My first successful nebula - C20 North America
▲ 64 r/dwarflabofficial+1 crossposts

My first successful nebula - C20 North America

Preface by saying I’m not knew to photography, I do it passionately and professionally ☺️

Tonight the weather was good for trying from my backyard, with a bortel sky of 7, but clear and not humid. I’m on Long Island in NY.

I started at 10:30p in EQ Mode, Duo-Band, 30 second exposures, gain of 60 and went to almost 400 frames. Then ran it through Stellar Studio…first mind blown… and then took it into camera raw and Photoshop and did some spot color correction and level adjustments (plus sharpening, upscaling and noise reduction). Now mind absolutely blown!

I think the DwarfMini is now officially my most favorite Xmas gift ever. I’m going to enjoy the heck of this thing!!!!

I’m traveling to much darker skies next weekend and can’t wait to try it out there!

u/DangReadingRabbit — 4 days ago

My first images with the DwarfMini (not that impressive, but great to me…)

Not all that exciting and impressive to most, but to me a 10/10!

I got the DwarfMini as an Xmas gift from my spouse but was actually in the hospital Xmas day, had a lot of health issues and surgery in March so man, I just didn’t get a chance to use it.

Yesterday we took a spur of the moment camping trip and I brought it with me. In the afternoon I tried the eclipse (from New York). Two photos, two different modes.

Then last night I successfully got the EQ mode set up and tried a few things. Unfortunately it was a bit hazy and not the darkest sky where I was, but I thought this was pretty neat anyway for a first try and not a lot of time (this is about 60 images stacked I believe, 1/30). It’s the NGC 6871 Star Cluster.

I’m looking forward to finding darker skies and trying longer capture times and really learning all I can. I so appreciate that technology has made entry into deep space and astrophotography a little more accessible. I’m a passionate photographer, for fun and for work, and have always wanted to do play more with space photography.

You all are amazing with the images here! I humbly share my first…

u/DangReadingRabbit — 7 days ago

[S] [USA-NY] Fuji Lenses:18mm f2 R and 35mm f2 WR and LensBaby 50mm

All photos: https://imgur.com/a/2AXE9kt

All prices include shipping in the continental USA. I won’t ship anywhere else. I’m firm on pricing.

I take Venmo or PayPal. I have a good reputation on eBay (but I’m trying to avoid their high fees for this sale). My name there is auctioneer-amy. I’ve bought and sold here too but it’s been quite a while. I reserve the right to sell only to people with a good history here and good karma overall.

The gear for sale:

Fuji 18mm f2 lens. Bought new on Amazon and used it once. It’s brilliant, I just don’t use it. Hard to part with, but it’s ridiculous for it to sit here unused. $280 SOLD

Fuji 35mm f2 WR. Bought new on Amazon and used it once, same situation as 18mm but Ive had it longer. It’s redundant in my kit. $275

Lensbaby Composer Pro II 50mm f2.5 Double Glass. These are fun. I have a few Lensbabys and enjoy them. But I use this one least. 50mm just isn’t my favorite focal length. $175

Comment below and then send a private message if interested. I priced them fairly because I want to sell them quickly. All come from a non-smoking home and are so very lightly used, in excellent condition. Have always been in a bag and in a dry photo cabinet. I will ship within 24 hours of payment.

Thanks for looking!

Edit: Here’s an old transaction I did here with a review.

u/DangReadingRabbit — 10 days ago

NYU Langone Hospital (formerly LI Communtiy / Brookhaven) - recent experiences?

Brookhaven was almost universally hated, because of bad experiences there… I myself had a terrible ordeal there many many years ago. I only know one person who even praised them, and it was their cardiac department for saving her husband’s life after he was stabbed.

All that said… they’ve changed hands, redone their ER and are supposedly trying to improve. I even had hand surgery there a couple of years ago with an NYU surgeon. My experience was fine, not amazing, not bad.

My preferred hospital has been Mather or St. Charles for years…. But with the recent Northwell-Fidelis split, I thought I’d ask around what people think of NYU Langone these day…

So what’s everyone’s thoughts? Any good or bad experiences? Been to the new ER? How’s their nursing care? Anyone admitted and have experiences? Are they better than they were as Brookhaven? Hard to imagine they could be worse 😂

Would love to hear…

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u/DangReadingRabbit — 19 days ago

Let’s Talk that Darn 2nd Row Cup Holder

As many of us know, Mopar’s official part number for the official Chrysler cup holder is way over priced (at $240). No one in their right mind would pay that. I had posted about it and u/tink00070007 even shared a link to a 3D model, so I kept that as an option if I couldn’t solve this another way.

I’m one of those people determined to get to the bottom of this kind of thing. I was pretty convinced that somewhere along the way Mopar made a mistake and somehow this cup holder ended up with the wrong price. It doesn’t make any sense… very similar cup holders from other cars are all a fraction of the cost.

So searching around on eBay I found a listing for a Genuine Mopar Console Cup-Holder 1VQ69BD1AA … this part number traces out to a whole bunch of models, but not specifically the 2023 Chrysler Pacifica, but based on the photo looking so similar, and the price being fairly inexpensive, I decided to take a chance. I ordered it.

This is coming from an auto parts store, so the seller had to order it to fulfill my order. I ended up sending him a message about compatibility and he wasn’t sure (since it’s not listed as being compatible). Long story short, we ended up having a very friendly in-depth conversation about all this and he discovered that somewhere along the way, the part number for the official cup holder for the Pacifica changed from 6EK261D2AA to 7JV65PD2AA. And in his system he was able to order the old part number for much much less that the $240 the new part number demands. He ordered one for me and I sent him the extra money for the second one.

Both came today. The 1VQ69BD1AA one and the 6EK261D2AA one. The 1VQ one came with a little rubber protection mat inside. The 6EK one did not.

6EK261D2AA fit perfectly! It’s absolutely the right one for the 2023 Chrysler Pacifica.

1VQ69BD1AA fit almost perfectly, but was absolutely close enough if it had been the only thing I could have gotten my hands on. I was going to just sell it, but I’m keeping it as a spare. As I said, that one came with a little rubber protection mat for where the cups sit, so I put that inside the 6EK261D2AA one. That’s how you see them pictured.

Sooooo all that is the long story way to say, there are solutions to getting a second row cup holder if you’re missing it… and without spending a crazy amount of money. Even the junk yards I called wanted either too much money (basing it on the “official part number price” or wanted me to buy the whole console).

I bought from PrestigeDodge on eBay … and he was the seller that was so helpful. The original part I ordered was the Genuine Mopar Console Cup-Holder 1VQ69BD1AA … but I told him if he can get more of the 6EK261D2AA one to sell he should. I don’t know if he can but it might also be a part number you can go into an official Mopar store and find… but you want that part number, not the new one that superseded it.

Probably no one finds this all as fascinating as I do, but thought I’d share it anyway. To me, there’s no way that $240 is the correct price for just the cup holder with part number 7JV65PD2AA.

Thanks all for your help originally, and I hope this helps someone else.

u/DangReadingRabbit — 22 days ago

Green Ghosting Warranty Return … did you have the issue a 2nd time?

I’m a lover of these reMarkable devices. Been a fan since their first one…. Still have and use my reMarkable One.

Last October I bought a Paper Pro. I love the color and light. I enjoyed daily use up until a couple of weeks ago when the infamous “Green Ghosting” showed up.

I’m now in the midst of waiting for a replacement… my warranty return and replacement was already approved. I shipped mine back, they got it Friday and they’re saying it can take 2-3 more weeks to get the replacement. I do hope it’s faster than that. Ugh.

Anyway, for anyone who had this Green Ghosting experience…

What was your experience with getting a replacement?

Did you ever have Green Ghosting again, a second time with the replacement? In other words, did your replacement ever start to show Green Ghosting too?Did you have to get another warranty replacement?

Also, I had issues with their website. I had issues with emailing them. It hasn’t exactly been smooth. When I do communicate with a human, they are very nice, but I can’t say it’s been an easy experience to get the replacement (I’m a tech nerd and used to work in IT, so it wasn’t a problem in my end LOL)

Any insights appreciated…

Update: I communicated with a human again at reMarkable and they apologized for the issues I’ve had. They also said my replacement was preparing for shipment. It has a FedEx label number now but hasn’t yet shipped. With any luck I’ll have it before the weekend.

u/DangReadingRabbit — 30 days ago

Anyone know the part number? On the hunt for this cup holder…

The circled item is what I need (that’s a photo from the internet). The other photo shows mine is missing.

Just bought the car and love it… didn’t think anything was missing until I saw some photos online and realized there was supposed to be a cup holder in there.

I have two problem… seems hard to find used, and also seems ridiculously expensive new. Has anyone 3D printed one? 😂

Edit: maybe I lucked out… I found one on eBay that looks like the exact same thing, comes from a dealership and was listed for only $35, so I ordered it. We’ll see if it is what it claims to be!

u/DangReadingRabbit — 1 month ago

Overnight Oats Recipe - High Fiber Breakfast or Snack - 8 Grams

Just tried this recently and fell in love with it!

My Recipe

1/2 cup [rolled oats](https://a.co/d/07SJBZco).
3/4 cup almond milk of your choice - I use unsweetened vanilla.
1 tablespoon [chia seeds](https://a.co/d/0e2bQaiu).
1 tablespoon [peanut butter powder](https://a.co/d/07Ya75fE).
A little sugar and cinnamon.

Mix it all up and put it in the fridge with a lid overnight. I bought [12oz containers](https://a.co/d/0hPzE4Fk) on Amazon.

You could use oatmilk, regular milk or any milk of your choice. You can adjust the amount for thicker or thinner (mine was pretty thick).

I also tried chocolate peanut butter powder and that was good too!

You could use maple syrup instead of sugar.

Today I added some grape jelly to it (as a topper right before I ate it). I’m going to try cacao nibs this week!

What combinations and recipes do you like?

*This is for anyone not currently in a flare. When you’re actively suffering acute diverticulitis, stick to a low fiber diet for a few weeks and until you’re pain free. Also, as always, drink lots of water.

u/DangReadingRabbit — 1 month ago

My First Big Trip Since Surgery (Four Months Post-Op)

If your followed my story from the beginning and through my surgery , you’ve heard me say I travel a lot (both for work and pleasure). I just returned from my first big trip since having surgery. It’s now four months since surgery.

I was a little nervous about traveling. I still poop anywhere from 2-4 time per day. I’m trying to maintain my high fiber diet and drink lots of water. When we travel I usually have a large travel van with a bed and portable toilet with us, but that needed its own surgery recently and was still in the shop. But, we also always have a portable toilet in our other vehicle, our minivan (okay, let’s call it what it is, a luggable loo… a bucket with a toilet seat on top LOL)… so at least for an emergency, it’s better than having nothing. It’s piece of mind.

So we hit the road with a tote bag full of fiber snacks and my husband’s diabetes snacks and set off on our 12 hour drive from New York to Tennessee.

The next necessary nicety was a self filtering water bottle. Since my flare in December and since surgery I’ve been maintaining 64-90 ounces of water a day. I didn’t want to go broke buying bottled water or having to carry around cases of water. I bought one of the Brita self filtering water bottles and it worked out really well. I could fill it up anywhere and didn’t once have to buy water either on the road or in hotels.

Exercise … I thought about using hotel treadmills and that was always an option, but doing walk-in-place exercising for 30 minutes in the morning and again in the evening worked out just fine. Plus during this trip it was for work, so I’m on my feet a lot at photoshoots, so there was no shortage of being active. I was averaging 12k-14k steps per day.

Eating Out … obviously when we’re away from home we’re eating out a lot. The key takeaway is that I had to be sure to get my fiber. Breakfasts or Brunch always had oatmeal or blueberries or avocado. Lunches were often salads or included sweet potato fries. Dinners I’d have broccoli or beans (or both) or avocado or sweet potato in some form. It wasn’t hard to include something with fiber in it. And as mentioned, I had my fiber snacks with me, so could have one in the afternoon or evening if needed. All of this worked out just fine and kept me regular.

Pooping … we were away ten days and in that time I mostly pooped 2-3 times per day. Always in the morning before we left for the day, always in the evening when done for the day. Sometimes we’d come back to the hotel before dinner to do some work and email and I’d poop then too (maybe a little less than half the time). There was only one day I had an urgency to poop that needed to happen right away, and we found a public restroom (large gas station) where I could take care of business. I would have had the bucket otherwise 😂

Finally, It was so good to be traveling again. I felt like I was “smelling the roses” more if you know what I mean. I was sick quite a while, through the holidays and all before my surgery, and then recovering from the surgery itself… so this really felt good, to get back to our normal life and just enjoy the trip. We saw some really good sights: Atomic History stuff in Oak Ridge, Old Prison, amazing thrift store and record store, old school house, a bunch of Roadside America stuff and more. We met some nice people and ate some great food. I was finally just feeling like myself.

So that’s my four month check-in. If you want the previous episodes: Micro-perforation Adventure || Prep Day || Colonoscopy || The Surgery || Recovery from Home || One Month Since Surgery || Three Months - How It’s Going

u/DangReadingRabbit — 1 month ago

Green Ghosting - Questions

I’ve owned the Paper Pro since October 2025. I have the subscription and extended warranty because of it (and purchased obviously before the new cut off for that extended warranty).

In the last 24 hours, I’ve gotten some green ghosting. It’s clearing itself with refreshes, but I’ve never seen the distinct green colored ghosting like this before. Is this a sign the display is failing?

I hate the idea of having to send it back and wait for a new one. I use it daily, and I really hate that they don’t take a credit card and cross-ship.

Any chance my display isn’t failing? I know that unlikely. Like I said, this ghosting is new and is very different, darker and distinctly green…

reddit.com
u/DangReadingRabbit — 2 months ago

Three Months After Surgery - How It’s Going

For those who don’t know, here’s the links to my story up to now: Micro-perforation Adventure || Prep Day || Colonoscopy || The Surgery || Recovery from Home || One Month Since Surgery

So how am I feeling now that it’s been three months since my Laporoscopic and Robotic Sigmoid Colectomy (with a side of Appendectomy)?

I’m feeling pretty darn good. I can’t say I’m 100% because I think it just takes the body up to a year to be fully “normal” again, whatever that really means. But here’s the rundown:

My incisions are healed… mostly. For me this prolonged healing is unique because I had an allergic reaction to the surgical glue. I still have one scabby area on one incision, and the others are discolored but healed. I expect a year from now they’ll be barely noticeable.

Pooping: I poop more, and I think that’s because of having less colon but also from eating a high fiber diet now. I’m never constipated. I poop better than I ever have. No pain, no cramps, no straining; as long as I’m sticking to the high fiber diet…

Eating: I’m eating healthier. As mentioned, I’m eating a high fiber diet now. I’m at between 25-30 grams of fiber per day. I also drink at least 80 ounces of water per day.

I can eat whatever I want (except popcorn and corn, as per surgeon). I’m avoiding red meat and alcohol for now. Mocktails are my new treat on date night instead of 1/2 a beer 😂 (I was never a big drinker).

Going out to eat is great, I just make sure to add fiber to whatever I’m having… broccoli, veggies, salad or beans, depending on the restaurant. I can also take some Benefiber when I get home if I don’t get enough (that hasn’t happened yet).

Exercising: I’m walking 3-4 miles per day most days. My husband and I walk 2.5 in the morning and then I do 1-2 in the evening.

Weight: I lost 30/35 pounds when I was so sick before my surgery. I actually needed to lose it, so I’m trying to maintain (and even lose a little more). Diverticulitis is a terrible way to lose weight, but losing more is harder now that I feel so good and can eat whatever I want. It’s a good problem to have honestly.

Life: I’m back to work. I’m back to getting out of the house to be social. I’m back to going to family functions. I’m back to traveling! I’ve taken one short trip so far and my first big trip is planned for the first week of July. Unfortunately, during my whole health thing, our travel van decided it needed surgery too… she’s getting a new engine right now (eek). So our first big trip will be without her.

Overall I’m feel great. I still have little pangs of very low level pain here and there… but it’s low. Like a one. I occasionally have little bouts of diarrhea or really soft poop, but it’s way less than ever before, and I can usually track it to something like candy with red dye in it (always a sensitivity of mine). Life feels mostly back to normal.

My only remaining “concern” … I do poop more often. So I’ll worry a little about that on our first big trip being away from home for ten days. If we had our travel van, no worries… it has a toilet. But we won’t, so… yeah. I don’t think it’s a problem, and I won’t know until I go and do it. So wish me luck in that regard. I refuse to let it hold me back from life; it just may require more planning.

I’ll have a follow up with a tumor specialist in the next few months (because they found a rare one in my surgery). I’ll have a CT for the same reason. I’ll have a follow up with my primary doc just for good measure too. All of that will happen in September. I’m supposed to get another Endoscopy too (for esophagitis they found when I had the colonoscopy/endoscopy right before surgery).

So that’s it’s I think! Rating Diverticulitis: 0/10 ⭐️ Surgery experience: 9 ⭐️ (…now that it’s over. 1 star deduction for allergic reaction LOL)

I’m so thankful to all my amazing doctors.

Any questions, feel free to ask!

Previous episode

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u/DangReadingRabbit — 2 months ago

I Really Wish reMarkable would implement a Sticker locker room or category/saving system

These are just some of the silly and fun one I have saved in their own notebook for future cutting and pasting, but it’s not at all ideal as the amount of them grows. The way SuperNote does it is awesome, and I wish reMarkable would come up with something similar, or some way to save and categorize them.

u/DangReadingRabbit — 3 months ago

AI Data Centers and Long Island (By Jon Guercio on Instagram)

Not my Instagram, just thought people should hear the info. There’s also news articles about it, here’s one of them:
https://pix11.com/news/local-news/long-island/long-island-town-approves-moratorium-on-data-center-after-public-pushback/amp/
Sorry, there’s a lot of ads, but it’s not behind a pay wall.

I posted about it in the r/LongIsland group too, but someone messaged me and suggested I post it here also, with the original Instagram.

It’s something we all have a vested interest in paying attention to. No matter your politics, these centers use a lot of water, can cause noise problems, and utility costs to go up.

Just something to keep an eye on… and get involved if you see fit.

instagram.com
u/DangReadingRabbit — 3 months ago

Long Island town approves moratorium on data center after public pushback (be informed)

Sorry for all the ads, I tried to find an article not behind a pay wall. I saw a recent Instagram Post also talking about AI Data Centers on Long Island (not allowed to share it here) and just wanted to share the information. It’s something we all have a vested interest in paying attention to. No matter your politics, these centers use a lot of water, can cause noise problems, and utility costs to go up.

Just something to keep an eye on… and get involved if you see fit.

pix11.com
u/DangReadingRabbit — 3 months ago

Remarkable Paper Pro has me drawing more

There’s certain things I enjoy about having e-ink tablets in my life. I truly love having some of the benefits of technology, without the downsides of more screen time. This year my goal was to minimize time spent on social media and doom scrolling; so I’m journaling more, drawing more and reading more. My new reMarkable Paper Pro and Kindle Colorsoft have been essential in helping.

I love octopuses. They’re so smart and so cool. So I did a tutorial to learn how to draw one. I sketched it first, then outlined and stippled with the fine ink pen and used the shader tool (in grey) to add some depth.

Thanks for looking ☺️

u/DangReadingRabbit — 3 months ago

It’s frustrating without internal links, but I’m managing for now by using Tags.

But even tags have their problems.

For example, why does every tag I create show up in every notebook? If they are system-wide by default, there should be a checkbox to make them “this notebook only” when creating a new tag.

There should also be a way to sort them. As my tag list grows over time, sorted by “most recently created” isn’t ideal. And lack of sorting is made worse by the fact every notebook shares all tags.

Here’s an example. I have a journal and have a tag (January, February, March, etc.) at the start of each month. I have a knitting notebook. I have tags for each type of project (sweater, socks, scarf, etc.). I have a work notes and task list notebook, with tags like pending, external, group projects, long-term goals, to-do lists. My work notebook doesn’t need the knitting tags. My knitting notebook doesn’t need the monthly tags. My journal needs neither set of tags.

And why, when navigating to a specific page, isn’t there the option for last page? I realize you can type in the number, but just out of curiosity”first” and “last” next to “go to page…”

This is the kind of stuff that makes me realize the developers aren’t users. If they were, stuff like this would frustrate them as much as anyone else, and they’d fix it.

I love my reMarkable paper pro (and still love my rM1), but things like this drive me crazy. There really are some simple improvement they could make to the software that could make the user experience top notch.

Edit: I also realized this tonight: If you create a tag and tag a page with it, fine. But then if you untag that same page, it automatically deletes the tag completely? In other words, if no pages are tagged with “Tag-Name” then “Tag-Name” gets deleted. WTF?

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u/DangReadingRabbit — 3 months ago

To keep it as short as possible… I was diagnosed with fibromyalgia in 2001. No meds because I’m allergic to too many things.

I’ve been dealing with dry eyes the last couple of years. I always chalked it up to allergies until recently when it’s been much worse. I also have had very dry skin, dry nose all my adult life.

Have had chronic dental health issues as long as I can remember, despite good hygiene.

As part of my fibromyalgia, the usual: aches and pains, off and on fatigue, concentration issues.

And recently, had a bad case out of nowhere (so it seemed) of smoldering diverticulitis that led to major surgery.

My family is like an autoimmune repository 🤣 And I have it on both sides… lupus three generations back on dad’s side; rheumatoid arthritis and CREST syndrome on mom’s side.

I’ve never has a positive ANA (but not tested in the last two years). My inflammatory markers can often be up.

I’m going to talk with my doc about it, but just wondering others experiences with possible Sjogrens, dry eyes and related symptoms. I only learned about it recently because of this dry eye nonsense.

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u/DangReadingRabbit — 4 months ago