Posts Tagged ‘support’

Having a Caring, Compassionate, Understanding Friend

Friday, June 25th, 2010

When our lives are difficult, as they often are when we have a chronic illness, having a caring, compassionate, understanding friend can be tremendously helpful. A friend can give us hugs, and when we need it, a shoulder to cry on. A friend like that can be the difference between getting through difficult times or just giving up.

Everyone I have talked to about this has told me they know how much of a difference having a friend during difficult times in our lives makes, because they have experienced that difference for themselves. I’m sure you have too.

But not everyone has a friend like that. And even if we are lucky enough to have such a friend, it’s very likely that there will be times when we need caring and understanding, but our friend isn’t available to give it to us. Fortunately, if we don’t have a friend like that, or we do but he or she isn’t available, there is something we can do – something that very few people know about: we can be that kind of a friend for ourselves.

The reason we can do that is because as human beings, we are innately caring and compassionate. Without even thinking about it, we care about injured pets and other animals. And we have compassion for our children, friends, and partners when they are facing or going through difficult challenges. All we need to do to be the caring, compassionate, understanding friend that we need is to direct those innate qualities to ourselves.

We can do that in many ways. For example, we can by give ourselves hugs, and we can tell the person in the mirror how much we care about him or her. Doing that may feel strange and awkward at first, but over time it feels less and less so. And I know from watching my clients, as well as from my own life, that the difference being a caring, compassionate, understanding friend to ourselves makes is immense. So I strongly encourage you to be that kind of a friend to yourself.

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Group Coaching

Do You Hate the Effect Your Illness Has On Your Relationships with Your Children and Your Partner? Do You Hate Not Having a Life?

My coaching/support group can help you have better relationships with your children and your partner, and it can help you find new ways to manage your illness symptoms and challenges so that you, with small steps or big ones, start to create a fulfilling life despite having a chronic illness.
The next group will take place by phone on Thursdays at 5:00 PM PDT / 8:00 PM EDT starting on July 8th, and will continue weekly though August 12th (six sessions).
These groups offer the support that people with chronic illnesses often need, at a fraction of the cost of individual coaching or therapy. As a member of my list, you have the first access to this group.
To find out more about the content, the cost, or to sign up, go to Coaching/Support Group information.

How to Deal With Others When You Have a Chronic Illness

Sunday, April 11th, 2010

When someone wanted coaching session with me, I used to send them a questionnaire to fill out before the session. In it, I asked how they felt supported by their family and friends, and then I ask how they felt unsupported by those same people. From the large collection of answers I received over many years of coaching people with chronic illnesses, I learned what they want but don’t get from others, and I learned about the relationship challenges and difficulties people with serious chronic illnesses have. In this post, I’m going to share that knowledge with you. Then I’m going to describe some strategies and methods you can use to get support from the people in your life and have the kind of relationship you want with them.

The first thing I learned is that, more than anything else, there is one thing those of us with chronic illnesses are not getting from other people that we really want: understanding We want others to know how hard it is for us, both physically and emotionally, to live with a chronic illness. It’s not surprising to me that not getting the understanding we want is such a common problem,  because I don’t think it is possible for a person who has never had a chronic illness to truly know what living with one is like.

That said, it is almost always possible to get more understanding from others than we currently do. The best way to do that, in my experience, is to avoid complaining about not being understood and to not criticize the other person for not giving us the understanding we want. Instead, what works best is to tell him or her how important being understood is for us and how appreciative we are when they try to give us understanding. Then, to help the other person better understand our symptoms and pain, it can be very helpful to describe them by comparing them to pain the other person has experienced, such as a kidney stone, or pain they can imagine, such as having a root canal without anesthesia.

Another thing I learned from people’s answers to my questions is that many of us with chronic illnesses have family members and friends who either don’t believe we’re as sick as we say we are, think our problems are in our heads, or think we are sick by choice as a way to avoid having to do things like housework and going to social events.

There are several possible strategies and methods for dealing with that kind of situation. Which ones to use depends on who it is that doesn’t believe you, and how important he or she is to you. If the person is a distant relative or a casual friend, you may choose to just avoid interacting with them. But avoidance is not a good strategy if the person who doesn’t believe you is a good friend, a parent, or your spouse.

Before I give you a specific method to use to resolve or at least improve the problem I’ve just described, I strongly recommend that you give yourself extra compassion for the emotional pain that having someone important to you disbelieve the severity of your illness inevitably causes. If you’ve read my other posts, you know that giving yourself lots of self-compassion is something I recommend often, because I strongly believe it is very helpful for those of us with chronic illnesses.

Depending on whom it is who doesn’t believe you, the history of your relationship with that person, and other factors, there are several possible methods you can use to improve or resolve the situation. One that often works well is the following: Instead of trying to convince the other person that what you’ve told them about your illness and its symptoms is true, accept the fact that they don’t believe you and let them know that you’ve done that. Then politely ask them if they would be willing to imagine what it would feel like to have a chronic illness, tell someone important to them about it, and not be believed. If they do, and chances are good that they will, you will at least have gotten some understanding from them that you didn’t have before, and it’s likely that they will start to let in and acknowledge the reality of your illness and its symptoms.

The next thing I learned from my respondents’ answers was actually a confirmation of something I already knew from my own experience as a person with a serious chronic illness: people often ignore or tune you out when you tell them about your ongoing struggles. Some respondents said their friends did more than ignore them; they abandoned them. When people in your life do any of those things, I again recommend (at the risk of sounding like a broken record) that you give yourself lots of compassion. I frequently ask my clients to tape reminders to do that to their bathroom mirrors or suggest that they wear rubber bands around their wrists to help them remember to give themselves extra compassion.

In addition to ensuring that you’re getting extra doses of compassion, there are some other things you can do when people tune you out. One is to make it a point to temporarily set aside your illness symptoms and problems when you meet your friends, and ask them, in a way that shows them you really mean it, how they are doing, what their concerns are and what successes they’ve had. When you consistently do that, you will usually find that they will show you the same concern and give you the same support in return.

Another thing you can do when friends tune you out or when they abandon you is to find and make friends with people who have the same illness you do. You can do that face to face in support groups, by phone in telephone support groups, and via computer in online support groups. Most major cities have support groups for the more common chronic illnesses. If there isn’t one for your illness and if you’re willing to do so, there’s a good chance you can start one by first connecting with other interested people through the websites meetup.com and craigslist.org. The advantage of the telephone and online support groups is that you can participate without leaving your home, so you don’t need to be concerned about mobility issues and other challenges that might make it difficult to attend an in person meeting. The website yahoogroups is a good starting place for looking for an online support group, as there are groups for almost any illness you can think of.

I titled this post “How to Deal With Others When You Have a Chronic Illness,” but it’s ended up being about how you can get your need for understanding and support from others met. I hope the suggestions I’ve shared with you help you do that.

Do You Feel Like You’re a Burden to Others?

Thursday, October 29th, 2009

When we have a chronic illness, it’s easy and very common to feel that we’re a burden to our partners and our families. We often need them to do many things for us that partners and family members of healthy people don’t need to do. At the same time, there are often things we can’t do with them that they and we wish we could do. So it’s no surprise that many of us feel like we’re a burden to others.

The good news is that there are several things you can do to counteract that feeling. The first is to frequently let others know how much you appreciate all the things they do for you. We can get caught up in our symptoms and pain and forget to do that, but when we remember, it makes a big difference for them because they know that they’re not being taken for granted. From time to time, you can show your partner or spouse that you are especially grateful for their help by getting a little gift or card and hiding it someplace where it will surprise them, like in a sock or lingerie drawer. You can do similar things for others who help you (although you may need to find a different hiding place :) ).

Another thing you can do to counteract feeling like you’re a burden is to make sure you don’t dwell so much on your illness and symptoms that you ignore the other people in your life. Even though you may not be able to participate in all the activities with them that you and they wish you could, your caring, support and encouragement – including support and encouragement for them to balance taking care of you with taking care of themselves – can make a tremendous difference in their lives.

I wrote in this previous post about finding meaning in your life when you have a chronic illness. Doing that may not lessen the physical needs that you depend on others to meet, but can help you feel less emotionally dependent on them, which can also help counteract the feeling of being a burden.

Here’s one final suggestion: It really is a privilege for us as human beings to be able to serve others. Doing so fulfills us like nothing else can. So even though taking care of you and your needs may not be easy for your partner or spouse, family, and friends, they definitely get value from doing it.

A Special Kind of Love – Part 2

Thursday, October 15th, 2009

Back in August I wrote a post I titled A Special Kind of Love, in which I described the special ways my mother took care of me during those times when I was sick as a child, and how as an adult I eventually learned to take care of myself the same way. Today I want to tell you another story about a mother’s love for her child.

A while back I was coaching a woman – I’ll call her Wendy – who was struggling with ulcerative colitis. I wanted Wendy to see that she needed and deserved lots of understanding and compassion from herself. Wendy is married and has a very young son. Like most mothers, she would do anything for her son to help him be happy and healthy.

Knowing that, I asked Wendy to imagine that her son had grown up and was in college. I also asked her to imagine that he was struggling with ulcerative colitis. After she took a minute and did that, I asked her what she would say and do. She said that she would hug her son and tell him that she would always love him, that she would always be there for him, and that she would do whatever it took to help and support him so that he could live well.

Hopefully Wendy’s son will never develop ulcerative colitis. But since Wendy has it and is struggling with the symptoms and challenges of living with it, she needs all the understanding, compassion, and support she can get. From her answer to my hypothetical question, Wendy realized much more than she did before that she has lots of understanding and compassion to give. I strongly encouraged her to give them to herself, because she needs and deserves them. And if you have a serious chronic illness, I strongly encourage you to do the same for yourself. You deserve it!

Who Do You Support and Encourage?

Friday, July 24th, 2009

Earlier this year I coached a young man who had chronic fatigue syndrome and some other health challenges that made his life very difficult. But he wasn’t a complainer and he did his best to get through each day.

As I got to know him, I learned that he was single and that he got tremendous satisfaction from working with at risk youths. He gave those kids lots and lots of love and support, including encouragement when they needed it and hugs when they needed them. Greg, as I’ll call him, was clearly a very caring young man.

I told Greg that I knew someone who could really use the love and support that he knew how to give. Out of curiosity and because he gets so much satisfaction helping others, Greg wanted to know who that person was. So I started describing him. I told Greg that the man I was talking about was a very giving person and very supportive of others and that he was in his late 20’s, and I provided some other information about him as well.

When I told Greg the person I was referring to had some serious health challenges, he realized I was talking about him. In an aha! moment, he also realized that he had been giving way more support and care to his at risk youth than he had to himself, that he wasn’t getting nearly as much support and care as he needed and that he could give them to himself as well as to at risk youth. And he started and continues to do that. How about you?