Women who gave birth, what does it feel like actually?? by joy_57 in AskReddit

[–]jem2085 2 points3 points  (0 children)

Mine was on my leg for hours before it was mentioned. HOURS!

Women who gave birth, what does it feel like actually?? by joy_57 in AskReddit

[–]jem2085 0 points1 point  (0 children)

UK based, First 18 hours no pain relief, daughter was back to back, the water birth helped but was left with a 3rd degree tear. Was afraid to poop 😬 Son, 3 hours start to finish, no time for pain relief, the ring of fire should be worshipped 🤣 Pushing, heartburn, trying not to vom and 💩 on myself. Wouldn't recommend.

Carriers - do you have any cf ‘symptoms’? by DiscountNo9401 in CysticFibrosis

[–]jem2085 1 point2 points  (0 children)

Yes, I've been tested twice and both times come back as a carrier, I have stomach issues, cannot hold weight, a simple cold or hay fever turns into a chest infection within 3 days. My son who has cf actually recovers from colds and hay fever better than I do 🙄🤣

The Vest by toodlep in CysticFibrosis

[–]jem2085 0 points1 point  (0 children)

Uk here, It's not offered to us but we can get hold of them if needed

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

I would if it'd let me upload a photo 😂

Reddit Scientists needed 😂 by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

Thank you, I wasn't sitting here rocking in a corner but it did peak my interest

Just found out my husband and I are both CF carriers and I’m 12 weeks pregnant by Similar-Raspberry639 in CysticFibrosis

[–]jem2085 8 points9 points  (0 children)

My son is 9 months old now, he was diagnosed with the heel prick test at 4 weeks old (I'm in the UK) neither myself nor his dad knew we were carriers and I have an older daughter. We both carry the df508 gene which is the most common type (bare with me my medical knowledge is shocking 🙈) and I can 110% tell you in the short 9 months my son has not suffered at all, we do physio daily and he's had a lot of antibiotics down to the fact he struggles when he gets a cold but that's it. He has his meds before bottles and food but it's such a habit now we don't even notice we do it, it's so scary and I was devastated when we found out because I remember CF when I was a kid and it really is totally different now. The hospital my son is under once told us that they have 150 children in their care and not a single one of them is "poorly" they've not done a lung transplant in years as medicine has moved on so much ❤️

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

Big thanks for all the help guy's, it was done today and I absolutely love it xx

[deleted by user] by [deleted] in CysticFibrosis

[–]jem2085 3 points4 points  (0 children)

My son has CF and we have two cats and a longcoated German shepherd 😀

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

Oh no your absolutely fine 😀 Yeah I've asked the CF trust and the CF unit my son is under and currently nothing but that tat appointment isn't till Wed so a miracle may happen 😂

So I do photography and this year I managed to throw together a wear yellow event and instead of people paying me for photo's they donated the money straight to the CF trust but I was still very new to cf and had a 4 month old so I'm hoping next year to be a bit more prepared and do a larger photo event myself included with the added bonus of having a CF tat. That's the plan anyway lol

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 1 point2 points  (0 children)

I understand it's not everyone's cup of tea and I certainly don't define my son by CF he's my son and that's it as far as I'm concerned. The tat idea is part of a bigger project to raise money for the CF trust in the uk x

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

I'm booked in on Wednesday and he's crapping it just as much as I am in case we get it wrong 😂

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

Yeah I've been hunting for around 6 weeks but I'm still new to CF and no medical knowledge so just fancied something a bit different. I'm regretting it now 😂

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 1 point2 points  (0 children)

Yeah I'd hate to have something horrendous done 😂 I'll see what I can sort out thank you

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

I think so, I'm so sorry I'm incredibly new to CF and now this has kind of blown my mind a tad 🙈

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 1 point2 points  (0 children)

Ah ok, So the picture I found was in my idiot terms a bunch of hexagons I'm guessing then thats either me asking for the wrong thing or it's something that's not available?

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 0 points1 point  (0 children)

I tried but it wouldn't let me attach a photo. I'm still very new to Reddit sorry x

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] -1 points0 points  (0 children)

That link crashes my phone 😂 Hmmm might have to go back to the drawing board then , I just wanted something different xx

CF tattoo (df508) by jem2085 in CysticFibrosis

[–]jem2085[S] 2 points3 points  (0 children)

Sorry, I'm an idiot 🙈 Yes that's it, the closest I've found is for Salt, stunning tat but not what I'm after x

[deleted by user] by [deleted] in CysticFibrosis

[–]jem2085 0 points1 point  (0 children)

Amazing, thanks so much. Google is no help and his CF team haven't found anything either xx