Traumatic Brain Injury and Post Concussion Syndrome For traumatic brain injury (TBI) and post concussion syndrome (PCS).


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Old 07-10-2012, 02:41 PM #1
Lagr Lagr is offline
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Default First Summer with PCS

I'm wondering if others here find that their PCS symptoms are worse in the hot summer months. I'm particularly curious about headaches. Mine have been getting pretty bad this summer, despite upping my topamax dosage. Every day my head hurts.

A couple weeks ago, I saw my neurologist and he told me to exercise more. Well, I haven't been able to take his advice because the headaches have become so bothersome.

Any strange chance topamax could actually cause headaches? Or is this most likely a result of summer heat and humidity? I would hate to think my headaches are getting worse the longer I have pcs. Ugh!
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43 yr young female, suffered a mTBI with PCS August 2011 while playing ice hockey. Symptoms included dizziness, nausea, exertion headaches, trouble sleeping, fasciculations, sensitivity to light and noise, occasional numbness to extremities.
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Old 07-10-2012, 04:23 PM #2
postconcussion postconcussion is offline
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Hi Lagr,

Sorry bout your headaches I do notice that the heat and humidity makes my headaches worse. And then it is harder to exercise. The only thing that i can really handle lately is walking in the pool. Best wishes.
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Lagr (07-11-2012)
Old 07-11-2012, 07:01 AM #3
SmilinEyesMs305 SmilinEyesMs305 is offline
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The summer months are h*ll for me and my PCS. My first summer it was so bad, that whenever I got overheated, I had to lay down on the floor with ice packs on my neck. I had no tolerance at all for heat and humidity. It was instantaneous. I would feel weird and 2 minutes later, I would have to be completely flat or I felt like I would pass out.

This year is a little better. The first week of hotter temps was really rough on me. The intense heat of last week, got me agian despite being in the AC most of the time. I'm still trying to get out of the "concussion hangover" from the strain on my systems from last weeks intense heat and humidity.

What you are experiencing is completely "normal" for PCS.

My advice: Make sure you are hydrated. Seems easy, but I mean drink as much water as you can. This makes a huge difference for me. Even when I think I drank enough, if I don't keep it up, I feel sick again. Once your body is dehydrated, all of your symptoms will spike. And you may not even realize you are dehydrated. So, always be drinking water!

AC as much as possible. Can you exercise indoors where its cooler?

Have you tried ice on your neck or head when things increase? It seems to help me cool down quickly and lessens my symptoms somewhat.
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What Happened: On 3/8/11 I was stopped waiting to merge into traffic when I was rear ended by someone doing 45 mph. I walked away from the accident, to fall into the pit of PCS 5 days later... (I have had 2 previous concussions, but neither developed into PCS.)

Symptoms 3 Years Post: Physical: migraines, infrequent vertigo, neck and back pain (from accident), tinnitus, visual field deficits in left eye, problematic light sensitivity, (including visual seizure activity), noise sensitivity, EXTREME fatigue, semi-frequent disrupted sleep cycles,
Cognitive: semi-frequent Brain fog after cognitive strain, limited bouts of impulsivity, unable to concentrate for more than short periods of time without fatigue, word finding problems, slowed processing speeds, impaired visual memory;
Emotional: easily overstimulated, depression, anxiety;

Treatment so far: Vestibular therapy; Physical Therapy; Vision Therapy; Vitamin Schedule; Limited caffeine; Medications; attempting to limit stress and overstimulation; Yoga; Cognitive Therapy
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Old 07-11-2012, 08:57 AM #4
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Thanks for the replies. I've been trying to stay in the a/c as much as possible, but still seem to be getting headaches. Towards the beginning of the summer I was able to make the headaches go away by going to the pool. I think the cool water had some sort of effect. That doesn't seem to be helping anymore, maybe because the water has warmed up so much due to the continuous high temps here. It's almost like bath water now!

The pain has been so bad that I haven't even been exercising much at all. Went to the gym maybe once last week. Went for a long walk last night. This is such an evil cycle. Headaches mean less exercise, which means less of that good fatigue at the end of the day, which means less chance of quality sleep.
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43 yr young female, suffered a mTBI with PCS August 2011 while playing ice hockey. Symptoms included dizziness, nausea, exertion headaches, trouble sleeping, fasciculations, sensitivity to light and noise, occasional numbness to extremities.
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Old 07-11-2012, 12:40 PM #5
rosebower rosebower is offline
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Quote:
Originally Posted by SmilinEyesMs305 View Post
The summer months are h*ll for me and my PCS. My first summer it was so bad, that whenever I got overheated, I had to lay down on the floor with ice packs on my neck. I had no tolerance at all for heat and humidity. It was instantaneous. I would feel weird and 2 minutes later, I would have to be completely flat or I felt like I would pass out.

This year is a little better. The first week of hotter temps was really rough on me. The intense heat of last week, got me agian despite being in the AC most of the time. I'm still trying to get out of the "concussion hangover" from the strain on my systems from last weeks intense heat and humidity.

What you are experiencing is completely "normal" for PCS.

My advice: Make sure you are hydrated. Seems easy, but I mean drink as much water as you can. This makes a huge difference for me. Even when I think I drank enough, if I don't keep it up, I feel sick again. Once your body is dehydrated, all of your symptoms will spike. And you may not even realize you are dehydrated. So, always be drinking water!

AC as much as possible. Can you exercise indoors where its cooler?

Have you tried ice on your neck or head when things increase? It seems to help me cool down quickly and lessens my symptoms somewhat.
YES YES YES! I KNEW it wasn't just my imagination!! *HUGS!* And the water too! I learned that hydration made, oh maybe 50% of all the difference with my PCS. And it's SO much harder to stay hydrated in the heat. I'm very easily dehydrated and I feel like a 55 year old with hot flashes ( it's my first summer too!)
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Old 07-11-2012, 01:59 PM #6
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This is my first summer too but I don't feel the heat like most ppl. I went to the doctors in jeans and sweater when most were in shorts and T shirts. My hands were ice cold. Weird
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