Diagnosed with FFA about 18 months ago. Still just about able to cover hair loss but will soon have to resort to wigs. Married with two grown-up children and two lovely grand children - everyone very supportive.
Jean, I saw your comment today about the positives of having FFA. That was a good reminder. I have to ask a question. Is your hair loss to a point that you are in a wig daily? Have you lost a lot? And may I ask what medicines/treatments you've been on since diagnosis. Any info would be appreciated. Blessings, Lori. If you prefer to email me outside of this site, feel free. My email is lobertella@yahoo.com. Thank you so much.
Hi Jean, I hope that you FFA is still in remission, the problem I have with this support group is that long term members stop contributing, which leaves me to believe the worse that there is no cure and a hair piece is required. The literature says the disease burns itself out..if this was the case with you, would you be happy to answer a few questions..I am currently resisting medications due to toxicity and lack of results..bit would love to here your story..I know it's traumatic bit bome guidence would be great..hope you r one of the lucky one,
Lo
Jun 4, 2015
Plf
HHi jeanH
Apr 30, 2018
Plf
Hi Jean, I hope that you FFA is still in remission, the problem I have with this support group is that long term members stop contributing, which leaves me to believe the worse that there is no cure and a hair piece is required. The literature says the disease burns itself out..if this was the case with you, would you be happy to answer a few questions..I am currently resisting medications due to toxicity and lack of results..bit would love to here your story..I know it's traumatic bit bome guidence would be great..hope you r one of the lucky one,
Apr 30, 2018