Living with Chronic Illness Alone

One of the most common misconceptions about chronic illness and disability is the belief that no one is facing it alone. In reality, many people living with chronic illness or disability do not have a system of support at all.

Across the United States, millions of individuals are managing conditions that affect their ability to handle daily responsibilities, maintain their health, or continue working, and many of those individuals are doing so without consistent help from another person.

There is a widespread belief that serious illness or disability naturally comes with built-in support from a spouse, a family member, a close friend, or a paid caregiver. That belief is comforting, but it does not reflect the reality for everyone. Many people live alone, have family members who are unable to help, or find that relationships change over time in ways that leave them without the support they once expected.

The impact of chronic illness extends far beyond physical symptoms. It often interferes with a person’s ability to remain in the workforce, which can lead to financial instability and a loss of routine. Over time, that disruption can also affect a person’s sense of identity, especially when work and independence have been central parts of that person’s life.

When income is reduced or lost entirely, the ability to hire help becomes out of reach for many people. Even those who have Medicare or private insurance quickly discover that long-term daily caregiving is not covered in a meaningful way, and assistance is usually limited to short-term or intermittent services.

The cost of care places it even further out of reach. Assisted living facilities commonly cost between $4,000 and $6,000 per month, and in many areas the cost is significantly higher. Hiring a reliable full-time caregiver in the home is often even more expensive, and it requires not only financial resources, but also the ability to coordinate schedules, manage responsibilities, and oversee care while already dealing with pain, fatigue, and the effects of medication.

For individuals without financial means or personal support, the default option often becomes placement in a Medicaid-funded nursing home.

What is not widely understood is how closely nursing home placement is tied to the final stage of life for many residents. Research has shown that the median length of stay in a nursing home before death is only about five months, and more than half of residents die within six months of admission. Other studies estimate that overall median survival after entering a nursing home is approximately two to two and a half years, with a high mortality rate during the first year. While these numbers vary depending on age and underlying conditions, the overall pattern is consistent.

Managing a chronic condition requires constant attention, even on the days when energy is low and symptoms are worse. Medications must be tracked, appointments must be scheduled and attended, and decisions must be made in situations where there is no room for error. When there is no one available to share these responsibilities, the entire weight of that management falls on one person.

Research consistently shows higher rates of depression and emotional strain among people living with chronic illness, particularly when they are also experiencing isolation. While statistics can highlight patterns, they cannot fully convey what it feels like to face ongoing challenges without reliable support or to carry responsibilities that would be difficult even with help.

For many people, managing chronic illness alone means continuing to function without a safety net. It means making difficult decisions without guidance, handling setbacks without assistance, and maintaining a sense of stability without knowing who to turn to if something goes wrong. This level of responsibility requires a kind of endurance that is rarely visible to others.

It is important to move away from the assumption that people have support simply because they appear to be managing. A person’s ability to get through the day does not mean they have help, and it does not mean the situation is sustainable over time.

Taking the time to check in with someone who is living with a chronic illness or disability can make a meaningful difference. A thoughtful question, a willingness to listen, and a consistent effort to stay connected can help reduce the sense of isolation that so many people quietly experience.

At the same time, checking in is not the same as having a support system. Many people who are seriously ill are facing each day without anyone consistently helping them with the practical demands of daily life.

This is where the limitations of our healthcare system become especially clear. Even individuals who have worked hard, saved responsibly, and planned for their future can see their financial resources quickly depleted by medical costs and the need for care. Unlike other expenses, these losses are often permanent, with no realistic way to rebuild what has been spent.

As financial resources decline, the level of available care often declines as well. At the same time, a person’s physical and cognitive capacity to manage their own needs may also be diminishing. Tasks that were once manageable, such as organizing medications, keeping appointments, preparing meals, or responding to changes in health, can become increasingly difficult without assistance.

Over time, this creates a pattern that is rarely acknowledged. Health does not decline only because of illness itself, but also because of the absence of consistent support. Without help, small challenges become larger ones, and manageable conditions eventually become life-threatening.

This gap in care leaves many people without the level of care they need to remain stable, safe, and independent for as long as possible.  It is not a rare situation or an exception, but the predictable outcome of a system that does not provide long-term support for long-term conditions.  It is happening every day, and it will continue to happen until we acknowledge how many people are being left to manage alone and begin to address the gap in care that should never have existed in the first place.


Are you or someone you know living with a chronic illness alone? Leave a comment below.

When a Chronic Illness Becomes Part of Your Everyday Life

The author standing in a room using her modified upright rollator as an assistive device. Image is decorative in nature.

People sometimes ask why I speak so openly about my journey with chronic illness. The truth is that it’s become such a significant part of my life that it would be difficult not to talk about it. Managing medications, undergoing treatments, attending doctor’s appointments, facing hospitalizations, and working through physical and occupational therapy aren’t occasional events. They’re woven into the fabric of my daily life.

The rehabilitative process and the constant adjustments required to manage my health shape how I plan my days, how I use my energy, and how I move through life. These experiences influence my routines, my priorities, and many of the decisions I make. Chronic illness isn’t something that appears briefly and then disappears again. It is present every day and, at times, every hour.

Because it’s such a constant presence, speaking about it simply reflects the reality of my life. Sharing these experiences helps others understand what living with chronic illness actually looks like, and it allows me to connect with people who are navigating similar challenges. Silence would require pretending that this enormous part of my life doesn’t exist, and that would not be honest or helpful to anyone.

There are many people living with chronic illness who are still at the very beginning of their journey. Some may have just received a diagnosis and are trying to understand what it means for their future, while others have spent years searching for answers and have been dismissed or doubted by doctor after doctor. They know something is wrong with their bodies and they know their lives have been affected, yet they’re still waiting for someone to name what they’re experiencing.

For those individuals, the uncertainty can be one of the hardest parts. Living with symptoms that disrupt daily life while being told that nothing is wrong can create confusion, frustration, and self doubt. Over time, many begin to question their own experiences, even when their bodies are clearly telling them that something isn’t right.

People in this stage need information, guidance, and reassurance. They need to learn how to advocate for themselves, how to seek out the right specialists, and how to navigate a medical system that doesn’t always make those answers easy to find. Just as importantly, they need to know that they’re not alone. Others have walked this path before them, have faced the same uncertainty, and have eventually found the answers and support they needed. Sharing these stories can help light the way for those who are still searching for their own answers.

There are many people who have little understanding of what it truly means to live with a chronic illness. They often haven’t been exposed to accurate information about how chronic illness affects a person’s daily life, their abilities, and their long term well-being. Because of this lack of understanding, it becomes important for those of us who live with chronic illness to share our experiences so that others can learn what this reality actually looks like.

Without that knowledge, many people continue to believe harmful stereotypes. Some assume that people with chronic illness are lazy, unwilling to work, or content to live off the tax dollars of others. They imagine that staying home means a life of ease and relaxation while everyone else continues working and moving forward with their lives. These assumptions ignore the physical pain, exhaustion, medical treatments, financial strain, and constant uncertainty that often define life with a chronic illness.

Will sharing accurate information change everyone’s mind? Unfortunately, it won’t. However, it can change some minds, and that still matters. If even only a small number of people come to understand how profoundly chronic illness can limit a person’s quality of life, then speaking openly about these experiences is worthwhile. Greater understanding may not solve every problem, but it can replace ignorance with awareness and, in some cases, lead to greater compassion.

Chronic illness reshapes the way a life unfolds. It changes routines, priorities, and expectations in ways that are often invisible to others. Talking about it openly is simply a reflection of that reality. When illness is present every day and sometimes every hour, it is no longer just a topic of conversation. It becomes part of the fabric of our lives.  It has become an integral part of my life, and if my experiences can help even one person, it makes sharing my personal journey worth it.

Maintaining a Social Life with a Chronic Illness – Jan Mariet’s A Day in the Life

Accessibility Is Not a Privilege – Jan Mariet’s A Day in the Life

When a Chronic Illness Breaks What Was a Strong Partnership – Jan Mariet’s A Day in the Life

I Couldn’t Even Get in the Door – Jan Mariet’s A Day in the Life

I Couldn’t Even Get in the Door

A Rollator and Wheelchair User’s Experience Navigating Inaccessible Medical Offices

Often, when I venture out into the ‘real world’ on days I need my upright rollator, I’m reminded just how inaccessible that world can be for rollator and wheelchair users.  The places you would expect to be the most accessible, like doctor’s offices, are, in reality, often the least accessible.  This is especially true for the smaller medical practices in older buildings and at specialists’ offices.

Almost every doctor’s office I’ve visited using my rollator has been surprisingly difficult to navigate. First, many of the specialists I deal with have only one or two handicapped parking places in very overcrowded parking lots, and they always seem to be taken. 

I can understand that, and I park wherever I can, but often, the only way to get to the ramp that leads to the entrance if I’m not parked in the handicapped accessible parking spot means I have to walk in traffic to get to it, and that isn’t always safe.  So often, the sidewalks at medical practices lack curb cuts until you get to the actual handicapped ramp.  People who walk without assistance can utilize the sidewalks, but without appropriate curb cuts, wheelchair users and rollator users are forced to wheel behind parked cars that may back up at any minute, or risk rolling through the  driving lane.

I live in an area where the number of people with handicapped placards is much higher than the actual number of handicapped parking places available.  Our area has a large elderly population and honestly handicapped placards are held by a large percentage of our residents. 

I don’t judge people, if they have a placard, then their doctor certified that they met the requirements and that they need it; I’m not going to argue with that.  I realize many people have invisible disabilities, and I’m glad people get what they need. 

But I can’t imagine how hard it is for wheelchair users with so few accessible spaces available. Most need to extend a ramp to get in and out of their vehicle, and you can’t do that in a regular parking space; they aren’t wide enough.  So, if the accessible spaces are filled, they simply can’t get out of their van.

There are also people like me, who don’t necessarily need an oversized parking place, but I can only walk short distances.  I can’t tell you how many times I’ve had to call inside a medical office to tell them that I’m outside in the parking lot, but because I can’t find a parking space close enough that I can actually walk in, that I’m going to be late. It’s great that they have an overflow lot across the street, but I can’t walk that far, even with my rollator. 

Once I get there, and find a parking space that is close enough that I can get in, I’m faced with the fact that there are rarely automatic or accessible doors at doctors’ offices.  The doors at doctors’ offices are typically security doors, and they are incredibly heavy, and nearly impossible to open while using an upright rollator. If you have weak arms or hands, or are a person seated in a wheelchair, they are next to impossible to open.

You have to remember, not every person in a wheelchair is being pushed by a caregiver.  Many wheelchair users are on their own, and have lightweight chairs they can push themselves, or powerchairs.  The doors to most doctor’s offices are not made to be opened from a seated position, or when both hands are occupied by a rollator or crutches.

Once you get inside the doctor’s office, the check-in desk is usually too high for a wheelchair user which makes checking-in a bit awkward.  As a rollator user, I don’t have that issue, but it does make me stand further back from the desk, and if they hand me a clipboard and pen, I can’t carry it and hold on to my rollator.  Rollators, like crutches, take both hands.  Holding it under my arm makes it awkward, too.

I’ve noticed there is almost never open space for a person in a wheelchair to “sit.” Instead, there are rows upon rows of chairs but with no designated open areas for wheelchairs to remain while waiting, which means they end up parked in the walkway, and that’s really awkward.  It must be frustrating to be in the way and there is nothing you can do about it.

As a rollator user, I can tell you, there is rarely a place where I can sit and keep my upright rollator within reach.  Usually, there are tables, or other rows of chairs in the way. Often, I have to ask other people to move so I can find a place I’ll fit. 

People are very nice about it, and often move without me saying a word, but sometimes, they are absorbed in their own issues, or busy on their cell phone, and they don’t notice.  It can be uncomfortable to have to ask people to rearrange themselves for me.  It’s hard to ask strangers ‘for a favor’ because the waiting room isn’t set up for the assistive devices many people use.

My upright rollator is customized, and many people are curious about it.  I tend to field questions from other people in the waiting room about where I got it, would it work for their aunt or mother-in-law, and that it looks so much better than a regular rollator.  I don’t mind answering their questions, but sometimes when you are at the doctor’s office, you aren’t at your best, and you’d really rather just be left alone.

Once you are called into a clinical room, you often have to follow a medical assistant down a long, narrow hallway.  They tend to walk very quickly, which is something people using rollators or crutches aren’t really able to do.  I can’t tell you how many times the medical assistant disappears around a corner, and I stand there lost until they come back looking for me. 

If there is an exam table, it often lacks grab bars or any way to use it safely. The token two-step platform attached to most exam tables offers little help for people with balance issues or who cannot safely climb steps. Adjustable exam tables that lower for patient access and then raise for the physician do exist, but very few medical practices actually have them.

Fortunately, most exam rooms have chairs in them.  The only problem is that my upright rollator is quite large, and often, it takes up the only vacant space in the exam room, leaving no room for the doctor or nurse to work.  I’m often told by the nurse that they need to move it outside of the exam room but can’t leave it in the narrow hallway because that would be a fire hazard.  When they say this, I always wonder what I’d do without my assistive device if there were a fire and I couldn’t get out by myself, and I was left by myself in an exam room with the door closed.  

They say they will bring it back when the exam is over. I cannot tell you how many times, even after I remind the doctor that I need it, the doctor leaves quickly and no one returns with my rollator. It is not safe for me to try to go searching for it on my own.

So I am left there, waiting until someone eventually comes, usually when a medical assistant arrives with the next patient. Then there is a sudden rush to locate my rollator and return it to me so the room can be turned over. Often this happens 20 minutes or more after the doctor, who always promises to let someone know, has already left.

More than once, I have resorted to calling out just to get someone’s attention, so I do not have to wait indefinitely. It is embarrassing, but honestly, they are the ones who should be embarrassed.

I want to be clear, I’m not here to shame doctor’s offices or their medical staff. Many staff haven’t been trained to realize that separating a disabled person from their assistive device is simply not an acceptable practice.

Some offices have a larger exam room for power wheelchair users or for patients who are much larger than a typical patient, but these rooms aren’t always available because of the variety of disabled patients who need to use it.

I understand that medical offices must serve patients with many different types of disabilities, and I do not expect them to anticipate every possible need. But some accommodations should not be considered unusual or optional. Patients who use rollators or wheelchairs are among the most common mobility-impaired visitors to any medical practice, so spaces that can safely accommodate them should be standard.

Features such as doors that are easy to open, front desks that are not so high that a shorter person or wheelchair user cannot see the receptionist, and exam rooms large enough to maneuver with a wheelchair or rollator are not extraordinary requests. They are basic elements of accessible healthcare.

Doctors’ offices do not intentionally set out to be inaccessible. Accessibility gaps are usually not about intent; they arise from not seeing the space from the perspective of a patient who cannot even open the door. No one may be trying to exclude disabled patients, but good intentions do not erase real barriers or their impact.

Seeing a doctor is stressful enough. For someone with a disability, there is something quietly discouraging about pulling into the parking lot and immediately wondering, “Can I even get inside?”

From that moment on, every step requires calculation. Will I find a parking spot close enough to walk from? Is the ramp actually usable, or too steep or tight for my rollator to navigate? Will I be able to open the door without help?

Once you’re inside, there is the stress of wondering, will I be able to sign-in at the desk?  Where will I be able to fit in the waiting room with my assistive device?  Will I be able to get on their scale when they take my weight?  Will I be left behind by a medical assistant rushing to the exam room, when I just can’t walk that fast?  Will I even fit into the exam room with my rollator?

What assumptions are being made about me just because of how I walk? If I bring someone with me, will the doctor talk to her instead of me, as if I am unable to understand or speak for myself? (Don’t worry — I always set them straight.) Will I be treated as a capable, intelligent adult? Will I be treated with dignity?

Will my medical concerns be taken seriously, or will I hear that familiar line, “This is probably just part of your disability progressing,” without any effort to investigate the real cause? Will my physical limitations lead the doctor to assume I am not willing or able to do the hard work required to recover from a separate condition? Will certain treatments or options simply not be offered to me because I am less mobile? Will I be seen as a “poor dear” whose quality of life is not worth the effort or assumed to matter less?

All of these questions would make anyone’s head’s spin.  The stress of a doctor’s visit is so intensified for a disabled patient. 

And if you happen to be a medically complex patient, you have the added worry that the doctor will only look at one small part of your complex medical issues, and never look at you as whole person with multiple medical needs.

Some of these barriers are physical, like the heavy doors, the too-steep ramp, or the cramped exam rooms.  But there are also so many attitudinal barriers as well, such as your intelligence being discounted due to the fact you have a physical disability, decisions to move a patient’s assistive device out of reach, or failing to offer newer treatments because your life is assumed to be limited anyway.

People with disabilities already know the world was not built with us in mind. Realizing that the very places meant to help us, medical offices, often present additional barriers to care only adds to that burden. These obstacles do not merely inconvenience us. They quietly exclude us and, at times, openly diminish us. No one should feel shut out of medical care simply because their mobility looks different.

I am not sharing this because I enjoy complaining or want special treatment. I am sharing it to offer a small glimpse into what it can be like to seek medical care as a person with a mobility difference.

I don’t for one second believe that medical offices don’t want to be accessible.  Many practices do not own their buildings and may have little control over the parking lot, ramps, or curb cuts. Still, accessibility laws exist for a reason. Property owners can be required to make needed improvements if a tenant insists on them. Practices also make decisions about where they lease space, and they can choose not to occupy buildings that fail to meet basic accessibility requirements. Occupying a space that doesn’t meet basic accessibility standards is ultimately a decision.

Most of the improvements needed to make doctors’ offices more accessible are not expensive. Many do not require major renovations. Small changes can make a meaningful difference.

Installing automatic door openers or adjusting door pressure, leaving intentional open spaces in waiting areas instead of filling every gap with chairs or displays, ensuring there is at least one flat, accessible unloading area near entrances, and training staff to recognize barriers and offer appropriate assistance are all practical steps that can dramatically improve access.

Accessibility is not about special treatment. It is about equal participation and equal access. Disability is the one minority group that anyone can join at any time. The shift from able-bodied to disabled can happen in an instant, through one accident, one illness, or one unexpected medical event.

Accessibility is not about convenience. It’s about dignity, safety, and the basic ability to participate in our own healthcare. When medical offices remove barriers, they are not offering special treatment. They are simply making it possible for patients to be patients. No one should have to fight their way into a doctor’s office before they can even ask for help. No one should ever have to say, “I needed help, but I couldn’t even get in the door.”

How People Disappear

I’m right here. You may not notice me anymore, but I am still here.

You may think my smile means something. You may believe me when I say, “I’m fine,” because you want to believe me — and then move on.

What else am I supposed to say? When your body repeatedly falls apart, and there is nothing left to try to stop it, are you going to announce, “I’m desperately ill… again”?

I’ve learned that my reality makes people uncomfortable, because eventually, even compassion has a limit. But it’s still my reality.

My reality is more than you want to know, or maybe more than you can handle knowing.  But either way, I’m still here, handling it, because what other choice do I have?

Planning feels pointless when every plan dissolves before my eyes.  It’s hard to take action when your body repeatedly, relentlessly lets you down; when illness and medical urgency demand to be heard above all else.

I hold back even on the things I genuinely want to do, not because I don’t care, not because I don’t have desires, but because caring has become exhausting, and hoping has a cost I can no longer pay.

I’ve stopped imagining the future, not because I don’t care, not because I don’t want one, but because I no longer know where I fit inside it.  Every time I imagine a life ahead, it crumbles before my eyes, and no amount of work or effort changes that reality.

Hope becomes dangerous. Planning becomes cruel. When every plan is eventually taken from you, what is the point of hoping?

The dreams I held, and still hold, don’t disappear, I just quietly let them go as quickly as they appear.  My hand can’t hold the string tight enough, and I watch them, like balloons, disappear into the sky.

They linger as reminders that I am no longer fully living, and yet, I am not dead yet, either.  I’m living in the ether of illness.  I am slowly becoming a memory; someone old friends check in on once in a while before scurrying on with their real lives, that no longer include me.

Empathy becomes cruel when it is the only pattern left in your life. Sympathy is even crueler. 

When your choices are ‘hope and constant disappointment’ or
‘planning for something that will be taken from you and leave you emptier than before’, what do you choose? After a while, you stop choosing at all.

Do you sit and watch the world go by? Do you keep talking about the illnesses that quietly steal your life away? Or do you try to converse, carefully, briefly, until even that becomes too much for others to carry?

After a while, conversation seems useless, too.  You stop contacting anyone, and you imagine their great relief.  And in many ways, your voice starts to embrace the silence.  It’s just easier.

So, I read. I think. I write about things that seem important to fill the minutes and hours that I exist. I tell myself these things matter. And I try to believe it.

Then, even that becomes hollow, because I know, so well, that words are not actions, and the actions are beyond what I can do.  Naively, I thought maybe my words would enough, but slowly, relentlessly, I have realized that is not true – at least not for me. 

How desperately I want it to be true, how desperately I wanted my written words to become my voice, but desperation does not change reality.  Words unread are nothing at all. Words just become something to fill the relentless time that each day takes.

That is the rhythm of my life now.  I am a songbird that no longer has a voice.  I am an eagle that can no longer soar.  I am the broken-down old horse that grazes on a barren field, trudges to a cold stall at night, and searches for a slice of apple in the empty pockets of faceless people I no longer know. 

This is nothing like living.  I have lived and I remember what it feels like. I remember having a small spark that lit one person’s way. The spark is gone, the way has gone dark, and this is nothing like living.

I am the old dog who waits by the door for an owner that has passed away, and I have no idea – only long, empty, faithful days of waiting for a joyful reunion that will never come. 

I’m right here. You may not notice me anymore, but I am still here.  Please, someone notice me.

02/01/2025


Cancer Always Has the Final Word

Image of a teal ribbon, which is the symbol for cervical cancer.

It doesn’t matter if the ribbon is pink, or teal, or any other of a myriad of colors. It means another person has heard those heart-stopping words: You have cancer.

Once those words are spoken, disbelief does something strange. From that moment on, you barely hear anything else that is said. Or maybe you hear it, but you don’t understand it. You certainly don’t remember it. The words bounce around the room like sound effects in a movie theater, echoing without meaning, until everything turns into a kinetic blur.

And if you happen to be alone when those words are spoken, the first time you try to say them yourself, they come out one of only a few ways.

Sometimes they are choked out through sobs, leaving the listener struggling to understand what you are trying to say, only knowing that whatever it is has shattered you.

Sometimes they come as a low, gravelly whisper, barely audible, but powerful enough to silence the room.

And sometimes, you don’t say them at all. You keep them locked inside, afraid to even whisper the words you are certain you must have misheard, even though deep down you know they are true.

The unfairness hits hard. Why me?  Reality hits.  Why not me?

All the qualifiers the oncologist offers, “We’ve caught it early.” “The chances of getting this under control are promising.” “Surgery alone may take care of things.”  They ring in your ears. But your heart and your mind hear something else entirely. They see the worst. The awful realization that your life might be ending, and that there is still so much you planned to do. Wanted to do. Needed to do.

The people you might be leaving behind.
The good you always meant to do.
The changes you intended to make.
The challenges you believed you would someday meet.

All of it floods your thoughts and your body at once. It spins together into a blinding, hopeless spiral of the life you could have had, if only you had known.

But don’t we all know that life is finite? Fragile? And yet we are stunned when that truth becomes more real than we ever imagined it could be.

Reality is something we push aside while we live our daily lives. Sleep. Wake. Dress. Eat. Work. Repeat. Over and over, without much thought.

The plans we always meant to follow through on slowly slip away with each step we take and each quiet thought we set aside. The day-to-day cycle becomes the pattern. The pattern becomes everything. It spins until we barely recognize that there was ever anything else.

Until the word, barely spoken, speaks: cancer.  And the pattern changes so quickly it disarms us.

Now the pattern is appointments. Recovery. Radiation. Chemo. Maybe immunotherapy. So much stops mattering. The world shrinks almost overnight.

Nausea.  Retching. Exhaustion.  Malaise.  Shrinking.  An endless fog of confusion.  Alternating devastation and hope.

We live for the day this aggressive pattern ends. We wait to be finished. To be well. To continue our lives. We believe that once this is over, everything we dreamed of will still be waiting for us.  But cancer always has the final word.

For some, life itself ends the conversation. For others, the collateral damage left behind by the disease, and even more by the treatment, forces life to be reordered. Reorganized. Reassembled. Reimagined.

The things we mourned when we first heard that word are no longer possibilities. We recover. We mourn. We go on. But we are never the same.

Regardless of the ribbon color. Despite the unpronounceable name that both specifies and reduces our lives. Not even when survival is the outcome.

We return to a pattern. A slightly altered one. Waking. Dressing. Eating. Working. Resting. Dreaming. A life reshaped by a single word that still echoes, long after it was first spoken: cancer.


Cancer Changes Everything – Jan Mariet’s A Day in the Life

“I’m Fine” – The Reality of Surviving Cancer – Jan Mariet’s A Day in the Life

Products That Make Life Easier When You are Battling Cancers of the Mouth, Tongue, or Throat – Jan Mariet’s A Day in the Life

Products That Make Life Easier When You are Battling Cervical Cancer or Cancers in the Abdominal or Pelvic Area. – Jan Mariet’s A Day in the Life

Where Were You? – Jan Mariet’s A Day in the Life