July 19, 2025

Saturday, July 20, 2025

Saturday, July 20, 2025

Tonight's picture was taken in July of 2003. Mattie was a year old! It was his first trip to the Outer Banks of North Carolina. That day we went to see Bodie Light. I am a big lighthouse fan, and I wanted to pass along this love to Mattie. I figured you couldn't start too early. In fact, Mattie loved all our day trips far better than seeing the beach that year. 






Fast forward to July 2009, Mattie created a birthday card for me, with the
help of my in-laws, that was in the shape of Bodie Light. To me, this card meant that Mattie remembered our trips and our lighthouse adventures together. 







Quote of the day: When you are angry, you’re carrying the burden while the other person is out dancing. Irish proverb


Before leaving for the hospital today, I put together a big pot of homemade chicken soup. I had frozen chicken broth that I made months ago, and I defrosted it and threw in all sorts of vegetables today. I find after a long day at the hospital, by the time we get home, I do not want to cook, nor do I want something heavy to eat. I figured chicken soup has protein and vegetables and would be good for my mom and me. 





We arrived at the hospital at 1pm. My goal was to attend the 2:30pm occupational therapy (OT) session. My dad has been in the acute rehab of the hospital since Monday. It is NOW Saturday, and I have yet to meet the OT! Why? Because they keep changing the schedule on me. As we were walking in the hallway to my dad's room, a woman was trailing behind us. I turned around and she explained she was Sarah, one of the OTs. She isn't my dad's weekday OT, but was working with him today. She let me know that my dad completed all of his therapy for the day. I told her that couldn't be as he had a 2:30pm session and I was looking to observe the process. Keep in mind that I have already participated twice in my dad's physical therapy sessions! Needless to say Sarah did not know what hit her. I told her that I can understand the schedule changing once or twice during the week, but with my dad it is daily! I also told her I have yet to meet Aileen, my dad's OT and would be curious to know what they are working on! She said I sounded angry! YES I AM ANGRY! I am angry about a lot of things. 
But I think what sets me off regarding this whole situation is that his health care team doesn't take my input, doesn't care to know about his level of functioning before he was hospitalized, and even worse doesn't care to know the strategies we currently use at home. Instead, they talk to me like a clueless wonder who doesn't have the foggiest clue how to manage a 90 year old with Alzheimer's and considerable physical impairments! THAT SETS ME OFF!  

Shortly after complaining, in walked Aileen. Truthfully I was better NOT meeting Aileen. She was attitudinal and condescending. She told me she was working with my dad on how to use a sock assist. If you don't know what this is, I included a photo. It is a device used to help you put on your socks. What's the problem with this? 

Countless OTs have tried to use this device with my dad in the past. Cognitively it is very confusing for my dad. I would be the one who would have to do most of the work, so in essence it is counter productive. In addition, it already takes me 45 minutes each day to do my dad's morning hygiene routine. I have no intention of adding another 30 minutes to the process to use a gadget. A gadget that has led to lots of frustration in the past for my dad! This is where consulting with the family is vital! If she had asked me this to begin with, then she could be working on other tasks with my dad that we perhaps could actually implement at home. This is the great divide between healthcare and the caregiver! 

Once I got into my dad's room, he was up and in his wheelchair. Sarah told me that he was asking about me ALL morning and he even insisted that she wheel him into the room next to his, because he was sure that was where they could find me. I spend six hours a day in the hospital with my mom in tow. Any one who has spent any time in a hospital knows this time is debilitating! Any case, I was hoping my dad was more oriented to reality today, but unfortunately he was not. Today he was asking for his pack of cigarettes. My dad hasn't smoked since before I was born! SO A LONG TIME AGO! In addition, he wanted to play poker. AGAIN something we have never done! This confusion and disorientation comes with dementia and being institutionalized, which is why I try as much as I can to be present in order to ground him back to reality. 

You may recall that my dad's nurse yesterday was sure that he had cDiff, a bacterial infection of the colon. I told her I did not think my dad had cDiff, as my dad has irritable bowel syndrome and these bathroom accidents are a frequent occurrence for me. Any case, I asked my dad's nurse today whether they captured a fecal sample and what was the plan of action! You are going to love this! Yesterday's nurse did not chart this issue, nor did she consult my dad's doctor like she promised. So today's nurse just looked at me dumbfounded. Needless to say, I know my dad doesn't have cDiff and truly that is what matters. If I thought something was different or wrong, you can rest assured I would be all over the issue. 

However, as the day wore on, my dad got more ornery and started cursing at me. Again, it takes all the strength I have to keep it under control. My mom heard him and she reprimanded him. I stepped out of the process to regroup. Truly if the health care team wants to know why I am angry, I think they should walk my DAILY journey over the last two years, and see the impact on their own mind, body, and spirit. THEN WE WILL TALK. 

July 18, 2025

Friday, July 18, 2025

Friday, July 18, 2025

Tonight's picture was taken in July of 2003. Mattie was a year old. At that point, Mattie was toddling around and not walking independently. We took Mattie to the Outer Banks of North Carolina that week. It was our first trip to the beach! Mattie was scared of the ocean and hated the feeling of sand on his feet. So we spent a lot of time on the deck.... as you can see Mattie loved the hose and watering down the wood! Thankfully, we just kept introducing Mattie to the beach and the following year, Mattie graduated from the deck and made it to the beach! He loved making sand castles and beach combing!


Quote of the day: The disease might hide the person underneath, but there’s still a person in there who needs your love and attention. ~ Jamie Calandriello


This morning I thought I could sleep to 8:15am. That did not happen. At 8am, Indie was throwing her body against my bedroom door. She wanted me up because she was hungry. As I started to get up, I opened my bedroom blinds. I could see Steve, the fellow who helps me outside the house, was pulling up to the house in his truck. I figured my gardening company sent him over because their mowers broke the hinges in my backyard gate. I had no time to get dressed, so I literally threw a jacket over my pajamas and headed outside. While I headed to the front door, my neighbor text messaged me. He wanted me to know that I was going to hear two gun shots! THANK goodness he texted me, because I would have called the police otherwise. A deer got caught while attempting to jump over my neighbor's fence. Animal control showed up and they assessed that the deer was badly injured and suffering. So the deer was killed. Truly that sound and image have been with me all day. My neighbors told me that they text messaged me before the shots occurred because I have been through way too much and I am still juggling way too much. I thought their sensitivity was very kind. 

I can only imagine what Steve thought when he saw me, because usually I know when he is coming and I am put together. This morning, I am sure I looked wiped out, dazed, and confused. Steve understands everything I am dealing with and is a kind soul. I am convinced there is nothing he can't fix. As is typical, when Steve arrives, he thinks he is coming for one thing, but I always have other problems I need help with. Today's adventure was my backyard lights. After the rain storm two nights ago, the lights stopped working. I checked my circuit breakers, I checked the power chords going to the landscaping transformers and everything looked fine. So I concluded... it has to be the transformer. I was going to take on the replacement of the transformer this morning, but when Steve arrived, I tasked him to deal with it! And then there was light!

I got to the hospital about an hour later than I usually do. I typically try to get to the hospital to give my dad lunch and dinner. By the time I got to the hospital, all I can say is...............DEAR GOD! My dad was disoriented, very confused, and basically said his life wasn't worth living. He said he is insane and I should not have to take care of someone like him. Truthfully it was a combination of confusion and great sensitivity beyond himself. Typically with my dad's dementia, he can't think beyond himself and his needs. Today, I saw a glimpse of my real dad, the dad who wanted to look out for me and who always had my best interest at heart. 

My dad thought he was at work (not the hospital). In fact, he told me.... please don't tell them I am insane! Why? Because he was afraid he wouldn't be able to bring home a paycheck and then he would be leaving me and my mom destitute. No matter how debilitated my dad maybe, my point is, he was and has always been a FAMILY MAN! His family comes first, he worries about his family, and one of his important roles in life was to be a provider for his family. 

My dad thought my maternal grandmother was still alive. He thought that his brother (who died years ago) was down the hallway and he was telling us about conversations he had in his room today with colleagues from work. This acute change in his cognition caught my attention, so when his nurse came in, I asked her about my dad. She said YES, there was a noticeable change today, so much so, that my dad got out of his wheelchair, grabbed his walker, and was wandering the hallways this morning on his own. Keep in mind that my dad is NOT allowed any movement without help and supervision. When the nursing staff saw that he was wandering, they freaked out and now even in his wheelchair, he sits on a pad that is attached to a device that gives off a horrible alarm if he gets up! 

The nurse also told me about his massive bathroom accidents today. I am used to these, but they caught her by surprise. She feels that my dad may have C Diff. C Diff is a bacterium that can cause diarrhea and colitis (inflammation of the colon). C. Diff infections are often acquired in healthcare settings. 

My dad really wants us to sleep in the hospital room with him, but there is no way I can make that happen with my mom in tow, and me balancing the house and the cat alone. I have created a July calendar for my dad, I have cues and prompts all over the room to help him remember where he is, but truthfully there comes a point where even these cues and prompts are of no use. Today was very upsetting, but what I do know is our visits are crucial to keeping my dad mentally engaged and in touch with reality.  

July 17, 2025

Thursday, July 17, 2025

Thursday, July 17, 2025

Tonight's picture was taken in July of 2004. Mattie was two years old. By that time, Mattie was acclimated to the sand and surf. A big difference from the year before, where we spent no time in the sand because Mattie disliked the feelings of the sand on his feet and he was deathly afraid of the ocean. But by two, Mattie discovered that he could build and create with sand! That he LOVED! To me summer always meant a trip to the beach. It saddens me that I will never be returning to these places again. 




Quote of the day: Life's under no obligation to give us what we expect. ~ Margaret Mitchell


We got to the hospital today for our family team meeting. In attendance was my dad's doctor, the case manager, the rehab coordinator, and another physician. Given that I experienced these lack luster meetings in 2022, I knew the team comes in and out of the room and there really isn't much dialogue or time to process things. In 2022, the meeting indicated that my dad was going to be discharged that week. Today, we learned that my dad won't be discharged until July 26. So this means he will be in the rehab a total of two weeks. 

Truly for me it is hard to keep it together, because people in my outside world think that the only thing I am coping with is caregiving! Little do they know that my husband left me, I got divorced, I am managing a house myself, caregiving for both of my parents around the clock, and running Mattie Miracle. That is just a synopsis that truly doesn't address the daily juggling act I perform. Not to mention the deep emotional wounds I live with on a daily basis. Some days, I can put all that hurt in a box and other days, when stressed out and overwhelmed, I am angry and will push back on the care team if they are not meeting my dad's needs. 

Today at the care team meeting, they warned me that by the time my dad is discharged he may not be able to walk up and down a flight of stairs. So they mentioned a stair lift! I love these crazy suggestions! I say crazy because one, stair lifts are NOT covered by insurance, and two, the average stair lift costs $5,000. How do I know this, because after having a hissy fit, I text messaged my neighbor who installed one a year ago for his dad. He gave me the 411 on stair lifts! Any case, I am dealing with so much, why not throw something else on my plate to manage. Overall, I HATE having to make all these decisions alone, to be the only adult on duty, and to not have the support of my spouse. I assure you I would NEVER have signed up to do 24/7 caregiving, without being married. Yet here I am. Which is why tonight's quote is so apropo... as life is under NO obligation at all to give us what we want or expect.

It is clear that my dad's doctor can see I am under great stress and distress. Of course he doesn't know the full picture of why, yet without knowing the full picture, he suggested I try counseling! Hysterical! Truly hysterical. I endured a year of counseling. It was ineffectual as I don't need anyone giving me atta girls or telling me.... wow look how much you are have learned and accomplished! My response is BIG DEAL! I didn't need many of the horrors I have experienced to illustrate my inner strength. Despite this being my own profession, I have faced once again that there are things in life that truly can't be fixed, solved, or made better. NO amount of therapy will change what has happened or how I am feeling. Losing Mattie and the manner in which I got divorced are so awful, that if I survive this, the only way for me to cope with all these thoughts and feelings is a little bit at a time. 

When I got home tonight, I found my grass being cut and the lawnmower running right into my backyard gate and taking it down. Seems about right for my life. So I had to take photos and send it to the company. Something I will have to deal with tomorrow. Certainly my dad is where he needs to be now, because he doesn't have the strength to come home right now, but I have to say the daily visits back and forth to the hospital are very tiring. My mom and I spend five to six hours a day there. It is vital to keep my dad orientated to reality. Keep in mind that he has NO IDEA where he is, and most times thinks he is home. I have explained to him the time line of what has happened to him and repeat it every ten minutes. I have written some things down on his white board in the room, but tomorrow I am bringing in a July calendar so we can mark off days and include some information about his hospitalization. I am stunned that his therapists haven't done this in one of their sessions, but given my dad's confusion and frustration, I am addressing this ASAP. 

July 16, 2025

Wednesday, July 16, 2025

Wednesday, July 16, 2025

Tonight's picture was taken in July of 2005. Mattie was three years old. That week we took Mattie to Boston to visit my in-laws. We went on a strawberry picking adventure and "Farmer Brown" was in his element. Mattie absolutely LOVED IT! My mother-in-law raised two boys, so she knew how to keep Mattie engaged and moving. 


Quote of the day: Empaths did not come into this world to be victims, we came to be warriors. Be brave. Stay strong. We need all hands on deck.  Anthon St. Maarten


My morning routine looks very different now that my dad is in acute rehab. Typically I have to get up almost 90 minutes earlier to manage his shower, dressing, making the bed, and helping him with breakfast. So I have to say my dad being gone is a bit disorienting. 

This morning, my mom had physical therapy at home. Frankly I wasn't sure she could handle it. She is wiped out and even more wobbly on her feet this week since my dad has been hospitalized. While she was with her therapist, I went to return the bed rail I purchased for my dad's side of the bed and then I stopped at Lowe's and picked up "New Jack." 

In 2009, after Mattie died, my friends gave me a beautiful rubber tree fig, who I nicknamed, "Jack," for Jack in the beanstalk. When I first received Jack, he was about the same height you see with New Jack! Over the last 16 years, Jack grew over 5 feet tall. However, about a week ago, it dropped all its leaves and died (seems like a trend in my life). There was nothing I could do to resuscitate it! So this morning, I planted "New Jack!" There is something special about a rubber fig tree! They remind me of the beauty of the tropics. 

We got to the hospital today around 1pm and stayed until 6pm. I had the opportunity to meet my dad's physical therapist and attend one of his sessions. I got to see for myself if he could stand, walk, and do steps. Standing was challenging, walking was good but labored, and stairs did not look good at all. As the therapist said.... he is where he needs to be and there are goals for him. 

While I was in the therapy session, in walked Jennifer. Jennifer is the director of the rehab. I met her back in 2022, when my dad had a pacemaker placement. After one week in the hospital, my dad couldn't move from bed. The hospital wanted to discharge him to a nursing home. I wasn't having any of that, and networked my way around the hospital, until I discovered that the hospital had an acute rehab and I got connected to Jennifer. Jennifer was able to stop my dad's discharge until a bed was ready in her acute care. That may not sound like a big deal, but it was HUGE. Huge, because that one decision changed the course of my dad's future. He was given the intensive therapies he needed so he could come back and live with me. When Jennifer walked into the therapy room today, she came specifically to see me. There was no hand shaking, but hugs. That is how grateful I am to this woman! As she said to me today... "we are exactly the same, we both advocate fiercely for the ones we love." Refreshing that someone gets me, because typically I can be viewed as a problem. A problem because when I know what my dad needs, I DO NOT back down. I am like a bulldog, and those who eventually get to know me, land up respecting me for both the care I provide my dad and for having the courage to take on a dysfunctional healthcare system regulated by insurers! As Jennifer said... "your dad looks as good as he does at 90 because of you." Her feedback meant the world to me today, because there is nothing I wouldn't do for those I love. 

July 15, 2025

Tuesday, July 15, 2025

Tuesday, July 15, 2025 -- Mattie died 803 weeks ago today.

Tonight's picture was taken on July 15, 2007. How do I know the exact date? Because those burgundy and blue goblets came out ONLY on our anniversary (July 15th). My paternal grandparents were also married on July 15 (obviously many decades before me), and these wine goblets were given to them at their wedding. When they died, my uncle gave them to us. It was our tradition to pull them out to commemorate our anniversary. If you notice, even Patches, our cat, was part of our special day!


Quote of the day: It takes strength to face our sadness and to grieve and to let our grief and our anger flow in tears when they need to. It takes strength to talk about our feelings and to reach out for help and comfort when we need it. ~ Fred Rogers


Today was my 30th wedding anniversary. My first anniversary since the divorce. The traditional gift to mark this milestone is the pearl! There were no pearls, no gifts, and no cards. It is as if the day never happened, it has been erased. I heard from my maid of honor and one of my bridesmaids, and my mother in law wrote to me bright and early and she sent me flowers. As she wanted me to know that I am special and never forgotten. 
My mom and me right before my Roman Catholic wedding ceremony. Of course neither of my parents knew what today was and there is no point to discuss it with them as we are all deeply saddened. How can a beautiful day in 1995, turn out to amount to such great loss, betrayal and abandonment? 

Making a commitment before God, family, and friends means something to me. It is a lifelong commitment and my brain can not compute any of this nightmare. I have no other words right now, or at least none that I care to put in print. 








Today was my dad's first day in rehab. As you can see from his calendar, he was up bright and early. By the time I got to him, around 1:30pm, he was luggage. I found him resting in bed and he had no recollection of any of the sessions he did today! 
This is my dad's schedule tomorrow and we have a family team meeting on Thursday. At which point, I will hear their plan, which I am sure will entail a discharge date! My mom and I got home at 7:30pm, and the bed rail I ordered for my dad arrived. After a full day, I had to pull it out of the box and figure out how to assemble it. I am the jack of all trades. 

Any case, after an hour of putting it together and attaching it to the bed, I HATED IT! I thought it was flimsy and actually the sliding bar wasn't long enough and definitely wouldn't prevent my dad from getting out of bed. So that meant I had to disassemble this bloody thing and get it back in the box. Which proved to be worse than trying to assemble it. But I did it and back it goes tomorrow. It is in all these stressful moments, I can't help but reflect...... who would hate me so much to leave me managing the impossible? 




July 14, 2025

Monday, July 14, 2025

Monday, July 14, 2025

Tonight's picture was taken in July of 2002. Mattie was three months old. By that point I already nicknamed him Mattie Moo! So our family's unofficial name for this photo was Mom and Moo! I am not kidding, if you go to our electronic folder, this is how this photo is classified! 



Quote of the day: I’m gettin’ tired way past where sleep rests me. ~ John Steinbeck


Literally tonight, I am writing in bullet points! Why? Because I have been at the hospital today from 11am to 9:30pm. I am worn out on every level!

  • I herded my mom to the hospital this morning. I wanted to get there by 10am, but mornings are not my mom's thing. I literally packed up her breakfast to have in the car and told her we had to get to the hospital before my dad's physical therapy assessment. 
  • Keep in mind that the hospital wanted to discharge my dad on Sunday. I advocated for that NOT to happen, particularly because no one saw my dad get out of bed and walk. If he could not safely do those things, I wasn't taking him home, because he would fall again. 
  • When we arrived at my dad's room, we found he had a bowel movement and was sitting in it. While addressing this, Beth, the physical therapist, arrived. Therapists will say they DO NOT control where the patient goes (discharge or to rehab), but that is NOT true. Their recommendations drive the decision. 
  • Any case, I made it clear to Beth what had transpired at the hospital since July 9, and that I blamed the hospital for my dad falling at home. Beth listened and did a great evaluation of my dad. When I asked her what the plan was, because I knew the hospital was going to discharge him today.... she looked at me and said.... YOUR DAD IS GOING NO WHERE! He is NOT safe for discharge! I told her I wanted to kiss her! It was the first person who saw exactly what I was reporting! 
  • The entire team understood that I wanted my dad to get into the hospital's acute rehab program! Truly this is the only facility I will leave him in, because it is connected to the hospital and my dad's rehab physician runs this program. 
  • In the middle of managing my dad's care and multiple health care team visits, I also met several people who represent hospital leadership. They received my grievance and I have been told the letter has gone far up the leadership chain and a formal investigation is now underway. I was interviewed (round one) for this grievance today. 
  • By 2:30pm, I went down to the hospital's cafe to purchase lunch for my mom and me. While there, I ran into Althea! Who is Althea? She was the patient advocate in the ER back in 2022, when my dad was admitted for a pacemaker. Althea is younger than me, she is from South Africa, and she is truly an angel. She was so supportive to me and my mom back in 2022, I never forgot her. In fact, at that time she connected me with her boss, and her boss is now the director of nursing at the hospital. Someone I remain connected with, who truly is motivated to provide outstanding patient care. 
  • Althea did not remember me, but I told her what a difference she made to my life. She was so touched by our conversation, she actually came up to my dad's room and spoke to all three of us for 90 minutes. She is working on getting a certification on mindfulness and hopes to help first responders. Naturally we got into discussing mental health and traumas. 
  • At 7pm, we transferred my dad into the hospital's acute rehab. The last time my dad was admitted to that program was in 2022. So it is not new to me, and of course we know the director of the program, which gives me peace of mind. My dad is exactly where he needs to be and my focus is to try to get rest, because I am close to not being able to function. 
  • Of course in the midst of this, I always ask myself, how could my husband not be here to help and support me? I have no answers! Tomorrow, July 15, would have been our 30th wedding anniversary, and it would have marked 37 years together (dating and marriage). 37 YEARS! Not 37 months, not 37 week, not 37 days.... BUT YEARS!!!!!!!!!!!!!!

July 13, 2025

Sunday, July 13, 2025

Sunday, July 13, 2025

Tonight's picture was taken in July of 2007. Mattie was five years old and doing one of his favorite activities... bath time. When Mattie was a toddler, he hated water, and bathing him was painful. But by the time he was a preschooler, there was a transformation. I am not sure he loved bath time per se, but what he loved was playing with his cars and toys in the tub. His creativity would unfold in the water! This photo was classic Santa Mattie. He would give himself a Santa beard out of bubbles! 


Quote of the day: Words are tears that have been written down. Tears are words that need to be shed. Without them, joy loses all its brilliance and sadness has no end. ~ Paulo Coelho


I could not get out of bed this morning. I think I finally got myself up at 8:45am! Unheard of in my house! Even Indie did not wake me up. Of course my mom got up early for some reason and was waiting for breakfast to be made. During my morning routine, I got a phone call from a nurse practitioner at the hospital. She basically said my dad was ready for discharge! Seriously this woman had no idea what she unleashed. I basically told her that unless my dad gets out of bed and we assess if he can stand and walk, I am NOT taking him home! There are no physical therapy evaluations over the weekend, so she was stuck waiting until Monday. But I told her, I would see her at the hospital when I got there and we would discuss this more! I did meet with her and she turned out to be a lovely woman. I explained to her that my anger was not really directed at her but to the system. A system which can't wait to push out patients, whether they are ready to go home or not! She understood. So tomorrow I await a visit from the physical therapist and my dad's rehab doctor. But I am prepared for my dad to be discharged and as always I am going to have to figure this out alone. 

I told the nurse practitioner that I watch my dad throughout the day, but at night, I am not in my parent's bedroom. So in order to keep my dad safe and in bed, I have purchased a full side bed rail. This rail will prevent him from getting out of bed, until I am there and can safely monitor him. He won't like this change, but safety has to come first and I can't rely on my mom to oversee his evening care. 

When I first arrived and went to my dad's room today, his nurse greeted me and handed me and my mom gowns and masks, because they have put my dad on contact isolation. My dad has a virus. He has had a virus since admitted to the hospital, but just today, they decided to classify him as having contact isolation. When Mattie had cancer, there were many times, he had contact isolation. Therefore gowns and masks were required. I certainly understood why his healthcare team had to wear these things, as they were going in and out of patient rooms, and they did not want to spread whatever Mattie had to other patients. However, I never wore a mask and gown with Mattie. Our life was chaotic enough, Mattie felt very different already, he did not need to see his mom and dad in gowns and masks. Only to emphasize his illness! We never wore them! If I did not wear them with Mattie, you can rest assured I was not wearing them with my dad. I am not sure my dad's nurse ever had family members outright refuse her request, but I did it without batting an eyelash. Later in the day, this nurse came back into the room, and I could feel her level of respect for me, as she heard me dealing with the nurse practitioner and advocating for my dad! She also let me know how sweet and kind my dad is.... indeed! What is very clear about my dad is he was and always will be a family man!

Switching gears, for two days, I have been working on a formal letter of concern to send to the hospital's ER director. I finally finished it and sent it off tonight. It is below. Do note that I changed all the names of people and the hospital for this blog posting.................................................................................................


Dear XYZ,

Thank you for this opportunity to share my recent experiences in your emergency department. ABC is our medical home. We live outside the beltway, but we have purposefully chosen your hospital because of your high standards of care and your compassion for addressing patient and family concerns and needs. 

Our recent ER visit was deeply concerning and has given me pause about returning in the future. On Wednesday, July 9, I took my 90-year-old father to your ER. My dad lives with me, and I am his primary caregiver. My dad has Alzheimer’s, and I brought him to the ER because he had a 101 fever, chest congestion, a bad cough, and he was so lethargic that I had trouble getting him up to walk a couple of feet. Given that these symptoms came on quickly this week, I consulted my dad’s primary care physician by phone. He said it was important that I take my dad to the ER to rule out pneumonia. 

I have outlined below my concerns and timeline using bullet points. Overall, I believe my dad fell while at home on July 11 at 2am, because he was ill and he was discharged from the ER prematurely (July 10, at 4am) and against my wishes. If my dad had been admitted to the hospital on July 10, he would not have fallen at home, and his recovery would be more manageable. Now we are not only dealing with the symptoms he presented with on July 9, but we are also dealing with a fragile 90-year-old who has hurt his back (thankfully he did not break a bone), is in pain, and any movement causes him great discomfort. The fall was a major setback, and it was indeed preventable. 

July 9-10 

  • My dad entered the ER on Wednesday, July 9 at 9pm.
  • The ER was not busy, and we were brought back to Room 20 within 30 minutes of our arrival.
  • Thankfully I have access to my dad’s patient portal, because I could easily follow along with tests being ordered and see results in real time. I am not sure what families do without portal access. I say this because it was hours before we met Dr. WOW, the ER physician. Note that we only met with her because I asked for her to come to our room as I wanted to hear from her about my dad’s condition. In previous ER visits, we were always introduced to the physician almost immediately. Since the ER was not busy that night, there was no reason Dr. WOW was not able to visit with us sooner. 
  • Families come to the ER scared and concerned and with a 90-year-old even something minor can be a major health issue. In addition, it would be my hope that primary caregivers are considered valuable members of the healthcare team and therefore our observations are valued and taken into consideration. Not only did I not feel heard by Dr. WOW, but I also felt she had a condescending attitude, as she implied that having my dad admitted to the hospital would be committing insurance fraud. Who says this to a primary caregiver? Believe me, if my dad did not have to be in the hospital, I would not be at ABC. I took my dad to the hospital because he needed medical attention. Dr. WOW is all about the data, sticking to rigid admission criteria, and has therefore forgotten that patients are greater than their test results. The whole patient must be evaluated and considered when making sound medical decisions. 
  • On July 10, at 4am, my dad was discharged from the ER because Dr. WOW felt my dad did not meet the criteria necessary for hospital admission. She had no regard for the fact that I did not feel able to care for my dad at home in his current depleted state. I was left to figure it out and I told her I had a feeling discharging him was a mistake and we would probably be right back in the ER. Our family and friends asked me…. Who would discharge a fragile 90-year-old at 4am? They are not medical professionals, but even they immediately saw the problem with such a decision. 
  • Once we returned home, I monitored my dad’s vitals every four hours and shared this information with my dad’s primary care physician. 
  • On Thursday, July 10, I had the opportunity to talk with my dad’s primary care physician. He gained access to all the ER assessments, reviewed them, and shared my concern about being prematurely discharged. He felt that there was enough evidence to merit a hospital admission. But then again, this physician evaluates the WHOLE patient, not just the data. 

July 11

  • At 2am, my dad fell trying to get out of bed to go to the bathroom. 
  • After calling 911, six paramedics arrived and helped me get my dad off the floor, down the stairs, and into an ambulance. They wanted to take my dad to another hospital system. However, I refused that option. I wanted my dad back at ABC for two reasons. First, my dad endured extensive testing on July 9 and 10 at ABC and I did not want him to have to go through this again at another health system. Second, I believe it was important for your ER to see firsthand that it was the wrong decision to discharge my dad on July 10. My dad was clearly physically depleted, weak, and unable to function. His symptoms came on acutely, he was not acting like himself, and they significantly impacted his physical abilities. 
  • When we arrived at the hospital at 3am, I explained what had happened to the ER nurse, and I also told him that this time, we were not leaving your hospital until my dad was admitted. 
  • We waited from 3am to 7:30am, when a change of shift occurred. The change of shift made all the difference in the world. We went from the D team to the A team. The health care team was listening to our concerns, and Jay (our nurse) could hear how distraught we were, so he sent in Jasmin and then Chrissy to talk with me about my experiences. Chrissy promised that an investigation would be carried out, but I wanted to put these issues in writing. 
  • My dad was admitted to Room 505 on Friday at 3pm and remained in the hospital over the weekend. 

In addition, I wanted to share my observations of listening to and enduring another patient’s issues while in ER room 20. On July 9, there was a young adult who was in a hallway bed right outside my dad’s room. She was clearly going through withdrawal from drugs. She was agitated, crying, hysterical, demanding drugs, and wandering around. I found this so upsetting as I did not know who to focus on first, my dad or what was going on in the hallway. I have no doubt other patients and families were facing vicarious trauma from listening to this for hours. Naturally patients addicted to substances need compassionate care, but this care needs to be in a different location within the ER, where other patients do not feel threatened by what is happening outside their ER room. I experienced this same issue during our April 2025 ER visit, but this time the issue seemed ten times worse.

In closing, I would like to hear how this information will be relayed to Dr. WOW and all your ER physicians. Patients and families come to you for help. No one knows their loved one better than their family, and the insights and concerns of family caregivers must be considered when making healthcare decisions. Older adults are the foundation of our society, and I expect the healthcare institution that I choose to care for my parents to value this greater generation and partner with me to ensure not only their medical health but their overall quality of life. 

The medical data may indicate one thing, but even a minor virus can be deadly for an older adult and their well-being and safety to return to the community should be part of any ER assessment. There was no regard for my dad’s safety or my own when he was discharged on July 10 at 4am. Many thanks for your time and attention to my letter. I look forward to hearing from you about my concerns.