Where acceptance is all there is!
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Posted on January 27, 2016 at 11:44pm 2 Comments 0 Likes
My 7 year old daughter will be starting LDN this week. This drug does wonders for autoimmune conditions by blocking endorphins through the night. The body then releases an overabundance of endorphins the following day to compensate. The endorphins heal inflamation (of course anyone with alopecia is inflammed. C Reactive protien blood test will confirm this) and balance the immune system, targeting the true problem, rather than a temporary toxic drug. There are no side effects, not…
ContinuePosted on January 13, 2016 at 9:03pm 1 Comment 0 Likes
Hello,
I am wondering if anyone has taken this blood test and what your numbers were. It is a test for inflammation. My daughter was a 12.4. Normal is a 0.0 to a 4.4. Clearly she has silent inflammation, a very dangerous condition that is becoming chronic for her. After many blood tests, this is the only abnormality showing up. I believe the inflammation is causing the autoimmunity. I an curious if anyone else is having this experience. The name of the test is the C…
ContinuePosted on January 10, 2016 at 4:12pm 4 Comments 1 Like
Hello, We are in the process of bloodwork. It has been a year and I refuse to accept that my daughter will never have hair again.
Throughout our journey I have recently had much bloodwork done. My daughter's results showed extreme infammation in her body. Her C reactive Protien was a 12.2. This confirms that she is indeed inflammed. Silent inflammation of course if very bad news for long term health: cancer, stroke, diabetes, on and on.
We are doing an…
ContinuePosted on December 12, 2015 at 1:04pm 25 Comments 3 Likes
Hello,
I am wondering if anyone is going this route? We ditched the steroids about a month ago after 8 months of treatment. I am juicing organic fruits and greens each day. We have stocked our kitchen with vegan, non GMO, no gluten, no dairy, pure foods. Our new strict diet is of the highest quality and nutrition packed. Supplements include D3, Omega, B12, Calcium, and probiotics. It has been 6 weeks and hair is still falling rapidly. I was so hopeful it would slow by…
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I'm so sorry you are having a tough time. It's very difficult to watch your child go through this and not be able to do anything about it. Alopecia Areata is very unpredictable. It could turn around at any time and let the hair regrow, and never come back again. There is no viable treatment yet, but a lot of research is being done now and I predict that in a very short time there will be some good answers. To keep abreast of the latest news on treatments (there is no cure at this time, either), check in with www.NAAF.org, the National Alopecia Areata Foundation. You can trust this organization.
Hello and welcome!
How are you and your daughter today?