Experiences with

Post-exposure prophylaxis (PEP)

I saw this device on You-tube which helps control breathlessness. I would love to try it but because its made in America the postage is over £18.00 the device us £23.00 and honestly there's very little to it. Has anyone tried and tested this device. Would be nice to hear if anyone has. 🤔

So a good look 👀 in the mirror and a pep talk to the one staring back! Come on Annie, you can do this!!

Stack advice and. pep talks welcome. And for some reason HU isn’t coming up in my if I’m slow to respond that’s why. Thanks so much for listening.

What pep talk works to get you back moving again? I need all the help I can get.

They aren’t putting anything concrete in his 504 besides “extra time for testing, being able to have fidgets ect) he’s an anxious by nature kid and the size of the school has never really agreed with him (he leaves the pep rallies early, hates their crowded aftercare) he got offered a spot in a smaller

At 15 minutes I slowed to a walk while he gave his little pep talk at the end of the run, then I pressed 'resume' and set off again. Steve Miller singing 'Take the Money and Run' played, I sang along (don't worry, nobody within earshot :) ).

I was considering buying a PEP to try and keep my chest clear. Has anyone any advice on which to buy please? TIA

I get on ok with my aerobika but wondering if it’s worth spending £35 on the Evergreen Pari -o Pep? If it speeds things up I’d be interested in buying one 🙏

I'm not really looking for advice (fundamentally the answer is just that - it is bloody hard), but a bit of support and any words of pep you might have to spare please. As much as anything, I need to be able to get this off my chest. I'm nine months into PCS.

Bones be damned😀.I am very active which helps with bone loss and scoot around full of pep most days .So if you are very senior and on Pred and feel well just go with it . My goal is to get as low as possible and stay there ad infinitum

So, pep talk over, how is your Quest going now we’re into the third quarter of the month? Mine has taken a back burner. Four days in the car across Europe meant a whole lot of sitting still and no running so there goes my consistency.

Can someone give me a little pep talk and get me back into vacation mood?! The expectation to be having a good time coupled with the reality that my body is declining is knocking me down right now xx

I saw a different Dr today and was alarmed when she said my lining was "6.4mm" she then spent about 2 minutes silently scanning me whilst I came to accept that my lining was too thin and silently gave myself a hard pep talk about being patient and how it wasn't the end of the world.

constipation frightened to poop in case I "UNBLOCK" myself to the nasty stuff I just can't control I looked it up on DR GOOGLE and it came up with Proctalgia Fugax/ Levator Syndromeas I have all ready posted about my 2 colonoscopies 1 colon scans and don't want 2 bleat on I am taking Mebervine, Bucapans, Pep

Reading online made me realize it might be associated to PEP (or PUPPP).. even though I am not second/third trimester, and I did not gained weight rapidly. What can explain this? Haven’t take Beta test yet. 1 embryo transfer on Dec 19th.

Zytiga has given my dad an extra pep in his step (I think because of the prednisone.) However, I can see the cancer starting to come back. The urinary incontinence issues are slowly creeping back, he has had some back pain, and shoulder pain where there are significant mets.

I try my pep talks with myself but they don't last. How do I get out of this? LYME disease forums I see tells you so many remedies to try but they are so foreign to me, it's like being in another universe where I don't speak their language.

Such an army of support, advice, pep talk, and comfort is part of the improved survival rate for this disease..because it's so lonely to find yourself the only one with cancer in your social group...Those who have not been touched by this, really have NO IDEA.

The latest Patient Impact Statement has been released by the International COVID-19 Blood Cancer Coalition (ICBCC). Titled [i]"Navigating a post-pandemic world: A guide for immunocompromised blood cancer patients"[/i], it aims [i]"to help you navigate and manage the risks arising from the combination

The other therapist that I saw (and used all of my benefits coverage on) just wanted to give me pep talks about “thinking positively” and finding my “energy” and told me that I just needed to put myself out there and that everyone is nervous about meeting new people… And I have nowhere else to turn.