www.alopeciaworld.com
My daughter who at the time was 8 Nov 2016 was diagnosed with AA, like so many posts, articles, and treatments I did try the steroid injections, when the initial diagnosis was revealed to us. Its was complete shock to all of us. How Why what caused this??
AS you many know, they say stress induced, my daughter has been a chronic asthmatic since 2, and has been on many inhalants over the years. As a mom who listens to my intuition I know that the asthma played a roll just before her start of hair loss she it was fall and bouts of her asthma were acting up.
So i firmly believe that illness plays a role of the on set of AA. NOW with that being said, auto immune diseases do run in my family. My grandmother had a form of one as did I. Now no-one in our family had Alopecia or hair loss. partially what they say about auto immunes are true.
Since modern medicine in the state of Florida is "medicine" steroids, creams, ointments, you get the picture as we have all encountered. The first time at the demo, as we all cried, of course I wanted my daughter made whole immediately, so i didn't hesitate to their treatment. When I got home I did so much research on this disorder. No-one knows the cause of the onset or the whys? NOONE. Doctors can only predict and go by there protocol. which we all know.
I stated up spending great deal trying to find something for her to make this stop. I started to become writhing she educated so by the second demo appointment I know that these injections were just WRONG for her. My spirit was screaming at myself, as I wiped the tears from her face and mine and told her to be strong, this is going to help. I WAS LYING TO HER AND MYSELF!! So January of 2017 was the last time we walked into the demo. Now facing complete baldness, losing her eyebrows, all in a matter of less than 60 days, I started to notice the lack of life that is in my daughter. Her self esteem has crashed and she stopped doing everything she loved the beach, riding bikes, swimming, just going outside playing with her friends, playing dolls, and she turned to the computer something she can hide behind. This here has crushed me more than the hair loss, I feel as though I made decisions to hurt my baby girl. I have 3 daughters she being my youngest I can see her anger that she never had, she grabs at her sisters hair to lash out. When in our daily family prayer she is praying for eyebrows I had to make some serious decisions to help my baby.
My girls have always ate healthy not your normal kids. They love fruit (kiwi) vegetables (spinach) no soda, I make a lemon cucumber mint water, that she drinks all the time.
I started to research nutrition, and changing her diet. As this is the first part of the body healing itself and stopping the auto immune disease. Obvious her system is toxic and started doing a liver detox on her as the immune system is in the digestive system. I cut out sugar completely, and as far as fruit I limited that 2 2 a day. I got her tested in what she is lacking and what is going on through a sergeant. We found that she has a fungus in the digestive system, and as I figured her liver is toxic. So the new regiment I just started, is 3 enzymes in the morning and 6 different minerals 3 times a day.
Since we just started this that day, I noticed a change in her mood, she actually said she wanted to go to the store with me. Its this small steps I am rejoicing in at this point. If anyone has input on this approach to AA or has any info to share please do.
Many prayers sent out to you all who are going through this fight. Blessing CJ
Members: 1
Latest Activity: May 25, 2017
This group does not have any discussions yet.
Comment
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.
© 2024 Created by Alopecia World. Powered by
You need to be a member of Children with AA to add comments!