Well some people may see the name of my blog: THE PLACE FOR ENLIGHTENING, as preposterous given the fact that i am neither a prophet nor a preacher to start enlightening people. so as a result i would explain what is in the name of my blog.
T he main aim of my blog is to be a place where people would be given insights into the happenings around them, those happenings they have no clue about or may be they have some knowledge about the those events which unfortunately may not be the complete knowledge or the wrong one. It is supposed to be a place where cobwebs which are in the minds of people which prevent them from having complete understandings of happenings around them or situations in other parts of the world would be removed. This however does not in anywhere mean I am immuned from those cobwebs. I may be having the wrong perceptions of certain happenings around me, the way i understand certain things may not be the right way so you people out there would be able to give me some insight into those things so i understand them better. For example i dont believe in the saying: NO MAN IS PERFECT. I belive every man is perfect. I don't believe DEATH exists and i don't aslo believe that people fear death.
3 comments:
Thanks for visiting my blog our son was born with esophageal atresia, down syndrome, tracheomalacia, bronchomalacia,laryngomalacia, and developed atalectsis of the lungs but that has gotten much better he goes in every week for esophageal dilations. esophageal atresia is a 1 in 5,000 birth defect so it is pretty rare. You have a very awesome blog. and I wish you the best and i hope that i hear back from you.
I appreciate your comment you left on my site. I am trying so hard to get my site out there as it is so hard to keep a job with our son having the condition he has. I am trying to get my site to where it is atleast some sort of income for us. My site means alot to me. I FOUND YOUR COMMENT SO INTERESTING. I i guess i DONT understand what goes on i the other countries, How can they just let them die, I mean WHY wouldnt they send them some where where they can be helped and saved especially if america has all of this information. It just seems so scary. I could never loose hope in our son, and we have fought for him until the end. There where many times I argued with many doctors and nurses about what they insisted was right for opur son and I would beg to differ at one time they told us that our son had a 20% chance to make it off the vent seeings that what they didnt know was that our son was born fine breathing on his own. I made them extababte him and put him on some 02 and he blew them away. You can not tell a mother that has carried a baby for 9 months and then spent day and night by his bed side with no sleep how there baby is, some of the doctors only saw our son once a day, so they where going by what they where told, it got pretty complicated at times i thought I was going to not make it, it was so tough. We were very lucky to have a outstanding pediatric surgeon that loves our son very much that would do pretty much anything for him. I am so interested in knowing an finding out information on esophageal atresia from other countries. Any info I cna find i know it has to happen in other countries b/c there are 6 born with esophageal atresia every day and 27 in the world a day. So it is out there. I wish you the best and I want to thank you so much for staying in touch with me it means alot, I hope to hear from you soon. Kayla
Interesting input Kebba. I will encourage you to write more health stuff. People are unaware of many medical issues that can help them take care of their health. Like salt content, exercise, oily foods, and many more.
great
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