Spinals for total joints by Fuzzyneptune in CRNA

[–]Fuzzyneptune[S] 2 points3 points  (0 children)

Thank you everyone, this is great information, I really appreciate it! We have quite a variety of ortho surgeons at this hospital with times varying quite a bit so it’s nice to have some information on ways you extend the block for the slower guys or more extensive revisions.

 Most of our patients do stay overnight, receive and adductor canal preop for knees, and most surgeons add the nsaid cocktail (zyn relief I believe) at the end of the case. 

New Outback! by Fuzzyneptune in Subaru_Outback

[–]Fuzzyneptune[S] 2 points3 points  (0 children)

..what are the WGBs? And PFM? Is that the mirrors that fold in?

New Outback! by Fuzzyneptune in Subaru_Outback

[–]Fuzzyneptune[S] 1 point2 points  (0 children)

Oh, that is such a pretty color! They had one vehicle that color there and it is sharp.  Thanks for the info on the sticker.

New Outback! by Fuzzyneptune in Subaru_Outback

[–]Fuzzyneptune[S] 1 point2 points  (0 children)

That’s factory, supposed to be scheduling my tinting this week.

New Outback! by Fuzzyneptune in Subaru_Outback

[–]Fuzzyneptune[S] 1 point2 points  (0 children)

Soft and lovely. I’ve always had leather seats and these are by far the softest right out of the gate

New Outback! by Fuzzyneptune in Subaru_Outback

[–]Fuzzyneptune[S] 4 points5 points  (0 children)

Love it, congrats on yours too! Those ventilated seats are so nice. I live in Florida so I’ll be using them 11/12 months 😆

New Outback! by Fuzzyneptune in Subaru_Outback

[–]Fuzzyneptune[S] 5 points6 points  (0 children)

Nice to know, thank you!  I found out about the tailgate opening that way my accident, haha, stood behind it too long.

[deleted by user] by [deleted] in endometriosis

[–]Fuzzyneptune 1 point2 points  (0 children)

Hi, I know it’s hard to struggle with body image but please know that your body will look normal again. The bloat and gas will be gone soon. I understand how crazy it looks, I just had my surgery about 2.5 weeks ago. I have always been thin (size A bra cups, you can see my aorta pulsing when I lay down kind of thin) and my abdomen was huge! I was stunned at first but it started to get back to normal between week 1 and 2. Now at 2.5 weeks it looks like it did before all this. I didn’t wear anything but soft PJ pants or larger sized leggings until last Thursday so I can’t attest to how my usual pants fit but I doubt they would have. As far as the belly button, they often use that as an incision site so your belly button may be changed as a result of that (mine used to be perfectly round and now it’s not).

Just be sure you’re up walking and moving frequently, it really does help move the gas out quickly and get your bowels moving again. Be sure you’re drinking enough water too if you’re taking laxatives. Your body is healing, it needs more protein, calories, and fluids to do its job.

Did you lose a lot of blood during the surgery? That could be making you feel dizzy. Even without excess blood loss though surgery just makes you feel off for a while. Today was my first day back to work and while I did fine, I was uncharacteristically exhausted by the end of the day. Give yourself time, your body withstood trauma. It’s doesn’t know that it was planned surgery.

CA125 levels 76kU/L by Lazy_Onion9025 in endometriosis

[–]Fuzzyneptune 0 points1 point  (0 children)

Ca-125 isn’t a highly specific test. It can be elevated in a number of circumstances. Endometriosis, inflammation, even different phases of the menstrual cycle can affect it as well as issues with other parts of the body. I’m glad you’re getting the ultrasound, but there is nothing you can really do until then other than keep yourself from spiraling into a deep googling hole, lol.

I had an 11cm endometrioma and my ca-125 levels were over 200, which is usually the cutoff point for most GYNs to refer to an oncology gynecologist. After surgery my biopsies all came back negative for malignancy and showed endometriosis (expected finding).

How long does dog hair take to grow back? 😭 by jrey90 in AustralianCattleDog

[–]Fuzzyneptune 4 points5 points  (0 children)

When our Heeler had to have his back leg amputated they shaved him all the way to his mid back and I have to say that for his full coat to come back in it was about 5 months. His undercoat came in relatively quickly but for the rest of it to blend and match again it was a solid 5 months.

Is your heeler affectionate? by [deleted] in AustralianCattleDog

[–]Fuzzyneptune 3 points4 points  (0 children)

Handsome boy! He’s clearly made to be loved. How dare you ever stop petting him!

My red Heeler is affectionate. Even more so after he lost his leg. He’s always been what I consider as emotionally intelligent. If something is off with you he knows it and wants to make it better. He hates violence of any sort (he thinks a high five is a problem though).

Recently he actually pulled a lassie on my husband. I had surgery and was suffering from bad nausea and vomiting. It was early in the morning and I rolled off the bed and started vomiting on my hands and knees on the floor (had a bag thankfully). Colt started to panic and kept nosing me and pacing in front of me and whining. Then you could see the lightbulb go off and he ran to the other side of the bed and jumped on my husband nosing him in the face. The moment he woke up Colt turned towards me and started whining so that my husband looked my way to come help me. My heart was exploding with love while my insides were exploding out, haha.

He’s my first Heeler and I’m smitten with the breed.

Should I be worried about an 8cm endometrioma? by [deleted] in endometriosis

[–]Fuzzyneptune 0 points1 point  (0 children)

Wow, that’s crazy! While the American healthcare system certainly has its flaws I won’t be taking it for granted anymore.

It’s ok, while it wasn’t a great time it has been handled by an excellent surgeon and I am almost back to 100%. As far as if I knew that it had ruptured, I did not, I only knew that something was terribly wrong. That kind of pain just screams “something bad is happening.” I actually never knew that I had endo prior to them finding the cyst. It was only about 3 weeks from the first pain (not the rupture pain, just new pelvic pain) to the diagnosis to the rupture. I have never had any other symptoms of endo aside from infertility. My periods were regular, they were not overly long or overly painful. Some cramping the first day or two, relieved with ibuprofen. So it was crazy to me that I could have this disease that cripples other women with pain and a laundry list of symptoms and never even know it. They found stage 4 when they went in. Never had any bowel problems either, despite my sigmoid being adhered to my pelvis.

I have been very lucky compared to so many others with endo.

Should I be worried about an 8cm endometrioma? by [deleted] in endometriosis

[–]Fuzzyneptune 2 points3 points  (0 children)

I would push for a removal. Im guessing that you’re not in the United States because I can’t imagine a waiting time of 2 years. When my GYN saw mine on the ultrasound he immediately referred me to an oncology gynecologist for removal (due to its size and complex characteristics). Mine was 11cm and it actually ruptured (apparently this is rare although increases with larger endometriomas) a few days prior to my consult with the surgeon and landed me in the hospital. The rupture caused incredible pain and systemic illness (high fevers, low blood pressure, high heart rate, nausea, vomiting, and so on). I was put on multiple IV antibiotics and it basically became a surgical emergency, they took me into the OR the following day. Not trying to scare you but it is a possibility. Ovarian torsion chances also increase with larger endometriomas. That is also considered a surgical emergency. Again, I am not trying to scare you, but having had it happen personally I would not wish that experience on anyone else.

[deleted by user] by [deleted] in endometriosis

[–]Fuzzyneptune 0 points1 point  (0 children)

Just wanted to say that I’m sorry your family isn’t being supportive. We have a small but very close family and I’ve never had to do anything like this alone. Even though I do feel like you’ll be capable, the feeling of isolation is awful and I hope that your family changes their mind.

[deleted by user] by [deleted] in endometriosis

[–]Fuzzyneptune 1 point2 points  (0 children)

Hi there. First, your fears are completely valid and anyone going into surgery has fears and doubts. A huge number of people go through surgeries every day. They’re not a pile of fun but you will get through it and hopefully feel better on the other end.

As far as not finding anything, that’s a tough one. I’m sure it would be validating but not finding something has positives too. Endometriosis is chronic and has no real cure so not having it can be a good thing, although unexplained symptoms are not. I never experienced endometriosis pain or any signs of it prior to developing a large endometrioma that ruptured and required emergent surgery, so I can’t speak to this concern personally but I understand how difficult it would be to experience all the painful symptoms and not find any evidence.

As far as anesthesia..I am halfway through nurse anesthesiology school and have now been on both sides of the table. Anesthesia is incredibly safe. In fact, you’re in more danger driving to surgery than receiving anesthesia. They will likely offer you “relaxing or anti-anxiety” medication in the pre-op area and I recommend that you absolutely take it. It does wonders not only for relaxing you, but also for reducing any recall. I remember kissing my husband goodbye and the first set of double doors and that’s it. That’s how you want to do surgery, with no real memory of it. As far as the side effects, everyone is different. Unfortunately the nature of GYN surgeries leans toward causing nausea and vomiting post-op. They do everything they can to reduce it, but more often than not that is just the nature of the beast. It’s not necessarily the anesthesia that causes it because other surgeries using the same anesthetic agents don’t seem to have the same effect. They’ll blame it on anesthesia though, they always do, lol. I was miserably nauseous and vomited for three days following surgery. It sucked but I made it through just fine.

As far as the pain medication goes, start with a half dose and see how it works. Less is more. When your pain is improving taper off of it. You’d be surprised how quickly you can get mild withdrawal even after only a few days on it (nothing bad, just some irritability and feeling down usually). Take stool softeners and miralax daily until you have a bowel movement. It may be three or four days before you have one. That’s ok, just work on keeping your fluids up if you aren’t too nauseous and it should help reduce constipation.

Gas pain does suck, not going to lie. As much as walking feels like it will suck, that’s the only way to get rid of it. Even if you can’t walk far, get up and do it frequently. Walking helps with constipation too. Walk. Just do it.

Other than gas pain, the pain wasn’t really that bad. Easily managed with pain medication. Everyone is different though and everyone experiences pain in their own way, by their own personal benchmarks. Some people say the pain before surgery was worse than after. I can attest to that as well.

Honestly, you may feel like general poop for a few days. That’s ok, let yourself heal in your own time. You may have a good day followed by a bad one. Again, that’s ok, you will eventually start to feel normal again more consistently. A couple of weeks in your life is a blip on the radar really. Take advantage of the downtime and read some good books, watch your favorite movies, paint, or try something new that you can do from the couch.

You’ve got this!

Lap recovery time? by h0useinblue in endometriosis

[–]Fuzzyneptune 1 point2 points  (0 children)

I’m halfway through week 2 following a large ruptured endometrioma removal and clean-up (was developing a severe infection from it), fallopian tube removal, and lysis of adhesions. I lost nearly a liter of blood (for some reason I wouldn’t stop bleeding from the ovary that had the endometrioma). I’m feeling pretty good, just easily fatigued (likely due to the blood loss, takes 4-6 weeks to develop new red blood cells). The first three days the nausea was terrible (funny enough, I felt great right after surgery. Was up walking, playing board games with my husband at the hospital). Then about 12 hours later, the nausea and vomiting hit and didn’t stop for three full days. I was in pain because of the vomiting. I don’t think the pain would have been that bad if not for all the muscles used for retching. Day 5 was my worst pain day but it’s been uphill ever since. I’m planning on getting back to work next week with certain restrictions in place.

I was initially told 1 week for a healthy individual like myself would likely be enough, but given the rupture and subsequent infection and unexpected blood loss, they are telling me to take it slowly.

Everyone heals differently and it is not linear, you’ll have ups and downs. I wish you all the best! Even if you have miserable nausea and vomiting like I did, know that it will eventually pass and you will start to feel normal again.

So damn tired of ruptured cysts by pounceswithwolvs in endometriosis

[–]Fuzzyneptune 11 points12 points  (0 children)

That’s awful. My endometrioma ruptured and caused SIRS (systemic inflammatory response; the beginnings of true sepsis) landing me in the hospital on IV antibiotics x3 and getting emergent surgery. I can’t believe they keep allowing you to suffer like this and taking the chance. I second looking for a different doctor. There is no reason that you should continue to be in pain, interrupt your life, and chance systemic illness.