u/Boring-Temporary-340

I’m annoyed for letting this bother me, but it ended up ruining my round a bit and I’m intrigued to see thoughts 😂. Context we were playing a 2v2 9 hole friendly game of matchplay, no money on the line or anything just to make the back 9 interesting. After 4 holes we’re all square and myself and player on the opposite team have 2 putts that we should make for par, I go first hit an awful putt and pick the ball up as the opposing player has a chance to win the hole, he then lips out unbelievably (shocking putting from both of us) and taps in for bogey. He then says ‘we’re 1 up’ to which I questioned and it was because he hadn’t give me my putt for bogey and I’d picked it up. Now obviously I know per the rules this would be correct but my ball was like 5 inches from the hole and I thought nothing of it. Am I in the wrong for being annoyed by this because it’s the letter of the law or is he being a bit of a dick?

As the title says, I find myself wondering whether I’ve long Covid or am I suffering from chronic burnout as lots of the symptoms do overlap.

No disrespect to anyone in here (I include myself in this category) but I’ve been trying to look outside of this bubble at stories of people who have recovered. I’ve noticed a pattern from a lot of people that they improved once they mentally started to let go of the illness. From not worrying or searching symptoms to starting to live life normally with exercise and seeing friends etc. This does make some sense to me with a lot of issues coming from the body being stuck in a fight or flight state. Intrigued to see what people’s thoughts are and if they’ve tried this?

I’m 8 months in, and my main issues are neurological, brain fog, head pressure and vision issues. Now the more I look into DPDR it best explains my vision problems which I’ve struggled to explain to doctors. Early on there were times I’d look in the mirror and think it’s like I’m looking from outside my body, but at no point have I mentally thought I’m not real or the world around me isn’t real, it’s just my vision looks like that. Has anyone experienced similar and has anything helped?

What have people found best for relieving head pressure, my doctor has started me on propranolol today so I’ll see how that goes. I’m also seeing a long Covid specialist which is really expensive and he mentioned in my first session we could look at LDN. If people have tried both what have they found is best ? I should add I don’t really suffer with ME/CFS symptoms, it’s mainly dysautonomia type symptoms I’ve got.

I had a specialist long Covid appointment. And he’s mentioned taking famotidine, and the more I’ve lucked into it some of symptoms fit the LPR possibility. I’ve had a dry barking cough for 5 months (yet I don’t cough very often) I get shortness of breath and a tight burning sensation in my chest yet don’t really feel like I’ve got heartburn or lump in my throat. Is this other people’s experience?

Please tell me everyone else is hating golf in these conditions and scoring terribly 😂 like playing on a hilly car park

Context, my partner 28F has struggled with her mental health most her life and has come off her antidepressants early this year. The past month she’s been going into the pattern of being up and down through the week but nothing too bad, then once it hits Friday afternoon/evening her mood completely drops. Won’t talk to anyone, won’t get out of bed extremely irritable, can someone help me understand and what can I do to help?

Help me out guys! I’m a decent player and year round I’m playing pretty consistently, but every year if we have a dry spell here in the UK and the fairways get burnt out I can’t hit a pitch shot to save my life 😂 I’m sure it’s partly mental, but it’s an area I never struggle with during the rest of the year, but as soon as the grass goes and the hardpans out I either hit the dusty chunk or get overly steep and blade it. How can I play these lies consistently! (I should add, any full iron shots etc I’m fine with, just that 50-100 yard area)

Booked an initial consultation which has cost a small fortune, anyone found them to be good ?

I’m 7 months in and not had any ME/CFS type symptoms I’ve been all neurological and lung issues. I’m scared that if I start exercising more I’ll develop the other symptoms has this happened to anyone (for context I still exercise abit now occasionally go to gym and play golf every week)

Anyone had these symptoms and found out what’s causing them, im 7 months in and was feeling around 80% better, but this has come on out of nowhere and is causing me problems now.

I’ve left finalising my exams far too long, I’m 8 years as an accountant and around half way through CIMA. I need to finish my exams but don’t want the pressure of my company paying thousands for study and then me being tied to that company for years which is their policy. What’s the best free way to study and is it actually doable I’ve heard open tuition mentioned often.

Essentially i’d like to change jobs, I work in banking and came into the company as an assistant accountant and have since been promoted to management accountant (been in this role around 9 months). Now the issue comes when I’m trying to apply for similar roles. My assistant accountant salary was £55k and my management accountant salary is £70k. So I feel the job titles are actually quite undervaluing my roles and experience when I look at other salaries for those job titles. Would it be reasonable to change the job titles in my CV?

Anyone else experienced this, I think I’ve overdone it this weekend playing a round of golf then going to a golf tournament in the sun. So 35k steps over 2 days and I’ve woke up really short of breath and I’ve had this symptom a few weeks ago for around 10 days also. Is this a flare other people have experienced ?

I’m 6 months into this disease and around a month ago I felt 80% better, I was exercising daily and feeling good for around a month. The past 2 weeks I’ve developed a tight chest and some breathing difficulty (nothing major), but my RHR has climbed about 3 points in the same period and my HRV keeps dropping. I’m now worried I’ve developed myocarditis has anyone else had similar issues?

I’m nearly back to normal after 6 months, but now out of nowhere I’m really struggling with shortness of breath and a tight chest is this something other people have experienced or could I be dealing with something different?

Small backstory, I’m 6 months in and all my symptoms have been neurological, dysautonomia, vision problems etc. I’m feeling probably 80% better which I’m grateful for, but I’ve noticed if I drink which I have a couple of times recently all my symptoms worsen for a week or so. Is this the same for other people? have people recovered and been ok drinking since?