u/8drearywinter8

Question about rent stability (or increases) if renting from PEKA

I'm considering renting an apartment from PEKA. I was wondering if they tend to hold rent steady over time (if you stay years, does the rent you started with stay the same?) or if you should expect regular/annual increases as a renter? Do they try to retain good tenants?

I know what I can realistically afford to sign a lease for now, but know I couldn't stay long term with substantial annual rent increases over time, and don't want to sign on for a future I can't sustain (though housing/rent sustainability issues like this are common in Canmore generally -- no illusions about that).

Would love to hear experiences, so I can make the most informed decision possible. Thank you!

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u/8drearywinter8 — 6 days ago

People who got worse after Pemgarda or Sipavibart infusions, how are you doing months later?

I'm one of the people with long covid who got much worse after a Pemgarda infusion in November 2025. it's months later, and I'm still steadily declining. I hit a couple of temporary plateaus and hoped the decline had slowed/stopped... but nope... still losing capacity, have a lower PEM threshold than ever before, less energy, lower baseline, and more autonomic nervous system dysfunction than at any time in the last 5 years. I am sicker than I have ever been.

I know most people posted about their responses to monoclonal antibodies shortly after their infusions and we haven't gotten a lot of long term follow up. I'm curious whether others who got worse ultimately kept getting worse, stabilized at a lower baseline, ultimately started to get better again (better than before the infusion, or back to your previous baseline)?

Would love to hear longer term outcomes from others who got the opposite of the magic healing we were all hoping for.

I tried to post this to r/Sipavibart, where most of the monoclonal discussions were happening a while back, but for some reason that sub wouldn't let me do so. Hoping I can reach those affected here as well.
Edit: question is now successfully cross-posted to r/Sipavibart so if anyone reading this wants to see additional responses, check there too.

I don't know if I'm a statistical outlier as I continue to decline, or whether this is the norm for those of us hurt by a treatment we believed would help us.

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u/8drearywinter8 — 3 months ago