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Author Topic: Hair Loss Post Tx  (Read 10874 times)
Cordelia
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Posts: 2012


« Reply #25 on: March 31, 2014, 07:43:17 AM »

Hi lainiepop!

I wonder that too, if it just takes time to get used to the meds?   I completely side with you on that thought!         
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Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
MooseMom
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« Reply #26 on: March 31, 2014, 01:20:47 PM »

My hairdresser commented last time it had thickened. So maybe sometimes its a case of the body etting used to the drug changes?!

That's probably the case.  It's what my tx neph and coordinator keep telling me.

I know this is going to sound weird, and it's probably only an optical illusion, but it seems that I lose a lot less hair after I've had it cut.  I know it's probably because with longer hair, it just LOOKS like there's a lot more hair in the sink (and I guess there is, actually!), but my hair looks a lot more normal when it is a bit shorter.
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"Eggs are so inadequate, don't you think?  I mean, they ought to be able to become anything, but instead you always get a chicken.  Or a duck.  Or whatever they're programmed to be.  You never get anything interesting, like regret, or the middle of last week."
Cordelia
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« Reply #27 on: April 05, 2014, 07:08:28 AM »

Hi Lainiepop, I've wondered that too, if it takes time for adjusting. I know I had the same thing with dialysis. For the first 6 months on D, it was the worst.

That's really interesting MM, what you were saying about your hair, its so interesting to hear everyone sharing their experiences, it sure helps to know that I'm not alone!
Logged

Diagnosed with Polycystic Kidney Disease at age 19.
Renal Failure at age 38 (2010) came about 2 hrs close to dying. Central line put in an emergency.
Began dialysis on Aug 15, 2010.
Creatine @ time of dialysis: 27. I almost died.
History of High Blood Pressure
I have Neuropathy and Plantar Fasciitis in My Feet
AV Fistula created in Nov. 2011, still buzzing well!
Transplanted in April, 2013. My husband and I participated in the Living Donor paired exchange program. I nicknamed my kidney "April"
Married 18 yrs,  Mom to 3 kids to twin daughters (One that has PKD)  and a high-functioning Autistic son
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