Posts Tagged ‘street medicine’

When I was younger, I remember driving in the car across the country with my parents. I spent most of my childhood living in Kansas and Indiana but spending major holidays outside of Pittsburgh. This meant many long car rides and my mental curiosity (and predilection for asking endless questions) meant a constant stream of conciousness in the car (God bless my parents). I remember traveling down some road just off the interstate looking for a place to eat and passing a sting of ‘hotels’. I asked my parents if we were sleeping at each one- one after the other and of course the answer was no. In hindsight, they looked like aweful places to sleep with there run down fascade, their “No Vacancy” light that is missing the N, V, C and Y, their broken down cars in the parking lot and a predilection for worn out lawn chairs adorning each side of the door. How welcoming. My mother called these a ‘No-Tell Motel’ and it was only after I got older that I knew what she meant.

Most of us probrably think the same thing when we pass by these establishments that offer a cheap weekly rate, bring your pets, bring your cigarettes and whoever else you want since the front desk clerk seems to only be half in this universe and half somewhere else. An inherant bias that nothing good is happening behind those closed doors and the people who reside there are either up to no good or don’t have anywhere else to be. And afterall, idelness never leads to anything good. To be fair, I have stayed in some of these establishments in my travels and can report that nothing ill befell me, but the sour taste still remains even after plenty evidence of the contrary. Old habits, as they say, die hard.

Below is a story from Brett about how wrong we may be about the goings-on in the local No-Tell Motel. It has been edited with his permission and all relevent names have been changed.

Tom * is a 70 guy who wound up on the street medicine service after i discovered he was homeless during his nursinghome stay a few weeks ago. He worked as a truck driver his entire life until 2008 when he retired. He initially had an apartment after he retired but developed gangrene in his right leg requiring an amputation and a necrotic left heel ulcer requiring multiple surgeries. Almost all of his medical issues are related to his uncontrolled diabetes. He’s been in and out of Lehigh Valley Hospital and St. Luke’s for almost a year and was unable to keep his apartment as a result of his frequent hospitalizations. (kind of challenges that whole notion that the homeless are just alcoholics who eventually had to pay the piper huh?) He does get about $900/ month in social security, but the lowest cost apartments are $700/ month and his meds cost over $200/ month. With no support system, no family, and only 1 friend in a similar situation as his own, he became homeless.

After a recent hospitalization, he was discharged a few weeks ago from a local short term rehab facility to a “no-tell” motel. I pass this motel often and think about how horrible it looks, and the bed bug infestation that must be occurring as I drive by. My suspicions were confirmed by reviews of Trip Advisor and I wonder how anyone would let a human they cared for stay there. Not only is Tim 70 years old with severely uncontrolled DM but he also has a severe tremor making it impossible to check his own sugars. The rehab facility discharged him to the motel with all of his meds, but no supplies to monitor his sugars even if he had the ability. He also had no hime care services set up- no visiting nurse, no meals on wheels.

I visited him the day after discharge and brought him diabetic supplies and supplies to care for his leg wound. I was appalled at the condition in which he was living. He had no access to food and was living off pizza from the shop next door. His fluids consisted on soda from the machine outside his room. The bottle then became a urinal and he had multiple bottles of urine stacked up by his bed. He assured me he would be ok, which of course I didn’t believe, so I returned the next day. Upon my return I found him and his room covered in vomit and he looked like he was going to die. I checked his blood sugar and the meter read, “HI,” meaning his blood sugar was greater than 600. He adamantly refused to go to the hospital because he, “had it with those people and would rather die.” I cleaned him up and brought him some food, but despite my pleading, he stayed.

I called Area Agency on Aging, the VNA, and the Conference of Churches, anyone I could think of who might be able to help me. Two days later I returned to find him looking MUCH better. It turned out that over the past two days the motel clerk and another motel resident had been helping to feed and bathe him. They dressed his wound with the supplies I left, administered his meds to him, and cared for him like a family member. A few other motel residents who were diabetic were coming to check on him regularly.

I thought about community building that occurs when one is all alone, similar to the communities I find in the encampments. If I give a sandwich to someone who is hungry, they will always share with their friends. I don’t know if the same type support and love shown for my patient would have happened at the $200 a night hotel down the street. I realized my own unconscious bias for this motel and will never look at it the same again and I give credit to the fellow inhabitants of the no-tell motel who supported this man when our system let him down.

I stand corrected.

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In the Spring of 2013, Brett came across a conference being held in Washington, DC a few weeks later. We scrambled with our employees and our families to find coverage for the many hats we wear and off we went to the National HealthCare for the Homeless Council conference.  I have been to many, many educational conferences in my professional career and I can say that up until that point, none of them would be described as life changing.  Prior to our attendance, we had been running the DeSales Free Clinic since 2007 but had not really met other people who were doing the same things. Two things happened at that conference that changed the trajectory of our lives.

First, we were able to see that what we had created at the DeSales Free Clinic was as comprehensive and well thought out as many of the programs who were presenting their healthcare models at the conference. We always felt in our hearts that what we were offering was logical and right but we really had nothing to compare ourselves to. The second thing was that we were able to meet all of these people that were offering healthcare to their homeless population in ways we had never even thought of.

It was like a mental explosion.

I remember sitting at a restaurant with Brett after the conference was over.  We made a plan at lunch that day about what we wanted homelessness medicine to look like in our area. It was suddenly blinding that what we were doing was great but there was SO MUCH MORE that needed to be done. More people, more locations, more populations, more awareness. For both of us, a sudden and sharp vision (blessing)was born.

We wanted to start with developing a Street Medicine Program. We don’t really know how to do anything small and so considering starting something in a logical-one-step-at-a-time method is a nice theory but we know we’ll blow it right out of the gate. We knew that the biggest job was two fold- 1) convince important decision makers that the Lehigh Valley has a homelessness problem and 2) Get buy in for this never-heard-of-it-before type of medicine called Street Medicine.

A few months after the NHCHC conference, we attended the International Street Medicine Symposium in Boston, MA. Again- mind blown. The benchmark program- Boston Health Care for the Homeless Program- hosted the conference and I thought our heads were going to explode on the car ride home.

Today, Brett starts as a full time Street Medicine PA in the Lehigh Valley Health Network Street Medicine Program. He has worked tirelessly at the hospital and had more meetings in the last year than I think he ever thought possible. It’s funny but Brett is more of a do-er and less of a talk-er but he knew that he had to get people to see the vision as clearly as it lived in our heads. He met with grants people, finance people, security people, mechanics, community partners, HR, PR, IT, development, department chairs, managers…he learned about departments that we never knew even existed. And amazing people who were willing to help in any way that they could to give this idea legs.  Their eyes were opened and all of a sudden, they couldn’t imagine why we hadn’t thought of this sooner. He did lunch meetings, breakfast meetings, stand in the hall and chat meetings. The goal was to create an idea so big that once your ready to ‘go live’, it would be nearly impossible to stop. Their eyes were opened and all of a sudden, they couldn’t imagine why we hadn’t thought of this sooner.

Everyone has a different dream and I feel like very few get to wake up and do what is living in their heart all day. There is a pure joy that escapes unabashedly out of a person when they are doing what they love. Today is that day for Brett.  Dream big or don’t dream at all.

” It ain’t about the money you make, when a record gets sold, It’s about doin’ it for nothin’, ’cause it lives in your soul.”  – Eric Church

The weather has always baffeled me. In a strange way, weather has a way of forcing you into the next phase of the year, ready or not. Saturday had temps in the 90s with humidity so high that it made my normally very straight hair resemble the before shot of an antifrizz hair product commercial. Heavy rains came Saturday night and just like that, Fall arrived. Football, crisp morning air, windows open.  

Last Fall, Brett and I attended our first Street Medicine Symposium in Boston. The Boston Healthcare for the Homeless Program has been the program that all others compare themselves to. It is a huge, well established program that has the most comprehensive programs, resources and street teams. The tentacles of this program seem to reach into all the parks, shelters, hospitals etc. To say we learned a lot would be a stupid understatement.  I recall having a conversation with Dr. Jim O’Connell, president and founding physician of the Boston program.  We were talking about funding (of course) and I said I was amazed at the multi million dollar budget of his program.  He inquired as to the budget of the DeSales Free Clinic and the scope of services. After I told him our annual operating budget was $15,000 he response was ” jeez, we must be doing something wrong if we need so much money”. We then talked about how we operate on limited funds. This is the attitude in Street Medicine – no matter how big or small your program is, fledgling or benchmark status, we can all learn from each other.

A unique feature of these conferences is participating in street rounds with the hosting institution. We really got to see how the pros get it done. I was rounding with a case manager who was looking for one patient in particular- John. She had not been able to find him for the last two weeks and was worried about him. We checked all the usual places that he hung out. We met his street friends who had much to tell us – except for where John was. And so our search continued.

It was about 6pm and downtown Boston was bustling with people leaving work. The streets and the crosswalks were very crowded, horns blaring, quick feet. At a particularly busy intersection, we began to cross just as we see a large dip form in the sea of humanity. As we approached, we saw that our lost patient- John- was right at our feet.  Wheelchair bound, he had lost his balance and tipped right out of his wheelchair and onto the ground. I was impresssed at the number of busy Bostonians who stopped to help him and make sure traffic would not hit him when the light changed to green. We scooped John back into his chair and moved him to the sidewalk. 

John was a rather imposing figure, both in size and in scowl. When you close your eyes and picture a chronically homeless man on a wheelchair, you are likely picturing John. Standing, he was most likely over 6 feet tall. He was wearing many layers of well worn and tattered clothing. He had on an old navy blue winter hat that was a little lopsided so only one eyebrow was showing. He was missing most of his teeth and had a rosy hue to his deeply wrinkled skin. He was not particularly friendly toward me and answered the case managers questions in a short and gruff tone. Yes he had been drinking. No, he didn’t need anything. No, he wasn’t hurt. Then she asked if he was hungry- and for a second, the fiercly guarded wall came down. He was hungry, and thirsty too.  He hadn’t eaten in several days. 

While the case manager went into a Panera Bread, I had a chance to talk to John (or attempt). I started by trying to figure out if he needed anything else since it seemed the peace offering of food had opened the door just a smidge. He told me part of the reason he had a hard time eating despite the available soup kitchens and food vans was that he had a peanut allergy. A severe peanut allergy. Imagine the great lengths moms across America go to in order protect their childreen from inadvertant peanut ingestion. There is even a service through my children’s daycare to find them a playdate with a child whose allergies match your childs ( think match.com but for kids with allergies). Before John, I had never considered what it would be like to have a food allergy on the street. I asked him a few questions about his peanut allergy and then, apparently, crossed the threshold of number of questions allowed.  

I had squatted down to talk to him. Being at the same eyelevel of someone who is wheelchair bound (homeless or not) is extremely important for leveling the playing field. Suddenly, John looked angry. He was nose to nose with me and yelled with a slurred speech, ” Do you reaaaaaaallllllllyyyyy care?” Pause. ” Well, do ya?!” I told him that I really did care. He looked away and muttered, “Well, I don’t know why.” 

There was they key to this whole interaction. Imagine wanting to be helped but feeling inside that you are so worthless that no one in their right mind should want to help you. Therefore, you prophylactically refuse the help because somewhere inside of you, you believe that you are protecting yourself from the inevitable. The dissapointment you will feel when the person decides you aren’t worth it and that they don’t care. Self preservation is a vital survival tool when living on the streets.

We walked with John to a location across town that he liked to hang out ( we had actually been there earlier that day looking for him). He was greeted warmly by his street brothers. A fleeting smile crossed his eyes (but not his lips). As we walked away, I turned back to see John breaking his sandwhich into four pieces – one for him and one for each of his street friends while they passed the bottle of newly purchased lemonade around. A reminder that the parable of the fishes and the loaves is lived every day on the street. 

 

 

Yesterday afternoon, a few of my co-workers and I were walking to a picnic held on the DeSales University campus. We were admiring the beautiful weather and the beautiful surroundings. Despite my love for the urban and rural homeless population, I have to admit it is a quiet retreat to spend time on this beautiful campus of rolling hills and beautiful fields.We noted a tree that was already changing it’s leaves. This launched a whole discussion about how everything is in a hurry- A.C. Moore already has Christmas decorations for sale and emails are jamming my inbox with taglines reminding me how many Fridays are left until Christmas. I, for one, have never really enjoyed winter. If the weather could stop at late October and blend right into April, I would be happy. The prediction for our area this year is another unbearably cold winter with higher than average snowfall. Putting my own last winter-related, generator-finding-polar-vortex-enduring PTSD aside, I think to the other work in my life.

It was a Sunday at the end of February 2014.   Brett’s cell phone rang and it was Jackie, a parish nurse who works with Brett at the Soup Kitchen Clinic. She was calling because she had a patient with her who was desperate to find someone named Corinne who normally takes care of him. She wanted to know if Brett knew who this Corinne person was. Much to her surprise, he passed the phone to his right and she got her answer. It seemed that Kevin* had been asked to leave the homeless shelter he was previously staying in. He had violated one of their rules and as Kevin said, “That was that.” He was out of medications but more importantly, he was out of shelter . The only other place to find shelter was over full and Kevin had been denied entrance the prior two nights. The temperatures were drastically low and he was scared and cold. He had only been able to take the belongings that he had near his bed. All of his items in storage, he told me, were discarded. Imagine the attachment you would have to your belongings if you could count all of them on your own two hands. More concerning, Kevin suffered from incontinence. Not having a reliable place to use the restroom and clean clothes to change into worsened the situation.

Kevin has been my patient for the last two years. He comes to the Clinic religiously every Tuesday for a blood pressure check. The blood pressure check almost always reveals more information about his week, his life and his other medication conditions. Despite his chronic incontinence, he always smelled like cologne. Kevin was compliant, he was never late for an appointment I had set up for him and he never ran out of his medications. He is talkative, polite and wonderful with the students. He had often told me he liked helping the students get their education. The students felt responsible for Kevin, but Kevin also felt responsible for the students.

Kevin and I agreed to meet on Tuesday. I went to my PA students and explained Kevin’s situation. Most of the students knew him from the Free Clinic and were deeply saddened to think of him sleeping on the street. I could see it in their faces- homelessness just got real.

Being that Kevin is a very tall man, finding clothes for him would be difficult. But the students rallied and came up with clothes, toiletries, snacks and other things they thought he would need. I arrived to meet him a few minutes early. In a strange change in weather, the polar vortex had given way to an unseasonably warm that day with a high of 62. I had not even worn a coat as I walked from my car to the building and I passed a few overzealous locals in shorts and tank tops. A few minutes later, I looked out the double glass doors to see a man dressed like the Abominable Snowman. He was struggling with the heavy doors and as I walked closed to help him, I realized it was Kevin.

Everything he owned was literally layered on his body or crammed into a messenger bag that was ripped down one side. Over the course of 10 minutes, he removed from his body 4 winter hats/hoods, two pairs of gloves (both ripped), a puffy winter coat, a leather jacket, a windbreaker, two sweatshirts, a button up collared dress shirt and a long sleeved t-shirt. He had on three pairs of pants, all of which were soaked with urine. What bothered me more than his layers, was his facial expression. Minimal eye contact, soft voice. No smile, no light hearted upbeat Kevin. The Kevin was lost, buried in the pile of clothes sitting beside him. A sadness filled his eyes. He told me he was so embarrassed for me to see him this way, embarrassed to walk the streets literally wearing everything he owned. He didn’t know what to do, where to go. He was desperate. Then his phone rang and it was his mother. She wanted to talk to me. I could hear it in her voice. She begged. She pleaded. “Find him somewhere to sleep tonight! Please! Why isn’t there anywhere else for him to go? Where are all the other people who are homeless?” Her questions were valid. Her frantic tone of voice was justified. Her disbelief that we have nowhere to put our homeless at night. I apologized, I justified, I rationalized, I validated. But in the end, I had no answers.

Then it was my turn to beg and plead. Could he come home to her? Were there resources for homeless in her town? Could she think of a family member, a friend, anyone who would take him in? All the answers were no. And while she wouldn’t elaborate as to why, I could sense that her answer was non-negotiable. There was no answer for Kevin that night. He had nowhere to stay and nowhere to go. It was gut wrenching. As a health care provider, I felt horrible. As a mom, I cannot imagine laying in my bed at night wondering if my son was sleeping outside in the cold. As a friend, I felt helpless. I could work no miracles that night. He slept outside behind a YMCA and waited for another day.

Eventually, we were able to convince the shelter that had asked him to leave to reconsider their decision. Kevin was permitted to return to the shelter and has been diligently working on filling out government paperwork, attending doctor’s appointments and applying for housing. Last week, he proudly reported that he had work with a local resource to update his resume and had interviewed for three jobs. Progress was being made and I am so proud of his recovery trajectory. As summer fades to fall, I know that Old Man Winter is waiting just around the corner. He lurks and just when you have almost forgotten the bone chilling cold that makes you want to pack up and move South for good, he snaps you back into His frosty world reminding me that “Walking In A Winter Wonderland” could have only been written by a person who was housed.

 

I have been working weekly at several nursing homes in our area for the last few years. I could spend an entire posting talking about how I think our elderly nursing home population ought to fall in the ‘underserved’ category but I will spare you that soap box for today.   I am extremely grateful to have bosses who understand my predilection for the homeless population and for leaving no stone unturned when I’m interviewing patients. It never ceases to amaze me that was the right series of questions you can uncover a world of hurt that the patients been through. When we close our eyes and picture a typical nursing home patient we are stuck with an image of grandma- with her tight rows of freshly curled hair resulting in the beloved (and highly flammable) grandma-helmet-hair. Or maybe a shuffling old man proudly sporting his WWII VFW hat with pins from his uniform.

You are far less likely picturing someone whose reflection resembles yours.

Many of my younger patients have lived in our nursing home system for quite a long time for one reason and one reason only. No one realized they were homeless at any point during the hospital stay or early on in the nursing home stay. Once they started to complete the rehab goals, the social services team comes to the realization that there is no discharge plan. I sometimes referred to this phenomena is the “fog of war- medicine style”.   After 9/11, George W. Bush made many decisions that he later reflected upon in his book “Decision Points”. He realized that perhaps they were not ultimately the best decisions, however, he felt he had done the best he could with the information available and the time allotted to make the decision. He cited the fog of war it during the decision-making process. This is common throughout history and no one really (successfully) faults people for it.

This phenomena also happens in medicine.

It goes like this: Patients are banged up, super sick or maybe have had a decompensation an otherwise chronic stable medical condition which leads to the hospitalization. In the world of hospital medicine, length of stay in the hospital is looked at very closely. In the haste of making a reasonable discharge plan there’s often a lot of questions that frankly just aren’t asked for a variety of reasons. Case managers and medical teams have a difficult job and are often asked to do the impossible. But sometimes, I think we don’t dig deeper into the answers our patients give us about their living situation. For example, patients often say they are going to live with their friend after discharge. At face value, this sounds great. Discharge plan complete. Until you ask if they have talked to their friend about this plan. Often, the answer is no. Or, another common scenario- a patient says they were living with a brother, sister, friend etc. prior to coming to the hospital. Somehow, this is translated by the discharge team that the patient will be discharged back to their prior living situation. No one asks, and the patient doesn’t mention that they can’t or don’t know if they can return. The patient is discharged from the acute care setting (hospital) to their short-term rehab facility and everything seems great until a simple question like “Hey, where you going next?” is asked. The response – a blank look from the patient and then silence sets in.

In the time that Brett and I have been in the nursing home system, we’ve noticed a large variety of patients whose social situations and living situations perhaps were tenuous at best prior to hospitalization. Homeless or not, many people’s social support is based on superficial interaction. Hanging out, watching TV, playing card, shooting the bull (not to be confused with cow-tipping. I am from Indiana after all). In the face of acute illness, that social ‘support’ is tested and often disappears when these patients need the most. The couch is suddenly unavailable. The car has been repossessed because of missed payments. The housing has dried up. Perhaps your truck driver who is now an insulin-dependent diabetic or perhaps had seizures and is no longer allowed to drive the truck. Not only does this person suffer from a loss of employment but many truckers sleep in the cab of their truck. They don’t have permanent housing because they live a life on the road.

A few weeks ago, Brett and I asked case managers from three different nursing homes in three different parts of the Lehigh Valley how many patients they thought were homeless in their facility. Without consulting a census or really doing anything scientific, they came up with 22. That’s 22 patients who have absolutely no where to go if they were to be discharged right now. This is astonishing. What complicates the situation further is that case managers who work in skilled rehab facilities don’t have the training to find housing for patients who are homeless. This isn’t a typical part of any case management training and is purely learned on the job or because of personal interest. And therefore the patients who are easier to move out of the nursing home seem to move out of the nursing home. The homeless patients tend to sit … hang out… and stay. There’s nowhere for them to go and no resources by which to move them.

The Point In Time (PIT) is a physical head count of the homeless on one given night that is universally chosen. Over 3000 cities participate in performing the PIT on this date in an effort to count the homeless and attempt to extrapolate trends about homelessness in your area and nationally. The data is reported to the U.S. Department of Housing and Urban Development (HUD). While HUD says it “does not directly determine the level of a community’s grant funding” (hud.gov), it is required information to report when applying for HUD funding. It would be hard to imagine that those numbers are not somehow taken into account when determining distribution of funding. It is not a perfect sampling tool by any means (a different soap box for a different posting) but it is concerning that these ‘nursing home patients’ are unaccounted for. These are patients that if they were not in a nursing home would be in one of our shelters, on the street or perhaps (if lucky) squeezing out another couch to sleep on. In essence, they should be recognized and counted.

In the last post, I talked about recognition of existence in the context of being a fledgling street medicine program. This same concept applies here too. In order to properly allocate care to the homeless, we must first know where they are. To know where they are, you have to know where to look. The homeless are all around us, hidden in plain sight, waiting to be recognized.