BEST has created a virtual presence in Second Life for reaching out to those with brain injury and their caregivers. BEST hosts a variety of social events, small group discussions, workshops, and skills training.
Our goal in Second Life is to support those with brain injury engage in alternative and meaningful learning and peer support.
Our virtual office can be found on Etopia Island in Second Life. We also have a dedicated community center (PEER Center) which is the home of many of our activities and events.
Here is what’s happening at the PEER Center:
Join us in Second Life. All are welcome!
To get started, please click here.
Calling all Washington State support group facilitators!!
Thank you for facilitating and running support groups for those with brain injury and their families. Your continued commitment cannot be overstated or over-appreciated. You truly are the BEST!
Our dear friend, and also a facilitator, Bethany Davis is conducting research about our support groups and has posted a survey for you to complete at SurveyMonkey; https://www.surveymonkey.com/r/R53G3XH. We would appreciate your participation in this research.
Your answers on this survey will help inform areas of need in training, funding or resources for managing your group as well as provide a picture of what the support groups in our state look like.
If you have any questions please contact us at 877-718-2378. We’ll be happy to talk with you.
You can complete the survey at SurveyMonkey; https://www.surveymonkey.com/r/R53G3XH
(Editor’s Note: Writer, BEST guest blog contributor and brain injury survivor, Isaac Peterson, shares his personal coping strategies for dealing with brain injury in this comprehensive personal essay. KT)
Since no two brain injuries are alike, I’ll share some coping with strategies in general terms.
One of the most important things you can do to help yourself recover is to be open with your family and friends. Let the people you care about most, and who care about you, know what’s happened, how you’re feeling, and what you need.
Most people don’t know or understand what having a brain injury is like, so they can’t know unless you tell them. Family and friends are great support for those times when you feel worthless or helpless.
You may have those feelings while you are trying to adjust to your new normal. Some of those feelings can come from comparing the new you to the old one–the person you were before your brain injury.
My advice on comparing the new you to the old you is simple: don’t. There will undoubtedly be things you could do before but can’t do now, or things you can’t do as well as before. Don’t dwell on what you can’t do any more–focus on what you can do now. Always work to do those things better and better, and gradually work your way back to doing what you could before.
If you’re like a lot of traumatic brain injury (TBI) survivors, you’ve got less energy and different sleep patterns, coupled along with constant sleepiness.
That’s only natural; sleeping is the way your brain works to heal itself.
And if you’re like me you may even notice that at certain times of day you have less energy and may need to take time out for a nap; my low energy time of day is early afternoon. I’ve also had trouble sleeping at times. Prescriptions can really gum up the works—one of mine causes drowsiness and another causes insomnia.
What to do?
Two things that have worked for me with the down times is to try to set a daily routine where I’m not doing much of anything in the middle of the day. I recommend you set a routine that works for you and hold to it as much as possible. For the times I have trouble sleeping at night, taking a couple of Benadryl tablets when I go to bed helps me get to sleep. Benadryl doesn’t have nasty side effects like other sleep aids (check with a medical professional for possibilities that may work for you).
Every day things you could do without even thinking can be pretty hard to do now. You’ll need to come up with workarounds, alternate ways to get done what you need to get done. My brain injury made bending down to tie my shoes a real ordeal sometimes, but somehow I managed it. A simple thing like being able to tie my shoes was a major personal victory–that may seem like a silly thing to people, but those people usually aren’t people who’ve had a traumatic brain injury. Don’t let that get to you.
What I hope you’ll do is to celebrate every victory, no matter how small. Even tying your shoes again is a victory. Try to experience the joy and sense of accomplishment you experienced when you first learned to tie your shoes. Try to do that with every positive step you take and celebrate it.
Set yourself up to experience a series of small victories–make winning a habit. You can set yourself up to master small but manageable tasks—but make sure they are things you can manage to overcome in your present state.
As you master more and more of these tasks and keep winning, winning will become a habit. Make winning and keeping a positive outlook part of your new normal. But if you don’t meet your goal, don’t beat yourself up or quit. It’s not failure, it’s a way to get a better handle on what you need to work on and get better at. You’re not a failure until you give up. Just start again, be patient and keep going.
Try not to dwell on things you can’t do. Look at them as things you haven’t done yet.
One thing that will help is including exercise in your routine. Going out walking is an activity is something that’s been huge in my recovery. Exercise will help keep your body in better shape, and the better shape you’re in the better foundation you have to recover from your injury. And of course, a good diet can help with that. I recommend a heart healthy diet.
I can’t emphasize the value of patience enough. One thing that may try yours is the responses of other people who have never lived in your world. A traumatic brain injury, unlike a broken leg, is an injury that’s invisible to other people.
People will feel free to give you unsolicited advice. You may hear things like, you’re just looking for attention; get over it, it’s all just your imagination or if you’d just stop thinking about it, it will go away, and all sorts of comments that only show you how little these people understand or can relate.
I can’t really tell you how to cope with that kind of thing; all I can really advise is to try to patiently explain to that person. Encourage them to ask questions so it becomes an opportunity for that person to learn.
Having a brain injury doesn’t mean you can’t ever have any fun. As much as you’re able, keep doing the things you used to do for fun. As you move forward, you might actually redefine what fun means—you’ll want to have as much fun as you can, so be sure to include some fun time into your daily routine.
Keeping a positive attitude is key. I know it’s hard to do and I can’t tell you how to do it. Keeping busy when you can and doing things you enjoy will help. Surrounding yourself with positive, supportive people will help. Your loved ones can help, and joining a support group can go a long way. Being around people who are going through what you’re going through and can tell you how they cope with their own traumatic brain injury is huge.
There’s so much to learn and remember—I could spend the rest of the day telling you what I’ve learned.
And since every brain injury is different it’s hard to tell you exactly what can help. I’ve tried to cover some of the things that apply to most people with brain injuries.
One thing I can tell you with complete confidence, though, is simple: Your life definitely isn’t over; it gets better. Just give it time and don’t give up.
Click here for a catalog of more essays and articles from Isaac Peterson.
Isaac Peterson grew up on an Air Force base near Cheyenne, Wyoming. After graduating from the University of Wyoming, he embarked on a career as an award-winning investigative journalist and as a semi-professional musician in the Twin Cities, the place he called home on and off for 35 years. He also doesn’t mind it at all if someone offers to pick up his restaurant tab. Peterson also welcomes reader comments. Email him at email@example.com.
The Brain Injury Community Support Group in Spokane, Washington, created a memorable evening of celebration and giving thanks.
Utilizing the culinary talents of Holly Blomquist-Worley and Marysa Rogozynski, these two women prepared a Thanksgiving feast for support group members to savor and enjoy.
Held at the Multicare Valley Hospital on the evening of November 25th, BESTies enjoyed each other’s company, some delicious food, and had the opportunity to give thanks.
Judging by the smiles and this delightful meal in the pictures, a good time (and full bellies!) were had by all.
The Brain Energy Support Team (BEST) has just witnessed the most beautiful art of sharing and caring.
Thank you for helping to support the empowerment artists of the brain injury community and their families.
With your generous help, you are providing the support for more learning materials and educational opportunities to tap into creative tools, resources and strategies for brain injury survivors to live the BEST lives possible after brain injury.
You put the “giving” in Giving Tuesday yesterday, the international day of giving back to causes that make a difference in the lives of others.
Click here to contribute on our fast and secure donation page.
Donations of any amount are welcomed and greatly appreciated.
As we reflect on 2019, the art of living our BEST lives possible in beautiful color and texture was evident.
Through our large support group network in Washington State; Our BEST Space activities, educational opportunities and events; widely attended educational symposiums; the Washington State TBI Conference; Brain Injury Awareness Month; camping; picnics; barbecues; the Tacoma Art Museum, TAM Local Community Art Installation: “Superhero” show featuring BEST artists; Second Life online support and activities; and BEST community outreach, the art of sharing our care and supporting each other was nothing short of magical.
Looking forward to the new brushstrokes of 2020. Thanks for making 2019 so special.