Summer Vacation

Did I jump the gun? Is it too early?

I guess I might have taken an abrupt hiatus from blogging. It wasn’t intentional, but also wasn’t aimlessly forgotten.

Today I read a post of someone who said she disappears a lot and she talked about how that was okay. I agree with her. It is okay sometimes to not have anything to share, to take in the world, to absorb what others give, and hold onto it for yourself.

I have held onto a lot in the last week or two. And really asked myself a lot of questions. May is Mental Health Awareness Month, along with several more specific “Weeks” and “Days” sprinkled throughout. In the past I would pour my heart out in FB posts and urge awareness and stigma-destruction. This year, I needed to absorb it all.

I needed to see if the world was catching on. I wanted to believe that all our speaking out really meant something. And it is hard. It is not easy to see the impact of it all in the midst of growing mental illness crisis in our communities.

I ask myself, is this blog just here for me to produce mental health awareness? Or do I talk about the trivial things too, like the fact I joined a dating challenge this week? Does either mean anything?

I don’t intend to sound negative. I know there is meaning in any attempt to connect and relate with the world around me. It is just difficult for me to talk about seemingly menial things when there is so much to be said about the things that truly matter.

So when I get done with this mental vacation, we’ll see where I land. Til next time!

**oh and also, if you want to send me potential men to date, my DM’s are open LOL #challengehomework

Summer Vacation

To The Core

So much is going on in our social and political climate today that is matched with public commentary from all sides. I struggle to voice my opinion on these matters for several reasons.

I made two major decisions as I matured from adolescence into adulthood. One, I would stop being fake and hiding behind a mask. And two, I would not share or dispute my core values and beliefs with the world at large.

These may seem like contradicting rules of behavior. I think they are actually complementary. What I gain from vulnerability in being open to those that want to see the real me is actually empathy and tolerance for those that differ from me.

This is not a perfect science. Occasionally, I find myself in a discussion that lends to “opening a can of worms” in terms of debating controversial topics. I do have to remind myself restraint is more in line with my core and I pull back to sharing my experience rather than my opinion.

That is the key I think.

What we need more of is sharing our personal experiences and less of arguing our personal opinions. When you can truly understand a person’s journey in life, the core beliefs take shape without even voicing them.

And it leaves the door open to drawing conclusions about your own life. I have held strong to the thought that two people discussing a deep-set value which is opposite from the other person will never be productive in changing either person’s mind. Debate of controversial topics will only further ingrain the existing opinion of each person. It serves no purpose.

But when we share our experiences with no agenda, we unleash a new world where people find similarities and differences can exist, and both sides can coexist.

The battle within me to stand up for the things I care about is not an easy thing in this realm of blogging. I don’t want to be silent. I don’t want to let the intolerance of the world and comparison game to hold me back.

So I will not back down from sharing who I am, through life experiences. And I will never impose my beliefs on anyone who reads my blog. My hope is anyone who reads my writing will be influenced positively, even to the core.

To The Core

Lull After the Storm

It is severe weather season in Oklahoma where I live. Every year around this time, the daily weather report comes out and usually contains a heads-up warning of when to be weather-aware for impending storms that may produce dangerous conditions.

The days leading up to the storms are filled with anticipation, mostly from the meteorologists and storm chasers. They are amped and ready to go. Eventually, the conditions develop and the minute-to-minute coverage begins.

As the storms start to spark up to my southwest, I take the tv off of mute and watch, listening for any signs danger is heading my way. I stop scrolling Facebook and instead jump back and forth between the national Mesonet radar and news channel radars on my phone. Rarely does “the” storm come through my neighborhood. In fact, it hasn’t happened yet.

But the activity and hype certainly dominates my time. Family group text and random texts from friends are filled with check-ins and commentary on the weather reporting. All is a buzz for the few hours leading up to the storm front blowing through. Coverage lasts until the storms pass the viewing area and move on to the next news station and the next set of people who are just starting the process I am finishing up.

And then there is the lull after the storm. It is an eerie quietness – the tv is put back on mute, the texts die down almost from exhaustion, and I suddenly realize it is 11pm and I haven’t had dinner.

This happens in the course of our lives too, and I am not talking about weather. We start to see the signs of burnout, mental stress, and circumstances all pointing to the conditions needed for a potentially dangerous situation (PDS as our weathermen like to call it). Sometimes it hits us out of the blue but as we get wiser to the symptoms and we keep our eye on the radar of our lives, we can prepare that safe spot to go to and ride out the storm.

Last week was a PDS for me. Days prior, I received a new assignment for cleaning up a work project that was in addition to my 8 other projects, knowing 3 of them were needing to be finished by the end of the week. It was the final week of public accounting busy season. All the indicators of stress and mental struggle were showing in the disarray of my house and building up laundry and dishes. Friends and family were reaching out about impending crisis and wanting my input.

I weathered the storm. I shifted my energy into writing and produced five days of content that had been held inside for a long time. I stayed focus on my work tasks and gave myself grace on the housework. I kept going to therapy to offload everything that was happening. My mental health safe spot was ready and equipped with everything I needed.

You may have noticed I didn’t post anything this week. And I think there is a good reason for that. I think the lull after the storm is just as necessary as all the activity that happens when the storm is raging. We use it to pick up the pieces and process. And that is exactly what I did.

I have refocused and reorganized my work to do list. I have adjusted to the decrease in hours that will remain until the next busy season. I pulled out the trash bags and the vacuum cleaner, loaded the dishwasher and gathered the laundry. I checked my mailbox and opened my daily planner again.

I am not sure when the next round of storms is coming but I am ready. What I do know is out of every storm comes inspiration to do more and do better the next time. I truly hope I keep the motivation to fulfill those inspired thoughts. “Stay weather-aware” has taken on a whole new meaning for me now.

Lull After the Storm

Day 5: Discharge

**This week’s blog posts are dedicated to advocating for effective mental health treatment and educating patients, family, and friends in all areas of inpatient psychiatric care. The perspectives shared here are not that of a mental health professional, but rather someone with lived experience. Information shared may not align with every circumstance or viewpoint of readers, but is meant to offer guidance in an area that is often confusing and holds little resources.**

When the day finally arrives for the patient to be discharged from the hospital and return home, reactions from everyone involved can vary tremendously. The most common reaction is worry. Is she really ready to be released? Will he stick to the treatment plan? Am I being honest about feeling better to the hospital staff or do I just really want to leave and be in the comfort of my own home? The typical length of hospital stay in the United States is now a week or less. Is this enough time to assess, treat, and stabilize a person who was a harm to themselves or others just last week?

I have spent the majority of this week focused on practical matters to consider when you or a loved one is in inpatient psychiatric care. While I still want to provide that today, I feel there is a significant elephant in the room that needs to be discussed as well. For that reason, the second part of today’s blog will talk about the possibility of readmission due to inadequate length of stay in the hospital.

Getting out of the hospital may seem like the top goal in the minds of family and friends, but even more so in the mind of the patient. While there is the occasional patient who feels safe and comfortable and want to remain in the hospital longer, for the most part, asking when they will be released comes up regularly during their stay. Be aware that in any situation involving suicidal thoughts, plans, or behaviors, legal involuntary hospitalization becomes a factor and when to leave the hospital is not something the patient can decide for themselves.

Several factors appear to influence the length of stay for a patient. Mental state, including suicidality, are assessed continuously and weigh into the decision. Unfortunately, one of the other factors at play is the approved length of stay for the individual’s insurance policy whereby payment is agreed to be made. I have encountered a person who had been in hospitals frequently and said their stays were always exactly 9 days, regardless of how they were doing, when they realized this was the maximum number of days insurance paid. In any case, the date of discharge is largely out of the patient or family’s control.

In the days leading up to discharge, the facility will work to satisfy requirements for release. This includes scheduled appointments for follow-up outpatient care with a psychiatrist and therapist. The timeframe these must occur varies from state to state and even location to location, but typically a psychiatrist visit is set for within a week of discharge and a therapist within one month of discharge. This is in order to transfer the prescribing of medications to an outside doctor. In some cases, patients do not have the funds, transportation, or support system to make it to these appointments, thus having no refills of medications used to stabilize their condition, and starting what has been coined “the revolving door” effect.

As far as practical advice, here is the little I have to offer: Maintain expectations – The purpose of inpatient care is to address the immediate need of safety of the individual or others. It is not to see through to complete recovery of the current condition. This means, for the most part, people leaving a facility will still have many depression and anxiety symptoms that need to be addressed. Do not expect this person to re-enter their daily routine of work, child care, homemaking, or social lifestyle. While it is important to try and create an environment of normalcy, don’t carry any expectations and instead take cues from the person who was in crisis as to level of activity. It is sometimes helpful to transition slowly by maintaining the same schedule they had in the hospital for several days and focusing on setting up the treatment plan.

Below is some fascinating context provided for a large-scale study on readmittance of psychiatric patients within 30 and 180 days of discharge:

  • In 1955, the peak of state hospitalization, there were 560,000 beds available for an estimated 3.3 million American adults living with serious mental illness and other disabilities. By early 2016, after more than half a century of deinstitutionalization, there were slightly fewer than 38,000 beds for 8.1 million people with the same conditions.
  • Psychiatric hospitalization is the single greatest direct cost of serious mental illness. In 2013, schizophrenia hospitalization alone cost the United States $11.5 billion, of which $646 million resulted from readmission within 30 days of discharge.
  • Releasing patients faster creates more bed capacity without requiring new beds. Under the influence of widespread psychiatric bed shortages and pressure to reduce hospitalization costs, length of stay has been shrinking for decades. In 1980, the median LOS for an acute episode of schizophrenia was 42 days. By 2013, it was about 7 days.
  • More people are competing for an ever smaller number of inpatient psychiatric beds, where they stay ever shorter periods of time, after which they are more likely to be readmitted to the same hospital within weeks to six months of discharge.

Taken from the Executive Summary of the report:

“The analysis found a statistically significant association between shorter hospital stays and
rapid rehospitalization across the states. Among the findings:

  • Patients in states with the shortest LOS were nearly three times more likely to be re-admitted into a state hospital within 30 days or 180 days of discharge than patients in states with the longest LOS.
  • Eleven states had a median LOS of two weeks or less. In those states, 1 in 10 patients (10.8%) was rehospitalized within 30 days of discharge, and slightly more than two in 10 patients (22%) were readmitted within 180 days.
  • Nine states had a median LOS of four months or more. In those states, 2.8% (fewer than three in 100) patients were readmitted within 30 days of discharge, and 7.9% (fewer than eight in 100) were readmitted within 180 days.”

Some limitations of this study are they were conducted only in public state hospitals and only counted one readmission to the original admitting facility and did not factor in multiple readmissions. In my opinion, readmissions often occur to a different facility and private facilities are driven more by insurance standards. I believe these statistics to be under-reported with relapse and readmittance being more common than we know.

I wish there was more call to action I could present here. The only way for forward progress is unfortunately through the legislative system. Currently, Medicare excludes payment in any institution for mental disease (IMD) with more than 16 beds. This has resulted in the above 2016 statistic where there are only 12 beds per 100,000 people with a mental illness diagnosis. This is unacceptable and discriminatory. I suggest becoming active in advocacy and speaking to your local legislators to influence change. If you need suggestions on where to get started, please message me and we can work together towards a change to this system.

Day 5: Discharge

Day 4: Knowing Who’s Who

**This week’s blog posts are dedicated to advocating for effective mental health treatment and educating patients, family, and friends in all areas of inpatient psychiatric care. The perspectives shared here are not that of a mental health professional, but rather someone with lived experience. Information shared may not align with every circumstance or viewpoint of readers, but is meant to offer guidance in an area that is often confusing and holds little resources.**

One of the thoroughly confusing things the first times I was hospitalized in inpatient psychiatric care was who all the people who were not patients were and what their role was. For a while, I didn’t even know they had different jobs and would get frustrated when I would ask one person a question and they told me to ask someone else. It left me feeling as though I was an afterthought and they didn’t want to deal with my problems. At first, I just stopped asking questions. Eventually, a kind mental health tech explained the entire structure to me one late night and my stays were so much smoother from then on out. So here they are, in no particular order:

#1 – Mental health technicians – Sometimes just referred to as a “tech,” these are sometimes the hardest working, least appreciated employees in a hospital. You will find techs spending all of their time in the general population area, amongst the patients. They handle all practical requests such as needing an extra blanket, wanting to get into your room (if rooms are locked during the day), requests to take a shower or sharpen colored pencils, really anything you can think of. Their actual job is maintaining a safe environment, observing behavior, taking vitals in the morning and when needed, doing safety checks for individuals on suicide watch, and providing physical security if the need arises. They likely will be asking you questions throughout the day regarding your mood, level of depression/anxiety/suicidal thoughts, and charting the information for the nurses and doctors. They will lead group sessions with or without curriculum to teach coping skills, address concerns, or bring up morale.

#2 – Nurses – Nurses are usually stationed behind a desk or even a wall with a glass window that opens and shuts. They are there to monitor physiological and medical wellbeing and are rarely the right resource for general questions. They administer medications several times through the day to the appropriate individuals and chart any medical concerns. Occasionally, personal hygiene items will be held behind the nurses desk for check-out, but first ask the tech what the procedure is for receiving this at morning/evening/shower times. If you are not feeling well, aren’t sleeping well, feeling extremely anxious, or have any need for medical attention, you can go directly to the nurses’ station. They are not usually up for chatting or keeping company as their jobs are demanding and require every minute of their shift to complete.

#3 – Psychiatrists – The doctors will come in once a day, usually at different times. Some will come the same time every day (always the morning, or even late at night). You will be assigned to one doctor you will see throughout your stay and your first visit will be with them within 24 hours from arriving on the floor. From then, you will see them once every weekday and once over the weekend. They typically will meet with you for a brief time (can range from 2 minutes – 15 minutes). Any requests for items that have been restricted from you should go through your doctor. For example, if you brought a personal item like a stuffed animal that didn’t make it to your room, you can ask if they can write an order for you to have that comfort item. Be sure you know before-hand what questions you need to ask because you won’t have contact with your doctor for another 24 hours. Their role is to assess your mental state, prescribe medication and treatments, and determine readiness for discharge.

#4 – Therapists – There are several types of therapists you may encounter in a psychiatric hospital. The most common will be licensed counselors or psychologists. They, like the doctors, will come in throughout the week. Typically, they will only come once or twice a week. You may have a chance to meet one-on-one with a therapist for a 30-60 minute session, but these do not happen often. For the most part, therapists will come in to lead group therapy sessions or even educational groups about mental health. Another common type of therapist you could see, depending on the facility, is an occupational/recreational therapist. They will come to lead low-impact exercise group sessions or recreational game sessions. You can ask the nurses’ station if you would like to speak with a therapist to get put on their schedule.

#5 – Social Workers – This person is the main connection to the outside world for the patient. Along with updating authorized family members about inpatient treatment, they work to find resources for the patient after discharge from the hospital. Closer to the discharge date, they will meet more often with you to go over your plan for care in the days and weeks following discharge. Typically, protocol is to have an appointment scheduled with an outside psychiatrist within 48 hours of discharge and have first therapy (whether individual or outpatient group therapy) appointment scheduled to happen within 1-4 weeks of discharge. For people who are in need of other resources, such as housing, occupational, food assistance, healthcare, etc, the social worker will handle this as well.

It definitely takes a village to bring mental health to someone in crisis. In my experience, even the other patients can play a process in your journey to wellness. The key thing to keep in mind is these people are really here for you only for this season. You very likely will never encounter the patients, the techs, the nurses, the doctors, or the therapists again in your lifetime. Some will make the biggest impact on your life and you will never know their last name. Be sure to show your gratitude while you can and thank them for what they do.

Day 4: Knowing Who’s Who

Day 3: From the Outside Looking In

**This week’s blog posts are dedicated to advocating for effective mental health treatment and educating patients, family, and friends in all areas of inpatient psychiatric care. The perspectives shared here are not that of a mental health professional, but rather someone with lived experience. Information shared may not align with every circumstance or viewpoint of readers, but is meant to offer guidance in an area that is often confusing and holds little resources.**

From the moment you walk away after helping a loved one to be admitted to inpatient psychiatric care, you can easily feel powerless and unable to provide any additional support. However, there are a few avenues of care that can still be maintained from the outside. Significant others and caregivers may feel a large range of emotions stepping away, from relief in knowing their loved one is finally in a safe place and no longer requires constant attention from them to helplessness in not knowing how to fill their time now they have been removed from the process of caring for that individual. Here are some steps to fill this gap:

#1 – Do your research – It is most likely you will receive very little information from the hospital, especially if you must part ways from your loved one before the admitting process takes place. In many cases, an ER will even transport your loved one to a completely different facility based on availability of beds without your knowledge. This can be a terrifying ordeal when trying to contact this person later, as confidentiality laws prohibit hospitals from confirming or denying the presence of a psychiatric patient. This is why it is suggested to demand for a significant other, family member, or friend to remain with the person in crisis throughout the process until they are walking onto the psych floor of a facility. The only other method of obtaining this information is by the patient initiating contact through phone once admitted (don’t forget to have full phone numbers written down on a paper the patient keeps with them in their pocket – they will not have access to their contact list on their phone once admitted).

Once you know the facility in which your loved one will be staying, search online for the facility website. Make notes of visiting hours and procedures, patient phone numbers and times open for incoming calls, and any other nurse or information phone numbers. Some websites will have general descriptions of the facility’s programs, daily schedule, or family resources. Typically, you will need to wait for the patient to make the first contact as communication with family can be restricted for the initial period of time they are hospitalized. In some cases, the admitting nurse will allow the patient to make one phone call when they arrive on the floor and that call needs to be mostly about obtaining the necessary information for future communication. Ask general questions of your loved one, such as: when can I call you next? what number do I call? is there a security code you set up that I need to give the nurses when I call? when can I first visit? what time is visitation? All of these questions could involve your loved one asking the nurse or tech close by for information.

#2 – Maintain contact with nurses and doctors – Families should designate the best person to be a main contact with nurses and doctors regarding the care of the patient. Don’t have too many cooks in the kitchen. This person should be someone who is assertive and proactive in obtaining information and persistent in contacting the nurseline daily at a minimum. Establish this relationship with the nurses early, calling within 1-2 hours of initial contact with the patient. It is a relationship that must be built and may not be fruitful in the first few attempts. Once the nurses, doctors, and social workers realize you are determined to stay involved in your loved ones care and feel respected by you, a cooperative effort in getting the patient well can start. The first contact can sound like this, “Hello! I am calling about my daughter XXXX XXXXX, her security code is XXXX. I wanted to speak to a nurse or her assigned social worker about how she is doing so far, and see if there is anything I can do to assist in her receiving the care she needs while she is there.”

Follow up the next morning, saying “Good morning! I am just checking in on XXXX XXXXX. I called yesterday and spoke to XXXXX. How did XXXX sleep last night? Will she be seeing a doctor today? I would also like to plan to visit during visiting hours today. Is that permitted at this time?” The more you become familiar with the staff working, the better the information you will receive and the more effective your help once your loved one is discharged from the hospital will be.

#3 Make regular phone calls to your loved one – Psychiatric hospitals usually have common areas for patients to spend time between time in their rooms resting, meals, and group therapy sessions, and have phones to make and receive calls from family and friends. It is better to start small, with only closest family and friends making contact and sometimes waiting for the patient to reach out to others. For this reason, it is best practice to let concerned friends and extended family know you will give your loved one their phone number for them to call when they are ready to talk. Ask your loved one when the best time for you to call them (does dinner happen from 5-6 when phones are open but they are in a different room? have they been going to bed at 8 even though phones are open until 10pm?). Set up a time you plan to call at least once a day so they will be in the area to take the call, and make sure your loved one knows they can call you as much as they want outside of that time. Set a reminder on your phone to call at the planned time and always make an attempt every day. Save the phone number you receive your first call from the community phones as a contact in your phone so you recognize it as them calling.

You may struggle at knowing what to talk about the first few times you get on the phone with your loved one. Avoid asking how they are feeling or if they feel better unless they have demonstrated to you they want to talk about these things. They are likely overwhelmed with a lot of techs, nurses, doctors, and therapists constantly asking these questions, and this should be a time they have a break from that and have contact with the outside world. Be ready with a few lighthearted stories about what has gone on in your day and your world. Ask about general, concrete things such as “Is your bed comfortable? Do you have a roommate? What did you have for lunch today?” Be ready to be the one who initiates the end of the conversation as your loved one will probably feel uncomfortable telling you they are done talking. Have a good excuse (“Well, I have got to get dinner started. Call me later tonight if you want to. Otherwise I will call again at this time tomorrow.”) Expect your first conversations to be very brief and generally for calls to last less than 10 minutes. It may not seem like anything to you looking in from the outside, but it will make a difference to the one on the inside to receive communication and love from the outside. It lets them know they are not forgotten and gives hope their life will be there waiting for you.

#4 Visiting the patient in person – This can be one of the most challenging activities in the entire experience for both the family and friends and the person in the hospital. While one hour at first seems like not enough time every day or twice a week (depending on the facility’s structure), you will find yourself searching for something to talk about ten minutes after arriving. Be prepared to see your loved one in a state different than you normally see them. They might be very nervous and even feel a sense of shame being seen in the hospital and can change the way they behave or communicate. Avoid making big sweeping statements such as “You look great!” or “You look like a trainwreck! Have you been sleeping at all?” Speak the truth of your observations but soften it. “It looks like you might be feeling better. Does it feel like that to you?” or “How did you sleep last night? Is it hard to sleep in a different place?”

Try to bring something to do together to fill the time with something other than talking. I have found one of the best things to have for visitation is a deck of cards. Bring it and set it on the table, maybe start shuffling the cards, but don’t have expectations of playing. Conversation may flow and your loved one may have a lot to talk about, but if the conversation lulls and awkward silences come in, suggest you play a game. Suggest a favorite game you have played in the past, or teach a simple new game. A somewhat competitive game can lighten the mood and even at times be a great release of positive emotions between the two of you. Be careful not to disturb the other visiting guests and patients. Even playing a game of solitaire together can help connect you. If you feel the visit has had quality connection only 30 minutes in, don’t be afraid to ask your loved one if they are ready to go back or if they want you to stay the entire time. Sometimes a short visit can serve a better purpose than sitting in silence to take up the entire time. Before leaving, ask if there is anything you can bring them next time they may have forgotten at home (slippers, more socks/underwear, chapstick, a new notebook to write in).

#5 Set up support for yourself after phone calls and visits – Remember to take care of yourself in the midst of all of this. The hospitalization may be happening to your loved one, but you cannot support that person very well if you do not have an outlet for emotion. Give yourself time to feel and reach out to someone outside your ring (see yesterday’s blog post) shortly after times you communicate with your loved one. It can be very beneficial to set up a few therapy sessions for the time your loved one is hospitalized to process the experience as it is happening.

I will close by saying the most important day to visit, in my opinion, is Sunday. For most facilities, groups, individual therapy sessions, doctor visits, and treatments occur Monday through Friday. Saturday seems to be a good day to rest from all the activity, but Sunday can feel very isolating and alone. Whenever I was hospitalized, I would tend to reflect a lot on Sundays about family and where I was and a full gamut of other things that generally would leave me melancholy. Suddenly, not receiving a visit can leave you feeling abandoned or trapped without outside contact. Remember, the self esteem of the individual in the hospital likely is at an all time low, so reaching out and asking for what they need is rare. Take the initiative to call daily, visit whenever available, and keep up to date on how treatment is going from the staff.

Day 3: From the Outside Looking In

Day Two: Ring Theory

**This week’s blog posts are dedicated to advocating for effective mental health treatment and educating patients, family, and friends in all areas of inpatient psychiatric care. The perspectives shared here are not that of a mental health professional, but rather someone with lived experience. Information shared may not align with every circumstance or viewpoint of readers, but is meant to offer guidance in an area that is often confusing and holds little resources.**

Oftentimes when we know someone facing a crisis, whether it be a close friend, family member, or just an acquaintance, we don’t always know the right words to say. We may also have a difficult time processing the crisis through our own emotions and actions and before long, the wrong words come out to the wrong people at the wrong time. Several years ago, I was introduced to something called the Ring Theory and it became a very simple tool to use in any crisis, mental health related or otherwise. It saves friendships, relationships with family members, and ourselves from embarrassment and bitterness.

Essentially, this is how it works:

  1. Draw a circle with the name of the person in crisis written in the middle. In our case, this is the person being admitted to a psychiatric hospital. This is the first ring.
  2. Draw a second circle and name the person(s) closest to the person in crisis in terms of relationship. This is most likely a spouse and any children.
  3. Draw a third circle and name close family that is not part of the second circle, such as parents, siblings, very close relationships with aunts, uncles, cousins, or grandparents. For minors, this circle would actually be the second circle.
  4. The next rings are completed unique to whomever is using the tool. For example, if the person in crisis is your family member, the fourth ring and beyond will people in relation to you from closest in relation to furthest in relation. These rings will likely be filled with people that may know of your family member but don’t know them directly, like your coworkers, friends, church leaders, and your personal therapist.
  5. Using the tool: When communicating about this crisis and how it impacts you, the rule is “Comfort In, Dump Out.” What that means is anyone in a smaller circle than where you place yourself should only receive support and desire to understand. Anyone in a larger circle moving outward from where you are on the rings are safe to vent to, seek advice, and generally receive support from. The closest outward ring from you is typically the safest group to disclose details in confidence and less details should be shared the further you get from the center. Likewise, be accepting of negative dumping from anyone in a smaller circle than you, including the person in crisis. See below for a diagram of what this looks like.

In practice, this would look like a close aunt to their adult nephew in crisis phoning their best friend to entrust their emotions regarding their nephew being hospitalized. But when she is getting updates from her nephew’s spouse, she should refrain from expressing these emotions (don’t say “I can’t handle this! I have never seen him like this. What in the world are you going to do?”). She would offer comfort, help, and advice if solicited to the nephew’s spouse, and dump out the stress and fears and emotions to her best friend.

So what do you do if you are on the same ring as someone else? How do you communicate to other close family members? or what if one of your tight-knit group of friends is hospitalized? This is where judgment comes to play. Evaluate if factors exist that would place you or the other person closer to the situation or the person in crisis and apply the theory. Seek an outer ring connection to be safe if it is unclear. But, in reality, this most often looks like mutual support, a give and take from both people. Share when the other person is strong to support you and be strong when they need support.

As the rings go in, the emotional stress of the situation increases. This means the highest stress level outside of the person in crisis is usually the spouse and children. In the same respect, the further in, the harder it is to reach out. Many times, a spouse struggles to share with anyone how the situation is making them feel. My best theory for why this is, is because when they are in personal crisis, their closest confidant is usually the one who is in the center of the rings at this moment. The person they usually dump everything on should only be receiving support right now. It can leave a person feeling isolated, alone, and seeing their negative emotions build up. Empathy and understanding in the silence can go a long way, and providing practical help is sometimes the only avenue we can take to support.

In closing, there is one person that trumps all of the rings. And that person is your personal therapist. Having a therapist, you can always rest assured you are dumping everything to an appropriate person without question and you can ensure you are receiving the support you need to be better equipped to be an asset to the ones closer to the crisis. It is typically overlooked when someone has a mental health crisis that anyone other than the person in crisis is in need of professional help. In reality, friends and family members having an outlet in speaking to their personal therapist actually is in benefit to everyone involved. Practice using this tool in small ways and prepare for when it can be used in the hardest of days.

For more information on Ring Theory and its origins, please click on this link.

Day Two: Ring Theory

Day One: Intake

**This week’s blog posts are dedicated to advocating for effective mental health treatment and educating patients, family, and friends in all areas of inpatient psychiatric care. The perspectives shared here are not that of a mental health professional, but rather someone with lived experience. Information shared may not align with every circumstance or viewpoint of readers, but is meant to offer guidance in an area that is often confusing and holds little resources.**

Whether you are the person needing acute psychiatric care, a loved one directly involved in the process of getting someone to help they need, or an indirect bystander, the first day in inpatient care can be a mind-numbing experience. Tensions and emotions run high, those directly involved are at a point exhaustion, and what’s important may rush past you before you know it. The most important factor to keep in mind through all of this is this is the necessary step to wellness and as is with all temporary things, it will get better.

#1 – Getting to the hospital – There are many paths this part takes. Some may take an ambulance to an emergency room from their home following a 911 call. Others may check in at an ER after a sleepless night in crisis. Walk-ins to standalone psychiatric facilities is yet another way. Based on what is to follow, I believe the best method in arriving for intake, if available, is to contact your established psychiatrist or psychologist to see if they have connections to nearby facilities so they can contact the facility directly and act in their capacity as a healthcare provider to secure a bed. This will make the rest of the steps much shorter.

#2 – Packing for your stay – This is a step that is not always available, but when it is, can alleviate a lot of stress and confusion along the way. Most psychiatric facilities hold similar restrictions on what items can be brought by a patient to be used during their stay. You will definitely notice what makes it to your room is much less than you arrived with, but all restricted items are safely inventoried and held by the hospital to be given to you at a later time (1-2 days after intake) or returned when you are discharged. Items to leave at home are tennis shoes with shoestrings, electronics, jewelry, any clothes with drawstrings, and spiral-bound notebooks. Personal hygiene items should be packed together (fit into a gallon ziplock bag as a rule of thumb – remember to pack chapstick!). You will not be given these items, but may be able to access them later in your stay. The hospital will provide the basic necessities. Generally 2-3 outfits are permitted. The hospital is very cold always, so pack layers – warm socks, house slippers, long sleeve tees, sweats, and a comfortable sweatshirt. Comfort items I suggest taking are a pillowcase from your bed at home and a small throw blanket. Know that you will likely not be allowed these items, but if you request these from your doctor the first time you meet, they can literally write an order/prescription for you to have these items and it makes a difference in an otherwise unfamiliar place. The last and most important item to take is a single piece of paper with names and phone numbers of anyone you could possibly want to contact, including therapists and doctors. Keep this on your person as you won’t know when the rest of your belongings will be processed and provided to you.

#3 – Hurry up and wait – While it may seem like a life-threatening crisis would instill a great sense of urgency to admit a patient, the reality is there is a huge shortage of beds available. In fact, the sad truth is in this system, the best way to be admitted quicker and to the best quality of care is having solid private health insurance. Be prepared to sit in an uncomfortable room guarded by police officers for 12 hours or more with very little communication or care. Don’t expect to be admitted to the hospital you arrive in, as they may have no beds available but are not allowed to let you leave once checked in. They will transport you via ambulance or police car to the nearest facility with the first opening that accepts your insurance. Ask if a family member or friend can sit and wait with you, though it will not always be allowed in the secure setting. If you do end up being admitted where you originally check in, you will speak to an administrative person to give insurance information, meet with a doctor/nurse practioner to assess whether you need inpatient care, and possibly be visited by someone to take urine and blood samples.

#4 – Parting ways with friends/family – This may happen at any stage from the moment you walk in to when you walk onto the psychiatric floor. Advocate for yourself up to the point of being admitted to have your loved one with you. If you feel comfortable, they can even be by your side as you talk with a professional, have labwork done, and wait in a secure area. Know that the moment you allow separation to occur, it is very hard to regain being together and it is also the moment any information to that support person ceases. In most cases, they will no longer have the ability to know where you are (even if you are transported to another facility) or any knowledge of visiting procedures, ways to contact you, or what care is being provided to you. In most facilities, contact with the outside world is restricted for 24-48 hours. This is where the written list of contact information is integral. Usually one phone call once the patient arrives on the floor is allowed. This person should be ready to take a call from an unknown number. Let them know the name of the facility, patient contact phone number, any required secret access codes in order for people to contact the patient (usually they will ask for you to choose a four-digit code that must be given over the phone before any acknowledgement the patient is in fact there), and information on times allowed for incoming calls. This person should then be responsible for searching online to find visiting hours and procedures and communicate to the rest of the family and close friends all of this information.

#5 – The first 24 hours – During the first 24 hours of being on the psych floor, it can be the most challenging and confusing time for everyone involved. The person on the inside will experience what feels like their dignity being stripped away as all of life’s comforts are immediately removed. The people on the outside can find themselves worrying more than before their loved one made it into the facility due to no contact and lack of information, as they have just handed the reigns over to strangers in the hospital. The expectations of emergency care quickly are realized to be very different from reality. In most cases, the first thing a person will do is be offered a meal or snack to eat while the nursing staff complete paperwork. Given the circumstances of how long their wait was and if they have been up all night long in the ER, the patient may be shown to their room and given a sedative to sleep or rest. At some point in the first 24 hours, you will be seen by the doctor who will be meeting with you daily. This is a very short visit typically (sometimes lasting only a few minutes). Be sure to ask as many questions as you can, request your comfort items (you won’t have a chance to do this again for another 24 hours), and give a good history including any medications you are currently on or have had success with in the past. Remember to give yourself time to breathe, let your body rest, and relax in knowing you took the hardest step in getting help. Ask when the next group is meeting and if you can attend. Generally, they will not disturb you in the first day while resting to attend every group, but the sooner you participate in the process, the sooner you will feel better.

Day One: Intake

When the disease takes control

TW: suicidal ideation

Today was a hard day. A person I care about required immediate intensive care for suicidal plans. I have mulled over and over what to speak on in this post. The last time this happened for them, I was inspired in the moment to begin a YouTube channel. I think I even created it and made the first video post introducing myself. But that was all I did. From my lengthy experience with severe mental health treatment, I have carried a deep passion and vision for changing the mental healthcare system. I don’t know how or when my impact in all of this will come to fruition, if ever. What I can do now is advocate and speak up in the midst of the way things work in today’s world.

Let me preface everything I am about to say with this statement: The most qualified and equipped people to provide guidance in effective change to the mental health system are ones who have needed the mental health system. Yes, even more than the doctors and therapists trained in all specialties and definitely more than politicians and policy makers. With that in mind, know that everything I have learned about how the system could work better came during a time when I was mentally ill, but was developed and fine-tuned when I was mentally well.

The best advice I can give to anyone facing a severe mental illness and their family and friends is to remember what you are fighting for and what you are fighting against. So often, when the disease takes over control, it seems as though we are fighting every tactic and justification and pleading of the person we love to get them help. Know this is far from the truth. You are fighting against the disease and fighting for the person locked inside. It is just at this very moment, your loved one has lost the ability to fight the disease any longer. We all have the same enemy, the disease. Too often, the desire to maintain control looks like the mentally ill person fighting against any help from family and like the family is fighting against the mentally ill person to strip away their freedom. If we do not step back and instead give in to this idea, this is when the disease thrives.

So what can we do? When emotions are at an all-time high, and words and actions are internalized by everyone involved? When a life is on the line? When we feel powerless? We can join together and turn our anger and frustration away from each other and place it all on the despicable monster, the disease. Take the power away from the disease! Tell all its secrets, lies, and manipulations! Expose it for what it is and deny it any more power. For a time, this has to be carried by the family and friends. Speak truth in love, maintain as much dignity and control as possible for the person suffering, and know when action must be taken. And trust in the body’s natural response to threat to life. Just as when we naturally fight to breathe when drowning, the body will fight for that last ditch step to save their life.

I realize much of what I said is conceptual and not practical. This practical guidance is what I hope to achieve into the future, and plan to shift gears this week. I will dedicate my blog posts to a beginner’s guide to inpatient psychiatric hospitalization this week. Please feel free to share with anyone you know could use this now or in the future.

When the disease takes control

This is Us

If you are following along, you may have noticed there was a missing post yesterday. While I aim to blog once a day, I recognize the need to always give myself grace. And there are just some days when nothing comes to mind and a post would really serve no true purpose. That is not to mean I will not ever post random ramblings, because I feel like that could happen.

I have been contemplating all the topics I could cover in my blog, and truly there is nothing off the table. For now though, this blog is the start of a conversation if you will. A way you get to know me in my entirety as a person. It might be a one-sided conversation for now and maybe for a long time, but I am okay with that too. So, I thought today I could introduce myself as the divorced mother of two.

I was married at the age of 21, had my first son at the age of almost 26 and my daughter at 30. And I was divorced at 34, 13 years after marrying. It always feels strange telling people that I was married for 13 years and have been divorced now for 5 years. I definitely don’t feel old enough to have that much life experience in a marriage. And people often are surprised as well, thinking the same.

Tonight I was watching the most recent episode of ‘This is Us’ (may be some slight spoilers if you need to wait to read the rest of this), and I loved what was said by Kate right after she and her first husband Toby signed their divorce papers (I warned you of the spoilers!). She told him “Just because our marriage ends, it doesn’t mean that our story ends. We were meant to be together, and now we are meant to be apart.”

I know this is a fictional dramatic, emotional television show meant to pull at our heartstrings and end up with everything and everyone exactly in the path they are meant to be. But I definitely feel like this part is my story. Believe me, I didn’t always see it that way. I, like Toby in the show, wasn’t sure I could ever see it that way. I might have had a great deal of hope and desperate longing to reach this point of mutual understanding and respect, but when it all was happening it was like an unreal night terror.

I know this isn’t every person’s story too. For some, healing doesn’t bring reconciliation. For others, safety of one’s physical and mental wellbeing requires distance. So why is it different for me? Luck. That’s it. I was going to say God’s protection and blessings, but that really isn’t right either. God doesn’t choose to protect my relationship with my former spouse and ignore others. It’s not that we are more enlightened as human beings, or better people. We just are lucky. We have two amazing children with two engaged parents who are now meant to be apart. We are better apart. And how weird is that?

Whenever I am on a first date and the man asks me, “So, why did you get divorced?” (btw, men should not be focusing on exes ever on a first date), I always respond, “We just couldn’t make decisions together anymore.” I guess I don’t know how else to explain it. It was more than that, obviously. But that is the most concrete reason I can come up with. Whenever any decision, big or tiny, we needed to make as a married couple came up, we found ourselves on opposite sides of the world. Compromise wasn’t even a possibility because any “give” from one person would “take” it all away from the other side.

However, today, I would say we do exceptionally well in making decisions. It really wasn’t about the decisions. It was about us, feeling free to be who we really were in our core. I couldn’t be who I was without feeling like I was infringing on his ability to be who he was, and vice versa. It took me learning exactly who that person was over several years to realize this, and to realize that we were meant to be, just not anymore.

I don’t think I will ever be the ex-wife who wears matching jerseys with my ex-husband and his wife or goes on joint Disney vacations with both families. I know they exist, but that is the exception. I am grateful that I am the ex-wife that can have a twenty-minute text conversation about what exactly we can do with our 8 year old daughter’s hair that gets so tangled we spend hours getting the knots out, or sending a sweet picture of our kids being silly just to share the moment. And that is what we have become. We had a great marriage for a time when we needed it, and now this is us.

And here you were, thinking you wouldn’t get a random ramblings post!!

This is Us