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Does anyone have any good suggestions on how to find a place to live. It is easier to just live alone when you have a TBI.....it is my experience that marriage is not a wise decision. I am on a…Continue
Started this discussion. Last reply by Kerry Mischka Oct 5, 2012.
I am so touched by what you wrote and I live in Trinity, Florida...Tampa is right around the corner. I want you as a friend, but don't know how to do it. It would be so much fun to get some other…Continue
Started this discussion. Last reply by Kerry Mischka May 30, 2012.
I sustained a severe TBI on August 23rd, 1997. I never got SSI and totally depend on God to help me financially. Can anyone help me and tell me what to do. My family took over everything while I…Continue
Started this discussion. Last reply by Kerry Mischka Mar 18, 2012.
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Kerry Mischka replied to Kerry Mischka's discussion Finding a place to live.
Glen Brist said… Kerry, I am surprise that in re-hab you were taught not to nap.....I was so tired I slept allot.....and they encouraged it because it is allot like a babies brain,,, it is busy growing, (in our case , reconfiguring, ) and they said that is why babies sleep allot... my Dr. suggested the sleep med (Ambien) mainly to shut my brain down , Often our brains run around , in my case I am taking care of the home ranch, so I have had to plan, organize, and also work physically hard, and at my age, I just could hardly do it.... hence the need for naps.... There again, age is a major difference will all of us... Actually, my Dr. encouraged me to work out at the hosp. sport center, which is good for our selves, and If I had lots of errands to run in town, and I felt my brain getting tired, I would put "projects" aside , and drive home. There are allot of things that can just wait, my driving safety, and mood, and making proper choices are more important, so "whoa" " I am going home to nap " Sometimes my family would say " go take a nap " probably if I was getting a little on edge, and at first I resented it, it to me was like they were saying to a child, "go to your room, we don't want you"....and sometimes I would cry, so I realized "it" was my problem, so thanks to God, I was able to make adjustments within ... best let this be all for now...
Glen Brist said… Kerry, my Dr. says that I will face a fatigue issue the rest of my life.... If I do not nap, I am toast... easier to get along with others (family) if I nap, but I have also learned to relax and let things slide.....tbi has taught me that one can squabble over things so minor,, life is to short for that so I am glad for faith and also support group therapy, that has helped me to accept and compensate.... I take a Dr. prescription for going to sleep, wish it would keep me there the full night.... but there again.... nothing wrong with naps..... Thanks for sharing what you did, sorry I have missed your profile till now....
Daniel Trapp said… Kerry,
Interesting. Do you get regular sleep, by that I mean are you able to go to bed at the same time every night, are you able to get 6-8hrs of uninterrupted sleep, and do you use sleep aids (glass of wine, shot of whisky, or sleeping pills) to help you get sleep?
Also, concerning the mechanism of your injury, did you suffer any blunt force trauma to a specific area of your head?
Daniel Trapp said… yes, that is the case. Forgive me for not responding, I leave the website up and do not log off when I am not here.
I am currently taking a disabilities class and the Professor has asked us to get involved with a blog/support group. I have some TBI related issues so I have chosen to do more research on how TBI effects the lives of people, the difficulties one faces on a daily basis, and also the frustrations with having a disability that society is pretty clueless of and not very understanding of. My goal is to gain new perspectives on how this unseen disability is very real to those who have it.
Kelly Sanford said… Kerry,
I have not been on the site in a while. Good to hear from you. How are you doing? I am starting vestibular therapy related to my head injury. Do you know anything about it?
Kelly Sanford
In less than three weeks Congress will meet to vote on the PABI Plan. The PABI Plan would create a seamless, standardized, evidence-based system of care for the millions of American families suffering from the number one leading cause of death and disability in America’s youth: Pediatric Acquired Brain Injury.
(If you’re not sure who your Congress person is please email your name, City, State to: ted@thebrainproject.org for contact information)
About the PABI Plan:
http://www.thebrainproject.org/pabihome.php
Message to leave in voicemail (or if the receptionist insists on taking the message, please make sure they repeat it back to you so you know they wrote it down correctly):
"(Legislative Assistant’s name), my name is (your name) and I am (insert position/organization or hometown). I wanted to thank Representative (Insert Name) for considering to serve as a co-sponsor of HR 2600, the National Pediatric Acquired Brain Injury Plan Act. As you know, over 130 bi-partisan Members of Congress have signed on as co-sponsors of HR 2600 and we would greatly appreciate Congress (man/woman) (Insert Name)’s continued support of the millions of American families who have a child with a brain injury. If you need to contact me, please feel free to call me at (your phone number)."
Email to send after VM (please cc ted@thebrainproject.org): “Per my voicemail, my name is (your name) and I live in (your hometown). I would greatly appreciate if Representative (Insert Name) would agree to co-sponsor HR 2600, The National Pediatric Acquired Brain Injury Plan Act, which would create a seamless, standardized, evidence-based system of care for the millions of American families suffering from the number one leading cause of death and disability in America’s youth: Pediatric Acquired Brain Injury.
Thanks very much for your support and that of congress (man/woman) (Insert Name), and please do not hesitate to contact me with any questions.
If the receptionist asks what it is regarding, tell them it is about HR 2600, The National PABI Plan Act as they are aware of the bill.
Thank you, Craig Sears
Geo Gosling said… No. I don't think it is possible for someone who has not suffered a TBI to understand what it is like to live with an injured brain. Therefore, they could not make much of a helpful comment to someone who has suffered a TBI. I am not being critical of anyone; that's just the way it is. It's a fact of life.
I agree, you couldn't describe what it's like to give birth unless you have given birth yourself. I, or any male human being, could never describe what it is like to give birth.
I was extremely f!@#$%^ pissed-off for a good 10-12 years after I suffered my TBI. I'm still pretty pissed-off but nothing like I was. Time does not heal all wounds but it does make them less "painful"...I guess. The best thing I did for my anger was to keep myself busy. I did that by writing a book where I "vented" about all the shit I have had to put up with because my brain has been severely injured. Then I wrote another one.The books are: TBI Hell: A Traumatic Brain Injury Really sucks followed by: TBI Purgatory: Comes After Being In TBI Hell
Click here for TBI Hell (in print)
Click here for TBI Hell on iTunes
Click here for TBI Hell from Google eBooks
click here for TBI Purgatory (in print)
Click here for TBI Purgatory in iTunes
Click here for TBI Purgatory in Google eBooks
Click here for TBI Purgatory for the Kindle
Yes. Life does suck...for a while (it could be a long while) after one has suffered a severe TBI. Your life will never be the same, at least mine won't. But...life is a funny thing - it's all how you look at it. I was suicidal, homicidal, omnicidal (I would have killed anything and everything) for a good 10-12 years after my accident. Then, I don't know, I decided that I hate feeling like this and thought "Well, I'm pretty f!@#$%^-up, I can't do what I used to do, but I can do...this, that, and the other thing, so I'll do this, that, and the other thing."
Plus, I figured with my luck if I tried to commit suicide, I'd fail and end-up worse off than I am now, and if I killed someone I'd be caught and thrown in prison for life. Then I'd be in prison with a TBI...not good.
stephen d. cunningham said… Hi Kerry,My PTSD is not combat PTSD. It is life and death expereance when i was in the hellicopter crash thats when i also got my first TBI 12-25-1972 my second came in 1975 for following orders. Alot of inhumane things happned to me after the crash until i got discharged then i ran for my life.
stephen d. cunningham said… Thankyou Kerry I was taken off medication causing me lots of side efect hopefull its for the best.Thanks for calling me A Hero but Iam not a hero .Iam a Surviver thats all.The photo i found it on FB i search for funny photo helps the time and the ringing in the ears move along.Keep smiling it makes others feel better. STEPHEN
Kelly Sanford said… April 24, 2013 at 6:30pm to August 28, 2013 at 8:15pm – St Lukes rehab
May 23, 2013 at 8am to May 24, 2013 at 4pm – Seatac marriot
May 31, 2013 at 7:15pm to June 24, 2013 at 10:15pm – EVERYWHERE
July 15, 2013 at 10am to July 21, 2013 at 11am – North Skookum Lake

TBI Survivors Network replied to Cheryl Green's discussion Brain injury survivor Kris Haas is doing an incredible, inspiring art project
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