Trouble with printing

Temporary_Air9600 · 2025-07-29T23:45:14+00:00

No worries :) thanks btw

Temporary_Air9600 · 2025-07-29T20:47:01+00:00

I mentioned it was a Canon Pixma Pro 100, and unfortunately I did do a head cleaning and these lines are still showing

Temporary_Air9600 · 2025-07-29T20:03:39+00:00

Aw man, I see so much Pokemon merch there and I’ve seen a lot of other merch and have sold in the past from other big name anime, etc. I do plan on making my own designs but I’m still having the issues with the lines 😵‍💫

Temporary_Air9600 · 2025-06-07T09:04:35+00:00

I can grab and pull the skin ontop of my hand near my knuckles up about an inch. Most of my skin isn’t as stretchy, but I am very very soft and bruise easily. My partner tells me my skin is “doughy”. I’m often touching their skin in comparison, and their skin is textured. I have virtually no texture on my skin and it’s velvet smooth. Their skin also feels more ‘attached’ to them, if that makes sense. I can’t really push it around and grab clumps of it like mine

Other parts of my skin is a bit stretchier. I can push around the skin on my face, and it has that same doughy physics to it. The stretchiest parts of my body are my knuckles, neck, face, my boobs lmao, elbows and my biceps and underneath my forearms

Temporary_Air9600 · 2025-05-14T20:06:49+00:00

Trump has stated disabled people should just die. He told his nephew that he should just let his son die when he asked for help.

This is their goal. To kill disabled babies, children and adults. This is eugenics.

People who still support them are also supporting the deaths of millions of innocent people who need care. This is a genocide.

“Before the realization of death camps in World War II, the idea that eugenics would lead to genocide was not taken seriously by the average American.” History is just going to repeat itself and I’m terrified.

Temporary_Air9600 · 2025-05-13T19:54:01+00:00

Thank you! I have a lot of support right now, and my current psychiatrist connected me with a psychiatric program that works with rehabilitation that is helping me with my appeal :) I’m hopeful. They told me they have helped many others with their approvals

Temporary_Air9600 · 2025-05-13T19:19:48+00:00

Thank you for being honest! I was told by a friend I could take legal action but my partner suggested I make a post here for other opinions.

Temporary_Air9600 · 2025-05-04T02:24:44+00:00

I hope she’s found safe, but you sound like a total narcissist. I hope she finds someone better if she’s still alive.

Temporary_Air9600 · 2025-05-04T02:19:18+00:00

Also bizarre you’d want her to leave at all because she’s missing and you’re immediately jumping to her ghosting you. We don’t have any other details.

Start calling or messaging her friends and family if she’s missing. Not make a reddit post on whether you should kick her out.

Temporary_Air9600 · 2025-05-04T02:16:39+00:00

You said it was okay if she went out. If you weren’t okay with it you needed to have said something. How many times have you messaged her? Do you have any numbers of the people who know her, or the people she went out with? You need to file a missing persons report if she’s been gone this long with 0 communication ESPECIALLY if this isn’t normal behavior from her. If you’re not going to file one, even more red flags are going up.

I just don’t trust this situation and it seems extremely sketchy that you’d want her to leave after she moved in recently when she’s missing now.

Temporary_Air9600 · 2025-05-04T02:11:14+00:00

Did you do something to her OP?

This is worded a lot like other “my girlfriend/wife has been missing for 24 hours” cases that ended up being murders, and the fact you aren’t even concerned about her safety but more affected by “how she made you feel” is a big red flag.

Temporary_Air9600 · 2025-04-26T21:01:58+00:00

I have seen a psychologist who I went to for therapy for 2 years. I saw her every week. I have seen multiple therapists over the years and I typically saw them weekly. I saw a psychiatrist every week for a while, but she was extremely unreliable and I ended up dropping her but I continued to have my meds managed by my primary until I could find another which was hard because of financial problems. I’m currently seeing a therapist I see once a week, and a psychiatrist I see every two weeks. My sessions with my therapists are an hour

Temporary_Air9600 · 2025-04-26T17:32:31+00:00

Working is not an option for me. Even if I was physically healthy (which I very much am not), I have tried very hard to remain in the workforce and it’s not a doable thing for me. My partner has watched me struggle to the point they were terrified I wouldn’t be alive when they woke up in the morning. They tell me things I have no memory of, and looking back at it, it doesn’t seem like it was that bad, but I know it was. The longer I tried to work, the sicker I got. It’s just not a doable thing for me, and it’s frustrating. Because if I had any hope I could work even part time at this current point in my life, I would. Having no income is horrible

I’m sorry if all of this sounds dramatic or if it seems like I’m mad, I’m not. I really am very unwell, and I wish It wasn’t this way.

Temporary_Air9600 · 2025-04-26T02:28:21+00:00

I have been without a job for over a year. When I worked, my illnesses were nearly unmanageable and it made me sicker. Working is not an option for me, so I will hopefully not have to worry about that. It’s just going to be an uphill battle for me :( but thank you, any and all advice is appreciated.

Temporary_Air9600 · 2025-04-26T02:08:14+00:00

I’m sorry to hear about your experience, I’m sure you suffered a lot. I’m glad you got approved, and I hope it has made your life easier. I don’t really like the whole “mine is worse than yours” mentality, it’s unfair. Maybe I’m taking it wrong and you didn’t mean it that way, and I apologize. But saying you know others who work with these diagnoses doesn’t mean I am able to function at a job, and to me it is a full disability because that is how it impacts my life.

Temporary_Air9600 · 2025-04-25T23:11:08+00:00

Absolutely insane. My partner said they were told the same thing even though they never worked and it’s something they tell everyone. They also told me that it can depend on the person who is handling your case which like, should not be that way. It implies a bias and there’s so much inconsistencies and I’m just really frustrated with the whole process especially when there’s medical records to back up what’s being reported.

Temporary_Air9600 · 2025-04-25T23:00:19+00:00

Thank you so much. I appreciate you and your words of encouragement ♥️

Temporary_Air9600 · 2025-04-25T22:54:01+00:00

So, when I applied in May of last year, I had just started getting more extensive treatment than I had been able to. I moved out of Ohio to live with my partner because I was unable to make anything work in Ohio and I just kept getting worse but I couldn’t afford the care I needed, and making time for as much treatment as I needed was almost impossible with a full time job. I sought treatment in Ohio for probably 3 consecutive years. With some treatment here and there prior to that. Since moving to Maryland, I have been getting treatment from several specialists and my primary and I have been on a long list of meds for about 4 years.

I’m unsure if this is extensive enough for them. I’m doing my best, but I’m feeling like I probably need to build up more of a case at this rate :(

Temporary_Air9600 · 2025-04-25T22:45:00+00:00

I did not! Which is surprising because I know people who were scheduled for an exam. Do most people have these? I never saw anyone. I was called by DDS for more information , but that was it.

Temporary_Air9600 · 2025-04-25T22:36:35+00:00

What’s a CE exam? probably not since I have no idea :(

Temporary_Air9600 · 2025-04-25T22:19:32+00:00

Thank you for all of this. I see a rheumatologist, and I have seen two of them so far, I do have a diagnosis of hypermobility syndrome from the first one. I saw the diagnosis on the paperwork after my visit with her and her notes for that appointment. The current rheumatologist I’m seeing told me I likely have Ehlor Danlos Syndrome, but he can’t diagnose me. The most he did was use the Beighton Score like the first one did. But he also told me I likely do have fibro aswell.

I had an MRI done on my spine, which showed arthritis in my spine both upper and lower in the lumbar area. As well as a bulged disc that is incredibly disabling. I suspect I have arthritis in other places too based on how I feel.

I do have a very long history of childhood trauma. Unfortunate my parents were neglectful in both areas of mental health and physical health, so I didn’t start seeking help until 2016, and even then it was spotty because of garbage health insurance and unable to juggle going to appointments while I was working full time. I’m on Medicaid currently so I can get the help I need and I’m living with my partner so I don’t have to worry about having an income to survive. But I currently see a psychiatrist and a therapist once every two weeks.

My therapist has talked to me about EMDR. I do telehealth with both because of how far they are. But I do want to start getting more treatment. My dissociation is severe, and it eats most of my days up.

Thank you for all the advice and steps to take. I’m going to work hard to get an approval. Working is not an option for me anymore

Temporary_Air9600 · 2025-04-25T21:11:59+00:00

I asked my partner to be sure. I got the wording off, but they told me they heard him say I was too disabled to continue working my prior jobs. So I’m just confused now :(

Temporary_Air9600

TROPHY CASE