherapy last Sept/Oct, and I was staying over in her hospital room one night when she had 4 ‘grand mal’ seizures, each lasting 2 and a half minutes, was transferred to intensive care, in a coma for 3 days, and when she woke up she said she was paralysed from the waist down.
Her nerve endings are coming back and she is having to learn to walk all over again, on a zimmer frame and crutches.
She had waist length blond hair, and is heartbroken as she is now bald (she had planned to study a hair and beauty course last September).
She has completed 5 weeks of chemotherapy, 9 weeks of immunotherapy, and another 5 weeks of chemotherapy, and is now on ‘maintenance’, which is lower level chemo.
She will be receiving treatment until October 2025. We are all broken as a family. I don’t think I will ever mentally recover from this.
I went back to work in January, and work 3 days a week, mostly from her hospital room using the hospital wifi, and caring for her in between, as she can’t do anything for herself.
Its heartbreaking. And my 13 year old boy has found it very difficult, as I’m mostly at the hospital and hardly at home.

Although we had hoped she would be in a position to start college this September, having deferred her place from Sept 2023, the reality is that she will need a further year of rehab before she is able to progress onto college.
I am utterly desperate for success stories, parents of other teenagers who were affected by leukemia who have come out the other side, and whose teenagers have gone on to lead normal lives.
Anybody who can give me some inspiration, please do

TidyQuail · 03/09/2024 19:22

I don’t know if this forum is active and its my first time posting, so will eagerly anticipate any replies.
My daughter Lily turned 17 on 10th May, and is now an outpatient at Alder Hey, but has to return every single day, 7 days a week, for an antifungal infusion, and will do for the next 6 months.
She only became an outpatient 8 weeks ago. She was an inpatient for 10 months.
She was diagnosed with ALL (Acute Lymphoblastic Leukemia) on 22nd Sept last year, and my world collapsed. I honestly felt like I would die of a broken heart.
And I still feel this way.
She had 5 weeks of aggressive chemotherapy last Sept/Oct, and I was staying over in her hospital room one night when she had 4 ‘grand mal’ seizures, each lasting 2 and a half minutes, was transferred to intensive care, in a coma for 3 days, and when she woke up she said she was paralysed from the waist down.
Her nerve endings are coming back and she has having to learn to walk all over again, on a zimmer frame and crutches.
She had waist length blond hair, and is heartbroken as she is now bald (she had planned to study a hair and beauty course last September).
She has completed 5 weeks of chemotherapy, 9 weeks of immunotherapy, and another 5 weeks of chemotherapy, and is now on ‘maintenance’, which is lower level chemo.
She will be receiving treatment until October 2025. We are all broken as a family. I don’t think I will ever mentally recover from this.
I came back to work in January, and work 3 days a week, mostly from her hospital room using the hospital wifi, and caring for her in between, as she can’t do anything for herself.
Its heartbreaking. And my 13 year old boy has found it very difficult, as I’m mostly at the hospital and hardly at home.

She is now living back at home again to work on recovery, rehabilitation, mobility and nutrition, although as I mentioned, we have to return every day for about 5 hours for the i/v antifungal infusion.

Although we had hoped she would be in a position to start college this September, having deferred her place from Sept 2023, the reality is that she will need a further year of rehab before she is able to progress onto college.

LittleSparklyStar · 03/09/2024 19:27

TidyQuail · 03/09/2024 19:22

I don’t know if this forum is active and its my first time posting, so will eagerly anticipate any replies.
My daughter Lily turned 17 on 10th May, and is now an outpatient at Alder Hey, but has to return every single day, 7 days a week, for an antifungal infusion, and will do for the next 6 months.
She only became an outpatient 8 weeks ago. She was an inpatient for 10 months.
She was diagnosed with ALL (Acute Lymphoblastic Leukemia) on 22nd Sept last year, and my world collapsed. I honestly felt like I would die of a broken heart.
And I still feel this way.
She had 5 weeks of aggressive chemotherapy last Sept/Oct, and I was staying over in her hospital room one night when she had 4 ‘grand mal’ seizures, each lasting 2 and a half minutes, was transferred to intensive care, in a coma for 3 days, and when she woke up she said she was paralysed from the waist down.
Her nerve endings are coming back and she has having to learn to walk all over again, on a zimmer frame and crutches.
She had waist length blond hair, and is heartbroken as she is now bald (she had planned to study a hair and beauty course last September).
She has completed 5 weeks of chemotherapy, 9 weeks of immunotherapy, and another 5 weeks of chemotherapy, and is now on ‘maintenance’, which is lower level chemo.
She will be receiving treatment until October 2025. We are all broken as a family. I don’t think I will ever mentally recover from this.
I came back to work in January, and work 3 days a week, mostly from her hospital room using the hospital wifi, and caring for her in between, as she can’t do anything for herself.
Its heartbreaking. And my 13 year old boy has found it very difficult, as I’m mostly at the hospital and hardly at home.

She is now living back at home again to work on recovery, rehabilitation, mobility and nutrition, although as I mentioned, we have to return every day for about 5 hours for the i/v antifungal infusion.

Although we had hoped she would be in a position to start college this September, having deferred her place from Sept 2023, the reality is that she will need a further year of rehab before she is able to progress onto college.

Hi, I’m so sorry to hear what you’ve been going through with your daughter. I worked as an oncology nurse for many years and saw so so many children and teens go on to make full recoveries even after awful things like your daughter has been through. I will keep you all in my thoughts.

Allthehorsesintheworld · 03/09/2024 19:29

My friend’s son was diagnosed with acute myeloid leukaemia the same time as Gary Linnerker’s (sp?) son so more than 30 years ago. Things looked very bad at times, he was barely 5 when diagnosed. Thankfully he had a bone narrow transplant from a sibling ( brave child, brilliant hospital staff who explained everything carefully) and made a complete recovery.
That seems so long ago and treatments have improved hugely since then.

AllThePotatoesAreSinging · 03/09/2024 19:30

I know someone whose son was diagnosed with leukaemia at 6 months. He had a lot of treatment and a transplant 8 years ago. He is 10 now and healthy x

StillWantingADog · 03/09/2024 19:31

One girl I know had it when very small and has just started high school. Another had it more recently and now in remission for some time.
the nhs is on the ball with stuff like this and it’s very treatable.
I suspect the journey will be a tough one for you all, wishing you all the best

ifonly4 · 03/09/2024 19:34

The son of someone I used to work with had it around the age of 4-6. He was fit and well on leaving junior school and as far as I'm aware everything is ok with him (still see colleague in passing) and he's around 14 now.

TidyQuail · 03/09/2024 19:50

Thankyou so much everybody from the bottom of my heart. These postings mean the world to me as it feels like an isolating experience so far. None of my work colleagues, nor friends, nor family members can relate to the experience. I still have flashbacks to the 4 grand mal seizures she had last october during the first round of chemo which put her in a coma and is the reason she still can't walk. Even though the nightmare began last August, its still so raw, and I find myself obsessing about relapse, and constantly asking the nurses if adolescents can go on to live a normal life, as a lot of these postings refer to very small children, less so 17 year olds, but I have to think positive for lily's sake. I will probably post regular now that I have found you guys

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