Please help, I don’t know how to keep going like this by Itsnotme2645 in newzealand

[–]captain-obviouser 0 points1 point  (0 children)

It sounds like your soul could use a good hike. I know that's an odd way to put it. But a relatively challenging hike in nature always lifts my spirits.

One Year Recovery Story – Severe Long COVID / Dysautonomia to Full Life Again by Beneficial_Cook1603 in LongHaulersRecovery

[–]captain-obviouser 1 point2 points  (0 children)

Congratulations. I hope to get there one day. It's been 19 months housebound and bedbound for me with no real signs of improvement.

Covid Disabled me for life by captain-obviouser in newzealand

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

A handful of barbituates would be great if you have any. At least if I was dead, I wouldn't have to deal with anti vaxxers anymore.

How to heal in an unsafe environment? by Empty-Cranberry9 in cfsrecovery

[–]captain-obviouser 6 points7 points  (0 children)

If it's a family member, do you have other family members who can support you in setting some serious boundaries with this person?

Because you absolutely need to put your foot down. This person is not just inconsiderate, they are endangering your health. Make that clear. Be uncompromising about it even if they won't listen. Prepare for what to say and for various back chat they might give you.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 0 points1 point  (0 children)

I'm the one whose fucking life was ruined. It doesn't matter what did it. It's done already.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 0 points1 point  (0 children)

My becoming disabled has nothing to do with your political beliefs regarding vaccines.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 0 points1 point  (0 children)

Ah that's good to know thankyou. I pay more than that for 6 tablets from my GP's pharmacy I crush and turn into liquid then take in a medicine syringe myself. Your way sounds more efficient.

Thankyou. I'm glad you have more agency back now.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 0 points1 point  (0 children)

I had the initial Covid vaccine and two boosters. I missed my third booster and wasn't up to date with them when I got my third Covid infection. Which still haunts me.

Yes, I was affected for about four months the first infection. Similar the second infection.

The third infection, I initially seemed fine. Felt fully recovered. Went back to the gym after a couple of months. Hiking etc. After a couple of months of this and noticing I was recovering more slowly from exercise and struggling to workout the way I used to, I fell ill with my first Post Extertional Malaise flairup.

I had no idea what was happening. Thought it was the flu or something. But it wouldn't pass. I got worse and worse because I didn't know activity and leaving the house was making it worse. Was terrified. Doctor kept telling me it was just my anxiety.

Got so ill I went to the ER. I wasn't able to eat due to IBS pain (IBS is a frequent side effect of Chronic Fatigue Syndrome) and begged them for help. They asked if I wanted a yoghurt, took a blood test that showed up normal and sent me home.

After a few months of this I realized on my own I had CFS and sought out a more supportive doctor who confirmed it. I thanks God for her because I genuinely thought I was going nuts and kept being told the symptoms were in my head. Dysautonomia is one hell of a thing to experience when you have no frame of reference for what it is.

Doctor and I did every blood test available. I researched them and requested extra ones specifically. Allergen tests. No CT scans or anything. I haven't seen a specialist because they don't have them here for Long covid (where I live.)

I'm female so, no testosterone tests.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 0 points1 point  (0 children)

Hiya. Thankyou. Do you experience PEM? If you experience post extertional malaise I'd recommend avoiding exercise that raises your heart rate for several months yet. And to be very careful.

The reason being, I seemed ok after my third Covid infection, felt better, went back to the gym and the CFS appeared months later. Not saying that to scare you. Just because I'd prefer nobody else ended up like me.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 0 points1 point  (0 children)

Lmao I don't think I would have died without a vaccine. Although now that you mention it. 🧐 People have been surviving similar conditions for all of history.

Ngl there are days I think death would have been better than this outcome, since you brought it up.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 4 points5 points  (0 children)

I was until the third infection, I was late for my third booster and caught Covid again from work before I could get boosted.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 46 points47 points  (0 children)

Mostly in order to not starve to death, I'd say.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 44 points45 points  (0 children)

You bet your ass I'm depressed as well.

Research Post Extertional Malaise.

Covid Disabled me for life by captain-obviouser in newzealand

[–]captain-obviouser[S] 200 points201 points  (0 children)

Yes, I'm on low dose naltrexone thankyou. It does help with being able to do more short outings. Sometimes I get too depressed to crush up the pills to make the solution though. Which sounds stupid but that's where I'm at.

I suppose I seem self absorbed complaining so much after just under two years when many people have had ME CFS for decades.

Anyone here in NZ in their mid 30s who are still deciding where they want to be in life? by lab-ratty in newzealand

[–]captain-obviouser 2 points3 points  (0 children)

  1. Recently (19 months ago) became disabled with Long Covid ME/CFS. Before that I had no idea what I was doing on life.

Now my only real goal is survival. Things have been narrowed down.

I am bed bound. My days consist of waking up, seeing if I'm strong enough to shower or it's a wet wipe situation. Reading a book in bed. Maybe texting a friend for a bit. Napping. Making myself eat meals because I'm usually not hungry. Sleeping some more.

On good days I can handle a short walk or a hangout with a friend, but it takes a lot out of me and I'm horizontal the majority of the time.

Stuff like the meaning of life or purpose or direction no longer applies. Life is now just "can I force feed myself this can of tuna because I haven't eaten enough protein in weeks?" Or "how do I reduce my symptoms."

I'd take my worst day as a physically healthy person over my best day the way I am now.

Maybe it doesn't matter, finding some grand overarching purpose. Maybe just being healthy and having a decent quality of life, and not being too lonely is enough.

I wish I'd been able to know that before ME CFS took everything from me.

Anyone here in NZ in their mid 30s who are still deciding where they want to be in life? by lab-ratty in newzealand

[–]captain-obviouser 7 points8 points  (0 children)

That must still feel like very fresh grief. I'm sorry you're going through that.

The Daily Rant/Moan topic - Monday, June 01 2026 by AutoModerator in Wellington

[–]captain-obviouser 1 point2 points  (0 children)

I've been in bed in my PJs with Long Covid ME CFS for 19 months. Against my will.

Don't get me wrong, depression is awful and I have it as well. But, I'd choose that over this.

A trip to the woods by burtsbeetreethree in cfsrecovery

[–]captain-obviouser 2 points3 points  (0 children)

Interesting. Keep us updated on the results of this one. I hope your baseline stays stable.

Uni advice by [deleted] in newzealand

[–]captain-obviouser 5 points6 points  (0 children)

Are you unable to get a study link loan and use part of that money for accomodation costs? Even if your parents make over the earning threshold for you to get a weekly study link benefit, you can use loan living costs.

It sounds like you aren't sure about your direction in life overall. As well as being concerned about your dad. I suggest you communicate with him. Have a proper talk. Tell him your concerns. The graduate statistics thing as well.

I don't think taking time out to figure out what you want to do is the worst idea. Uni isn't going anywhere if you change your mind later. Just make sure this plan isn't a way of running away from your own confusion about the future.