This list is not meant as an endorsement or promotion of any kind. It's simply to educate and pass on information. My hope is to assist you in your search and cut out a few steps for you. I would like you to find support if you need it.
Alopecia (hair loss)
Anxiety and Depression
Anxiety and Depression Association of America
Anxiety and Phobias
Inspire, empower and support arthritis patients
March of Dimes
Tools and resources
National Birth Defects Prevention Network
Offers publications and webinars
WIC Works Resources System
Blind (Vision loss)
American Council of the Blind
American Foundation for the Blind (AFB)
National Federation of the Blind
Body-Focused Repetitive Behavior
This includes trichotillomania ( hair pulling), dermatillomania/excoriation (skin picking) and onychophagia (nail biting). (Also subtypes).
The TLC Foundation
(The TLC Foundation has given permission to list them. They offer many support groups for these disorders and helpful information). 10/05/2020
Visit www.BeautyByCheryn.com or call 866-324-0908 now!
For a free consultation please visit: www.chailledefaria.com or email Chaille directly at email@example.com
For more information, please visit: www.habitware.com
Phone: (970) 644-5333
www.JoanKaylor.com Online Coaching and Counseling
For US calls: 561-299-4911
https://trichotillomaniablog.com/ Trichotillomania Blogger. Naturally-Minded. Jesus Obsessed. Empath by Lesley
trichyhabit.tumblr.com trichy blog for support
@pickingmefdn (Picking Me Foundation)
Raising Awareness of Male Breast Cancer
Support groups for breast cancer in men
National Breast Cancer Foundation
2600 Network Blvd. Suite 300 Frisco TX 75034
Support groups for breast cancer
National Cancer Institute
(ACPA) American Cleft Palate-craniofacial Association
Reach Out Ages 14-25
S.A.F.E. Alternatives (Self Abuse Finally Ends)
American Diabetes Association
the Diabetes Site
Centers for Disease Control
The International Dermal Institute
Postgraduate Education in Professional Skincare
1535 Beachey Place, Carson, CA 90746
National Eczema Association
National Eczema Society
Zainab Danjuna on YouTube
Just a regular girl from London, with an itch that needed to be scratched (Eczema)
Glaucoma Research Foundation
http://www.glaucoma.org accessed 01/24/2021
http://glaucoma.uk accessed 01/24/2021
links to the site are encouraged & permission is not required
International Glaucoma Association
http://glaucoma-association.com accessed 01/24/2021
The Glaucoma Foundation
http://glaucomafoudation.org accessed 01/24/2021
online discussion group (APUP) Adult Patients Under Pressure
info on clinical Glaucoma trails
The National Eye Health Education Program
http://nei.nih.gov/nehep accessed 01/24/2021
National HIV/AIDS Hotline
(800) 344-7432 (Spanish)
Hyperhidrosis (Excessive Sweating)
Maria Thomas blog launched in 2011 to raise hope and awareness one drop at a time.
Working to improve quality of life for those with lupus.
US in Lupus
Support lupus patients in US
U.S. National Lyme disease
(The U.S. National Lyme disease (lymedisease.org) has given permission for this listing). 09/15/2020
Lyme disease association
research, education, prevention and patient support
Stories of Lose and Survival with Melanoma
Find stories of patients and survivors.
North American Menopause Society
Disclaimer: This website is for informational purposes and not for diagnosis. More details.
Men’s Health Network
National Alliance on Mental Illness
National Multiple Sclerosis Society
Association of Professional Piercers
https://www.memberleap.com/members/directory/… (By State directory)
The International Federation of Psoriasis Associations
National Psoriasis Foundation
(National Psoriasis Foundation has given permission for this listing though it was not needed.) 09/14/2020
https://www.psoriasis.org/talk-psoriasis/ support for psoriasis and psoriatic arthritis
Chronic Pain Kit for tips and resources to help you:
https://www.psoriasis.com/ (Free beneath the surface kit)
The Psoriasis Association
International Rosacea Foundation
National Rosacea Society
This organization has been around many years, doing research and providing information pertaining to rosacea. I was once on the newsletter mailing list.
(National Rosacea Society has given permission for this listing). 06/11/2020
http://rosacea-support.org this is a support forum started Oct 1998 by David Pascoe. The website also contains information on rosacea.
another rosacean who has a blog
Advice Support Community
British Association of Dermatologist
British Association of Skin Camouflage
skincancer.org offers Robins Nest program for support and guidance to help you through your skin cancer diagnosis.
OHBAAT (One Human at a Time)
"Turning your New Normal into the ideal life". A religious based site to support your life after Post Corona. "Personal Media".
American Thyroid Association
a public site accessed 01/11/2021
If a description is to be provided with the link, ATA® would prefer the following wording:
The American Thyroid Association® (ATA)® , founded in 1923 as the American Goiter Association, is a nonprofit professional medical society comprised of physicians and scientists dedicated to enhancing the understanding of thyroid physiology and pathophysiology, improving diagnosis and treatment of thyroid diseases, and promoting the education of physicians, patients, and the public about thyroid disorders.
In the 95 years of its existence, the ATA has grown to more than 1500 clinicians and research scientists in the field of thyroidology. Thyroid diseases are among the most common disorders of the endocrine system, affecting almost 13 million Americans alone. Advances in understanding the causes and improving the clinical management of thyroid diseases are evolving at a rapid pace in the current era of biomedical discovery.
mom blogging about hypothyroidism
https://hypothyroidmom.com/ accessed 01/09/2021
Thyroid Federation International
https://thyroid-fed.org/ accessed 01/09/2021
My Vitiligo Support Team
MyVitiligoTeam is not a medical referral site and does not recommend or endorse any particular Provider or medical treatment.
No information on MyVitiligoTeam should be construed as medical and/or health advice.