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Son aged 7 newly diagnosed, I'm so upset

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Cheryl76

New Member
Relationship to Diabetes
Parent of person with diabetes
Hi. So, I knew my son wasn't very well and took him to the doctor's first thing Monday. Wee test and blood test then we're in a ambulance to hospital. Quickly diagnosed with type 1 diabetes and we came home last night. Should have the support team visit today. No family history of this.

I just feel devastated. I can't stop crying and I just want to say help, please help.
I don't really know what I'm wanting just feel so alone. I'm married but my husband couldn't care any less about me right now and just ignored me while I sobbed. I'm scared for my son and for myself as selfish as that sounds. I just have no one to talk to right now. Thanks for reading.
 
Oh Cheryl, I'm so sorry to hear about your son's diagnosis :( Don't worry, you are NOT alone, there are lots of friendly, knowledgeable people here who know very much how you are feeling, and can help you with your questions and concerns 🙂

There is a very steep learning curve with Type 1 diabetes, but things will become easier in time, and it doesn't have to stand in his way of doing anything he wants to do. People live full, happy and healthy lives with diabetes and can excel in any field (think of people like Sir Steve Redgrave and PM Theresa May 🙂) I would suggest having a read of Adrienne's essential guide for parents of newly-diagnosed children, written by one of our members whose daughter was diagnosed within hours of her birth. You should also get a copy of Type 1 Diabetes in Children Adolescents and Young People by Ragnar Hanas - considered to be the 'bible' for children and young people on insulin regimes, and an essential reference, it will help you get to grips with all aspects of living with diabetes. I'd also recommend looking at the Children With Diabetes website. They are a UK organisation of parents of Type 1 children and have lots of information about things like schools, care plans etc.

How is he feeling about things, is he coping OK with the injections? What insulin has he been given? Please let us know if you have ANY questions, we will be more than happy to help 🙂
 
Hello Cheryl, Welcome to the forum. I am sorry to hear about your sons diagnosis. I can only imagine how worried you must be. We have quite a few mum's and dads on here plus some very knowledgeable people who will be along soon. I just couldn't read and pass on by.
This is a good place for friendly support and advise , I'm sorry to hear your husband is not being very supportive ATM. Could it be he is numb with shock ?
 
He's having 3 day time injections of a fast acting insulin before meals and a slow night time one. Sorry if all the terminology is wrong. He gets very upset and tearful with the finger prick tests and the injections. My heart breaks a little seeing that.
Unfortunately my husband doesn't care about me and the marriage has been crumbling for a while. He couldn't get away from the hospital quick enough so feeling very alone. He may be struggling with it but he won't discuss his feelings.
 
He's having 3 day time injections of a fast acting insulin before meals and a slow night time one. Sorry if all the terminology is wrong. He gets very upset and tearful with the finger prick tests and the injections. My heart breaks a little seeing that.
Unfortunately my husband doesn't care about me and the marriage has been crumbling for a while. He couldn't get away from the hospital quick enough so feeling very alone. He may be struggling with it but he won't discuss his feelings.
I'm sorry to hear this, it's a shame you don't have your husband's support :( I hope at least that your son is being shielded from this at such a difficult time for him.

Hopefully, things will become clearer when you get your visit later on, I hope you have a good team to help with things 🙂 He is on a good insulin regime, which should be flexible for him, so that's a good start. Rubbing the injection site with an ice cube can sometimes help take away any sting, but often it is the tensing up and anticipation of the injection that causes pain - once he becomes more relaxed they should be practically painless. There are different sizes of needles too, so there may be a shorter length that he finds better (shortest are 4mm). This little guide might help with the finger pricking.
 
Welcome to the forum, Cheryl.🙂 I'm sorry to hear about your little one's diagnosis. It's only natural to feel upset but, as Northerner says, you're not alone on this forum. I hope the visit with the team goes well later and they help you start coming to terms with the new situation. In the meantime, fire away with your questions...we're here to help and support you.🙂
 
Welcome Cheryl, it is a big shock, but well done for acting quickly and getting your son medical help. If you haven't already, get a pen and a pad and start to write down any questions you have, and issues you have come up with etc, so that when the team comes round you don't forget anything. Also, write down what they say, as you probably won't remember it later. Best of luck and we are all here to support you . 🙂
 
Welcome.
It is still very early days for you. Have you got any other family or friends around to support you.
There are a number of parents of recently diagnosed children who may be along to offer you some pointers.
 
Welcome Cheryl. I'm really sorry to hear of your sons diagnosis and also the fact it's compounded by other problems.
I hope today's visit helps you feel more confident and wish you both well.
 
He's having 3 day time injections of a fast acting insulin before meals and a slow night time one. Sorry if all the terminology is wrong. He gets very upset and tearful with the finger prick tests and the injections. My heart breaks a little seeing that.
Unfortunately my husband doesn't care about me and the marriage has been crumbling for a while. He couldn't get away from the hospital quick enough so feeling very alone. He may be struggling with it but he won't discuss his feelings.

Welcome to the forum Cheryl, and sorry to hear about your little boy's diagnosis. My son was diagnosed aged 4 (he's nearly 16 now) and I have a vivid memory of the diagnosis, the shock and devastation, and how it turned our world upside down. You are experiencing a kind of bereavement and it will take time to adjust - but please let me reassure you that your son will still be able to lead a full and happy life, eat a normal diet, play sports, do well at school, etc etc. Sending you a big hug from one Mum to another 🙂

You are in at the deep end, and there's a steep learning curve, but you'll be a type 1 expert very quickly - I highly recommend the Ragnar Hanas book that Northerner mentioned above - this book is written in a clear approachable style and is positive and upbeat, and I found it invaluable in the early weeks, especially when I needed advice out of hours. I also recommend if you're on Facebook joining the group "CWD - Main Group", to connect with other parents of children with diabetes and draw on our collective experience. There is usually someone online on that group at any hour of the day or night!

Re your son getting upset over the injections and fingerpricks, I well remember that as being one of the most upsetting things - I literally had to pin my son down to inject him as he screamed and pleaded, heartbreaking :(. But the fear is worse than the actual feel of the needles - make sure you have 4mm or 5mm needles, much gentler. For the fingerpricker, use the lowest (shallowest) setting - this is relatively gentle compared to the butcher's device that they use on the wards! Only prick the sides of the top part of the fingers, never the pads (these have the most nerve endings and so hurt more), and avoid pricking index fingers and thumbs. He will get used to it before long and it will be much less traumatic, but in the meantime you need to be brisk and no-nonsense about it, and then move on to doing nice things immediately afterwards. Don't let the clinic push your son to do his own injections unless he himself wants to - some kids are happy to do this, but most want the support of an adult at that age - my son didn't self inject until he was 11.

Sorry also to hear about your husband's attitude. I was married at the time my son was diagnosed, but although his Dad did care in his own way, he didn't get properly involved in learning about the diabetes care, and certainly wasn't supportive of me. We have since divorced (unconnected with the diabetes), and though he regularly sees our son, he doesn't have him overnight because he can't/won't support him with his diabetes. That doesn't mean that he didn't care/grieve about the diagnosis, and it could be that your husband is upset but can't express his emotions. Whatever the situation, is there any other family member who could offer you some support, and maybe even come along with you to clinic and learn about your son's diabetes care? I speak from experience when I say I feel vulnerable as a single parent with nobody to fall back on if I were ill. None of my family live nearby and none of them know anything about type 1 management. So do try and get Grandparents or aunty/uncle on board from the start if you can.

{{{hugs}}} xx
 
Hello and welcome Cheryl.

I'm so sorry to hear about your little one's diagnosis, it is a huge shock and one steep learning curve to take on the running of something that just used to happen. The technology for managing diabetes is improving daily with great blood glucose management gadgets and gizmos which will enable your son to manage his diabetes very effectively. Young children are amazing resilient and seem to adapt quite quickly to the new normal,plus they are so tech savvy they really won't puzzle over how to set the right measurements on a glucose meter!

There are lovely people on here who have lived very well with type 1 for 50+ years without the benefit of todays fantastic meters, pens and pumps so there is every reason for a very happy healthy outlook. The blocks of living with diabetes will slowly start to fall into place and hopefully life will start to seem less frightening for you.

This forum is a fantastic resource for help and support and as the others have said please ask away and between us all we can answer problems you may face.
I wish you and your son well with getting to grips with his diagnosis 🙂
 
Thanks so much for the replies, and especially to Redkite for the mum hug.

I feel very much like I'm grieving and like somehow he won't be the same. I have to keep being with him to remind myself my little man is still the same Mario obsessed, funny, caring little person.

I feel scared to feed and water him as though everything I do might not be exactly right and I'll damage him.

Fortunately his school have been awesome, and I now know that 3 teachers have children with type 1. I feel boosted by hearing stories of achievements of those that had it from a young age.

My son is being protected from his father and my ill feeling. I don't sob infront of him. I'm honing my duck skills, calm on the top and turmoil on the bottom.

The Children's Diabetes Team are visiting at 2pm so I'm feeling better about that. Just confused with prescriptions as the GP said they have the info from the hospital but I need to tell them what I need and how much. They might as well ask me to Chinese.
 
Great news that school is being supportive (lots aren't so that's a BIG positive). Children are very resilient and at his age he won't have all those fears about the future that adults have - for him it's more about still being able to have that big 99 ice cream (and yes he can, but with insulin). He will still be the same lovely little boy as before, it's just he will need help and support, and things that you could do spontaneously like running outside to play in the snow will need a bit of forethought, ie a blood glucose test and a snack to prevent hypos - all this will become second nature before too long. My son (also a big Mario Karts fan at that age, and a Lego Star Wars fiend too!) carried on with swimming, gymnastics, beavers/Cubs/scouts, taekwondo up to black belt, tennis, and last year did the Duke of Edinburgh bronze award expedition. He's in Y11 now and in the middle of mock exams, and is a typical teenager really, grumpy when I prize his phone out of his hand and make him do some revision, but usually a lovely lad 🙂. Type 1 isn't the end of the world 🙂
 
Thank you, it's really reassuring to hear about life with your son. The diabetes consultant at the hospital said if relatives buy him diabetic chocolate he can throw it back at them
I think I worry about him being denied things.

His little sister is 5, she's been great but got upset watching his test and injection yesterday. I'm trying to take all her feelings into consideration too. It's tiring.
 
Thanks so much for the replies, and especially to Redkite for the mum hug.

I feel very much like I'm grieving and like somehow he won't be the same. I have to keep being with him to remind myself my little man is still the same Mario obsessed, funny, caring little person.

I feel scared to feed and water him as though everything I do might not be exactly right and I'll damage him.

Fortunately his school have been awesome, and I now know that 3 teachers have children with type 1. I feel boosted by hearing stories of achievements of those that had it from a young age.

My son is being protected from his father and my ill feeling. I don't sob infront of him. I'm honing my duck skills, calm on the top and turmoil on the bottom.

The Children's Diabetes Team are visiting at 2pm so I'm feeling better about that. Just confused with prescriptions as the GP said they have the info from the hospital but I need to tell them what I need and how much. They might as well ask me to Chinese.
I would order more than you think you need,or maybe the Diabetes team may be able to guide you. Most surgeries require 48 hours notice, of ordering. Unfortunately not all areas or surgeries work in the same manner. Have you looked on the website or asked if they can walk you through the system.
 
HI Cheryl, I was in the same boat as you. Marriage was crumbling, then my 3 year old daughter was diagnosed with type 1 on 23rd sept. she was completely traumatised with all the finger pricks and injections, we had to pin her down screaming and kicking just to give her insulin. She soon got used to it though after a couple of weeks. Now she doesn't bat an eyelid when getting her insulin, and likes to set up her blood glucose meter herself when getting her finger prick. Kids seem to adapt to it all so well. Better than us adults.
2 weeks after her diagnosis, my husband and I split. On top of this I was 8 months pregnant. I now have a 3 week old son as well as my daughter to look after, and we are all doing great. 2 months ago, I never thought my life would be like this. I was worrying constantly about my daughter, and what the future holds for her. I do still worry about some things, but feel so much better about it all now. Once you have had all your training and clinic appointments, you do feel so much better, and realise that it is manageable. It is a lot of info to take in at first, but with anything it does get better, and you learn more over time. I am still learning a lot now, the diabetes Nurses here are fab, and this forum is a great help.
I wish you both well
 
Welcome Cheryl. So sorry to hear about your sons dignosis, but as you have found already, you are very definitely not alone and there is loads of help available on here.

It is great to hear that the school are being so supportive. That can make so much difference, and with the teachers' own experiences of children with T1 they will be able to help your son at school.

The Ragnar Hanas book is excellent and provides a good reference book in the future is, so try not to be out off by the price of it. It really is excellent. I have been diagnosed for nearly 9 years now and still refer back to it as it has an excellent index making it easy to find the info you need.

Just keep asking any questions, and let us know how the appointment goes today.
 
Thank you, it's really reassuring to hear about life with your son. The diabetes consultant at the hospital said if relatives buy him diabetic chocolate he can throw it back at them
I think I worry about him being denied things.

His little sister is 5, she's been great but got upset watching his test and injection yesterday. I'm trying to take all her feelings into consideration too. It's tiring.

Yes avoid the so-called diabetic foods unless you enjoy tummy cramps and diarrhoea! You'll learn all about food, carbs and insulin dosing in time, but as a newbie you'll probably start off by avoiding large carby snacks between meals, because these would need an extra injection. My son used to get his "fix" of treats (e.g. mini packets of haribos or treat-sized chocolate bars) either as a pre-exercise snack or added on to the end of a meal, so that the carbs would be included in his meal injection. He has been on an insulin pump for several years, which among other benefits makes it easier to take insulin for snacks (something you might want to think about in due course). He doesn't have siblings, but when he had friends or cousins over I'd make sure he could be the same as them, whether that meant an extra injection for a treat or everyone else having theirs when he did. It wouldn't be fair on your daughter to feel restricted because of her brother's diabetes, but if you make it a whole family approach to meals and snacks, e.g. no sweets between meals is the family rule, not a diabetes rule. We used to have "sugary Saturday" when he was allowed to have Coco Pops and the like, and on other days more ordinary cereals - but this was something I'd have tried to do even if he didn't have diabetes. Now he's a teenager he eats non-stop, a lot of junk as well! But somehow we manage to keep his blood glucose levels within acceptable parameters 🙂.
 
Hi. So, I knew my son wasn't very well and took him to the doctor's first thing Monday. Wee test and blood test then we're in a ambulance to hospital. Quickly diagnosed with type 1 diabetes and we came home last night. Should have the support team visit today. No family history of this.

I just feel devastated. I can't stop crying and I just want to say help, please help.
I don't really know what I'm wanting just feel so alone. I'm married but my husband couldn't care any less about me right now and just ignored me while I sobbed. I'm scared for my son and for myself as selfish as that sounds. I just have no one to talk to right now. Thanks for reading.
Welcome Cheryl. Well done for getting him to the Drs ! Life ! its not meant to be easy is it ? I was diagnosed more than 50yrs ago at the age of 3. (the dark ages) I know a lot of T1s & its hard but worth learning & managing to cope 🙂
 
Hi Cheryl
I'm new here too. My son is 16 and was diagnosed Monday this week. I'm divorced and have no partner, although my ex and I are on very good terms. Like you, I feel very alone. I have cried a lot. I don't want my lovely little man to change. We're having issues with injecting as he has a phobia. I'm doing it for him at the moment. I've already had people telling me I'm wrong to do that, but I'm going with my heart on this one. I'm going to be on the same steep learning curve as you and I am more than happy to do it with you if it will help. If you're anything like me you're feeling completely overwhelmed at the moment.
Much love and hugs x
 
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