December 15, 2025

Monday, December 15, 2025

Monday, December 15, 2025

Tonight's picture was taken in December of 2004. Mattie was two years old! My mom always sent Mattie a new Christmas sweater every year. Mattie would wear this sweater and pose for a photo that would be featured on the front of our family holiday cards! By age two, Mattie understood the whole notion of photos and once our tree was up, it was time to snap photos of Mattie. This was one of many taken that year. It wasn't the one featured on our card, but nonetheless, it was a cutie! When I look at this tree, I see the tree skirt and the ornaments. All of which I still have, it would never have dawned on me in 2004, that years after this photo was taken the only thing left of my family would be the tree skirt and ornaments.... Mattie and my marriage disappeared. As if they never existed. When I receive holiday cards in the mail and see happy faces, and children all grown up, I can't say it doesn't pain me. It leaves me asking why is everyone living their lives, and mine has been destroyed?


Quote of the day: I wish I could press rewind and bring you back — just for a moment. ~ Unknown


Before I tell you about the nightmare of today, I wanted to show you a photo of Mattie's beautiful memorial tree... a white swamp oak. Something told me yesterday (before I knew my dad was going to get discharged!), to go visit the tree when I had the time! Thank goodness I did, because now my hands are tied. Despite Sunday's cold temperatures, I added 15 Christmas ornaments to the tree and tied a red ribbon around the tree. NO MATTER what I have going on, I want Mattie to always know his mom remembers! 


I truly did not know my dad would be discharged on Sunday! I thought I would have a few more days to get things done like grocery shopping and the Foundation's newsletter. Now I have time for nothing! 


When I was married, I used to have Blanca come and help me clean our house every two weeks. I have known Blanca since 2008, when Mattie was diagnosed with cancer. My neighbor introduced her to me, and he felt I would need this help because I was rarely home, yet our apartment needed cleaning and organization. So I met Blanca when I was under great distress! She got to know Mattie! I can't tell you how she cried when he died and even now, when we reflect on him, it pains her with what I have and continue to face. Blanca and I have been through many ups and downs in each other's lives. Now given all I am juggling, I am lucky if I have Blanca over once every two months. I had scheduled her to come today and I did not want to switch dates, but I warned her I would be home and she would have to work around us. 

So between cleaning going on (not being able to find a quiet space) and managing my dad, I truly thought I was going to jump out the window. My dad is in severe pain, and as I mentioned yesterday the hospital forgot to send a script into the pharmacy for pain meds. UNETHICAL on every level. His pain level is almost bordering on too hard to manage at home. He has lidocaine back patches, which are doing nothing, and I have a heating pad on his back! Given his brain bleed, he can't take Advil, which would do a whole lot more than Tylenol. There is something very, very depressing about being quarantined at home, with someone screaming in pain, disinterested in helping himself by moving his body and walking. I have noticed another level of cognitive decline in my dad with this hospitalization. I am hoping that with more time at home, and finding a way to address this muscle pain, that things will even out. 

Then adding to this mix, a friend of the Foundation wanted to stop by to drop off a holiday donation. Very kind, but very difficult for me. I truly limit my socialization with the outside world. When I wonder why I do this, then a day like today happens, and I am reminded why! Why? Because I get to see my dysfunctional life through someone else's lens. I can see how my life scares people and also I can see people questioning..... why do you give so much to everyone, and care so little about yourself?! 

In the midst of chaos today, I wrote a letter of complaint to the hospital. I felt things needed to be documented. I included it below in case you wanted to read it. It is now 9pm, and all I know is my own back is killing me from helping lift my dad and holding onto him so he doesn't fall. The next two days, he has doctor appointments. Which I also find hysterical! He was just released from the hospital and is in bad shape..... how do they expect this 90 year old to get to these appointments? The answer is THEY DON'T CARE! It is my problem and the only way I can transport him is by using Mattie's wheelchair. My dad is unable to walk very far without screaming in pain. Thank goodness I kept Mattie's wheelchair over all these years.... even now, Mattie helps his mom! 


Letter to the hospital..........................

Dear ABC Patient Relations,


I am writing to express my concerns about my dad’s recent hospital admission. I am my father’s medical power of attorney. My dad, is 90 years old and has moderate stage dementia. He was admitted to your hospital, through the ER, on Sunday, December 7, with a brain bleed. Though we live outside the beltway, we consider ABC our medical home. This year alone, my dad was admitted to your hospital three times. I will bullet point the issues below and I would like to specifically know how each of these issues will be addressed.

  • My dad was in Room 318, and on Sunday, December 7, my dad was transported to have an x-ray at 5pm. Typically I go with him for his scans, but I was unable to do so on that occasion. My dad was gone from his room for 2.5 hours and when I asked his nurse what was taking so long, she explained that there are not as many transporters available on the weekends. When my dad returned to his hospital room, he was very agitated, upset, and scared. When my mom and I asked him what happened and what was bothering him, he explained that the transporter dropped him off and he was left alone the whole time. In my dad’s mind, the transporter “died,” and he was going to be left in this “dungeon,” unable to get back to us. Since I was not with my dad, I do not know for certain what occurred, but it is clear to me that no one was present to alleviate his concerns. I am bringing this to your attention because patients who are vulnerable need much more oversight, support, and check-ins to avoid further confusion, anxiety, and fear. In fact, a chaperone should be available for such vulnerable patients. In any case, I would like your insight into how this can be prevented during future hospital visits. 
  • Throughout my dad’s admission, my mom and I were eager to get my dad placed in your Inpatient Rehab Center (IRC) once he was discharged from the hospital. My dad entered the hospital with no back pain, but with all the transfers from his bed to transporter beds and scanning tables, he developed significant muscle spasms and pain. Pain which he has returned home with, and we are having a very difficult time managing. While at the hospital, we shared our concerns with case management, nursing staff, doctors, and anyone who approached us about my dad’s care. Despite my dad making significant physical strides on Saturday, December 13, as he got out of bed, stood, and walked 15 feet with a physical therapist, he was still denied admission to the IRC. This was very upsetting for us to hear, and when we asked for the criteria used to make this decision, the only definitive answer we received was that from their perspective my dad would be unable to withstand three hours of therapy a day. We feel that this decision was made in haste and it was also very subjective. On Sunday, December 14, Theresa (case manager) entered my dad’s room and bluntly told us that my dad was denied placement into the IRC and instead presented us with two Skilled Nursing Facility (SNF) referrals. My mom and I proceeded to ask Theresa questions, explained to her that we were not interested in a SNF placement, and then wanted to know the specifics regarding why my dad was denied into the IRC. We were insistent, specifically because we saw the great progress he made on Saturday. Theresa did not like my tone; she did not like me questioning this decision and proceeded to walk into the hospital hallway and within minutes two hospital security guards were in my dad’s room. They escorted me out of his room, and wanted to talk with me, as Theresa implied that I was verbally abusive and threatening. I never cursed at Theresa; I never moved near her or touched her. I proceeded to tell both officers the medical ordeal we have been through these last seven days and shared that I am the full-time caregiver of both of my 90-year-old parents. The two officers immediately could recognize that I was just a distraught, overwhelmed, and passionate daughter and caregiver. If these two officers could assess this quickly, why couldn’t Theresa? It was completely inappropriate for her to call security on me. You may ask any of the nursing staff from 3A about me, as I was never abusive to a member of your staff, and in fact pulled 6–8-hour days in the room each day trying to help and meet my dad’s needs. I would like to make a formal complaint about Theresa. As a fellow licensed mental health provider, I view her behavior as totally out of line. Families of patients are going to get upset, angry, and advocate strongly. That is our role… to love, protect, and ensure the highest quality of care for our loved ones. It saddens me that Theresa showed no empathy, no compassion to me or my mom, and did not use intentional listening skills to form a connection with us, to help the situation and to help alleviate our stress. Finally, I would like an apology from Theresa, and I would also like some assurance that no other family is going to be wrongly accused by her.  
  • My next issue relates to discharge. During the discharge process, I requested that home health care orders (for PT and nursing) be sent to XYZ Home Health. When I called XYZ this morning, they said they received no notifications or orders from ABC. I then quickly contacted Dr. A's office and requested that the script be faxed over. I am juggling a lot with my dad’s full-time care and pain management. It would have been helpful if I did not need to do this extra legwork. In addition, when my dad was discharged, new medications were prescribed and sent to CVS. In the discharge orders it says that my dad should take Oxycodone. However, CVS never received a script for that pain medication. Given that my dad is in significant pain, how ethical is it to send a patient home without the needed pain medication? If that was not bad enough, the medical team prescribed insulin (a drug my dad has never taken at home prior to admission). CVS received the script for insulin, but no script for needles. How is a patient supposed to take insulin without the needles? I will be visiting my dad’s primary care physician on Wednesday and will be discussing whether insulin is necessary. However, I think these two oversights are significant enough to be mentioned as patients and their families rely on your medical team to discharge us with all the necessary medications needed to manage in-home care.

Thank you for your attention to these matters. I look forward to hearing from Patient Relations about these issues and the steps being taken to remedy each one. 

December 14, 2025

Sunday, December 14, 2025

Sunday, December 14, 2025

Tonight's picture was taken in December of 2004. Mattie was two and a half years old and by that time, had some understanding about Christmas. As packages arrived for Mattie from family, I would store them under our staircase. But as you can see, both Patches and Mattie really wanted to explore those boxes! Patches was an amazing cat and truly she just got it.... as soon as we took Mattie home after he was born, she knew he was precious cargo! Mattie learned how to love and care for animals from Patches, and she was a great teacher! When Mattie was sick with cancer and in the hospital, he longed for Patches to visit. The hospital never allowed that to happen, even as it was his last request while dying. Something I will NEVER forget. 


Quote of the day: If I had a flower for every time I thought of you … I could walk through my garden forever. Claudia Adrienne Grandi


The past three nights, I have had very vivid dreams. Typically I am so exhausted that I go to sleep and wake up and have no memory of anything in between. But that wasn't true the last three nights. Each night, in some shape or form I had a dialogue with my former husband. Perhaps I will discuss this in another blog posting, but tonight, I wanted to share my horrific day! I truly wonder about the state of our healthcare system, and God forbid you are in the system without a family advocate..... because I can assure you the system is about numbers, data, and insurance reimbursement! If you don't meet numbers and insurance won't cover a treatment or stay, you will be shown the door! Even if it isn't in your best interest as a patient, and don't get me started about the family caregiver. The system cares even less about us!!! 

I would like to know why hospitals are so eager to discharge older adults and send them to a Skilled Nursing Facility (SNF, or plain and simple a NURSING HOME). With the frequency of their referrals to SNFs, you would think there is a financial incentive involved for the hospitals. Other than by getting rid of you, they check the box off that they helped a patient and now freed up a bed for another paying customer! Why was today awful? Because I had the unfortunate opportunity to meet Theresa, a case manager. She wasn't the case manager I had been working with all week. The original case manager doesn't work on the weekends, so I got Theresa instead. Theresa came in with a total attitude and said my dad was not accepted into the hospital acute rehab program and instead she presented me with a print out of two nursing homes willing to take my dad for rehabilitation. When my mom and I pushed back at her, trying to get specifics about why my dad was denied, she kept reiterating that we were already told why he was denied! TRUST me, I don't have dementia! No one reviewed the criteria with me as to why specifically my dad was denied. All they tell me is that my dad doesn't have the stamina for three hours of therapy a day! That is ridiculous, specifically since therapy is NOT back to back in acute rehab, there is time in between to rest! He could do acute rehab, but they weren't willing to give him a chance! 

Yesterday's physical therapy session, in my presence, went very well! That is because I know he can push through the muscle pain and I also know what he is capable of doing! I am quite certain if I had been present for the other physical therapy evaluations (which always happened before 9am!), my dad would have qualified for rehab today. But without me present, the therapists were hesitant to move him, as he moans and screams in pain. Part of it is naturally my dad and part of it is his dementia. He can perseverate on certain things and then blow them way out of proportion. They would know this, if they even consulted with me throughout the week. So note to self.... in the future, with any other hospital admission, I will demand that I MUST be present for all therapy sessions! Otherwise, we will face exactly what happened today. They see a 90 year old with moderate dementia, and truly the system writes him off. In fact, the hospitalist said to me at one point.... maybe your dad doesn't want to do the work and rehabilitate. Maybe he just wants to sit, watch TV all day, and relax. I am sorry...... if that is what this doctor wishes for his own dad at age 90, good for him, but my dad is capable of having a fuller quality of life than this doctor imagines. 

Any case, back to Theresa! Theresa did not like my tone when I asked for clarity about the rehab center denial and literally she went out into the hallway and called hospital security. I KID YOU NOT! Within minutes two very large police officers were in the room and escorted me out of the room. They then interrogated me in the hallway! I SWEAR I can't make this stuff up! They wanted my perspective on what was happening! I explained the whole situation calmly. By the time I was finished with them, they were on my side and gave the social worker a talking to! I under no circumstance ever threatened her, never cursed, and never moved toward her! I disagreed with her, and she did not like that! Seriously if she can't understand the anxiety, fear, and anger of a family caregiver regarding the poor discharge process of a loved one, then I think she needs to find another line of work! Working with something that doesn't have a pulse to be very specific! In all my life, NO ONE has ever called security on me, and as I told the officers my role is to advocate for my dad and when I see an injustice, I speak up and confront it. They understood immediately! 

So bottom line, I decided to discharge my dad from the hospital tonight and I took him home. He would decline at a rapid pace in a nursing home, not getting the attention he needed, and also given little to no movement each day. He will get more movement from me and also be in a non-clinical setting, which I think is more normalizing. Of course the burden and work are now on me. On discharge they reviewed all the new medications my dad was prescribed. One of which was insulin. Prior to hospitalization, my dad wasn't taking insulin, only an oral med. When I got to the pharmacy tonight, Stacey, our wonderful pharmacist said.... they did not prescribe needles to go with the insulin! She told me that if I paid for needles out of pocket that will be over $50, but with a script it is fully covered! DEAR GOD HOW STUPID ARE THESE PEOPLE!? While at the pharmacy, I contacted my dad's primary care doctor. I told him I wasn't getting the insulin and why! Why? Because in the hospital oral diabetes meds are not given to patients. Instead, every patient with diabetes gets insulin. However, now that my dad is home, the hospital wanted him to take his oral med and the insulin! I questioned this.... after all they never gave him both in the hospital and I never gave him both at home before! How do they know that this combination of drugs won't produce hypoglycemia (low blood sugar)? My dad's doctor agreed with me and so for now, we are holding off on insulin, until I see the primary care doctor this week. On top of which the hospital prescribed pain meds for my dad, but guess what??? They never sent a script to the pharmacy for it! This level of incompetence is too much for my mind and heart to handle tonight! 

It is now 9:20pm. My dad had dinner, I applied his pain patches on his back and attempted to take him up the stairs to bed. I know that sounds aggressive, but I want him to get back into the routine and fully use his body. Do note, that he has NO MEMORY, NONE, of being in the hospital this week or being discharged tonight. This actually works in my favor, because for all my dad knows, he has been doing this for the last week. Meaning, that he wasn't opposed to going upstairs. My goal was to see how he did on the first few steps. If I deemed him unsafe, I would have aborted the process. But guess what, with direction, and a couple of pauses, he got upstairs and into bed. I am very proud of him and my hope is he continues to make progress. His in-home care team (PT and nurse) will begin once again this week, and I am so thankful I already have these professionals to turn to, as they have worked with us now for two years!