As those of you that are on my facebook will know, my son had peri-orbital cellulitis in September. This post is just for our reference of how/when/what happened. It is very long and photo heavy.
Sunday 11th September
Around 6:30pm I noticed a slight swelling to your right eye. I thought nothing of it and presumed you must have knocked it at some point earlier in the day.
Monday 12th September
Midnight: you climb into bed with papi and I and fall asleep until 7am. A clear indicator that something is wrong(you only sleep with us when you're ill)
7am:We see your right eyelid is now swollen soo much you can't open your eye at all.

8am: Drs appointment is made for 10am, which is the earliest they have available.
10am: Dr says it's most likely an allergic reaction. She prescribes a double dose of antihistamines and says she'll ring this afternoon to see how the swelling is.
11:30am: We arrive back home and I post on MamaPacks forum to ask their advice. My heart tells me it's not an allergic reaction due to it coming on too slowly and being localised to one small area. Toots responds by saying she thinks it looks like peri-orbital cellulitis and a quick Google search provides me with images that match how your eye looks.

1pm: I call the doctor to say the swelling has got bigger. She says to give it more time. I'm not really happy with this, so prepare a bag ready for hospital just in case.

2pm: Dr rings back, I say it's really not got any better. She says to wait until this evening as she is sure it's just an allergic reaction. I tell her I'm taking you to casualty now.
2:30pm: Arrive at casualty
3:30pm: Dr takes one glance at you and says he doesn't need to examine you as he can see clearly that you have peri-orbital cellulitis. He tells us that you'll need to be admitted to hospital for IV antibiotics for 2 days. My heart sinks, but not as much as it could have due to preparing myself for it being P-O C.
4pm: Admitted to childrens ward(assesment unit)
5pm: Cream put on both your hands to numb them in preparation for the cannula.
5:30pm: Papi arrives
6:45pm: You're getting very tired, grumpy and keep asking to go home. You have the mother of all meltdowns. I ask for some food for you because they haven't given you any tea! They bring you beans and toast with a spoon and a fork. You're soo hungry you use both utensil simultaneously to shovel beans into your little mouth. All whilst shaking profusely.
7:30pm: Drs attempt to put a cannula in. They try twice in your left hand, once in your right. All of which failed. The noise you make whilst trying to fit the cannula is heartbreaking and I break down in tears. It's a good job papi is here to hold you. We're told to go and have a little break to give you(and me) chance to calm down.
8:30pm: Nurse finally comes to put cream on your feet.
8:50pm: A nurse tells us that if the cannula isn't put in by 9pm then it won't get done until 10pm due to the shift change. We silently wish it gets done before 9pm. We're all tired, especially you as you've been up since 7am and haven't had a nap.
10:30pm: A cannula is finally placed in your right foot. flucloxacillin and benzopenicillin are administered.
11pm: Finally you're allowed to sleep.
11:30pm: I quietly cry myself to sleep. It's been one hell of an emotional day!
Tuesday 13th September
Papi took the day off work to be with you.
7am: You woke up when the nurse started to administer IV meds.




We spent most of the day in the play room.
Midday: IVs administered.
2pm: ENT visit and prescribe nasal drops and steriods to help speed up the reduction of the swelling. We then push you in a hospital pram(which you loved) to your opthalmist appointment. He says your eye is clear(huge releif!) and makes a follow up appointment for the following Tuesday.
3pm: I ask a nurse to bring you some food as you were never brought lunch!
4pm: Steroids administered
6pm: Next dose of IVs due. Cannula has failed and needs to be redone. We're promised it will be done before 9pm.
7pm: Cream administered to hands and feet.
7:30pm: We notice your eye is starting to open!

9pm: We're told the switchover will only take 10 minutes.
10:15pm: Drs are ready to try fitting another cannula. Tried again in your hand, failed. Finally got one in left foot. IVs and steroids given.
10:30pm: Bedtime at last!
Wednesday 14th September
1am: Meds administered. You woke up, cried but went back to sleep swiftly.
7am: More meds administered. Then playing in the playroom. Your eye is open almost half way and you can now see out of it.

9:30am: Drs rounds. He says we're not allowed to go home today. I'm soo upset I struggle not to cry. Practically everyone said we would be home on Wednesday.
We spend the day playing, mainly with you in the pram being 'a baby, mummy' and me walking around with you so you can go 'light spotting' and point out the lights the don't work.

Grandma visited again with a little present(as she did yesterday), but you sleep through it(again!)

As Grandma is leaving you wake up, then Nana arrives. She brings you ribena as always.
8pm: We attempt to put you to bed at a reasonable time....You don't fall to sleep until 9:30pm!!
Mummy and Daddy go and eat KFC in the parents room whilst you sleep. Then papi goes home.
Thursday 15th September
1am: Time for meds. You scream and thrash more than usual. The nurse checks your cannula-it's fine but she asks me if I think you're in pain. I do. She goes to ask the Dr if she can remove the cannula and start oral antibiotics as you've had the stated 48hrs of IV meds(anything extra is a bonus). She doesn't put the bandange back on your foot(or your sock) therefore you scream like a banshee and hurl abuse at me. (You hate seeing it and are only calm when it's covered up with your sock)You start pointing your finger at me screaming 'NO!' and other words I can't understand but they clearly contain malice and contempt for me. You start screaming for daddy because you're no longer my friend. After what feels like an aeon they send a different nurse in to remover the cannula whilst the previous nurse gets your oral meds ready. As soon as the cannula is out you're silent.
I give you the oral meds(with relative ease) and you try to go to sleep. You don't want me to touch you because you're still upset with me for holding you down so you couldn't pull the cannula out.
7am: You're eye is almost fully open!! You're much happier today(presumably due to no IV meds)
More playroom time.
9:30am: The Dr says we can go home! But we need to wait for your prescription(which could be some time). Your blood cultures come back negative.
10:30am: You ask to go home(again), so I go to see how long we'll have to wait. The prescription still isn't ready but the nurse says you can have your next dose of meds at 11am then go home. All we have to do is go back to collect you prescription when it's ready. They'll ring us when it's ready.
11:30am: We're home!!!!
12:00pm I put you to bed for a nap as you're shattered. You sleep until 4:55pm!!!!
4:50pm: Hospital ring to say your prescription is ready for collection.
4:55pm: You wake up. We wait until daddy gets home at 5:30pm so we can all walk together to collect your meds. As you needs feeding and changing before setting off.
We get to the hospital and they tell us you need 6.5mls of flucloxacillin and 3.5mls of phenoxymethly penicillin four times a day for the next 8 days. You also need nasal drops twice a day for the next three days.
Monday 19th September
Dr B rings to see how you are as she's recieved your discharge notes. I tell her you're doing ok and that we didn't get out of hospital until Thursday. She tells me it was a 'good spot' with your eye and 'well done for taking him to hospital'. All the time I'm thinking- 'if you'd done your job properly he could have started treatment sooner!'
How she failed to see what Toots saw from a mere photo(and Charlotte for that matter) is beyond me. But thanks to me for knowing in my heart that it was more than just a mere allergic reaction, the lovely ladies on MamaPacks and Charlotte, you got the treatment you so desperately needed. I dread to think what could have happened if I listened to the GP.
Tuesday 20th September
Follow up appointment with the opthalmist. He declares your eye completely clear and discharges you. :o)
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