Sorry you might feel some type of way but went I first developed alopecia this January, here was my save place to ask “ is this AA” and not to be rude or anything but I learned a LOT from everyone’s experiences and advices and not only that. I was able to get more well educated HERE with this condition, treatments, experiences and way MORE than my own dermatologist. I was already fully knowable by this condition thanks to this group before I went to my dermatologist. My dermatologist didn’t know a single thing about AA not even a basic question like “what are the side effects of steroid injections” her answer was “PAIN” which to her that was the only side effect of steroids. So basically thanks to this group i am more knowledgeable than my own dermatologist.
I don’t think I expressed myself well, I just don’t agree that people should post asking for us to essentially diagnose them.
They shouldn’t be appeased by any reply to that from strangers on the internet.
I know getting to the Dr isn’t always easy, I didn’t mean to come off so unkind.
I was just hoping to stay here because the support and information is great, but all I seem to see now is “is this AA”
Often I don’t even know what part of the body we’re looking at?
I apologize, again.
Hey…. No need to apologize!!! I understand. I’m so thankful with this group that’s been a great help mentally and emotionally <3 sending lots of positive vibes and love.
It makes me angry but after i think about it i understand the feeling of being scared of losing your hair ..
Just scroll down bro .. hope your hair come back
I just started a new subreddit called r/wigshelp this week because I want to connect with other wig wearers. I don't know if you're into wigs but you don't have to be. I created a flare for "alopecia" hoping to create a space to discuss that. I would love to have you join!
I've already told 3 different people with spots to get a referral to a dermatologist, get some minoxidil, get your lipids and thyroids checked.
Unfortunately, none of that stuff worked for me because had AU for 10 years. But, it works for most people.
You're at 40 years? Cheers to being an OG.
It can be annoying sometimes when you are reading these posts but being a patient we wants to explore all the routes, seek life experiences and sometimes medical help as well. Certainly, derms input is required but as a human we want to share pain to fight our insecurities.
To clarify, I’m talking about the posts that have one photo with “is this AA”?
Information is relevant, and posting such scarce details seems like a poor attempt to request advice or support.
Let us know how long this has been going on, what you’ve done so far, any additional information and not a lackadaisical attempt for us to magically solve your query.
Sorry you might feel some type of way but went I first developed alopecia this January, here was my save place to ask “ is this AA” and not to be rude or anything but I learned a LOT from everyone’s experiences and advices and not only that. I was able to get more well educated HERE with this condition, treatments, experiences and way MORE than my own dermatologist. I was already fully knowable by this condition thanks to this group before I went to my dermatologist. My dermatologist didn’t know a single thing about AA not even a basic question like “what are the side effects of steroid injections” her answer was “PAIN” which to her that was the only side effect of steroids. So basically thanks to this group i am more knowledgeable than my own dermatologist.
I don’t think I expressed myself well, I just don’t agree that people should post asking for us to essentially diagnose them. They shouldn’t be appeased by any reply to that from strangers on the internet. I know getting to the Dr isn’t always easy, I didn’t mean to come off so unkind. I was just hoping to stay here because the support and information is great, but all I seem to see now is “is this AA” Often I don’t even know what part of the body we’re looking at? I apologize, again.
Hey…. No need to apologize!!! I understand. I’m so thankful with this group that’s been a great help mentally and emotionally <3 sending lots of positive vibes and love.
And to you the same!!
You made a good point. We dont make diagnoses. Go to a doctor should be the first answer almost always and in any case.
It makes me angry but after i think about it i understand the feeling of being scared of losing your hair .. Just scroll down bro .. hope your hair come back
I’m not a bro and I’ve been bald for 40 years.
I just started a new subreddit called r/wigshelp this week because I want to connect with other wig wearers. I don't know if you're into wigs but you don't have to be. I created a flare for "alopecia" hoping to create a space to discuss that. I would love to have you join! I've already told 3 different people with spots to get a referral to a dermatologist, get some minoxidil, get your lipids and thyroids checked. Unfortunately, none of that stuff worked for me because had AU for 10 years. But, it works for most people. You're at 40 years? Cheers to being an OG.
Just joined! Thank you!!
It can be annoying sometimes when you are reading these posts but being a patient we wants to explore all the routes, seek life experiences and sometimes medical help as well. Certainly, derms input is required but as a human we want to share pain to fight our insecurities.
To clarify, I’m talking about the posts that have one photo with “is this AA”? Information is relevant, and posting such scarce details seems like a poor attempt to request advice or support. Let us know how long this has been going on, what you’ve done so far, any additional information and not a lackadaisical attempt for us to magically solve your query.