Posts Tagged ‘symptoms’

Look for the good things in your life, but do this first

Wednesday, June 16th, 2010

As I’ve written in several other blog posts, I follow and participate in several online support groups for people with chronic illnesses. In a group for people with Crohn’s disease, a woman – I’ll call her Kathy – recently wrote to say how upset and stressed she was because the drug her doctor had prescribed two weeks earlier hadn’t helped her symptoms – symptoms that included going to the bathroom up to 20 times a day.

A man I’ll call Gary responded. He shared with the group what had worked for him, and what hadn’t, when he had been in a similar situation. He wrote that he reminded himself that feeling down and sorry for himself always makes him feel a lot worse. So instead of doing that, he thought about all the things he loves about life, including his friends and family, and all the things that are important to him. Then he told himself that he had the inner strength to face and handle his pain and symptoms one day—and sometimes one hour—at a time, and he resolved not to let them beat him.

I think Gary gave Kathy very good advice. But I think it would have been even better if he had told her to first give herself lots of compassion and understanding. In the same way a parent – especially a mother – comforts her child when he or she is sick or in pain, Kathy can comfort herself. When I do that for myself first, I am much more able to follow Gary’s good advice and think about all the things I love about life. I have no doubt that Kathy will have the same result: if she first gives herself lots of compassion, she will find it much easier to find her inner strength and focus on the good things in her life.

My next Coaching/Support Group for People with Chronic Illnesses will start on Wednesday, June 30th. For more information, go to Coaching/Support Group Information.

Do you have TLCC Deficiency Syndrome? Here’s how to treat it

Tuesday, May 4th, 2010

You won’t find TLCC Deficiency Syndrome in a medical dictionary, but in my many years of coaching people with chronic illnesses I’ve found that it describes what many of them have. TLC, of course, is an acronym for “tender loving care,” and the last “C” is for compassion, so TLCC Deficiency Syndrome is the condition of lacking the needed tender loving care and compassion that people with chronic illnesses often experience.

Many things can cause TLCC Deficiency Syndrome. Some of the most common are new symptoms or a worsening of symptoms that are already present. I’ve observed that when people have flares or develop new symptoms, they usually get the treatments they need to combat those flares and new symptoms, but they often ignore the need for extra TLCC that almost always accompanies them. I’ve also often seen people’s families and friends provide lots of logistical support, such as rides to doctor visits, advice, etc. in those situations, but overlook or not fully recognize the need for extra TLCC their friend or family member has. As a result, the TLCC Deficiency Syndrome goes untreated.

So what do you do if you have TLCC Deficiency Syndrome? First, let your friends, family, and others in your support network know that you need more TLCC, and ask if they would be willing to give it to you. Chances are good that many of them will.

However, there will inevitably be times when you are suffering from a TLCC deficiency, but your friends and family aren’t able to give you the TLCC you need. When that happens, it’s up to you to give yourself the extra tender loving care and compassion that you need and deserve!

Here’s how: First let in and acknowledge to yourself how unpleasant and painful living with the symptoms of your illness has become. Now you may find doing that to be difficult and uncomfortable. However, the discomfort won’t last long and your TLCC Deficiency Syndrome treatment will be much more.

Once you’ve accomplished the step of letting in and acknowledging how painful your symptoms have become, then complete your treatment by giving yourself the same compassion you would give to someone you feel close to and care about, such as a child, a spouse or partner, or a dear friend. When you do, I’m certain that you’ll feel much, much better. Not only that, but you may find, as I and many of my clients have, that the treatments you’re undergoing for your illness become more effective.

Tom Robinson – Life Coach for People with chronic illnesses

www.chronicillnesscoach.com

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.

What small New Year’s Resolution Can You Make To Improve Your Life?

Wednesday, December 30th, 2009

Those of us who have chronic illnesses usually want to change our lives in major ways. We want our pain to go away, we want to be able to eat a normal diet, and we want the fatigue to go away so that we have all the energy we used to have. In short, we want all of our symptoms to go away so can have the quality of life we had before we became ill.

Most people with chronic illnesses spend a lot of time thinking about all those changes we want, which is completely understandable since so many of us have symptoms that are very painful and difficult to live with.

But in doing that, we can-and often do-overlook the many small things we can do to improve the quality of our lives. And some of those small things can result in big improvements.

One experiment I’ve read about that was carried out many years ago made me realize the difference small things can make. Researchers Ellen Langer and Judith Rodin divided the residents of a nursing home into two groups, and introduced very small changes  into the lives of those in the experimental group. They were given the option of seeing a weekly movie and a choice of two nights on which to see it. They were given the choice about whether to see visitors in their rooms, the lounge, or outside, and they were given the responsibility of taking care of a houseplant. Only one change was introduced into the lives of those in the control group: they too were given houseplants, but they were told that nursing home staff people would take care of them.

The difference in the quality of life between the experimental group and the control group was dramatic. Those in the former were much happier, and their mortality rate for the 18 months following the experiment was half that of the other group.

The results of that experiment don’t mean you should stop wanting your illness to go into remission, but they do demonstrate that small changes can lead to big improvements.

Since the new year is only a few days away, I will leave you with this question: what small New Year’s Resolution do you want to make – and keep?

Is Your Life Better Than You Realize?

Monday, May 11th, 2009

A while back, I had a client whose arthritis was so bad she couldn’t walk. Many tasks, from cleaning her apartment to buying groceries and cooking meals, were very hard for Maria to do. On top of that she was in a lot of pain.

On the other hand, Maria had lots of friends whose company she enjoyed and with whom she got together on a regular basis. In addition, she was building a business making things she loved, and she had just taken up painting and was enjoying it very much.

In one of our coaching sessions, Maria was feeling very negative and told me that she hated her life. It was obvious to me that that wasn’t true, so I responded by telling her that she didn’t hate her life – that what she hated was her illness and her symptoms. Maria replied that my observation was correct. Then, without glossing over her painful symptoms or pretending they didn’t exist, she was able to acknowledge the many things and people in her life that she enjoyed and that gave her pleasure. And doing that made her much more able to get through her hard times and difficult days, and have a much better life overall.

I’ll conclude by saying that I know that for some of you reading this, right now there are very few if any things in your life that you enjoy. In that case, I think you will find some of my previous posts helpful, and I will give you more helpful suggestions in the future. And you can always contact me for a no cost consultation.

But if you are one of the many people with a chronic illness who focus and dwell on their symptoms and pain (which I even did myself at one time)  and overlook the positive aspects of their lives, then I invite you to fully acknowledge all the people you connect with and the things you do that you love and enjoy. I know you’ll be glad you did.