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#1
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hot weatheri am in the uk, and for us we have had extremely hot tempertures, my epilepsy has got worse, but my work is trying to make things hard. I have an appt with my neurologist on 4th sept. I take tegretol R and keppra. Any suggestions. i was diagnosed 6 years ago, i have tonic clonic , atonic, myocloinc and absences. theresa |
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#2
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| Hi Theresa, welcome to the forum. ![]() Sorry to hear that your seizure activity is getting worse. You are taking a lot of anti-epileptic drugs right now, so I assume that you have been on the "cocktail tour" for a while. I'd advise you to take whatever measures you can to stay cool as heat can be a seizure trigger. Do you spend a lot of time outdoors? A cool, wet towel around the back of neck can help cool you down. There is a lot of info posted in this forum. Search around a bit and you may run across something which strikes a chord with you.
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. Would you like to help support this forum? We recently had a bunch of new neurofeedback practitioners agree to offer CWE members discounts for service. See post #12 for the list of all participating practitioners. |
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#3
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weather Hello no i dont spend much time out door in the summer, as i also as a side effect of teg r i have sensitive eyes, iwear tinited prescription glasses. Is there anything official stating that hhot weather effects epilepsy? I would help my case at work. i have been looking but so far nothing has jumped out at me theresa |
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#4
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| Perspiration and medication Alert on Overheating in People Taking Topamax Quote :
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. Would you like to help support this forum? We recently had a bunch of new neurofeedback practitioners agree to offer CWE members discounts for service. See post #12 for the list of all participating practitioners. |
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#5
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thanks think that will help in my case, also found some other info. theresa |
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#6
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| OK. One other thing though - Quote :
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. Would you like to help support this forum? We recently had a bunch of new neurofeedback practitioners agree to offer CWE members discounts for service. See post #12 for the list of all participating practitioners. |
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#7
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| Isn't it really strange that I never found any triggers and I kept careful records? Despite my age and the fact that I had a total hysterectomy BEFORE developing epilepsy, took HRT, my seizures followed a catamenial pattern. Every neurologist I saw said this was completely impossible. Huh? In the past two years I lost that great predictable pattern, my precious auras, everything I "needed" . At least now I haven't had a seizure. for 6 months |
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#8
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diary I do keepo a diary, but that not enough for them, trust me. They want it in black and white from either neurologist or some E organisation, as defined as a possible trigger. |
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#9
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| Quote :
Quote :
same info also attributed to Epilepsy Toronto 2005 ‘Safety & Epilepsy’ Epilepsy Matters, Volume 1 (Issue 3) Fall 2000 Quote :
Quote :
__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. Would you like to help support this forum? We recently had a bunch of new neurofeedback practitioners agree to offer CWE members discounts for service. See post #12 for the list of all participating practitioners. |
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#10
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| Hi everyone. Re Heat and how it effects epilepsy, Recently I had my semi-annual appt with my neorologist and I mentioned how the hot wether was causing me to lose my balance more, my gait was worse and my co-ordination was worse. His reply to me I found extremely interesting. He said that when the wether is very hot, it can have a negative effect on your meds and cause you to act like you're drunk because you lose so much of your medication though your perspiration (I sweat ALOT) bringing your blood syrum level down. If my medication level were to be increased, the meds could go toxic in my system causing a whole new set of problems. also increased because I also take meds for ulcerative colitis. Before he changes any of my meds he ordered a special type of blood test that most labs won't do because it's so expensive, "Blood Syrum Unbound Fraction" to see how much of my medication is being lost through perspiration. I'm not totally sure but I think he explained that it shows how much of the medication is actually in the blood and how much is being stored, that's the "unbound fraction". It's a very rare type of test and the tech. that took my blood has never seen this done before. In my 28 yrs. with epilepsy, I've never heard of this before and find it quite interesting. I always knew that you lost some of your medication though perspiration, but not that much, (maybe it's because I perspire more than most people, I also have "hyper hydrosis" which is extreme sweating) Randy diagnosed with epilepsy and Ulcerative Colitis in 1979 - current meds are: 275mg dilantin/day 120mg pheonobarb/day 3,000mg Mesasol/day
__________________ Diagnosed with epilepsy and ulcerative colitis in 1979, Been on meds ever since. 275mg-dilantin/day 120mg-pheonobarb/day 3,000mg-Mesasol/day |
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#11
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| Very interesting! Neurologist down here says they see LESS Seizures during the summer time down here than they do during the Fall, Winter & Spring! And I live in a tropical place! |
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| hot shower, triggers |
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