Searching for Alopecia Areata Support Community information? Find all needed info by using official links provided below.
http://www.worldalopeciacommunity.org/
Jan 22, 2016 · The focus of World Alopecia Community, Inc. is to enhance the overall well-being of those affected by all forms of alopecia, through evidence-based education, wellness activities, and community support. We want to teach people to not just live with alopecia but how to thrive. Whether you are new to alopecia or have had it for years, you will benefit from being a part of the World Alopecia ...
https://www.naaf.org/find-support
The NAAF support network offers different ways to create a sense of community among individuals with alopecia areata and their families. If you would like to discuss your experiences with alopecia areata in a group setting, the Support Group Program will be the best fit. It is a great way to get support and know you are not alone.
In just one month, this community of 149 supporters helped raise over $139,700 to combat the forces of alopecia areata that try to bring us down — a feat made possible by each and every special Super Human Strength shared to celebrate Alopecia Areata Awareness Month. READ MORE HERE
https://www.hairlosstalk.com/guides/alopecia/universalis/treatments/
Alopecia Universalis Support Groups. This is an online support community for hair loss sufferers of every kind. We’d like you to go to the forums, register, and scroll on down to the Alopecia Universalis section. Post your story. Share your experiences. Throw it out there, and give people time to respond. They will.
https://www.hairlosstalk.com/guides/alopecia/areata/
First off, we’d like to invite you to our online community of Alopecia Areata sufferers. It’s brand new, so we hope you will register and post to introduce yourself. We’ve created it just for you, and there are many others with your condition who you can interact with: Click Here to …
https://www.facebook.com/alopecia.hair.loss/
World Alopecia Community - Alopecia Education & Support, Clayton, Delaware. 4,875 likes · 15 talking about this. World Alopecia Community's (WAC) mission is to enhance the well-being of those...5/5(3)
https://www.heralopecia.com/
Alopecia Areata is a type of hair loss that affects about 2% of the population; it can strike children and adults randomly, even those in good health. Over 4.5 million people in America are afflicted by it (NAAF), and about 25% of those with Alopecia Areata have had a family history of this particular type […]
https://www.facebook.com/groups/alopecia.areata/
The focus of World Alopecia Community (WAC) is to enhance the well-being of those affected by all forms of alopecia, through education, wellness activities & support. We want to teach people to not...
http://www.worldalopeciacommunity.org/introduction-to-alopecia-areata-2/
Jan 22, 2016 · Alopecia areata (AA) is most common in people younger than 20, but children and adults of any age may be affected. Peak incidence appears to occur from age 15-29 years. As many as 44% of people with alopecia areata have onset at younger than 20 years. Onset in patients older than 40 years is seen in less than 30% of patients with alopecia areata.
https://www.smartpatients.com/communities/alopecia-areata
The Smart Patients Alopecia Areata community is an online discussion forum for patients and caregivers affected by an autoimmune skin disease called alopecia areata that results in hair loss and emotional pain. Members share information, advice, and emotional support for patients, caregivers, and others dealing with alopecia areata.
How to find Alopecia Areata Support Community information?
Follow the instuctions below:
- Choose an official link provided above.
- Click on it.
- Find company email address & contact them via email
- Find company phone & make a call.
- Find company address & visit their office.
