LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » dry saggy scaly skin- anything to help????

 - UBBFriend: Email this page to someone!    
Author Topic: dry saggy scaly skin- anything to help????
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
my skin has not been good in years- now I know why- these buggers!

Since I am on abx it has gotten worse- it looks like it is old saggy, white , dry and I can see the outline of each segment on there and I have line after line- looks similar to pic in the link below on the left- but mine looks worse.

 -

I don't really wanna try any more creams since I have tried just about everything for years. *note- I am slightly allergic to coconut so I can't take internally.

It started on my legs years ago, went up on my arms, now on my neck and I am seeing a little on my face- call me vain- no offense intended but I don't want to look 80 when I have not earned those lifetime badges yet. [Wink]

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
I see link I posted didn't show up!

try this?:::

http://www.dailymail.co.uk/femail/article-2270786/Adonia-StemuTone--24-miracle-cream-sells-10-000-units-48-hours-going-sale-UK.html

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
Umm water.

I use prai cosmetics amd they seem to help
Also have heard positive things about cocoa butter

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
MichaelTampa
Frequent Contributor (1K+ posts)
Member # 24868

Icon 1 posted      Profile for MichaelTampa     Send New Private Message       Edit/Delete Post   Reply With Quote 
Water was my first reaction to this question as well.

If you didn't have lyme disease going on, that's what I'd be telling you. Maybe you're doing the right amount of water and you need extra, or maybe you're doing all that your body can handle but it is having difficulty using it, ... who knows ...

There have been times that I have had trouble assimilating water, and adding Willard Water helped a lot. I wonder if doing that would help your situation, if you're feeling you're drinking enough. Do you feel thirsty? Do you ever drink some and then walk around and hear the water jiggling around in your stomach as if it is not being assimilated?

Posts: 1927 | From se usa | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Water, yes, very important. Fish oil, too.

And liver support

(because the skin is a major organ of detoxification and the liver & kidneys are overwhelmed as they are with any chronic toxic infection so the skin has to take up the slack and lot of stuff we can't really see is being "pushed out" through our skin).

Work from the inside out.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=030792;p=0

LIVER & KIDNEY SUPPORT & and several HERXHEIMER support links, too.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Lyme also attacks collagen. So addressing lyme will be of great help to skin in the long run, too.

In the mean time, Gotu Kola can be a nice support to collagen, from the inside out.

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/3/32567?#000000

GOTU KOLA - Informational Links Set
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Kudzuslipper
Frequent Contributor (1K+ posts)
Member # 31915

Icon 1 posted      Profile for Kudzuslipper     Send New Private Message       Edit/Delete Post   Reply With Quote 
Water is important. but also , sealing in the moisture after a bath or shower... never get out of water without moisturizing! I know that this probably has chemicals in it...But I love Nivea skin firming lotion with Q10. I am also allergic to coconuts and shea butter...so know there is none in there. It's really hard to find a moisturizer without one or the other of those.

any oil internally is good, fish oil , olive oil, and pasture raised organic butter is supposed to be good too. (obviously in moderation)

Posts: 1728 | From USA | Registered: May 2011  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
My skin looks like that on my lower calves. Awful! I think mine is related to candida/yeast and to Sjogren's.. it makes my body dry.

I drink tons of water, seemingly to no avail.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Good point made by Kudzuslipper about moisturizing right after bathing while skin is plumped up. To keep the moisture in but also let the skin breathe, be sure to avoid any products with any petroleum chemicals and additives / dyes.

To find safe personal care products:

http://www.ewg.org/

Environmental Working Group
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
jjourneys
LymeNet Contributor
Member # 39813

Icon 1 posted      Profile for jjourneys   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
My legs have been like this for about 3 yrs now. I started treating for lyme in jan 13, amazingly, after a few months the skin cleared up.

I've been off ABX for a month, the skin mess is coming back! it is so embarrassing that I refuse to wear shorts.

Posts: 250 | From East Coast | Registered: Jan 2013  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
I drink lots of water, if I drink any more I will explode. I use lotion and in 5 minutes it is dry again. I was looking for an internal suppliment. no creams have worked.

I will see abuot trying what has been suggested above that I have not tried, thanks.

Michaeltampa, yes, sometimes I get slushing sound.

jjourneys like I said I have had this for yrs and yrs. I started abx 5 weeks now and it looks worse.

I always use only natural products and I always moisturize after bathing- if I didn't I would look like a cracked flaking mummy

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
glm1111
Frequent Contributor (5K+ posts)
Member # 16556

Icon 1 posted      Profile for glm1111     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dry skin is on the list for parasites. Google parasite symptoms. Also google skin parasites and visit the PARASITE WARRIORS SUPPORT THREAD.

Gael

--------------------
PARASITES/WORMS ARE NOW
RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS*

Posts: 6418 | From philadelphia pa | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Maybe mine is worse because I ran out of coconut oil 2 wks ago. I just got more.

I'm upping my usage and will see if it gets better.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Lisa [Smile]

If you've read some of my posts then you know I'mm the Queen of Rashes. Had dry peeling scaly skin called guttate psoriasis (actually RMSF and lyme), for the last 12 years.

Since abx the rash has gone away...BUT when I had the rash I tried everything.

The best, and please take my word for it, it organic grapeseed oil with a few squirts of natural sheeps lanolin in it, and a few squirts of castor oil (hexane free).

The lanolin is actually absorbed by the skin instantly and repels water for hours.

Internally I found nothing helped me.

Don't waste your money on creams or lotions...safer cheaper and more effective to make the oil and put it on after a bath or shower.
Biotin and silica didn't help me.
Good luck.

PS. Don't spill the oil in the shower tub or on the floor-you'll have a wipeout. Just squirt some of the mixture in your hand and rub it in your skin.

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
TerryK
Frequent Contributor (5K+ posts)
Member # 8552

Icon 1 posted      Profile for TerryK     Send New Private Message       Edit/Delete Post   Reply With Quote 
When my LLMD saw my dry skin he put me on thyroid meds right away. Dry skin is a common side effect of thyroid issues Ask your doctor to check your thyroid.

I have the wrinkly skin too and my LLMD told me it is damage from lyme. Don't know if that is the case for you.

Terry

Posts: 6286 | From Oregon | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
I used lanolin when I was pregos- yes, that might work! thanks Greta!

boy castor oil sure is a good thing. Why don't people use it like they used to?

Lymetoo, I used to use coconut oil before I found out I am allergic. I really liked although it didn't help greatly, it did help more than most creams.

100% Pure makes a nice body cream. It used to work on me up until recently. They make cosmetics all out of fruit - great products!

Parasites- yes, on my list!

I did notice since on (day 5 today) of azithro that I am having tons of skin things going on. I am getting a nightly itch and redness on my chest and clavicle bones. I just remembered how for years I have been getting night sweats with tons of itching on those bones!

So I figure the abx is hitting that area now and killing off those stupid bugs and that is causing a more dramatic action there. ??

It always perplexed me tremendously why I had this rash and sweats there- it was always so strange!

well, one thing this journey sure isn't- BORING!

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lisa K said:

"I did notice since on (day 5 today) of azithro that I am having tons of skin things going on. I am getting a nightly itch and redness on my chest and clavicle bones. I just remembered how for years I have been getting night sweats with tons of itching on those bones!"

-
That is exactly where I often get a YEAST rash. So heads up, youngin! [Smile]

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been doing a ton of research on this, because I have horrible issues on my elbows. How can two small areas of the my body drive my crazy. They do. Painful, itchy, flaking.

What I've found is something called ACA acrodermatitis chronica atrophicans. Yes, caused by lyme disease. ACA known in the medical world as Herx disease.

Research says it comes from the European strain of borellia?????????? What, how would a Euro strain get in Kentucky? Believe me it wasn't from any other place.

Sounds like I'm real lucky that it has stayed contained to my elbows since it came up in '07.

Pam

I've yet to find anything that helps.

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've heard of other Lyme patients who have this. Is the skin discolored?

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
It has several red hard nodules under the skin. Then the next stage is itching, painful sensations. Then it goes to scaly, flaking, and swollen.

I've tried steroid cream rx, coconut, essential oils, naturopathic creams. Anything I've tried has to be applied multiply times daily to relieve the need to pick at it.

This phases happen over and over again. It's a never ending cycle. I'm so blessed it's just my elbows. Some of you I'm sure have areas as bad as the pics on the web. OMG!

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
Carol in PA
Frequent Contributor (5K+ posts)
Member # 5338

Icon 1 posted      Profile for Carol in PA     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lisa, look up information about "cigarette paper skin."

This is atrophy of the skin, and is related to the Lyme bacteria affecting the collagen.

When I was working in the hospital, I took care of so many old, sick people who had this.


Fish oil helps with the dryness, and will improve skin integrity.
You may need to increase your dose.


Rough dry elbows are one of the symptoms of low thyroid.
I have a friend who had rough elbows as a child, and developed an autoimmune condition as an adult.

Posts: 6947 | From Lancaster, PA | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
yeast rash?!?!?! what is that?????


Map- is it psoriasis?? sounds so similar.

My daughter gets psoriasis on her elbows.

Carol, my skin is not discolored like the photos I see of cigarette paper skin.

I have also noticed a lot more brown spots all over me too- the "age" type spots that you can sort of peel off.

I will keep taking oil and see if it improves. Hopefully I will know soon

I do feel extra dry though since on zithro. especially my mouth0 it feels like I ran for an hour with my mouth open

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have hastimoto's. Was hypothyroid long before becoming ill. My thyroid gland has no visible blood supply to it.

Dead organ? If I was a super smart bacteria, I'd hang out there too. That's why my immune system is attacking it.

I know the truth of lyme & co. But finding a specialist, whole different world. My PCP won't increase my meds based on sx.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'll be back later regarding the yeast rash... found this:

http://www.youtube.com/watch?v=JNQ8caxC6ac

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
map, I wish you luck with that! craziness. I regret never going to med school. I would be the RIGHT kind of dr!

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
LisaK
Frequent Contributor (1K+ posts)
Member # 41384

Icon 1 posted      Profile for LisaK     Send New Private Message       Edit/Delete Post   Reply With Quote 
My fish oils seem to be helping! yay!

http://www.carlsonlabs.com/s-22-fish-oil-liquids.aspx

--------------------
Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen

Posts: 3558 | From Eastern USA | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm using lemongrass essential oil every night. My elbow thing is one of the bad guys. I'm trying to stop it's life cycle. At least in my elbow.

Covering up the symptoms is worthless.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.