Neurophsch test...
 

So I did my testing on Friday... It was awful!! I do not know I have ever felt more stupid! Also really opened my eyes in that I had not realized how much I had really lost until this test.. Tests I had..

I had to remember numbers as they were read aloud.. I could not do 4 numbers...

Had to repeat numbers backwards as they were read to me forward... ex.. 369, I would say 963... could not do 3 numbers...

Other test that I failed miserably was; I was read 3 simple sentences like.. Joe ran home.. at the same time I had to answer simple questions like, Where did Joe run... at the same time I had to remember the last word of each sentence and write it on the following page when told... I could not do more than 2 sentences.. it was horrible!

I was also read a short story and could not remember many details 10 minutes later...

I have never felt so stupid! On top of all of that... I had the worst headache when I was done... some brain fog and was dizzy... went back to my parents, took a 3 hour nap and still was not good...

I am so very happy that is over!

Sarah,

You got a mixed blessing. It sounds like you have serious difficulties but now, others will have a proper understanding of your condition.

With the new knowledge you will get when the report is done, you can seek help with ways to work-around your limitations rather than fight against them. When I learned of my memory dysfunctions, I could finally stop getting frustrated and find another way to deal with memory needs. I still struggle with memory issues but I do not get nearly as frustrated, if at all.

Now, you need to just rest to recover from a hard day yesterday. It may take a few more days. And, try to be patient as you have to wait for the report.

My best to you.

I had the same problem and I was told to follow the order like A1,B2,c3 and I sucked at that and had to say the alphabet each time.....I was very nervous about going so I couldn't concentrate... Your not alone

My memory is pretty much the same. I ask my child if she wants milk or juice and, by the time I've reached the fridge, I can't recall her choice. Now, I'm grateful that, at least, I remembered she wanted a drink, and just put both jugs on the table.

As, after seven years, it seems unlikely that my memory will return to its premorbid function, I just do whatever I need to do to get done whatever needs to get done. If I need to write things down, set timers, ask for assistance, etc..., I just do.

I'm over being embarrassed. If I had an injured leg, I wouldn't feel shame over using a cane, so why should I feel that way about the memory aids I need for my injured brain?

In fact, I've come to realize that some of my workarounds are downright clever. Necessity, as they say, is the mother of invention.

Yes Mark it is a mixed blessing, I just think I was more shocked at how bad the deficits are... and the big question is.... will I find enough of a work around to go back to work? and is this permanent?

Shady- I had to do the same thing... forgot about that one until you brought it up...

Hockey- I do the same thing... I hope I can learn some work arounds!

My neuro-psych report was pretty devastating. I was so far gone, I didn't even realize how badly I was doing on parts of it.

Once I got over the shock, the neuro-psychologist began using the report to recommend therapies. That's how I started Attention Processing Training. Without the test, I would never have got APT - and it did make a big difference to my day to day functioning.

I know it's hard, but try not to despair. The report is just your starting point.

I took mine like almost 2 weeks after I hit my head and I didn't know I had a concussion for like a week so I would of done so much worst if I knew I had a concussion like right after it happen.

Shady,

I doubt you had a NeuroPsych Assessment. They are rare and expensive. You likely had a Computerized Neurocognitive Test like an ImPACT, CNS Vital Signs or other system or a SCAT I or SCAT II .

Knowing one has a concussion should not change the result of a NPA or CNT

My test was part of a study that I am in with The University of Texas... i do the initial testing.. then 8 weeks of therapy and then a final testing... I will find out the details of the therapy tomorrow...

Mark,

I don't know what It was called... I just thought it was the same or close because they asked me around the same questions... I think it might of been SCAT II because I saw the same questions on a paper my doctor told me to fill out and I saw it when I searched SCAT II and it was the same thing...I know it wasn't Impact because it wasn't on the computer....some doctor asked me those questions and say the months backwards and I did a balance test which I failed terribly

Hopefully you get answers to your issues.

I was freaked out about how I did on the test, some users who I bugged will tell you how paranoid I was of it.

Luckily I learned a lot, and did a lot better on some of the tests than I thought too. At the same time I did worse on some parts that I thought I did good on.

It really gives you a sense of relief when you finally know the answer.

I hope you come back with positive news!

Kev- what are you doing about your results? are the therapy's that they are doing giving you any help?

That's great that you'll get therapy and a follow up test. Putting aside how tiring it is, I'd love to do another neuro-psych to measure my progress.

I do so hope your get improvement from the therapy. Don't be discouraged if you get very fatigued, especially after the first few sessions. When I started APT, I'd come home and flop on the chesterfield for the rest of the day.

Well im going to be doing vestibular therapy for my balance issues.

He implied that my body has surpassed the natural healing phase. Basically saying im stuck with it.

Luckily ive been through cognitive therapy where I have learned some workarounds. Now im also discovering new ones on my own.

Kev, I can't remember (big surprise) when you sustained your TBI.

Even pretty old school neurologists tend to think that improvement is possible for up to two years.

Modern research indicates that the TBI brain can continue to improve indefinitely.

Yes, improvement comes more quickly, and effortlessly, in the beginning, but therapy can continue to pay dividends. I'm seven years post injury, and my cognitive function has continued to get better. The brain is amazing - don't give up.

Sounds good, I believe in infinite healing as long as I keep myself in check, and dont worry, I dont believe in the word quit! :)

Hockey- Kev is about 7 months out.. we got here about the same time.. his accident seems much worse than mine for sure!

Hockey, you to can join the study... http://www.brainhealth.utdallas.edu/...ch/participate
they are constantly looking for people... my dad is a war vet and is part of the study too..

Kev- what classifies as too long? does that mean I am stuck with this as well???

After 1 year of issues I had an Occupational Therapist assess me in June of this year. The treatment plan was denied. I just had my internal examination done today by the insurer's OT. Wish me luck. I hear about all of the therapies you are all receiving and hope I can be a recipient of those too.

good luck!