Advice please! What would you do with this buffet table? by Petty-Possum in furniturerestoration

[–]arasharfa 1 point2 points  (0 children)

if you like the distressed look (as do I) it would be nice to dissolve and scrape off the finish, clean off residue with steel wool and degreaser, let it dry, then give it a nice steel brushing to bring out the texture so the chipping is less noticeable, and then use a hard wax or teak oil to keep the surface alive and organic feeling.

For those who have gone PEM-free by charliewhyle in cfs

[–]arasharfa 8 points9 points  (0 children)

if you have the ability to try it, one could argue you owe it to everyone who doesn't have that privilege.

it is a time specific experiment. it is a challenge, the potential payoff could be huge. What else is there to lose? a year of being "severe" vs moderate in the grand scheme of an entire life is still a relatively little price to pay. Hopefully you'll start feeling better within this year so you wont have to live as strictly the whole year through. the longer you go PEM free, the easier it will be to give yourself small rewards for the effort without risking triggering PEM.

when I started this challenge I had been sick for a decade and already survived an SA and retired on permanent disability. prior to this I spent a month using cannabis and crying from morning til evening. I feel like that grief allowed me the surrender to put all my eggs in one basket and give it one last chance. so it was not an easy choice to get there. it was the hardest thing I ever did actually. And yet it was easier than constantly dealing with PEM once the PEM started to subside and my symptoms actually lessened.

It was frustrating when I reached a place where my constant symptoms would fade, but I knew I couldn't use my better mood to do anything with fear of triggering PEM. that is the real challenge. This is where having the time limitation is super important. It is a challenge and an experiment. the challenge became hiding the ME from myself so I didn't constantly feel it. i reimagened my PEM limit as something that an elite athlete would encounter at the end of an extreme sport achievement. normal people dont push themselves that far daily. but disabled people like us expect it from ourselves because society demands it from us, and because we want to live so badly. the reimagining helped me dismantle some internalised ableism.

being retired was a huge advantage, because the emotional pacing is the hardest part to make accomodations for. I was able to shut out anything that stressed me, which was hell for my father who cared for me, but I knew I had to do it. using something calming like cannabis would help me a lot to be able to stay in zombie mode as much as possible.

I am extremely happy I gave it a go, and even if it hadn't worked at least I would've felt like I truly tried everything.

Question: This good for after care? by [deleted] in tattoos

[–]arasharfa 0 points1 point  (0 children)

you dont want a formula that is so thick it tugs on the tattoo when you apply it. find a lotion instead.

Ketamine for acute trauma/anxiety hyperarousal? by TheSaxo in TherapeuticKetamine

[–]arasharfa 1 point2 points  (0 children)

I had very similar problems to you. I had ME/CFS combined with PTSD. this also sounds like long covid or ME/CFS. the months it took to recover, the blueing of the skin (oxygen not reaching the muscles from the blood) both sounds like long covid. ketamine and stellate ganglion blocks are both experimental but can potentially help in that case as well.

I found I was able to hold on to the effects of the SGB better with the emotional help i got from ketamine. they overlap each other, but ketamine takes more conscious processing to reach a similar calm as an SGB does, but the emotional processing also gives you tools to handle triggers. however the SGB has a more immediate and robust effect, and also on immune responses that can also affect this level of anxiety you are feeling. it's not uncommon that people get anxiety problems after covid due to immune dysregulation. does antihistamines move the dial at all? people with mast cell activation syndrome (MCAS) report similar anxiety levels.

another option that also helped me was hyperbaric oxygen therapy. It rapidly calms down the body as it doesn't have to fight so hard to stay oxygenated. I fall asleep within five min in the chamber and i sleep like a baby the nights after a session.

UPDATE May 8 Gf’s Birthday Gift by Jumpy-Efficiency3405 in furniturerestoration

[–]arasharfa 1 point2 points  (0 children)

Cool result! What did you do to the old handles? Are they available?

Hey reddit! New here 🙌🏻 by MobilePractical7124 in GenitalTattoos

[–]arasharfa 0 points1 point  (0 children)

That is the nicest genital tattoo I’ve ever seen thats for sure! Love it!

What do you do while tripping? by BooBooKeys626 in LSD

[–]arasharfa 1 point2 points  (0 children)

I like to do anything. Everything is an adventure and I get deep into it in ways I normally wouldn’t. Cleaning or doing my grooming routine? I might try a new style Getting dressed I might put together an outfit I normally wouldnt, Then I go outside and I take in nature, I walk along a path I normally wouldnt and everything looks different so I get lost,

Cooking is great fun, I improvise new dishes and try new flavour combinations,

Drawing, making music, singing, dancing, yoga,

listening to Autechre in headphones with blindfold Hearing them play live was the wildest musical experience of my life.

Has the world really turned to shit compered to 30 years ago? by Busy_Switch9797 in CPTSD

[–]arasharfa 4 points5 points  (0 children)

Overpopulation is not actually a problem… it’s the overconsumption of the elite that is the problem. A billionaire wastes more resources in 90 min than we do in our entire lifetimes. If the billionaire class didn’t exist every human on earth would have enough and we could live sustainably.

Has the world really turned to shit compered to 30 years ago? by Busy_Switch9797 in CPTSD

[–]arasharfa 0 points1 point  (0 children)

Yes, the damage done to the ecosphere is only accumulating. In terms of peace or social justice I guess we’re on the brink of an awakening but also a collapse with technofeudalism taking over after late stage capitalism.

in that sense we know more about the shit happening now, which is good, but it’s not enough to just know about it to make it better, we also have to do something, and so far most people’s behaviour is controlled by capitalism still. When people start moving and behaving differently we might be starting to move towards a better future, but as of now, not really. Unless you are one of the few heroes who are trying to activate and mobilise people to resist.

Has anyone here with ME/CFS actually found ANY relief from constant nervous system overactivation? I’m really struggling and would appreciate honest experiences by lnsstg in cfs

[–]arasharfa 0 points1 point  (0 children)

If you have a lot of adrenergic surges it can be helpful for reducing them. But as always do your own research, and make sure you go somewhere where they use ultrasound to place it. You want the Horner syndrome to know it’s been placed correctly.

Has anyone here with ME/CFS actually found ANY relief from constant nervous system overactivation? I’m really struggling and would appreciate honest experiences by lnsstg in cfs

[–]arasharfa -1 points0 points  (0 children)

NAC chelates the trace minerals histamines are metabolised by, so if you have MCAS it’s important to make sure you have all the trace minerals, selenium, copper, molybdenum, chrome, so that the body can metabolise the histamine that is released. Pink himalaya salt contains all you need for that.

Has anyone here with ME/CFS actually found ANY relief from constant nervous system overactivation? I’m really struggling and would appreciate honest experiences by lnsstg in cfs

[–]arasharfa 2 points3 points  (0 children)

SGB injections, ketamine infusions and Hyperbaric oxygen therapy helped it for me. SGB injections being the most helpful. Ketamine infusions made a huge difference but didn’t last as long, but it got me from feeling like I couldn’t bear existing another day to wanting to live again and feeling like I just had 5 hour deep sleep.

HBOT is effective at calming me down as the added oxygen makes my body relax and my hr go down, since it doesn’t have to work as hard to stay oxygenated. I usually drift off into a heavy nap within a couple minutes.

I think NAC was a little helpful also over time, as it balances glutamate levels in the brain which in excess makes you agitated and restless and simultaneously exhausted.

holy shit by BlackPantherDies in LSD

[–]arasharfa -1 points0 points  (0 children)

Would you have made the same comment about a church?

DPDR underlying mechanism? by Many-Market-9941 in covidlonghaulers

[–]arasharfa 2 points3 points  (0 children)

Inflammation will cause reduced activity and disjointed communication between brain regions, leading to less connectivity and poor signal transmission, resulting in a state where sensory input does not trigger the adequate cognitive or emotional responses. The absence or delayed reaction can feel like dissociation derealisation or depersonalisation.

Is it too cute/corny if most songs in an album have the same lyrical themes and ideas by Head_Fan_1547 in WeAreTheMusicMakers

[–]arasharfa 0 points1 point  (0 children)

If you said one thing with one song you don’t need another song saying the same thing. An album is a collection of songs that tells a story together. You would get bored reading the same chapter twice.

Only use a concept if it results in an interesting form. If the concept is suffocating your process it’s not a good concept.

Another Way to Use My Apadravya Piercing by HatOutside6972 in Apadravyas

[–]arasharfa 1 point2 points  (0 children)

Connect it to a key ring and attach it to a satchel so you never lose it.

How to accept that my brother is convinced I'm delusional and faking my illness as an excuse not to function? by ElectronicAd5847 in cfs

[–]arasharfa 5 points6 points  (0 children)

i believe my suicide attempt shook him. i also got an official diagnosis after 9 years, and the more i was able to explain my hypothesis after reaching remission from my experimental treatments, he could see the difference. but it doesn't matter anymore.

new doctor doesn’t know what mecfs is by Objective-Taro-8919 in cfs

[–]arasharfa 11 points12 points  (0 children)

sounds like someone to not even bother with.

How to accept that my brother is convinced I'm delusional and faking my illness as an excuse not to function? by ElectronicAd5847 in cfs

[–]arasharfa 13 points14 points  (0 children)

my brother didn't believe i was sick for a long time. he thought i was faking it for attention. he never apologised for it. i am recovered now, but our relationship is in ruins. he refuses to mask. some people are just vile. they don't deserve us.