| Ways to Handle the Bipolar Journey |
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| The Journey Now, as we all know, this journey can be a bit bumpy at times. It can be filled with some major pot holes and some unreal sort of curves -- and it's those times that we need all the coping skills possible. The trick is -- and this is important -- to stack up as many coping skills as you can during the smooth times, so that when the bumpy times come, you'll be ready. Trust me, if you've got a great set of coping skills at hand, and a great support group or safety net as some folks will call them, ready, then those bumps and curves don't last nearly as long and, sometimes, they don't seem quite as bad. Some of the things that help me cope: When I'm feeling myself go down I do my best NOT to merely sit and dwell on things. Just muddling over things is horrible for me because it continues to focus my mind on the depressive things that are bringing me down. Getting up and doing something to distract my train of thought helps -- even when it's the LAST thing I want to do. It's in my nature to want to sit there and muddle -- I have to at times will and force myself up and moving to do something else other than that. Not always easy, but mucho better for me. I have a great support group -- both online and IRL (in real life) -- I'm blessed, truly. When I'm slipping up, I often don't even notice it -- mania is very tricky like that -- it feels so darn good that often times you don't realize you're "there" until it's too late. I've got several friends that I trust that know me very well. They know when to say, "Hey -- are you taking on a few too many projects?" "Hmmm is that red lipstick you've got on?" "You spent HOW much on your credit cards?" Those friends know how to tweak my buttons when I need them tweaked -- the thing is simply that I have to be willing to pay attention to them when they start say these things. It's so easy to just brush off the comments and be like... "Oh, don't worry... it's nothing..." But the thing is... quite often when I'm manic, I don't see the things that others see... it pays me to listen. Again -- not always an easy thing. And these same friends -- I know if I feel myself slipping downward, I just have to contact them and they will be doing anything to help me back on the road to what what I call "the sweet spot." Again -- it's one of those things... I have to call them for them to help me, if I don't call, they won't know.... Many folks tend to isolate themselves when they are going into that downward spiral. This is one of the worst things you can do. I heard it described this way... Think of this -- Have you ever watched the Discovery Channel? What happens to that lone little antelope that wanders off alone from the pack? You guessed it! That isolated antelope becomes cheetah bait! You need to hang with the pack. Don't go wandering off alone. We don't want anyone here becoming cheetah bait. Whenever you think you want to just go off by yourself, you want to be alone, you want to isolate, you want to turtle, whatever you might call it -- just remember the Discovery Channel lesson. I know folks get tired of hearing this -- they heard it from their mama's when they were younger, they heard it from teachers in school, they hear it now from psychiatrists and counselors -- and now you'll hear it here: sleep is important. Bipolar disorder is very much tied to sleep and study after study supports this. Sleep is to the bipolar patient what a balanced diet is to the heart patient. Make sure you get enough sleep -- and not too much -- you need the right balance. Medications -- one thing I had to realize is that just because one thing works great for someone else it doesn't mean it's gonna be the same for me. And conversely, just because someone had a rough experience with something, doesn't mean I will. I have friends that both lost and gained weight on the same medication. Different medications afffect different folks different ways. And also, just because a medication is designated for one illness doesn't mean that it won't work for another. When I was first diagnosed I was really confused as to why on earth I woulg be taking medications for epilepsy, when I wasn't epileptic. Then I was on another medication for Alzheimer's for a while -- and though I may have my moments, I'm not an Alzheimber's patient. But I benefited from the medications. Try not to let the "labels" trouble you. Look at the results, not the labels. Along the lines of medications -- please be careful of "over the counter" medications. Just because it is over the counter it doesn't mean that it won't interract with the medications that you're on. Always check with your doctor before you start taking other medications. Also -- if you see more than one doctor, make sure that each doctor is fully aware of ALL the medications you are on -- if your family doctor doesn't know that your psychiatrist prescribed certain medications for you, then he or she might prescrible something that doesn't mix well with what you're taking. Be sure to tell what you're taking -- it is very important. With every new medication and every medication adjustment expect some changes -- it's rare that there aren't a few. I like to think of it like this -- your body is sitting there and WHAM! all of a sudden it's hit with this new medication -- picture (if you can) your body's eyes getting really big and looking at you and saying, "What the heck?!!" Your body has to adjust to the new medication -- some medications take longer to adjust to than others. Each med has their own set of side effects. Each medication has its own timeframe for how soon it will start to work. Eventually your body will settle back down and get back into the swing of things -- it's just a time issue. For some medications it can take a week or so and for others it can take several weeks or even a couple of months for the true effects of the medication to be seen. Be in contact with the doctor during the time of adjustment -- he or she will let you know what side effects are "normal" and which ones indicate that you need to come off a medication. And that leads us to the next thing that I've found so very helpful. Communication. Being open and honest with my psychiatrist has not always been easy. But the more open I am and the more willing I am to communicate and let myself be heard, the better I have gotten. The same is true for therapy. I've seen the most results when I've been willing to have the courage to say things that I really didn't want to say and to tackle subjects that I really didn't want to tackle. It's true -- therapy is work. But it's worth it. If you've been diagnosed and you're simply trying to go through this with just medication, then I'd suggest that you see a therapist as well. For me, I have been in therapy since my diagnosis and it's made all the difference. I've been able to work through things with my counselor as they came along and in turn she's helped to equip me with many coping skills that have become invaluable. And finally, but not lastly, my Christian faith has played a major role in my journey. I have a strong support group at my church and prayer has become a vital part of my life. If you don't have a place of worship, then I would suggest that you start looking for one. You'll find something there that no Friday night bar will ever give you... I have more peace now than ever before. If you've never listened to the Brooklyn Tabernacle Choir Be Glad CD, then please -- go out, buy one today. I'll add more coping skills as I think of them... I hope that these help... On our message board, I've posted this as well -- if you have a coping skill that has been especially helpful for you, then please, go over and share it with us... it's been said that knowledge is power. For those that have bipolar disorder, the more coping skills the better. We look forward to seeing you on the message board. (((BIG HUGS))) "Obie" |
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| Page last updated on October 1, 2005 Questions and comments can be sent to the webmaster@bipolarhope.org. © 2004-2005 Bipolar Hope All Rights Reserved |
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