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How to explain your chronic condition to loved ones?
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karm!nR
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karm!nR
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Number 6 is so important: 6. The exhaustion that results from a chronic disease is real.
I wish people and family would understand that it is not that I am not paying attention or that I Do not think what you are saying is important... it is that my mind is fatigued from my pain and sometimes my mind focuses on that pain!
karm!nR
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karm!nR
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It focuses on the pain no matter what I do.
Somya.P
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Somya.P
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Hello everyone,
How are you today? 😊
The holiday season involves reconnecting with family and friends, and explaining a chronic condition to them can be challenging. Have you seen this ongoing conversation offering some tips? We'd like to hear about your experience!
@Becholz66 @thecrohnsbook @PatsFan2623 @Marajade @Radman @Sherman @Dorene @Nana400 @Dashel47 @farare @Rockie @Advocate55 @Bs1020bs @Azlalilo @BrokenWing @brianyun @Jillk60 @Mrkittybuddysmom @Fordjonp @CXMavrick @Donna54 @Mocha461808 @Ezequiel @Amy1957 @Scooter197152 @Pamela_Levi @chrisg0116_2 @RAwarrior63 @PeterStyle @supportgirlies @Sarabiddy1977 @lorrainegrula @walters291 @riteway211 @dkstine
How did you describe your chronic condition to loved ones? How did they react? How has their support helped you?
Don’t hesitate to share your questions/thoughts/advice with us here!
Take care,
Somya from the Carenity team 🌼
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Somya from the Carenity team
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SallyAllen
SallyAllen
Last activity on 11/18/2024 at 8:06 AM
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I have Multiple Myeloma, a blood cancer that has no cure; however, there are treatments that allow us to live longer than in the past. What friends and family don’t understand is that the treatments (often chemotherapy) are given the rest of our lives. The initial (or induction) treatment is usually harsh and involves long hospitalizations to get to remission. People hear remission and think we’re cured. I often tell friends or family that I will not be able to attend a function because I’ll be having chemo that day. Their response is often, “I thought you were done with that.” And then I have to explain again that I will be doing this the rest of my life. And it won’t be the last time I have to explain. I often hear, “But you look so healthy!” I feel mean saying, “Well, I still have cancer.” Only my husband, adult children, and my kids-in-law truly understand the disease and the toll it’s taking on me. The rest have to be educated and re-educated. And that gets tiresome.
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gommer1
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I have COPD as well as peripheral artery disease don't know which will kill me first all my friends and family are fully aware
Crystine
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I am lucky that I have a great support at home and at my doctors offices but I still feel like a burden to everyone. Nobody makes me feel that way, its within me. I went from being healthy to having everything taken away from me with my chronic illnesses. I would love to go back 5 years ago when life was easier
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Christine Fabian
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gommer1
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@Crystine my problem getting support from drs I need it is always a 4 mo. or more wait
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SallyAllen
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The last bullet point under topic 4 brought tears. Yes, I talk to people diagnosed with the same chronic illness as I have and I always tell them this: you need to put away your old life and learn to embrace the new reality that living with this disease causes. You might still be able to garden or do holiday baking, you just won’t be able to do it as long as you did before. A whole day in the garden will become an hour or two, followed by a nap. Instead of baking all day, you might manage one or two batches of cookies. Friends and family don’t understand this. You might look normal, but they don’t see the underlying fatigue. They might think you are trying to get out of doing things you’ve always done. It’s up to us to educate them. And re-educate them.
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Lee__R
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Amy Stenehjem, a doctor with a chronic disease, recently published an article in the Huffington Post. Unable to leave her home for five years, she wants to raise awareness to as many people as possible of the daily difficulties she and others dealing with chronic conditions face as a result of their conditions. She lists 12 things a person should know when it comes to those who are dealing with a chronic disease.
Perhaps some of these points will resonate with you and will allow you the opportunity to educate your loved ones more on what you are going through. We hope this article helps you and your loved ones mutually, and for that reason we have chosen to transcribe this article for your reading.
A chronic disease is "an illness, condition, or injury that can affect someone for a lifetime and generally is not able to be cured, even if the patient may go into remission in certain cases. Its severity varies, some people are abe to work and live a "normal" and active life, while others are more negatively affected and often are forced to become more isolated. Many people with chronic diseases have no visible symptoms and the seriousness of the condition is sometimes not noticeable, which can cause others to misunderstand or make assumptions about the person and can also lead to lack of support from doctors, family, and/or colleagues."
Here is the list of points that Amy shared:
1. No one wants to be sick.
As a doctor, I have never met a patient who was thankful for their chronic disease. It is the mere opposite... most were very active individuals, and suddenly found themselves with an injury, condition, or disease and began the search for treatments to alleviate insurmountable symptoms.
2. Many doctors do not understand chronic diseases.
For years, it was common in the medical community to beleive that some of these illnesses were the result of depression or an anxiety disorder and that seeking mental health would be the only effective treatment.
But despite many medical advances, many doctors refuse to keep up with the latest developments and do not know how to deal with these patients. At the risk of worsening their symptoms, some patients therefore lose valuable time looking for a doctor who will listen to them, correctly diagnose them, and prescribe appropriate treatment.
3. Not being able to go to work is not the same as a vacation.
Being unable to work because of a chronic illness is not a pleasure. It is a daily struggle to perform the simplest tasks, such as getting out of bed, getting dressed, cooking, etc. Illnesses often force patients to isolate themselves and stay inside, besides attending medical appointments, because they are too weak to set foot outside.
You've probably been stuck at home because of bad weather or a bad flu. Remember the frustration you felt because you couldn't get out of the house. Now, imagine if you were stuck at home for weeks or even months. That would be frustrating, wouldn't it?
4. Having a chronic illness can trigger many emotions.
A chronic condition can alter the biochemical composition of the areas of the brain that control one's emotions. There are also other factors that can influence a person's mood and make them depressed or more worried:
- waiting for or seeking a diagnosis
- inability to work and the feeling of not being effective
- changes in the way the couple/family operates
- a loss of social interaction that leads to isolation
- financial stress
- the constant struggle with, and battle against, symptoms and trying to perform simple daily tasks
- Chronic diseases often create a sense of emptiness. It is not unusual for patients to go through all stages of grief (denial, anger, bargaining, depression and acceptance). They are mourning the loss of their lives as they knew it before and the life now that they are forced to have to endure.
The feeling of isolation is very strong; even if the patient wants to interact socially, his symptoms can prevent him from doing so. He then finds himself unable to make a phone call, write an email, or post a message on Facebook.
5. The symptoms of a chronic disease are very complex.
Symptoms vary according to the disease, and patients may have one or more symptoms at a time. Here is a non-exhaustive list: intense fatigue, pain, headache, inability to concentrate, nausea, and dizziness.
There is nothing unusual about these symptoms appearing and disappearing regularly, sometimes even within an hour. Planning activities in advance becomes a real headache. A "good day" for a patient with a chronic disease could be considered a "bad day" for someone else.
6. The exhaustion that results from a chronic disease is real.
Exhaustion is a common symptom that can be very severe, and even debilitating. A common activity or a more important event, such as Christmas and New Year's Eve celebrations, can trigger one's mental and/or physical exhaustion. Patients then have to "pay the price" and need several days or even several weeks to recover.
They, therefore, need a lot of rest and often cancel outings at the last minute. This does not mean that they are lazy or that they are isolating themselves because of choice. When exhaustion strikes, he or she has no choice but to stay home and rest. It is as if the body hits a wall and cannot go any further, no matter how much effort. If you want to better understand the exhaustion one with a chronic disease experiences, I invite you to read the article on "the spoon theory".
You may have been in bed for a few days after the flu or undergoing a surgery. Think back to how you felt: you could barely get out of bed and simple gestures exhausted you. Imagine that you feel this every day, constantly, for months or years.
7. Pain is a common symptom of chronic diseases.
Very often conditions are accompanied by severe pain, which can be in the form of headaches, arthritis, muscle, lumbar, abd/or cervical pain.
8. Not thinking clearly is extremely frustrating.
It is a complicated symptom to describe. Mental fog is a common cognitive dysfunction, and it can manifest itself in different ways: it is difficult to find words, difficult to concentrate, and/or difficult to remember things. People who suffer from it know what they want to say, but often cannot find the right words.
9. The risk of infection is higher.
The immune system can be weakend in those dealing with a chronic disease. Instead of tackling infections, the immune system wastes its time time and energy fighting against the patient's own body organs, joints, nerves, and/or muscles. Many people with these disorders take medication to regulate this problem and must avoid contact with those who are sick because a common cold can turn into a serious infection.
10. Certains foods can make symptoms worse.
Some foods can make the symptoms worse. The most common culprits are gluten, dairy products, sugar, soya, yeast, alcohol and processed foods. These triggering foods can cause inflammation, which in turn causes an increase in symptoms. These can last for hours, days or even weeks.
And because all these foods are part of our daily diet, it is often difficult to identify those responsible. No longer integrating them into our plates becomes a challenge.
11. The sense of smell is more developed.
Some odors, such as perfumes, household products, or cigarettes, can trigger migraines, mental fog, nausea, and other symptoms. Underdosed versions of drugs used for cancer treatments are sometimes prescribed. This sensitivity to odors is similar to that observed in pregnant women or patients treated with chemotherapy.
12. Living with a chronic disease requires a lot of effort.
Individuals diagnosed with chronic diseases need to be disciplined in making sure they get a good night's rest, avoid triggers, and take medication at the right time as to not worsen their medical condition. These individuals desire to feel" normal", perhaps by eating a slice of pizza or staying up late, and is understandable, even if they will "pay for it" later.
Despite this struggle punctuated by suffering, isolation, and debilitating symptoms, those with chronic diseases (and their caregivers) continue the fight. They struggle daily to better understand their bodies and accomplish things others take for granted. Those around them - family, friends, and colleagues - rarely understand the difficulties they face, and, therefore, struggle to be able to suport and help them effectively.
This post was originally published on The Mighty and reprinted by the Canadian HuffPost.