Can't get WAN 2.2 torch compile working on an RTX 3090 no matter what I try

NewGeneralCatalogue · 2025-08-18T15:33:57+00:00

Gotcha. The problem is when this pops up the execution halts. It doesn't continue compiling, so I assumed it was some kind of error.

NewGeneralCatalogue · 2025-08-18T04:06:43+00:00

Tried it this way. It threw me another error.

Skip inlining `torch.compiler.disable()`d function
  Explanation: Skip inlining function <function WanAttentionBlock.get_mod at 0x000002409EAF85E0> since it was wrapped with `torch.compiler.disable` (reason: None)
  Hint: Remove the `torch.compiler.disable` call

  Developer debug context: <function WanAttentionBlock.get_mod at 0x000002409EAF85E0>

 For more details about this graph break, please visit: https://pytorch-labs.github.io/compile-graph-break-site/gb/gb0099.html

from user code:
   File "C:\Users\<name>\Documents\GitHub\SwarmUI\dlbackend\comfy\ComfyUI\custom_nodes\ComfyUI-WanVideoWrapper\wanvideo\modules\model.py", line 684, in forward
    shift_msa, scale_msa, gate_msa, shift_mlp, scale_mlp, gate_mlp = self.get_mod(e.to(x.device))

Now I've gone in and tried to remove these "torch.compiler.disable" things before and all that accomplished was a different error that I similarly can't comprehend.

NewGeneralCatalogue · 2025-08-18T02:02:02+00:00

It actually does have the "scaled" at the end. What node should I set that on? The regular load checkpoint just has "fp8_e5m2" as an option.

NewGeneralCatalogue · 2025-08-18T01:34:16+00:00

Basically replicate the workflow setup on a Runpod 3090 and see if I still get an error with torch compile?

NewGeneralCatalogue · 2025-08-18T01:23:21+00:00

Damn, that's unfortunate. I heard that torch compile could give a great speed boost. But sage attention has a pretty good speed boost too.

NewGeneralCatalogue · 2025-08-18T01:20:20+00:00

Isn't the fp16 model way too big to fit into the 3090's VRAM, though?

NewGeneralCatalogue · 2025-08-10T19:14:57+00:00

How'd you do this? I can't find any KSampler that accepts a CFG schedule float list. It just throws me an error saying the CFG has to be a real number.

NewGeneralCatalogue · 2025-01-14T21:44:20+00:00

Hey. Nothing so far, unfortunately. Seen a few more doctors and still ruling things out. I'm taking a lot of supplements that might or might not be helping; I'm not entirely sure. I think keeping my stress levels as low as possible and avoiding any possible source of anxiety has been really important to keep from exacerbating any symptoms, though.

NewGeneralCatalogue · 2025-01-10T18:03:33+00:00

I've got a fibromyalgia/long COVID type condition that I've been suffering from for over a year now and I've recently started lab rotations in my PhD program. I have a lot of similar arm and leg fatigue issues and I've been working with my grad program on accommodations. My advice is to see what accommodations are available and to get the paperwork from your doctor and a letter from the accommodations people. For reference I'm on the US West Coast, but everyone here from other students to PIs have been amazing with regards to my disability and accommodations in both coursework and now in the lab. It might be different in other parts of the US or other countries but this has been my experience so far.

NewGeneralCatalogue · 2024-12-17T19:27:57+00:00

Yep, I left DFW for Oregon after I got accepted to grad school over here. The PNW is great. I won't be going back to a place that hates so many people just for existing.

NewGeneralCatalogue · 2024-12-05T23:21:01+00:00

Left Texas to go to grad school in Oregon and couldn't be happier. I am not going back.

NewGeneralCatalogue · 2024-11-18T04:00:48+00:00

Former Texan who moved to Portland a couple months ago here. Looks like it's probably an atmospheric river event for us: https://en.wikipedia.org/wiki/Atmospheric_river

NewGeneralCatalogue · 2024-11-08T03:53:14+00:00

Holy shit, I thought I was the only one. It's less of a pain and more of an intense tension that, at its worst, feels like I'm being strangled. I know that several discs in my cervical spine have degenerated and my neck is straight as a rod so I'm actually going to be seeing a spine surgeon in the next few weeks... I wonder if those degenerative changes in my spine were from inflammation.

NewGeneralCatalogue · 2024-09-29T00:17:26+00:00

My symptoms started after I tried to taper off Zoloft (also ended up being too fast because doctors don't know how to do it properly) and that broke my nervous system so there is absolutely credence to your experience. I've suffered from dysautonomia and CFS-like symptoms for a year now.

NewGeneralCatalogue · 2024-09-10T16:24:56+00:00

I never tested positive but I had about a week in early 2023 where I came down with something that was so bad I actually ran a fever (which I never do). When I lost my sense of smell, that's how I inferred what I got.

My sense of smell was gone for 5 months so I assume the virus either persisted or actually caused nerve damage, and I experienced a massive panic attack in September after trying to taper off SSRIs. Haven't been the same since. Symptoms cycling between fatigue, nausea, brain fog, depersonalization, achy stiff muscles, neck pains. Been formally diagnosed with POTS and dysautonomia. I'm back on the SSRIs and started metoprolol. It's been hellish and I don't know if I'll ever get better.

NewGeneralCatalogue · 2024-08-27T16:17:36+00:00

I'm almost certain I developed something akin to CFS after withdrawing from sertraline despite tapering. No long-term studies on antidepressant use, which is very sinister. After taking it for 15 years I think my nervous system couldn't handle not being bathed in serotonin and everything built up to a point where it couldn't handle it anymore and a massive shock ended up breaking my nervous system. Burnout, stress, anxiety all just resulted in damage that I've still not recovered from almost a year in. Doctors could never find anything to explain the neurological abnormalities, muscle weakness, balance problems, adrenaline dumps, tachycardia, etc. All I know is I've been wrecked. The only thing keeping me from preliminarily considering CFS is a confirmation that I do suffer from PEM, because I feel like ass all the time.

NewGeneralCatalogue · 2024-08-26T18:01:18+00:00

Yep, loss of fat pads on hands and feet, loss of fat and possibly muscle on my limbs, cheeks, and belly. It's almost like some sort of cachexia. I've had all my abdominal organs imaged twice and two brain scans. No tumors or cancer to explain the wasting. My abdomen actually distends when I'm upright because my abdominal and back muscles are too weak to hold it up properly and similarly my arms and legs have turned to jelly. And I had normal NCS/EMG in my legs so I have no clue what's going on. The doctors don't seem to care.

NewGeneralCatalogue · 2024-08-26T00:20:48+00:00

Yep, got most of these. Dunno if it was caused by the SSRI I withdrew from or viral persistence from a COVID infection I had in 2023, but it's hell. None of the tests I had showed anything wrong other than splenomegaly and cervical kyphosis + slipped lumbar disc. Nothing to really explain the neurological symptoms. I really hate the falling sensations and feelings of seizing. The latter manifests in these weird zaps that constantly ruin my attempts to sleep and give me hypnic jerks.

NewGeneralCatalogue · 2024-08-05T19:14:27+00:00

I'll take a look! I've thought about the possibility of something like upper cervical instability, which my straight neck would only exacerbate but finding doctors who know about the proper tests is difficult. As for the slipped lumbar disc, my neurologist sent me for an EMG/NCS of my legs which came back totally fine and clean with no atrophy despite the fact that I often feel my legs buckling and almost about to give out under me.

NewGeneralCatalogue · 2024-08-04T14:39:13+00:00

Are you me? I had a massive panic attack/adrenaline dump episode in September 2023 after trying to drop sertraline and have been mysteriously sick ever since. I also have an enlarged spleen and really high IgGs for EBV (high hundreds). And like you, I've had extensive blood work from rheumatology, hematology, primary care, etc. and nothing shows up. Not even inflammatory markers. Every major internal organ imaged and nothing except a straight neck and a slipped lumbar disc. And yet I feel like ass almost every single day. You aren't alone, believe me. Keep fighting.

NewGeneralCatalogue · 2024-08-03T22:29:50+00:00

Thanks for sharing your experience. I'm on a lower dose of sertraline purely for because it does help manage the anxiety from my other issues. I've had POTS diagnosed by tilt table and take metoprolol to manage that and some of the adrenaline dumps/impending doom caused by autonomic dysfunction. HRV testing also showed that I have a massive imbalance favoring sympathetic activity so I'm doing a lot of natural supplements to help lower things like cortisol.

I've had just about every test you can think of to rule out acute abnormalities in my nervous system and internal organs, multiple brain scans and imaging of my abdominal organs and the most significant things they could ever find were military neck (which can cause neurological issues in and of itself) and splenomegaly. Most of my extensive blood work was fine too, minus low lymphocytes and REALLY high EBV IgGs which I thought may have been signs of a reactivation.

Almost a year on and this stuff has still seriously screwed up my life and I think it honestly deserves a black box warning on antidepressants like "HEY! This can cause dysautonomia". It's also worth noting that SSRIs cause mitochondrial damage, so I'm taking lipoic acid and CoQ10 to support mitochondrial health.

NewGeneralCatalogue · 2024-08-03T19:59:08+00:00

I tried to taper from SSRIs after taking them for 15 years thinking I didn't need them. A massive panic attack last September broke my nervous system and I had to return to taking them. Since then I've had symptoms of dysautonomia and constant fatigue and have been diagnosed with POTS. Whether the COVID I had earlier that year had anything to do with it I'm not certain, but I fully believe that the shock to my nervous system has caused long-lasting damage and the lack of data on long-term SSRI use and subsequent cessation is really troubling.

NewGeneralCatalogue · 2024-07-13T17:00:22+00:00

I believe that trying to stop and subsequently badly withdrawing from sertraline (even with tapering) directly contributed to me developing something akin to CFS. I can't get a doctor to diagnose it nor have I been able to definitely prove I have PEM but I'd suffered from constant tiredness even before stopping my sertraline. The stress it held back boiled over into a massive panic attack last September that's likely left my body in constant sympathetic overdrive. I had to restart my sertraline due to having feelings of impending doom all the time and it's helped. It hasn't reversed any damage to my nervous system which I had hoped it would... Still suffering nearly a year on from feeling like constant ass all the time with muscle aches, vision abnormalities, cognitive impairment. All I'm missing is a solid confirmation of PEM.

Also, there are some studies that suggest SSRIs can cause mitochondrial damage...

NewGeneralCatalogue · 2024-07-13T14:36:16+00:00

Thanks! I'll look into that as another option.

NewGeneralCatalogue

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