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#1
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sorryI dont know whats wrong with me im just really trying to hard to figure all this crap out..... I am sorry love angel |
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#2
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| That's OK. It can be tough at times (for everyone) to keep things in perspective. It sounds like you have a lot going on.
__________________ New to CWE? I suggest reading the proactive prescription and epilepsy 101 threads. Also check out this chart of alternative epilepsy treatments and this page on EEG Neurofeedback. More great stuff can be found in the list of the best forum threads. Would you like to help support this forum? |
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#3
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| Angel its ok we want to help each other and keep each other safe and healthy. We try to support each other ,but we are also aware its the net and its harder than in person . But believe me we all want each other to be healthy and seizure free ,but nothing comes over nite . Wishing you the seizure free ,depression free , healthy ,happy life!!!!!! ((((hugs))))) Riva
__________________ Riva's Memorial |
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#4
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| Angel: Just hang in there, and stay in tune with your Neurologist. Never be afraid to say I need help! If you are experiencing depression, frustration, or side-effects and aren't receiving anything from your neurologist ~ You can ALWAYS phone your PRIMARY CARE DOCTOR! After all he/she is the "Head Honcho" of your well being; while the other Doctors are just specialty Doctors. Have you ever spoken with your Primary Doctor? Discussed anything with them? If not, you should. We are concerned about you, because we care! Are you aware that the Primary Doctor has the power too to control your meds and change if necessary, even the Doctor you are currently seeing if he/she feels that they aren't treating you properly. |
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#5
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my neuros office is going to be helping me with cost of meds and trying to help to find some other options as i have no ins and we are running out of money... so i panic i guess and start trying to find excuses as to why i shouldnt take my meds... which is wrong ..... im not going to go to my neurologist today we all kinda worked things out on the phone they helped me to calm down..... just stress weve all gone through at one time or another I GUESS im just more verbal about somethings... dont know when to be quiet... love angel Last edited by angel; 10-17-2007 at 04:15 PM. Reason: took out city and names |
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#6
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everyone. Where you want to pull your hair out and you get to the point where you don't even make sense. And like you said, You feel like the world is all crashing down on you. We all want to be healthy. We all want to be normal. And oftentimes we sit there and say "WHY ME? WHY COULDN'T IT BE SOMEONE ELSE?" People react to stress differently, for me, I used to just sweep it all under the carpet and pretended it didn't exist. I was in denial. I didn't want to admit I had "it". I'd rather tell people I was deaf than to say I had that "e" word, or I'd just say I have a neurological problem. The hardest thing to battle with is - Letting IT control YOU or YOU controlling IT? We sometimes feel like we're fighting or beating air and loosing. Or even beating a dead horse: ![]() There is absolutely nothing wrong in posting a post to say "I WANT TO VENT!". Trust me, I've shed tears out of frustration. I've punched my own pillow because I hate Epilepsy so much and it's a stress reliever and you don't hurt your- self .... TRY IT ... grab 4 or 5 soft pillows that you sleep on and pound on them as hard as you can on your bed and release it all off. It's ok to cry. When my little son told my neurologist what I would do sometimes, he smiled and said what I did was fine, and he understood but I was a little embarrassed that my little boy blurted that out to him, but I was surprised that when he told me that he's told his patients to do the same thing to relieve the stress off; because it was safe and it worked. But I would only be in there for about 10 minutes or less though. I would feel better afterwards and moved forward and get my other housework and things done. |