Sarah, what would the osteopath do?

Joe,

Osteopaths have a variety of skills beyond what an MD would do. They usually use Cranial Sacral Therapy techniques. CST is controversial. Some will try to manipulate your skull bones. Others will just work on your neck and spine. Some are grounded in medical science. Others can get very 'out there' in their beliefs (energy work, etc).

An MD specialist in Physical Medicine and Rehabilitation known as a Physiatrist may be helpful.

The biggest problem is that I cannot walk any distance at all. Since I tried to return to work 7 weeks ago, I have been unable to walk even a block, whereas in all my other recoveries I was able to build back up to walking longer and longer distances within 2 weeks Does anyone have any tips to building up tolerance and stamina for walking?

What Mark said... my DO does CST and works on my neck... small movements.

As for walking... I wish... I am in the same boat...

Hi Joe,

I'm very sorry to hear about your current struggles.

Does the LA in your handle mean Los Angeles?

I live in Los Angeles.

I was in a car accident on the 10 FWY heading through downtown from the West Side to get to work and the concussion I sustained in the accident caused me to be home-bound for over a year. That was the first diagnosed concussion I ever had.

I also became weak from 6 months of bed rest until my second neurologist ordered a spinal tap which relieved me of having a very severe, ongoing headache that required me to live in the dark with total quiet during that 6 month period of bed rest. Her thinking was that I had an increase of intracranial pressure that wasn't able to be seen on the MRI.

Have you had an MRI yet? Have you had a CT?

What is the diagnosis of the headaches? Do they think it's migraines? Post-Traumatic Headache? Tension Headache? Anything specific?

Is there a specific location where your headaches are located?

Eventually, I was diagnosed with pituitary dysfunction. (When the pituitary glad is being pressed upon, like by an increase of intracranial pressure, it is very painful and is usually felt behind the eye.) Now that I'm taking hormone replacements I am finally getting better.

Since you have a history of concussions, I recommend that you see an endocrinologist to get your hormone levels tested. This can be problematic because most endos are not experienced with pituitary dysfunction that is caused by a concussion. My endo is on the West Side - he does not take insurance, but if you have a PPO you can be reimbursed for the visit.

Some pituitary damage can cause headaches that are often misdiagnosed for a long period of time.

I agree with Mark that you need at least light exercise if you can tolerate it.

When I returned to work, I worked a 12 hour week and increased very slowly and gradually. I am still only working 35 hours a week but I intend to increase to 37 or 38 in the next couple of months.

Does your neurologist have a lot of experience with multiple concussions?

There is a great concussion specialist program going on at UCLA that you might want to look into.

You definitely need to rest as much as possible and whenever your symptoms become exacerbated.

You are very lucky to have your mom there to help you through this.

I colored pages some and read very simple, short articles. Coloring books are made with adults in mind.

There are also some "brain injury" work books that you might be interested in working with...

After I got a little bit better, I also started watching some light TV as I could tolerate it (after enjoying a 10 year reprieve from TV for a more active lifestyle) to help keep myself entertained.

Are headaches the only symptom you are experiencing that is keeping you from living a more normal life?

What kinds of symptoms are you having that is preventing you from walking?

Do you have brain fog inside the head or physical headaches outside the head? (I hope this question makes sense...) And how painful is it? Or is it just debilitating and uncomfortable?

EsthersDoll, thanks so much for your detailed response. I am sorry to hear of your struggle also.

I moved to LA - Culver City - from the East Coast last August for a new job and almost immediately became disabled due to a second concussion in Sept. and then a third in December.

I have Kaiser insurance and am in the process of transferring it to COBRA coverage since I am no longer working. I have tried to get an appt. at the UCLA TBI clinic, because I believe they are the experts in the area but it is very hard to get through their bureaucracy if you don't have PPO insurance. My mother said she would pay if necessary but that does not help in getting them to return our phone calls requesting an appt. I also have been approved for Medi-Cal, but they say it will take 90 days to get to the point where I can see UCLA doctors with it.

My Kaiser neurologist ordered a spinal tap but I was feeling so poorly on the day they scheduled it that I didn't go. If I knew what you just told me about how much it helped you, I would have gone and dealt with the resulting headache later. My neurologist said he did not see increased pressure when he looked into my eyes, so I thought the spinal tap was not really necessary. But maybe I was wrong, based on your experience.

I am seeing the Kaiser headache specialist April 7 and maybe I will get a diagnosis of the headaches from her. The headaches are across the front of my head. Not as low as the eyes.

I am also scheduled for an MRI next week. Not sure if that is necessary either since the last one after the 3rd concussion was normal and so was the EEG.

Can I ask who your endocrinologist is? It may save time to go to someone you recommend for our problem rather than trying to deal with the Kaiser doctors, who are more generalists. And my doctor is not familiar with multiple concussions - he is mystified by my symptoms.

The headache is my serious symptom. It is what is keeping me from walking and even talking. I have been unable to walk for 7 weeks, but the talking strict limitation is what got worse this week. I try to avoid any activity that gives me a headache and right now, that is almost everything. The pain is about 7/10.

Thanks again for all your good advice. Joe

Hi Joe,

Funny enough, I lived in Culver City when I was in that auto accident. I miss living there. I had to move closer to work because I can't drive or travel like I used to be able to - but at least I'm working now.

My endocrinologist is VERY good. His name is Dr. Theodore C. Friedman He has his MD and a PHD and he teaches medicine at UCLA.

But he is primarily a researcher, so he only takes cash (checks and debit cards) and he only sees patients on night a week.

Here is his webpage: http://goodhormonehealth.com/

I did not see him until one year ago, which was more than 2.5 years after the accident I was in.

He will probably want you to get the spinal tap done ASAP. Even though I had a spinal tap that relieved the pressure I had two years before I met him he still wanted me to get another one.

The spinal tap order should have written on it that your intracranial pressure is to be measured. It's very important.

The problem with an increase of intracranial pressure is that it isn't always seen or present despite having an increase of intracranial pressure. I took this passage from a website that I am going to include the link to below.

I didn't show any papilledema.

"Is it possible to have IH without papilledema?

While many physicians believe papilledema must be present in order to confirm an IH diagnosis, others argue that papilledema does not always have to be present. In some instances, a patient with intracranial hypertension may not show papilledema because of a time lag between the initial rise in cerebrospinal fluid (CSF) pressure and the development of papilledema. Therefore, at the time of diagnosis, papilledema is not seen.

Another theory is that the actual increase in CSF pressure may produce headache but is not high enough to produce papilledema.

Anatomy may also play a role. Variations in the micro-anatomy of the optic nerve can restrict CSF and prevent it from entering the optic nerve’s subarachnoid space. Or CSF pressure may be directed to a point of lesser resistance, such as the sella turcica (pituitary gland fossa) which then produces the appearance of an empty sella on imaging studies.

Other evidence of intracranial hypertension without papilledema is found in the fact that it’s possible to have asymmetric papilledema, in which the optic nerve swelling is either worse in one eye or only develops in one eye, rather than both."

Here is the link:

http://www.ihrfoundation.org/intracr...sion/info/C140

You can find a lot more information about other symptoms and details about increased intracranial pressure on that website that might help you out a little bit. You *may* be experiencing some symptoms that you aren't even able to pin point - that has happened to me quite a bit over the last few years.

You may or may not have an increase of intracranial pressure.

And you may or may not have an hormone/endocrine deficiency or problem.

If you see Dr. Friedman, he will cost more than just the amount of the first visit. He is very thorough and I highly recommend him. I saw three other endocrinologists who wouldn't even order the tests to be done for me to get a diagnosis (one of whom is a prominent endo who teaches at USC) because they just weren't informed enough about the damage a concussion can do to the pituitary gland/pituitary stalk or hypothalamus. They were insulted that I brought in the research to prove that it's an under diagnosed and misdiagnosed problem - Dr. Friedman quoted the research (right down to the levels considered to be necessary to have further testing conducted after mTBI and everything) and I didn't even take it out of the folder I brought it in.

Dr. Friedman will probably want you to have a very special MRI done on a very detailed machine called a T3. There are only 2 in the area, one is in Torrance and the other is at Cedars. Going to Cedars is more expensive but they have better radiologists there who can read them better.

He will sit with you for an entire hour to discuss the problems that you have during your first appointment.

You may end up spending a lot of money for testing that doesn't indicate or prove that you have a hormone deficiency.

My thinking was, if I didn't have any hormonal deficiencies (but I had done my research and I was pretty sure that was what was wrong with me) then I would move on and try something else. I have been very determined to get better.

Luckily for me, it seems that my journey to recover lead me to know that I need hormone replacement treatments in order to get better and in order to function and I didn't have to try other things.

I am so sorry to hear that you have such severe headaches. Even though your headaches are awful, please post your other symptoms if you get the chance because it might help someone figure out another possible solution for you.

You may also want to get an MRI of your neck, but I'm not exactly sure how you got your concussions. Sometimes nerve issues cause pain because the neck was injured and an MRI might show that.

Please feel free to PM me or keep replying in this thread and I'll reply as I am able.

Hi Joe

I too am a teacher, but have made it back to work full time. I don't run a big classroom anymore though, but I still get to have a small one and work with others.

For some brain resting activities you can try

listening to gentle music
audio books
planting something simple in dirt
run your hand through dirt
fold clothes or fold things -- paper

Hang in there. This site has helped me sooooo much and I hope it helps you too.

Sincerely

pm

Joe,

I have the same problem with not being able to walk. Over the months it has gotten better. I did vestibular therapy that got me stable enough to walk with out someone at my side, but I still have no endurance.

I try to at least pace length of the house here and there to get movement in. I live on a hill and around the block there is no where I could just stop sit and rest except in the middle of the sidewalk. I will sometimes go to the store with my husband and walk holding the buggy for dear life, but it is still walking and we go to stores that are not busy or too large and they do not play music, also I can go to the car if needed. Car rides are bad though so that is a hit and miss thing.

I listen to audio books quietly to pass the time while resting in a nice dark room. Many libraries have electronic downloads available if you are a member.

I also have bad headaches, but I have eye and ear involvement with my concussion.

Best of luck to you, I hope you get in to the clinic quickly!

Hi Joe,

I was the same way, massive headaches, every single noise bothered me so much, walking hurt my head, tiny noises sent me insane!! my head felt like it was exploding with every walking step, it was awful but did get better over time.

Mind you a year later I am still so sensitive to noises.

Walking was so hard and I went in to vestibular therapy as I couldn't walk in a straight line and I had a problem with my right eye. My OT told me everything is connected so very important to get our eyes and ears checked out.

Even lying down in a dark quite room did not help the headaches. Over time they became less thank God.

I have to write everything down, cannot remember anything.

You have good advice here though, I totally understand those headaches, I'd ask people to please don't talk!! it hurts my head!

I so hope you start to feel better very soon, everything had to be quite around me but it did improve, just took time.

Oh, and months later when I started to feel a little better it all came back which made me feel I was back to square one, I was told this can happen and to keep moving forward, take good care of yourself...