 |
 |
|
|
|
Alopecia Areata Support and Help
You are Not AloneIt's pretty obvious that you will definitely be shocked if you find your precious locks of hair falling down in large quantities. Not to mention being hysterical and completely lost in wondering why is it happening the first. That is usually the feelings for people who first face with Alopecia Areata. The main issues with facing Alopecia Areata are not knowing what to expect and whether the condition with improve or regress further. That thought alone can be a cause for anxiety and depression for most people. While there is indeed a great deal of Alopecia Areata treatment options, none can offer an absolute peace of mind. Women are especially hard hit because they usually have a higher regard of their hair then most men and going bald because of AA is not an acceptable option for most of them. Sadly to say, there is no way of avoiding Alopecia Areata from happening to you and like many things in life whether good or bad, the only way to survive it is to accept and adapt to it. Further to that, you should know that you are actually sharing an adequately common disease with almost 2% of other people so it's a pretty common condition too. What you need to do now as an Alopecia Areata sufferer is to find people that share your plight and experiences with them. That way, you can further understand the condition better and know what your options are.
The Helping Hands
You don't have to face this problem alone or lock yourself up in the closet. Lift your hand and find an Alopecia Areata support group to help you get back on your feet and you can life happy and productive lives.
Where to GoNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), Information Clearinghouse, National Institutes of Health The Purpose of NIAMS is to support the research of many forms of arthritic, musculoskeletal and skin diseases including Alopecia Areata. Their research has yielded many articles and clinical studies that you might find particularly helpful in understanding the disease. They also seek patients for studies and tryout of new medications and treatments. If you are looking for more information and data on the disease, you might want to check out their details below. 1 AMS Circle National Center for Complementary and Alternative Medicine (NCCAM), National Institutes of Health The NCCAM is another health related government institution that is dedicated in complementary and alternative medicines. Their site is a good source of info for you if you are looking for alternative treatments for Alopecia Areata. A good list of information that involves various herbal remedies, supplements and acupuncture can be found from their website. P.O. Box 7923 American Academy of Dermatology (AAD) The American Academy of Dermatology offers you a great way to find a certified dermatologist in the USA that can help you with your condition. If you are facing Alopecia Areata, it's best that you seek professional medical opinion before deciding on other options. The website also offers up to date information about the latest dermatological research and resources that you will definitely find useful. P.O. Box 4014 National Alopecia Areata Foundation (NAAF) As the name says it, the National Alopecia Areata Foundation is a dedicated Alopecia Areata support organization meant for all AA sufferers. It offers products, guides, meetings, conferences and events specifically for the condition. Anyone from around the world can join this non-profit organization and I strongly recommend you to if you just confirmed your diagnosis of Alopecia Areata. If you are from the USA, you can also participate in their regularly held functions and events for Alopecia Areata patients. 14 Mitchell Blvd. Alopecia World Alopecia World is an online community for anyone that faces hair loss. It's a good place to share, chat and discuss about anything alopecia. Just launched in 2008 the site has a commendable amount of regulars and it's a place to share your pictures, blogs and videos. The site is a social media very much like facebook for people with hair loss. So if you need someone to share your thoughts, you know where to go. http://www.AlopeciaWorld.com Locks of Love Surviving-Hairloss.com has always been a proud supporter of Locksoflove.org for its cause and help it provides to children hair loss sufferers. A non-profit organization with operations in the USA and Canada, Locks of Love helps provide free natural hair prostheses to children to help them restore their self-esteem and their confidence enabling them an uncluttered future. Whether you want to donate your locks or looking for one for your kids, this is the right place to start. www.Locksoflove.org Bald Girls Do Lunch If you have seen the Youtube clips on this site and NBC, you should realise that Bald Girls Do Lunch is picking up on posterity and fame. Created especially for women with Alopecia Areata, founder Thea Chassin, an AA sufferer herself bonded a bunch of girls that share the same plight together and formed this unique not for profit organization. If you are a woman who just lost your hair to AA, then contact this organization and you will find that you will be in great tender loving hands of the group. www.Baldgirlsdolunch.org Alopecia Areata Support Community An Alopecia Areata support group based in the UK, AASC is another online community for you to share your stories and find the necessary support. You can use AASC as if it were your very own place to share your fears, share your joys, and vent your frustrations. Most important, it's a place to get the right Alopecia Areata support that you need. http://www.alopeciaareatasupport.co.uk/
Many Many More!Don't let Alopecia Areata destroy your social life. There is more to you than just your hair. If you are really down and need help, these Alopecia Areata support groups and organizations are ready for you but you will just have to stretch out your hand first. Good luck.
 Return to top of Alopecia Areata Support Back to Alopecia Areata Return to Surviving-Hairloss.com All information here are written by a hair loss sufferer based on experience and self research.
It's best to seek a medical professional regarding any health problems. |
ToolsFree NewsletterRecommendations If you are looking for a topical treatment for Male Pattern Baldness, this might be the right one for you. Spectral DNC is one of the latest and positively reviewed products for treating genetic baldness. Combining the FDA's approved Minoxidil with its proprietary Nanosomes technology for better scalp penetration, this product is indeed unique. Check out our reviews about it here or GET IT NOW from  .
Featured Story A Case of Telogen Effluvium I'm a 22 year old male who was diagnosed with TE about a month ago. 3 weeks before my diagnosis I suddenly noticed I could see more of my scalp when I got out of the shower... Read More Sponsors |
Start HereYour SolutionsStuff That MattersResources
Hair Loss Articles |
||
Copyright ©
2008-2010 Surviving-Hairloss.com. All Rights Reserved. |
||
There are many organizations and Alopecia Areata support groups that are willing to lend a hand in supporting and helping you with your condition. While most of these organizations are based in the USA and United Kingdom, there are definitely local communities and support groups around your area that you can source online. Besides that, there are many forums and websites that are dedicated to people facing alopecia, especially Alopecia Areata.