Where acceptance is all there is
All Autoimmune disorders(Alopecia etc) have a dysfunctional cytokine reaction component to it
For the purposes of inhibiting ACE and reducing cytokines, the following foods and compounds seem to be the best choices:
• Green tea (ACE inhibitor, reduces cytokines)
• Black tea (ACE inhibitor, reduces cytokines)
• Quercetin (possible ACE inhibitor, reduces cytokines)
• Pomegranate juice (ACE inhibitor)
• Red wine (ACE inhibitor)
• Turmeric (reduces…
Added by Mike Staffieri RHN on June 28, 2013 at 11:00am — No Comments
I live in Italy, but I will go to the USA in september to attend a conference (I am a PhD candidate in anthropology).
I have gone to many doctors here, but nothing worked except a corisonic treatment that intoxicated me, many years ago. Do you know if there is any GOOD doctor I could go to in the USA? An expert in Alopecia, obviously.
I will go to Dallas, Washington DC and NYC... Thank you
Another year has passed. We're on on are way to St Louis for NAAF 2013.
This is my 6th Conference since my diagnosis of alopecia in 2007. I am so grateful for all the support from all of you!!!
Hope to see and meet many of you in person!!!
So, I'm tired putting myself out there when it comes to dating! Men in LA are so shallow, you know in life somebody should like me for who I am! it just makes me sick how this guy I met he asked me, and I told him on third date and showed him my head, and he ran but the funny thing he said it didn't matter, its what's in the inside. Sorry Jermey you are shallow and think you are perfect when all you are is fake!
In 1998, when I was in 4th grade, my mom noticed a small patch of hair loss while she was brushing my hair one morning. She told my dad (a physician) about it, and he decided to take me to a dermatologist. The doctor told my parents that I had alopecia areata, gave me the steroid injections (every 8 year old's nightmare), told me to apply a cream (looking back, I believe it was an irritant) and come back every few weeks.
I don't remember my initial…Continue
I was diagnosed with Alopecia Areata in September of 2012, 3 weeks after I transferred to a new college with a grueling schedule. I had only loosely heard the term "alopecia" but never paid attention to what it was. My hair was my favorite feature, and I have been happily dying it an array of colors for over 10 years. I had been behaving myself and had only highlighted the crown once in the year leading up to my hair loss. I don't heat style. I don't pull my hair out in my sleep or anything.…Continue
Added by Simone on June 24, 2013 at 12:32pm — No Comments
I have had alopecia areata since this February and in this time I have lost all of the hair on my head. I remember at the beginning the smallest dime sized patched being the biggest deal and freaking out. Looking back I realize how lucky I was to have 95% of my hair at the time. I am 18 and this is my first wave of it. I have had an extremely stressful year and attest my initial hair loss to excessive stress. I now have over an inch of hair all over my head and have little to no shedding…Continue
After about a year of having lost my hair (all of my head, my eyebrows, eyelashes, legs) I have lots of little hairs popping up. I am trying hard not to get too excited because I don't want to be disappointed. For anyone who has had regrowth, is there something I can do to encourage and hang onto the growth? Keeping my fingers crossed.....
Added by Roslyn Brown on June 23, 2013 at 5:28am — No Comments
I have honestly come to the conclusion that most dermatologists.... suck. No, seriously they are horrible and don't know what to prescribe they just give any type of drugs and hope it will work. Not cool! Today, I actually had to tell me new dermatologist that no, you cannot give me cortisone shampoo while on squaric acid because it defeats to whole purpose of the acid. So, I have come to the conclusion that in college I will study pharmaceutical science and either become a dermatologist…Continue
Does anyone have hair from the Hair Club? i'm just curious if you ever use reg shampoo/ conditoner or only there stuff....
Added by jewels on June 20, 2013 at 12:00am — No Comments
Had steroid jags for the first time in a long time yesterday. Don't know if it's because it's been so long since my patches were as bad or what but slept for almost 24 hours and today still feel woozy and sleepy and very emotional :-(
Added by Jo-Anne on June 19, 2013 at 3:18pm — No Comments
I feel really bad that I didn't keep up with stuff after my regrowth. In fairness I have been in and out of hospital for 18 months with bi-polar and that time was awful, strangely I had a full head of hair throughout all that. But about a week after finishing my uni exams for my second year, which had been deferred whilst I had been ill, my hair has started falling out again. It's been happening for about a week but it's pretty fast like usual.
Luckily I'm pretty ok with it. This is the…
I've had alopecia for about 5 months now, not even sure exactly what kind yet ( i'm seeing a rheumatologist soon).
I lost about 40% of my hair, but the last month or so most of it started growing back, i couldn't help but get excited. I had little fuzz covering nearly all my head again. Well the past few days i started noticing smooth spots on my regrowth.
How can i keep from getting too excited when i see regrowth? I don't want to get my hopes crushed, but i also don't want to…
Added by JessKa on June 17, 2013 at 9:00pm — No Comments