Saturday, July 14, 2018

Home at last!


We're All In This Together
You're Braver Than You Believe


Friday, June 29 – Friday, July 13

In this day and age, that is a long time for anyone to spend in the hospital. I was reminded of this when I went down to the cafeteria to get dinner on Thursday night and the cashier asked me for my ID for she could give me the employee discount. When I told her I didn't work there, she said she was surprised because she recognized me. When the random cafeteria staff think you work there, you know you've been at the hospital a long time.

We were excited when we finally started hearing on Wednesday that she would probably be discharged on Friday, because that meant she was out of the woods and doing well enough that she didn't need around-the-clock medical supervision. On Thursday, it was pretty much a foregone conclusion that we'd leave on Friday, so I started packing up all of our things. It's amazing what you accumulate in two weeks, and perhaps aside from my mom's health, I was most looking forward to not living out of a bag! Yesterday morning, we had the usual suspects come and check on my mom, and then the last thing they did was remove the wound vac temporarily. They did not want her traveling with it, and the hospital version is a large contraption compared to the home unit she will be attached to after it is administered later today.

So although my mom looks fabulous in this photo, it is a bit misleading because she was actually in a lot of pain, but we were both filled with adrenaline at the prospect of going home.

Right before we left the hospital!

The reality is that there will be very tiring days, weeks, and months ahead as she recovers. Some people with a wound vac take six months or a year to recover. Until that happens, my mom cannot drive, so we (C, G, J, R, and myself) will have to take her to all of her appointments, which are numerous. She needs medication every two hours right now. At the hospital, someone else did the cooking and cleaning, but it will be our job to prepare all of her meals, do all of her laundry, change her linens, make sure she is eating and drinking enough, make sure she is walking and doing her breathing exercises for her pulmonary fibrosis…the list goes on and on. We've only been home for 22 hours and already it is very apparent just how much work this is going to be. The only support we will have at home is that a home health nurse will come three times a week to change the wound vac.

However, we are more than happy to do it and both our dogs and my mom's dog, Ava, are thrilled she is home. I am viewing the entire healing process as a marathon and that as long as we are all moving forward, sooner or later we will get there! We keep reminding her of that Disney Cruise we booked for her birthday next June, so that is our goal…to have her completely well by then so we can all celebrate!

Just to show how far she has come, here are just a few photos of what she went through:

I have many more graphic and gruesome pics, but I will not include those here! I am just so proud of her progress because this has not been easy. She has survived an insane ordeal!

This was a very scary sight for me

So many tubes and cables and machines

I felt helpless just watching her

Finally moved the the Trauma Step-Down Unit

Getting a respiratory treatment

I didn't see any fireworks on July 4,
but I saw something even better...
my mom smiling!

Waiting to get a CT scan

The day before she was discharged


We cleared out our library and rented a hospital bed so she'll be able to rest comfortably at night and not have to navigate any stairs. C also made a hilarious sign for the door!

Her temporary bedroom

If you are a Seinfeld fan, you will get the name

The 24/7 joke is because this is exactly
what is posted on the library door
at my YaYa's assisted living home!
The asterisk/explanation is just too much!
LOL!!!


This will probably be the last update about my mom for a while…assume that no news is good news and when there is something to share, I will!

You can read the whole story here:

52 Hours

Still at the hospital...

The saga continues...

Getting Ready to Fly the Coop

Happy Tails to you!

Thursday, July 12, 2018

Getting Ready to Fly the Coop


Just a quick update today…

Since my last post, things have been steadily improving! The CT scan was clear, the infection has subsided, and one of the specialists from the lung clinic spent a great deal of time with us yesterday afternoon to answer questions and listen to my moms lungs and suggest some things she can do to ensure her lungs stay as healthy as possible during the healing process.

I was also able to watch them change the wound vac yesterday morning and it was nothing short of fascinating. I will, however, spare you the gory details! While it was a very painful process for my mom, and one that will be repeated every two to three days for the coming weeks and months, it appears to be working! I'm no doctor, but the wound looked SO MUCH BETTER than just two days earlier! Even the wound nurse was pleased with the progress! On Monday, the dimensions of the wound were 17 cm x 6 cm x 4 cm and yesterday they were 15.5 cm x 4 cm x 4 cm! That might not seem like much of a difference, but believe me, IT IS!!!

One thing that has made a huge difference for my mom has been my niece. She is 13 months old and having her visit has really boosted my mom's spirits. She saw my mom in the ER, in the Trauma ICU, and several times while in this current hospital room. My mom just lights up and it is so heartwarming to witness and I'm incredibly grateful to my sister R for bringing her as often as possible!

My mom has been slowly building up her endurance by taking short walks. Yesterday, my niece did three laps around the unit with my mom! I mean, LOOK AT THIS PHOTO! So precious! All the heart eyes! All of them!!!



Today is Day 15 in the hospital and I finally feel confident saying that things are definitely looking up! The current plan is for my mom to be discharged tomorrow and I'm hoping the next time I write an update, it will be from home instead of the hospital! Including tonight, I will have slept at the hospital for 11 nights, so I am very much looking forward to being home! It's amazing how much you miss the convenience of a fridge and a washing machine! 

Maddy and Ginny have no idea how much love smothering they are in for when I get home, and I know my mom has really been missing her dog, Ava, so that will no doubt be a very sweet reunion as well!

Read all about this ordeal in my previous posts:




Happy Tails to you!

Tuesday, July 10, 2018

The saga continues...


The last update I posted was Saturday morning and since then there have been a few developments.

The first actually happened Saturday morning but I did not write about it because I was so angry. There has been a group of surgical residents who have come to check on my mom each morning during rounds. Most of them are wonderful. Most. There was one who was extremely condescending every day and dismissive of my mom's experience. I kind of sat by and watched it happen every morning because later on each day, a surgeon who must oversee that group would come in and I trusted his expertise.

As many of you know, my dad is a retired OB-GYN and despite the fact that he and my mom are divorced, he has been kept in the loop throughout all of this and I've asked him questions along the way to confirm that he agrees with the treatment. It is interesting that after I shared with him what was going on at hospital #1, he actually suggested EXACTLY what ended up happening in terms of the surgery the next day when we came to hospital #2. Over TEXT MESSAGES. From the OTHER SIDE OF THE COUNTRY. I still am blown away by the incompetence of hospital #1 when my mom was right in front of them!

In addition to my dad, my brother is friends with an OB-GYN here at hospital #2 (a strange and wonderful coincidence, I know!). She also correctly suspected what was wrong while we were at hospital #1 and was supportive and instrumental in our decision to leave hospital #1 against medical advice. Yes, another OB-GYN who did not see my mom in person was able to determine what the problem was. Again, what is wrong with hospital #1?!?

So back to Saturday morning. This friend of my brother (who I will now refer to as our family friend because she visited my mom in the Trauma ICU and brought food and asked questions and was absolutely amazing to us) questioned a few things they were doing for my mom, so I had these questions to ask the residents when they came in on Saturday morning.

I've already described how this one in particular treated my mom throughout the week, and Saturday was no different, even though my mom had been through an insane ordeal the day before. I said I had a few clarifying questions about what was happening, and immediately she became extremely defensive. Rude, really. She questioned who this family friend was and stated that OB-GYNs know nothing about bowels.

UMMMMM…excuse me?!? Two OB-GYNs were able to diagnose what was wrong with my mom SIGHT UNSEEN. So clearly they DO know a thing or two! The fragile ego on this resident was embarrassing. To be so threatened by questions?!? Utterly ridiculous!

As soon as she left the room, I called for the charge nurse and I made it clear that I was very angry and that she was NOT going to treat my mom any longer and that she was not even welcome in the room. LIVID is the only word I can use to describe my emotions. I'm a very laid back, go-with-the-flow person most of the time (or at least I try to be!). But when you mess with my family, and especially my mom, who is in pain with a gaping wound in her abdomen, you will see a very not nice side of me.

Another surgical resident came in to speak with us and assured us that particular resident was removed from my mom's case and we would not being seeing her again. I explained that while I might only be one person, I am representing my entire family and that it is MY job to ask questions and it is THEIR job to answer them. Frankly, the fact that my brothers and I have been here around the clock has made the hospital staff's job easier because we are the ones who help her in and out of bed, get her water, adjust her pillows, settle her in the chair or bed, walk laps with her around the unit, cover her with blankets, adjust the temperature, and handle all of the other countless little things she needs. And we are excellent company for her as well, if I do say so myself!

This whole business with "excusing" that resident was right about the time I was writing my previous blog post and my mom was resting, so I decided against including that story until I had calmed down!

Everyone else here has been spectacular. Truly. But I have learned in a very short that I have to speak up. As great as everyone here is, the reality is that WE, her family, are the ones who will be taking care of her after she is discharged and we have to not only understand, but also be comfortable with the decisions being made. We are not morons – on the contrary, my brothers and I are intelligent, thoughtful people, who are far more familiar with medical language, procedures, medication, and so forth than most non-medical people. So my takeaway is that it is my responsibility to speak up, ask questions, and be my mom's advocate at all times. And to not be shy about it or apologize for it. Period.

So, on to how my mom is doing…

Saturday was a pretty good day (after that terrible morning). My two brothers, my sister, and my baby niece came to visit and to give me a break. I had been at the hospital from dinner time on Wednesday until lunch time on Saturday, and I was really suffering from dog withdrawal. As soon as I got home, I had a bite to eat, and then I took Ginny upstairs to bed with me (she is an expert-level napper...Maddy, not so much!). I slept for the rest of the afternoon, and then after dinner C and J went back to the hospital (G had stayed there all afternoon), while I hung our with my sister and niece. It was a nice break. C and J got home late, and G spent the night at the hospital. At one point during the evening, the nurses had to do something for my mom and they asked C, J, and G to step outside for a few minutes. One nurse said to my mom, "Your sons really love you!" and that made my mom's night.

On Sunday, J, R, and my niece visited my mom while I was able to run a few errands to pick up some things she needed before going back to the hospital to relieve G. At this point, we are a well-oiled machine! The rest of Sunday was thankfully uneventful and my mom was feeling a little more comfortable overall and the infection seemed to be improving.

On Monday morning, I had a meeting right down the street from the hospital. I waited until all of the usual morning rounds were done and my mom had eaten a little breakfast, and she assured me she would be fine while I went to my meeting.

One thing that's been happening is I can be in this room and not see another person for up to four hours at a time – just when my mom's medication or vitals are due. Long stretches of time when it's just my mom and me. I'm not complaining about that at all, but most of the time, we are left alone.

But if I leave the room? It's like a parade. If I go to the cafeteria to get something to eat,  someone comes in the room. If I step out to call a family member, someone comes in the room. EVERY.SINGLE.TIME. It's extremely frustrating. Sometimes it's a nurse or tech with updates, sometimes it's doctors to exam the wound and discuss treatment, and today it was the case manager to outline her discharge plan! I mean, seriously! I was gone less than 15 minutes today when I went downstairs for coffee!!! It has almost become a joke between my mom and me.

So, yesterday, I should have known something big would happen if I physically left the hospital.

While I was at my meeting, they put the wound vac on!!! Ahhhhhh! WHY? WHY? WHY? My mom said it was very painful and I have enormous guilt about not being here with her! I cannot understand why every time I leave, something big happens! They also did a chest x-ray while I was at my meeting because they were worried about her developing pneumonia (thankfully the x-ray came back clear aside from the existing fibrosis). Two big things while I was gone for a few hours!

The rest of yesterday went well, and having the wound vac actually seemed to make it a little easier for her to move around. C and G came to visit last night and they thought she looked pretty great considering all she's been through. We were feeling hopeful that maybe things were looking up. She did not have the best night of sleep, but part of that is because people are in and out of the room for various reasons.

As I mentioned, a case manager came in this morning and explained that the wound care team would be in tomorrow to change wound vac and then if they were able to secure the equipment for us to take home and arrange a schedule for home nurse visits, we might be able to go home tomorrow. Excellent news!

However, that did not remain a possibility for long, because one of the things they do during the night is draw blood, and the results today showed an elevated white blood cell count again. So just this afternoon, they've started her on two more antibiotics, meaning in addition to being on oxygen and the wound vac machine, she now has IVs in both arms. And since they don't know what's causing the white blood cell count elevation, she has to have another CT scan this evening. How much more must she endure?!? Honestly!

This pole is like an extra appendage
my mom has to drag around with her


I keep telling myself that it can only get better...and sooner or later those words will prove true.

Again, thanks for your messages and kind words. We wouldn't be able to do this without all of your support! We are so grateful for such loving family and friends!

Happy Tails to you!

Saturday, July 7, 2018

Still at the hospital...


As I write this, it is Day 10 of my mom being in the hospital (day 9 at hospital #2).

It has been a long and tiring week and so much has happened since my last post. My brothers and I have taken turns staying overnight with our mom and we've been trying to not leave her alone. She was alone for two afternoons this week for a few hours each time while I babysat my niece (a job she normally does!), but other than that and us running down to the cafeteria to get a drink or a bite to eat, we've been with her around the clock. I'm so grateful to my brothers for doing as much as they can while they are working full time…have I ever mentioned how much I love these two humans?!?

I know I was vague in my last post about what was actually happening, but I didn't want to include any medical details until my mom was able to give me permission, since this is really her story.

She had 32 inches of her small bowel removed. 32 inches of dead, diseased tissue. Her incision runs from several inches above her belly button, through her belly button, and extends several inches below her belly button. It is no joke. So many staples.

Throughout the week, every time she made progress, there seemed to be a setback. She's not only dealing with this, but also Type II Diabetes and Pulmonary Fibrosis, so they had to keep an eye on her blood sugar because she didn't eat anything until Wednesday and also her lung function and oxygen saturation levels. However, even though things seem to go well and then not so well, the general trend has been in the right direction.

On late Monday afternoon, she was transferred to a regular room. This alone was a big relief, because the Trauma ICU had many restrictions (which is perfectly understandable). We had to be buzzed in when we wanted to go to her room because it is a secured unit; no outside food or drink was allowed, meaning anytime we needed to eat or drink anything, we had to leave the unit (the same went for us using the restroom – we had to leave the unit and be buzzed back in); only two people were allowed in her room at any one time; and after 9 pm, only one person was allowed in the room with her. With her regular room, there is no limit to the number of visitors allowed at one time (although of course we want her to rest, so we don't want her overwhelmed with people) and multiple people can stay overnight with her if necessary (although my brothers and I have just been taking turns).

We had a really rough night on Tuesday. My mom was on a clear liquid diet and unable to keep anything down. As such, she was seen by two surgeons and they agreed that she needed her nasogastric tube reinserted to suction material out of her stomach (this had just been removed the day before). As you might imagine, having a tube inserted into your nose, having to SWALLOW, and then feeling it being snaked down into your stomach is a thoroughly horrific ordeal.

The procedure did not go well. Instead of the tube going into her stomach, it went into her lung. Beyond awful for anyone, but worse for someone with pulmonary fibrosis. After much consultation, it was removed shortly thereafter and there's been no further mention of that tube, thank goodness. What a complete nightmare.

She has slowly been taken off all of the machines…as of right now, she is on oxygen, which is normal for her on the best of days, and she has an iv for antibiotic fluids.

Which leads me to the latest setback.

We had high hopes that she would be discharged on Friday (we have plans to have her move in to our house for probably the remainder of the summer while she recuperates).

Obviously that didn't happen.

On Thursday morning, when they inspected her incision, they discovered it was infected. Not what we wanted to hear. They put her on antibiotics and drew a line across her belly to monitor the spread of the infection.

Yesterday morning, the inspection had spread beyond the line, so they removed a few of the lowest staples to allow it to drain and gave her more antibiotics.

Yesterday afternoon, after another examination, they decided to open up the entire wound. The WHOLE thing. Right there in her bed. And I watched. All the staples were removed and the newly healing skin was completely opened up. It was both the coolest and grossest thing I have ever seen. My mom was a rock star, lying in bed with her belly wide open so they could look down into to check on the interior sutures. I was in awe and completely shocked at the same time. Despite growing up in a medical family, I'd never actually seen the inside of someone (I mean, why would I have?), so it was fascinating. Sadly, even with my untrained eyes, I could see the infected tissue clear as day. I don't know how my mom handled all of that in such a zen-like manner. Honestly, I am the proud daughter of a complete badass.

They packed the wound with gauze and covered it up. The hope is that the antibiotics will help get the healing started, and once the infection is cleared up, they are going to use something called a wound vac to pack and seal it (this is be changed every two or three days).

As awful as all of that was, she said she felt better afterwards because the pressure was relieved. She was able to nap yesterday afternoon and slept fairly well last night. They came and checked it this morning, took out the packed gauze and put fresh gauze in there, so I was able to see it again. Her belly looks better than yesterday, so it would appear that the antibiotics are doing some good. I also think the fact that she was able sleep helped, although she is in a considerable amount of pain right now and is having trouble getting comfortable.

Thank you once again to the family and friends who are checking in. I'm doing the best I can with updates and I'm sorry if I don't respond to you individually, but know that I appreciate all of the kind words you are sending my mom from the bottom of my heart!


Happy Tails to you!