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#1
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Dilantin Question-VisionIs anyone on Dilantin that also wears glasses? When you can't seem to keep your level at a standard theraputic range, do you feel like your vision keeps changing and you need a different pair of glasses for a 5, 10, 15, or 20 level? |
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#2
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| Some of the anti-epileptic drug's I have taken have affected my vision but in time the body usually adjusted. I had more balance problems with Dilantin
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#3
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| I more than likely have to come off it for a while. I've taken it for about five years now and was usually at 18-20. It seems through chemo & radiation over the last year I can't keep a level for anything much less see the same way for any extended period of time. I guess it's back to the neurologist. Thanks. |
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#4
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| I know what you mean about your vision changing. One day my vision is blurry, the next it's ok???? I have been on Dilantin for 40 years and my level use to stay around 12-14. In recent years it jumps all over the place regardless of how many I take. My dosage is being changed almost monthly. I have blood tests monthly but lately I've been getting them every 2 weeks. I hope my level (and yours) stabilizes soon. Last year I had to buy new glasses twice and now I can't read a number a phone book. I refuse to buy glasses every three months. I'll just keep the magnifying glass near. I have balance problems too Birdbomb. Friday I fell and had to have some staples in my head. |
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#5
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| Dang, Jake! ![]() Did you get your arm healed up yet or are you still in a cast? When I broke my arm in Nov 02, my cast didn't come off until the end of Jan 03. Blah! My vision did the same as you described Jake. But now the prednisone has given me cateracts add halos to that. Dilantin affects the brain stem and does some evil things that are not reversable. But it kept those tonic clonic out of my life! I'd take it again in a heartbeat if my seizures started up again.
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#6
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| I feel better, I'm on my third pair of glasses and they spend a majojority of the time on the top of my head. All I want to do is see normal! I'm so sorry you had the head injury. Are you OK? I can only attest to being on Dilantin for ten years at a time becaue it has been "my drug." My issue is seeing normal to total blurry, I'll let you know what I come up with. One question for Birdbomb, I have a brand new bike and I can't ride it, I feel like the the bike is standing sideways, is that normal? |
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#7
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| You know Kam, I don't know if that's an effect from the Dilantin, but Ranman had some excellent information, You might want to send him a PM Long term effects of dilantin
__________________ Last edited by Birdbomb; 01-20-2008 at 11:43 PM. Reason: only half the fingers are workin |
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#8
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| Yep, I'm out of the cast and in my second month of Physical Therapy. I go for a bone scan next week. The doc said my wrist will never be the same and he doesn't expect the pain to be much better. He started me on Celebrex to go with the Duragesic and vicodin and whatever else I can find to take. Dilantin is a WICKED drug, but it does work for me. I've been on it for 40 years. |
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#9
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| I take Dilantin too... and hate it. it's tearing up my teeth. i used to wear glasses, but got the PRK surgery. It's the one where they actually cut your prescription onto the lense of your eye insead of cutting a flap with a laser and then fixing under the eye. I see much better. I'm so glad I did it. Sometimes I do not see as well as I'm supposed to, but I don't have to wear glasses anymore. I (eye)am supposed to be 100% healed at the end of the summer.
__________________ Love, Stace |
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#10
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| Dilantin? Problems with vision? Let me count the problems with Dilantin, 1) anti-depressant levels, 2) gums, 3) estrogen levels (don't ask), 4) vision,5) ability to concentrate. Let's see did that cover everything? Oops, no I forgot one: simple partials anywhere from 8:30 PM to 8:30 AM with no patterns and wrecked sleep most nights. Thank god I am finally off that ****. r97 |
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#11
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| Sorry, haven't logged in lately. Seems like I'm not the only one with vision issue. I never heard of the eye surgery you had Stacey, what do the initials stand for? I only had the eye surgery to correct the lazy eyes when I was seven. I went to my neurologist and she wants to get the "free" Dilantin level to see where I really stand, she said the vision should only be a problem if you're at a toxic level and I'm nowhere close (6.8 which is not the "free" level). Had that free level taken two days ago so I'll have that info soon. She feels that my "E" control w/ Dilantin isn't broken so let's not try and fix it by changing meds, and let's look at other areas. She ordered an MRI with & without contrast and she want's to focus on the occipital lobe. She also mentioned that in rare cases on continued use of Dilantin, she has come across Glaucoma, she gave me an Opthamologist that specializes in neurological issues, so I am trying to make an appointment with him as well. Birdbomb, I'll have to check with Ranman too and see if he has heard anything about this. Thanks. |
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#12
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| Had an MRI and everything is perfect from the scar tissue before & after chemo and radiology. Glaucoma is not an issue. My neurologist asked me if I was on the "red form" yet of Dilantin and I said "No". She said as soon as you see the change of color in Dilantin, call me often. She has a patient that was normally in the 20's go to 42 and my highest was 38. It took her patient four hours and very close to a grand mal; to break through to a theraputic range. She does not agree that the new Dilantin is a good sign... |
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#13
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__________________ Check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback |
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#14
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| I didn't have ANY side effects with Dilantin (Phenytoin) for years I've been on it ... until it finally took its toll upon me and that was .. it wrecked a havoc on my teeth and gums. I had to think if I had vision problems with Dilantin and the only time I can recollect was ONLY WHEN I was on other anti-epileptic drug's - especially with Dopey- Kote (Depakote) was when my vision was blurred; but I was lucky that Dopey-Kote was short lived and my vision returned back to normal. BUT - even before I was on any anti-convulsants (anti-epileptic drugs) I had visual problems: Brief Moments of: 1) 3-D going flat 2) depth of field / perspective lost 3) loss of color / hue - things would be in shades of gray / black & white (this also includes the loss of ability to see blends momentarily) 4) visual distortion - larger/smaller (aka Alice in Wonderland syndrome), fixed objects moving, fixed objects that are straight - being warped * I had to attend therapy for this problematic issue which took years; while these episodes happened, they gave me headaches - depending on how severe the hit was the headache would range from mild to extreme. I had to learn how to deal with this temporary brief loss which would last anywhere from 2 to 20 seconds long. And one being permanent nerve damage - neurological: 5) night-blindness that gradual in a progressive manner where by the time I was about 23 years old I was nearly completely night blind but it was not because of the medication, it effected me whether or not I was on anti-epileptic drug(s).
__________________ Sharon Advocate & Member of Head Storms - Resource Center " Vujà Dé - The feeling you've never been in here before!" |
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#15
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| Thanks for the link, I read that article, looks like something I may pursue. Trying to get into this "neurologist-opthamologist" is unreal, end of March is the soonest, he must be good. Does anyone feel severe pressure on the eyes that if you close them and rub them to relieve the pressure that you see what appears to be snow on a TV set or big bright circles? Brain, what kind of therapy did you do, what it at a neurologist's office or did you have to see an opthamologist? |
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#16
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#17
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Keep this one thought with you no matter what kind of neurologist you work with: everybody handles different drugs differently. Dilantin is cheap (in more ways than one), but is it the best medication for what you need it for? Ask questions if you are not clear on what they are telling you. And make darn certain you are clear. If they talk in circles or in medical jargon, get another doctor. My opinion based on 30 months with Neurologists. |
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| Thread | Thread Starter | Forum | Replies | Last Post |
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