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2 sad parents

Sat, 01/10/2015 - 07:24

Hello everyone, I am from Lima Peru, not write English, I use google translator, so do not make fun when I write, I am a humble person unlike units, which can afford private clinics, I have just the SIS and I'm waiting unlike those with money for private clinics, and thank there this page as many as we can habar the subject. My son today January 10 turns 3 months when I fulfilled the two months I began to have seizures, l I really desconosco this, when you drive to the hospital told me I had convulsions and had to see a neurologist who in the hospital no neurologists had my son in those days had convulsions followed until after 9 days left of convlusionar, high day December 23 and December 25 empeso 1l, for my wife and I was very sad again to bring to the hospital because unlike of you, my wife would sleep all day at the hospital where they had no neurologic PEDIATRA, after those days of agony I began researching the internet every night, until the day December 25 we got a pass to go to the hospital the child, where he saw the neurologist doctor and nurse who accompanied us her story everything that happened in those days my baby entonses neurologist and revised it so easy to just having the TOMOGRAFIA t reviewing my bebe said he had epilepsy, my partner cry it felt very sad, I said we will overcome, in those days I remain hospitalized, and unlike the first hospital, me and my mrs. no one could be with the baby until emergency ride to a stretcher on the second floor, had to spend days sleeping in uncomfortable waiting room throughout the day called us 2 times a day to tell us how the baby was still, after about subioal days second floor, and only my wife was looking after him, visits unlike the other where were coming many, just entering a person, and mom had to leave, no one in my family could come up to see me, my partner must wqlir outside to wait for me to come out, it is very sad that we saw other people in the class a and B took their children to a PARTICUPAR CLINIC, because unlike the hospital, we have to wait days for us dean an appointment with a neurologist, and my children in those days was still suffering, so much so that my partner lost all pasiencia and very sad it seems that would stay with my baby just always take care, it is very sad what I tell them, I am of the class D, and we are especially parents who cry for a baby not to blame for what happens on Sunday, January 4, 2015 my son was 4 days without seizures, just a few tips that gave but were not seizures, and was given high von medications I had to take them to their hours with our care, and research on the internet and talking with pdiatra told me that if I had seizures with more than 5 minutes what had to return to hospital the child, and PC, believe that my son will go up to the second floor eel ?? do not? has to undergo emergency, then they will ask again everything that happened from the beginning, and I have to wait days for you to come up to the second floor, and if it happened that denuevo always would repeat that, muna anxiety not having money, I started thinking about my poor child does not have the same care for having a low-income parents until now are almost 9 days and my son has had no convulsion, very sad and ashamed I feel that my partner when I retired from the hospital with my son said goodbye to all pascientes of all nurses of all the people passing by the hospital, and not knowing much about it I did not tell her that the baby will have seizures again, crying at night I thought if the baby becomes partner with the pain of my heart I will leave, he always happen that parents are strong in others only one, and in my case it seems that I will be one more group, at night you I pray and cry and ask God to take his soul and heal, I convulsions me and not ami son, I cry just thinking that vuelv to give a convulsion happens 5 minutes, and my partner tells me and can not, because I was already just what little savings he had, and return to the hospital financially would be very bad, I've seen that there are institutions that make their donations and raise money to help everyone to this cause, and I envy her great country there are many Organisations, here on google I found this and many pages in the world and in my country hardly esucha that, as I had money, so take my son to a dr. particular, could have helped me to donate money to all institutions, but if someone in your country asks for a donation organizing themselves resiben something, and that rest, I as a parent I am ashamed to ask for money, he is that nobody will support in my country, here neurologists charge a lot of money just for consultation, tomography and MRI, I have left free, the EEG, the 13th of eneeo 2015 we have an appointment with the neurologist, but like my son will gain sufficient assurance with your medications I also prescribed Pyridoxine and in my country do not sell, very sad just give me what they resetaron which are pHENYTOIN and KEPODEX, hopefully someone feel like me and understand the cry of a father who at least have a consolation'parte of you, since I became friends in facebook in a pediatric neurologist and asked him just that when my child has any reaction I dee advice as we are not the same country and I can not pay you, I said I'm reading and we have , yle did 2 questions but only the vee and never answered, sadly I write here to see if someone have mercy on my son of humble parents that the only thing you have to see our baby is the internet, which gave me the key to enter otherwise not tenria internet would not know anything about this, thanks for taking time to read my message, many blessings and good luck with your children with epilepsy, I hope to have a breath and know that someone has read and understood me, few tears heart say thanks to all.

they are appreciated:
My BABY TAYLOR M.

mi facebook https://www.facebook.com/elchamyx

Comments

It's a shame to see a child

Submitted by Anonymous on Mon, 2015-01-12 - 21:46
It's a shame to see a child having seizures unlike adults, I espereo your child recover, and I hope mine too.

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