Deleted User 298457
Deleted User 298457
All the rude boiis in London do.Yeah she got full support on WhatsApp. The person actually responds through voice messages on WhatsApp I've never seen anyone do that before
All the rude boiis in London do.Yeah she got full support on WhatsApp. The person actually responds through voice messages on WhatsApp I've never seen anyone do that before
Yes I knew that but there’s evidence to suggest that viral loads are much lower in fully vaccinated individuals.You do know the vaccine doesn't stop people from spreading it to others right?
It just makes their immune system stronger at fighting it to the point they don't develop the worst symptoms.
Yes I knew that but there’s evidence to suggest that viral loads are much lower in fully vaccinated individuals.
Okay. I only take the wee man out for walks if I can help it. The wife however just wants to take him everywhere and anywhere and I try my best to put to a stop to most things.
Whatever you do don't Google symptoms for babies or kids you will never leave the house again.
Nobody knows for sure how it effects kids and what long term issues there may be in years to come.
Like long Covid you just don't know there isn't enough info on it. I saw a kid on TV the other day on the news and apparently he's had issues with Covid for months on end now.
Basically you are taking a risk every time you expose them to someone else or within close proximity to someone else.
We will only know the answer to your question in several years probably a decade or two once it's ran through the population several times.
Personally I'd rather not take him anywhere and wife is complete opposite.
How do you cope as a couple? As in, does it effect your relationship? It goes without saying that the majority of us (all of us) will love our children unconditionally, regardless of their specific challenges. The difficulty surely lies in how mum and dad cope together through it.We have 3 boys 6, 3 and 1 year and I think I have mentioned before that the eldest has ADHD and ASD. He is under medication for his ADHD. He pretty much had trouble with sleeping since he was 3, getting up at night helping himself to food or drinks that were left out or in the fridge. He ran a bath one night when he was 3-4 years old. We were both sleeping and it was only a noise he made that woke us. Shook us both up it did. The thought of what could have happened....
Anyway this last 8 months or so he is a right pain to settle down at night. He will go to his room to play with lego around 6:30-7 and we tell him 8:00 is get into your bed and go to sleep time. From 8 right through till 10-11pm he is up and down stairs constantly. I am not exaggerating when I say he can be up and down 30-40 times in one evening. Its draining. We cant relax watching tv or eating tea. We have tea around 11pm some nights. Up and down is waking the other two lads. If the eldest is up during the night (which has reduced loads recently) he will be awake. ADHD is a ******* for that, once awake always awake full of energy etc. I will have to stay up so he wont do anything. Getting 4 hours sleep a night is a god send to me.
Theres been times he has got up and watched tv downstairs. I have caught him and also when I hear him come up stairs I will log onto the streaming services and youtube and check history. He has been up on many occasion 1am till 4/5am watching youtube stuff. Thankfully its mostly science stuff on the channel Kergustats or somthing.
fast forward to other day I rang his paediatrician and told her its getting worse and she did a prescrition for his normal medsa nd an extra batch of some melatonin tablets.. First one tonight at 6pm gone nite nite in 1 hour 15 minutes.... I know he will have medication all his life pretty much and its a shame but its best for him and us, plus his brothers.
fingers crossed they will help him out.. Anyone else with kids that has ADHD and/or ASD/?
Yep, both boys (7 and 3) have diagnoses of ASD. We had sleep issues with the eldest too, though once he's asleep thankfully he usually stays asleep. He still needs support to settle, one of us sits outside his room on the stairs. He'll come out a few times usually and takes maybe an hour and a half for him to fall asleep. Completely used to not having much of an evening.Anyone else with kids that has ADHD and/or ASD/?
That sounds hard on everyone. We had a period of maybe a year where my son would come in our bed during the might, and he's a wriggle sleeper so I sympathise with the lack of sleep. I also enjoy the precious "me" time when kids are in bed so it must be a struggle. Hopefully new medication is the light at the end of the tunnel.We have 3 boys 6, 3 and 1 year and I think I have mentioned before that the eldest has ADHD and ASD. He is under medication for his ADHD. He pretty much had trouble with sleeping since he was 3, getting up at night helping himself to food or drinks that were left out or in the fridge. He ran a bath one night when he was 3-4 years old. We were both sleeping and it was only a noise he made that woke us. Shook us both up it did. The thought of what could have happened....
Anyway this last 8 months or so he is a right pain to settle down at night. He will go to his room to play with lego around 6:30-7 and we tell him 8:00 is get into your bed and go to sleep time. From 8 right through till 10-11pm he is up and down stairs constantly. I am not exaggerating when I say he can be up and down 30-40 times in one evening. Its draining. We cant relax watching tv or eating tea. We have tea around 11pm some nights. Up and down is waking the other two lads. If the eldest is up during the night (which has reduced loads recently) he will be awake. ADHD is a ******* for that, once awake always awake full of energy etc. I will have to stay up so he wont do anything. Getting 4 hours sleep a night is a god send to me.
Theres been times he has got up and watched tv downstairs. I have caught him and also when I hear him come up stairs I will log onto the streaming services and youtube and check history. He has been up on many occasion 1am till 4/5am watching youtube stuff. Thankfully its mostly science stuff on the channel Kergustats or somthing.
fast forward to other day I rang his paediatrician and told her its getting worse and she did a prescrition for his normal medsa nd an extra batch of some melatonin tablets.. First one tonight at 6pm gone nite nite in 1 hour 15 minutes.... I know he will have medication all his life pretty much and its a shame but its best for him and us, plus his brothers.
fingers crossed they will help him out.. Anyone else with kids that has ADHD and/or ASD/?
How do you cope as a couple? As in, does it effect your relationship? It goes without saying that the majority of us (all of us) will love our children unconditionally, regardless of their specific challenges. The difficulty surely lies in how mum and dad cope together through it.
Best advice I can give you regarding Internet access is use something like this Deco Mesh WiFi system. You can administer your own network and assign specific devices their own protocol. For example, XXGb a day or no data after XXpm.
That sounds hard on everyone. We had a period of maybe a year where my son would come in our bed during the might, and he's a wriggle sleeper so I sympathise with the lack of sleep. I also enjoy the precious "me" time when kids are in bed so it must be a struggle. Hopefully new medication is the light at the end of the tunnel.
George ended up in hospital with RSV again last week, really disappointed in the doctors phoned them and they said because the symptoms match Covid they wouldn't see him even though he was panting, disgusting behaviour of you ask me.
Went to A&E and they rushed him in so no waiting, put him on a drip fluids and antibiotics to be safe while they tested, his SATs dropped below 90 a few times so they put him on oxygen as well overnight. He came home the next day after he perked up.
Hospital have advised us that in future if this happens to start force feeding him sugar water to keep his energy up.
What's most annoying about the doctors is George has a "pop up" in place so he should get priority care but they must just ignore it when it suits.
I know how it feels, our baby has a skin condition, no idea what it is. Our first telephone appointment involved us sending some photos of him and doctors 'scribed us some lotions. Sort of worked but kept coming back. Called again, same thing. They are refusing to see him to actually see what his skin is like, photos don't cut it. Its frustrating. I had to take the 2 youngest in for their jabs last week. You ring the bell and give details from outside via a speaker thing and sanitise your hands before going in, mask on obviously. Only 8 chairs in there, 2m apart all facing one direction so no face to face patients. You sanitise before going into the doctors room. You dont actually touch ANYTHING apart from the front door which you sanitise after walking through and the chair possibly with your hands. There is no need to not see anyone especially children, covid symptoms or not. Also to add, I am petty sure once I left the waiting room to go into the doctors room, the receptionist sprayed what looked like a Dettol spray where we were sitting, so even then the area which was used gets cleaned immediately. I will assume she did the same thing when I left.
I mean if you have COVID symptoms they should refuse to see you. They can diagnose a skin condition from pics tbf…what creams have they given you?
Cetreben is what my daughter has and it works.
They really shouldn't refuse to see children, especially ones with a pop up.I mean if you have COVID symptoms they should refuse to see you. They can diagnose a skin condition from pics tbf…what creams have they given you?
Cetreben is what my daughter has and it works.
George ended up in hospital with RSV again last week, really disappointed in the doctors phoned them and they said because the symptoms match Covid they wouldn't see him even though he was panting, disgusting behaviour of you ask me.
Went to A&E and they rushed him in so no waiting, put him on a drip fluids and antibiotics to be safe while they tested, his SATs dropped below 90 a few times so they put him on oxygen as well overnight. He came home the next day after he perked up.
Hospital have advised us that in future if this happens to start force feeding him sugar water to keep his energy up.
What's most annoying about the doctors is George has a "pop up" in place so he should get priority care but they must just ignore it when it suits.
They'll get a telling off soon as the wife updated his key worker and she wasn't best pleased.This is pretty standard at the moment. Hospital is bearing the brunt of all the stuff the GPs won't see and a normally quite chilled time of year is turning into a nightmare.
Primary care needs to grow up, they're all fully vaccinated and the risk is minimal yet the refusal to see anything "red" means that kids aren't seen at all.
They'll get a telling off soon as the wife updated his key worker and she wasn't best pleased.