Jenbissness
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  • Chattanooga, TN
  • United States
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Jenbissness's Friends

  • Jlhollow
  • HairJourney
  • Lauren@CornerofHopeandMane
  • Nave
  • molly

Jenbissness's Discussions

Short cycling

Started Aug 21, 2015 0 Replies

Hello Everyone,I am curious if anyone out there knows anything about short cycling... I was diagnosed with CTE and mild AGA per biopsy. My hair was shedding like crazy for 2.5 years (200+/day). In…Continue

Need advice for first wig

Started this discussion. Last reply by Nave Dec 13, 2014. 35 Replies

Hello Fellow Alopecians,I am currently shopping for my first wig and need advice. I have lost more than half of my hair and it is shedding more than ever, it is only a matter of time before I need a…Continue

AU question

Started this discussion. Last reply by Jlhollow Jul 25, 2015. 18 Replies

Hello All,I am reaching out to the AU people out there... just wondering a bit about your stories. I have been presenting with diffuse scalp loss for more than 2 years, about 6 months ago I noticed…Continue

Diffuse AA

Started Sep 28, 2014 0 Replies

Hello All,I am new to this forum, I am a 37 yo F who has been struggling with hair loss for almost two years. I have always had fine blonde hair, but a ton of it. In Dec 12, I noticed increased…Continue

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Relationship Status:
Married
Do you have alopecia?
Telogen effluvium
Are you age 18 or older?
Yes - I am 18 or older

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At 8:03pm on July 28, 2015, Jlhollow said…
So I live in NJ and the doctor who was recommended to me is a doctor who specializes in hair loss but I knew more about te and alopecia than her. She actually never really heard of diffuse aa. Can you believe that? She also works in NYC. So good news is that within that one month my eyelash gap did fill in. So I'm happy that my hair is growing back. I think I just got myself worried bc of the newly noticed leg hair that grows so slow bc alopecia according to the websites slows hair growth down until it stops growing. That has got me freaked out a bit.

My husband too thinks I'm crazy and I just need to stop worrying and it will go away. I really do try, but some days I'm not as strong as others. I feel like my hair rules my life. I have 2 kids, age 4 and 6 and I want to go swimming in the pool with them but I'm afraid of getting my hair wet bc I have to wash it again. And my hair looks horrible when it air dries and now it looks even crazier with thin hair and fly always. Ugh!!! I'm so glad you know what I'm going through.

I'm also on viviscal. 4 months now. I'm not sure if it's making a difference though. Do you think it is? It's pretty expensive. I'm also on biotin, vitamin d, multivitamin and selenium.

Do I get the applicator for the toppix? What else do you think I should get accessory wise with the toppix. It looks confusing. I'm such a tim boy so this whole thing is a whole new works to me.

So I'm going back to my derm August 18th. I am going to demand a biopsy again bc I need to know if it's autoimmune or not.

The thing that gets to me he most is the whole unpredictability of it. If I knew I had to wait another year of shedding then I would be fine. It's just the constant shedding all day long that gets to me. I did cut my hair chin length so I can't even put back in a pony tail but I wore a pony tail for about 10 months and I don't want to do that again.

Like I said before, I can't tell you how much I appreciate your help with this. I already feel better. Thank you so much.
At 6:31pm on July 28, 2015, Jlhollow said…
Hi Jen: I had a few questions for you regarding your experience.

Did the dr. Take just one biopsy or a few? I read an nih study that said they need 3 scalp samples to differentiate between CTE and diffuse AA. I can send you the study. They also said to look for black and yellow dots on the scalp and cadaver hairs.

Did you buy a wig? I'm not sure if I should get a topper or a wig. I'm afraid of the traction alopecia that a topper can cause.

I was thinking of using toppix. However I'm a brunette with blonde highlights so I'm not sure what shade to use. Have you ever used toppix before?

Since the beginning of the summer I've noticed it now only takes shaving my legs every 5 days or so where it used to take every day. This could've been since this all started since sept 2014 but since it was winter time I don't shave as often anyway so I don't think I noticed. I'm also seeing this with my underarm hair.

Do you lose 50 strands even on shower days? That would be great.

Thank you so much for reaching out to me before on this subject. I just feel so alone in this whole process. So it's nice to know there is support.

Thank you!

Jaime
At 8:15pm on December 13, 2014, Nave said…

Jen, If you want to call me you can. I can be reached at 931-742-0353.  Since we have both dealt with Stacey I wanted to let you know what I'm doing but didn't want to post it.  You can also email me @nancyave62@yahoo.

At 9:16am on October 3, 2014, molly said…

Hey Jen, I wouldn't necessarily recommend a scalp biopsy... unless there is uncertainty about whether or not it is alopecia. They wanted to check because it was also a possibility of stress/trauma causing hair loss which is what my family doc thought it was. It hurts like heck, and only gives a concrete diagnosis but no answers on how to treat it. That's just my experience! 

At 7:12pm on October 1, 2014, LeslieAnn Butler said…

Hi Jen,

I developed areata when I was about 26 and then universalis when I was 40 something.

At 11:09am on September 29, 2014, LeslieAnn Butler said…

Hello and welcome, Jen!

How are you today? I have universalis, too.

Leslie Ann

 
 
 

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