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Thanks for your reply, I found you on this website.
Yes, the headband wig is absoluetly fantastic. I would recommend getting a tight one so it doesn't move but this depends on you head shape ect...
It looked great, whilst I ran, did weights and worked out onthe step machine.
Cheers
Lisa
Thanks for your reply.
I found you right here on Alopecia World.
The headband wig worked really well at the gym, I ran on the treadmill and also went for a run outside, I also did my weights and it worked a treat! My partner came with me and he also commented on how well it stood up to the exercise. I could even put the wig up into a high ponytail, which I must say felt absolutely amazing (especially when you have no hair)
Please feel free to contact me anytime,
Regards,
Lisa
p.s. I just bought another headband wig (yes, I'm addicted to wigs!) :-)
Very nice to meet you! Yes I am still working as a RN....I work in the cardiovascular intensive care unit and currently looking for a different position. Kinda burned out of the ICU scene. I wish I could tell you about vacuum wigs but I do not know yet. I still have hair but it is quickly reaching the point where I am going to need to make a decision...UGH! I have hypothyroidism and despite my levels being "normal"..my symptoms worsen almost every day. :( I am going to an acupuncturist...he seems to think he can help me....guess we will see. There are lots of folks on here that know all about them. I do hear that they can be very hot though. Are you looking into getting one?
How are things going with you?
Did I tell you about the Boston Get-Together? It's actually in Medford. Not sure if thats close to you or not.
I have it posted on the Events page. Have a look.
Jeffrey
Jeffrey
I just was diagnosed with scarring alopecia and am beside myself. I am so upset every day... I need to get it together though because I need to still work, we just bought a house here in West Hartford and I have a mortgage now. My boyfriend has been wonderful but I am just so unbelieveably sad every day. I need to talk to someone. It burns and itches every day and the ibubropen i'm using isn't helping. I'm on clobetsol too and had injections from a Dr at NYU. I feel so helpless. If you didn't think it was weird I'd love to talk to you over the phone. I just am so sad and just need to talk to someone else that has gone through this. If you're ok with talking please let me know. My personal email is clbates01@hotmail.com. Thanks.
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