Prednisone and moon face

New Topic Post Reply Printable Version
46 posts in this thread.
Viewing Page :
 1  2 
[ << Previous Thread | Next Thread >> ]

Tammy B
New Member


Date Joined May 2007
Total Posts : 18
   Posted 6/3/2007 10:19 PM (GMT -6)   
Is this the idea behind prednisone and moon face:  the higher the dose and the longer you are on it, the more likely you are to get moon face?  Silly question, I know, but, I have been on prednisone for almost 4 weeks @ 40 mg/day without any sign of moon face...............until today.  I don't know if it's really there or that I am just anticipating that it will happen eventually.  My husband says that he doesn't see it, but, unless it was really noticable, he wouldn't say anything to keep me less anxious about it.  I am scheduled to go down to 30 mg./day on this week (yes!), and in two weeks down to 20mg./day.  I am anticipating getting down to below 10 mg./or lower to get rid of other side effects. 
 
Thanks for any input........................
 
Tammy
dx: fibromyalgia 2006; uctd/probable lupus 2007; hypothyroidism
 
rx:  Prednisone 40 mg./day; plaquenil 400 mg./day; levothyroxine .025 mg./day; sertaline 100 mg/day; allegra d; caltrate plus d 600 mg. 3x/day; multi-vitamin


Barbara Lee
Veteran Member


Date Joined Sep 2003
Total Posts : 2790
   Posted 6/3/2007 10:29 PM (GMT -6)   
Hi Tammy:

I've been on prednisone for 6 yrs now. I have to say in the beginning I didn't have a moon face, and that was at a dose of 20mg daily. My first 4 years on the pred left me w/o a moon face. The past 2 years my moon face has appeared. The higher the dose and the length of time really does make a difference.

I've been attempting to cut my pred use down, since I've been doing that I've noticed my moon face isn't as bad as it was last summer. I have other side effects that have left permanent damage to me. I've got cataracts, huge deep purple stretch marks on my breasts, underarms and top of my thighs as well as my stomach. I've got a huge buffalo hump on the back of my neck, I've also got more facial hair than I ever had. These are all side effects that will probably never leave me.

I know it's the pits to take pred, and I truly hope that you don't get a moon face. Good luck to you and it's nice to meet you.

Take care,
Barbara
dx fibro, SLE, glaucoma, cateracts, bells palsy, depression, migraine headaches, gastreopaersis, chronic anemia, MDS (Blood Cancer). Mediport and tons of meds.


okie
Veteran Member


Date Joined Dec 2006
Total Posts : 2818
   Posted 6/3/2007 10:31 PM (GMT -6)   
Hi Tammy, yes it does have to do with how much you are on. I have kind of a round face anyway so you can't really tell the difference unlewss I am in the hospital and they are pumping me full of the stuff in an IV. than I come out looking like the pilbury dough boy. I know no one wants to have this happen but try not to let it get to you too much. Remember it is not permanent. and if it is helping you than you need to take it. plus the anxiety isn't going to do you any good either.

I'm glad you are going down on it some. That's great news! hang in there.

Hugs
carol
God Bless
Carol
 
 Newly DX's Lupus.Possible CREST,COPD, high PB xanax,triam , vicodin.5x3, Evista for osteo,. oxygen Plaquanil800mil, . effexor. spiriva, xopenex. pred.10.mil.
 
Come ye, all that are weary and heavy laden, and I will give you rest!
 
 


Tammy B
New Member


Date Joined May 2007
Total Posts : 18
   Posted 6/3/2007 10:38 PM (GMT -6)   
thanks so much for the feedback. I am not a terribly vain person, but, up until I have been ill, I always prided myself on being extremely active and fit and taking good care of myself. It's not the end of the world, I know, and if it will go away, that is good news for me.

Thanks for your input - I really appreciate it!

Tammy
dx: fibromyalgia 2006; uctd/probable lupus 2007; hypothyroidism
 
rx:  Prednisone 40 mg./day; plaquenil 400 mg./day; levothyroxine .025 mg./day; sertaline 100 mg/day; allegra d; caltrate plus d 600 mg. 3x/day; multi-vitamin


CaptSue
Regular Member


Date Joined Jan 2007
Total Posts : 279
   Posted 6/4/2007 9:26 AM (GMT -6)   
Hi Tammy,

Good luck on the tapering. I have been on prednisone since last Sept. I only needed 10mg a day and have since gone down to 5mg a day. Even at that dose, I have a bit of a moonface. I detest it! My boyfriend says he doesn't notice (like your hubby, I suspect it's a white lie). It is an individual decision on the benefits verses the risks of this med.

Like you, I always prided myself on being fit and active. I've just had to revise the definitions as to what that means now. Keep in touch and let us know how you are doing.

Stay Strong,
Sue
Diagnosis: Mixed connective tissue disease (systemic lupus, scleroderma, polymyositis), Raynauds phenomena (both diagnosed in 2006)

Meds: prednisone (5.0 mg wish I could taper), Imuran (2X50mg), Prilosec (20mg), Prozac (off now)


applesk82
Regular Member


Date Joined Oct 2003
Total Posts : 262
   Posted 6/4/2007 10:45 AM (GMT -6)   
hi guys, now i'm not sure if it happens to everyone but i have been on prednisone for about 12 years now, and when i was at my lowest dose 5mg every other day, my moonface completely went away, right now its back cuz they had me on 60 mg of pred for a month and now i am tapering 10 mg every week, but for me most of the side effects go away when the dose of the prednisone is low, my doc said that i would never get down to 5 mg every other day like before, but 5 mg every day will not make a difference physiologically and she said that the side effects will go away again, except for the stretch marks, unfortunately those never go away, they kinda fade a little but they never disappear completely :( My hubby says that he doesnt notice the moonface either but like sue said, i think they are fibbing a little, but my strong belief is as long as he and i still like the way i look, i really dont care what other people think.
Hugs and prayers,
~Suzanne~
 
diagnosed in May '95 with lupus nephritis, hypertension,hypothyroidism, avascular necrosis (knee) '98, kidney transplant April '06, pseudo-cerebral tumor '07
prednisone, cellcept, prograf, lopressor, allopurinol, synthroid, diamox, OsCal +D


tink 2
Regular Member


Date Joined Jan 2007
Total Posts : 371
   Posted 6/4/2007 10:52 AM (GMT -6)   
Ok what is moon face?????
Lupus since 2005, MCT since 2005 polymysoitis since 2005,Arthritis since2005 sjogren's syndrome since 2005, vertigo since 2006,migrains since 2006, diabetes since 2006, Depression since 2004. who would not be with all of this.
 
       I just try to make it threw every day as best I can.
        God please remember I am on the diet platter.
                  So many beads so little time.....
 
                   Have a great Lupie Day Denise 


Butterflake
Forum Moderator


Date Joined Jun 2006
Total Posts : 1398
   Posted 6/4/2007 11:29 AM (GMT -6)   
Hi Tammy.  I also have a round face and if I smell prednisone I get moon face.  If I'm on more than 15mg I get the buffalo hump like Barb describes.  What is moon face?  Kind of like a round face with the areas between your jaw line and your cheek bones (jowls) puffed out like a croaking toads.  My moon face disappears quickly once I can no longer sniff the prednisone.  I'm having a bad flare right now and when I complained to my rheumy that I hate prednisone, all he said was, "Everyone does."  The "too bad" was implied.   

Dx: SLE, major depressive disorder, diabetes, fibromyalgia, asthma, gerd, sleep apnea, hypertension, IBS
Tx: plaquenil, methotrexate, Imuran, prednisone 10mg, flexeril, prozac, lamectil, celebrex, lisinopril, actos, lipitor, nexeum, seroquel, advair, arthritis tylenol  PRN: ambien, neurontin, promethazine, xanax, albuterol
supplements: multi vitamin, C, flaxseed oil, calcium/D
             Better living through chemistry :D    Donna
 


Tammy B
New Member


Date Joined May 2007
Total Posts : 18
   Posted 6/4/2007 11:43 AM (GMT -6)   
I can't tell you all how much these little notes help!!! My husband and friends want to and think that they do understand what this is like, but, like most anything, no one ever knows exactly how something feels unless you have experienced it first hand. I had heard about Lupus before I was dxd, but, never in a million years imagined that it was as devastating/lonely as it is. Everyone that tellls me that "at least it isn't cancer or something worse", is right, and I AM thankful that I don't have to contend with that, but, Lupus is just so invisible that at times I feel like I am always trying to "not feel ill" because no one can really "see" that I am in pain. I know that the moon face/weight is temporary and extremely vain and even silly to worry about, especially since the prednisone has been keeping my pain down from what it was. Definitely a love/hate relationship!!

Thanks again to everyone for the notes and encouragement!

Tammy
dx: fibromyalgia 2006; uctd/probable lupus 2007; hypothyroidism
 
rx:  Prednisone 40 mg./day; plaquenil 400 mg./day; levothyroxine .025 mg./day; sertaline 100 mg/day; allegra d; caltrate plus d 600 mg. 3x/day; multi-vitamin


tink 2
Regular Member


Date Joined Jan 2007
Total Posts : 371
   Posted 6/4/2007 5:23 PM (GMT -6)   
Thanks for explaining what it was. I am on Pred. now 60mg for 2 days 40 for 2 and 20 for 2. My drs do not want me on it all the time due to family history with it. I take it when the flairs are bad. I keep some at home. Thanks for the info . I did notice lots of red in the mask aria since on it and sugar leval elivated for 90's to 130's over night, and not sleeping.
Lupus since 2005, MCT since 2005 polymysoitis since 2005,Arthritis since2005 sjogren's syndrome since 2005, vertigo since 2006,migrains since 2006, diabetes since 2006, Depression since 2004. who would not be with all of this.
 
       I just try to make it threw every day as best I can.
        God please remember I am on the diet platter.
                  So many beads so little time.....
 
                   Have a great Lupie Day Denise 


PattyLatty
Veteran Member


Date Joined Mar 2006
Total Posts : 2559
   Posted 6/4/2007 6:31 PM (GMT -6)   
When I started tapering off 60mg of prednisone I was anxious to lose the moon face and all my puffiness and remember mentioning it to my rheumy. She told me that it varies from person to person but that in some people it can take up to a few months for it to completely go away after going off pred. So I wouldn't be too concerned if it doesn't go away right away, but eventually it will. Hang in there. It's miserable, I know!
Lupus, Rheumatoid Arthritis, Sjogren's, osteoarthritis, fibro, ibs, renauds, restless leg, hiatal hernia, double vision.

cellcept, neurontin, prednisone, plaquenil, synthroid, triamterene, cymbalta, tramadol, lunesta, actonel, meridia, tricor, aciphex, multivitamin, calcium w vit D, fish oil, aspirin


goldenwings
Regular Member


Date Joined Apr 2007
Total Posts : 81
   Posted 6/4/2007 7:06 PM (GMT -6)   

Hello here,

I had a moon face and put on weight when I was on 70-80mg sometimes more per day as a newbie to them.  Sounds very dramatic, but it was back in the days when prednisolone was the only thing that worked for SLE in relation to bringing the inflammation down and helping me totally.  I'm talking over 30 years ago.

As I dropped down the dosage over the months, the moon face disappeared as did the body weight gain.  I have never since then had either of these things happen, and I have taken steroids every day since I was first put on them after diagnosis.  I maintain a level and then when I am so unwell as to need to increase them I do so.  I always have done since being diagnosed over 30 years ago as I said.  

Take care.

goldenwings  sad

Post Edited (goldenwings) : 6/5/2007 5:18:00 PM (GMT-6)


Tammy B
New Member


Date Joined May 2007
Total Posts : 18
   Posted 6/4/2007 7:21 PM (GMT -6)   
Goldenwings~ Thanks for the good news! I was very happy that I hadn't developed the moon face/weight gain for the 3 weeks that I was initially on it. Funny how most people said that it was around the 1 month marker that it gradually started -- I'm in my 4th week right now!!! Today I started the weaning process going down from 40 mg. to 30 mg. for two weelks -- its amazing how exciting that is!!!!!!!

Love the input.......keep 'em coming!!

Tammy
dx: fibromyalgia 2006; uctd/probable lupus 2007; hypothyroidism
 
rx:  Prednisone 40 mg./day; plaquenil 400 mg./day; levothyroxine .025 mg./day; sertaline 100 mg/day; allegra d; caltrate plus d 600 mg. 3x/day; multi-vitamin


applesk82
Regular Member


Date Joined Oct 2003
Total Posts : 262
   Posted 6/5/2007 5:12 PM (GMT -6)   
i think pretty much everyone dislikes prednisone, but its the best thing that helps (atleast for me) but i do hate hate hate predinose, even though i dont really have a choice on taking it, but we do what we gotta do. and i dont think its really fair to compare what we have to cancer patients, that's like comparing apples to oranges, two totally different things (in my opinion). I use to work in an oncologist (cancer doc) office as a medical assistant before my transplant, and they use to do the chemo treatments right in the office, and just like us, some had it easier than others, but they hated it too. i am now down from 60mg to 40 mg but no physical changes yet, (not really surprised) but hopefully by the end of the year i'll lose the weight and most of the moon face.
Hugs and prayers,
~Suzanne~
 
diagnosed in May '95 with lupus nephritis, hypertension,hypothyroidism, avascular necrosis (knee) '98, kidney transplant April '06, pseudo-cerebral tumor '07
prednisone, cellcept, prograf, lopressor, allopurinol, synthroid, diamox, OsCal +D


lovexlife
New Member


Date Joined Dec 2009
Total Posts : 1
   Posted 12/7/2009 5:23 PM (GMT -6)   
hi, i'm 14 years old, and this summer i was diagnosed with auto immune hemolitic anemia. i had to go to school with a moon face. i would come home everyday crying because i would either get called "chipmunk" or "puffy cheeks" or "fat face". ive been off the prednisone for two months now, and the moon face is still very noticable, even though it has come down a lot. how much longer will i have to wait, because i honestly cant take anymore of this.

cured4real?
Veteran Member


Date Joined Dec 2005
Total Posts : 1942
   Posted 12/7/2009 11:02 PM (GMT -6)   
I got it from alpha interferon treatment for liver disease and its been permanent. I thought that with steroids it comes and goes. But when I take pred, my face often looks skinnier because the swelling in my parotid glands goes down and in my salivary glands.
Love, Marji
Ills--Sjogrens-Lupus cond., AI polygland. dysfunction 2, hyper/hypopigment, scoliosis,kyphosis,stenosis, deg.,O.A.,spine surgeries, salivary/lymphectomies, NASH, COPD, RLS, UT/GI bleeds, hystero, brain/nerve damage,TB
Meds--INH,Plaquenil, Evoxac, Metformin, Synthroid, HCTZ, HRT and Lidocaine patchs, Voltaren gel, Klonopin, Vicodin, Restasis, Albuterol, steroids


AmyTx
Regular Member


Date Joined Dec 2006
Total Posts : 185
   Posted 12/8/2009 12:41 AM (GMT -6)   
put it this way i was hospitalized when they put me on prednisone 80 mg..that was nov 30 of 2006 and by christmas i had a moon face... it does go away when you taper down though
Female: 38 yrs/old DX: Lupus (dx:'03) MCTD, Raynaud's, Antithyroid antibodies, Lupus Cebritis, Lupus CNS, Lupus Pneumonitis and Stage 3 & 5 Lupus Nephritis. 9 tia's and one pontine stroke,Seizures, Photosensitivity since childhood, vasculitis, left thumb and toe amputated from raynauds, Sjogren's
Meds: Plaquenil,Prednisone 30 Mg/Day,Miracle mouthwash,Xanax, Darvocet, Xopenex inhaler, Xopenex Nebulizer, Spiriva, prevacid, aspirin 325mg


PattyLatty
Veteran Member


Date Joined Mar 2006
Total Posts : 2559
   Posted 12/8/2009 9:48 AM (GMT -6)   
lovexlife,

Your face will go back to normal, but I know it's slower than you want it to. I've been tapering from 60 mg. for some time and my weight dropped 20 pounds, and I've been stuck there for a year. BUT, people are continuously telling me that I look like I've lost weight. Even those close to me. I don't see it, but they do.

I can't believe how cruel people can be, esp if they know that you're having to take medication for a medical condition. Stand high and know that you'll soon be back to normal. Your actions can teach others, esp the cruel heartless ones that there is a better way to treat people.

It will go away, and you'll get your pretty face back again. Join us here whenever you need to talk. This is a good place to come and hang out for a while, giving and getting support. Sounds like you could use a gentle ear.

((((Hugs))))

Pat

P.S Maybe one of the Moderators will start a new thread for you, or you can do it yourself.
SLE, fibro, renauds, restless leg, hiatal hernia, double vision, migraines, costocondritis.

prednisone, plaquenil, leflunomide, neurontin, synthroid, triamterene, actonel, niaspan, lyrica, tri-est, cymbalta, acifex


Bsime
Veteran Member


Date Joined Apr 2006
Total Posts : 1218
   Posted 12/8/2009 12:50 PM (GMT -6)   
Tammy,
 
Of all the possible and horrible side effects the moon face is not one of them.  It is merely a redispostion of fat (it can also occur inyour belly or back) that occurs with some patients on higher doses.  As you taper it will go away and you will return to normal.  I was on 60 mg for 6 months or more before I got it but it disappeared as I tapered in the following months.  I have not had a moon face or prednisone belly for the last 3 years even though I have been on prednisone for more than 4 years.
 
If prednisone is  controlling your lupus and not causing side effects that will harm you that is the most important criteria.  Listen to your doctor and don't make the mistake that many patients make getting off controlling meds too soon.
 
Bill
MCTD (lupus, scleroderma, polymyositis).  Diagnosed 2005.  Kidney, liver, GI tract, dysphagia, raynauds, Barretts esophagus, quadriplegic in 2005.  Recovered and now active in skiing, tai, chi, hiking, golf.  Meds: prednisone 2.5mg, imuran 25mg, amlodipine, benazapril, omeprazole, potassium, folic acid, vitamins, maxide and various supplements and vitamins.
 
Remain optimistic and you can overcome the odds.


caring
Regular Member


Date Joined May 2007
Total Posts : 26
   Posted 12/8/2009 12:50 PM (GMT -6)   
Tammy - I had "moon face" after having been administered high IV doses of Prednisone for about a week, and then tapered down (w/ pills) at home for 6 mos. It saved my life and I am so thankful for it. As I decreased the dosage, my face gradually slimmed down again. My husband had to be on high doses of Prednisone for a period of time and he never did develop the "moon face". I was always curious as to why. Anyway, although there are some neg. side effects of this med. - it can save lives, and did save my life ! Good health to you.

lunacygotme79
Regular Member


Date Joined Dec 2009
Total Posts : 34
   Posted 12/22/2009 2:34 PM (GMT -6)   
Tammy,
I am on 20mg of prednisone everyday and my face is swollen looking from it. I have been on it since about August. I have noticed the diference in pictures taken latley and it seems to be getting worse, although I have been gaining weight from the prednisone as well. I have noticed though if I split the dose, 10mg in the morning, then 10mg in the afternoon, it is not as swollen. I just came off a 6 day dose pack of Methylprednisolone for a flair, so I have been taken the 20 mg together and have already noticed the swelling, so I am going back to the split dose....... Since you will be tapering off it hopefully you won't even get the "moon" face. I hope you feel better soon!smile
 

Diagnosed 2009: Lupus (SLE);Rheumatoid Arthritis; Dermatomyositis; Optic Neuritis; Microscopicolitis; Chronic Gastritis; Cryptitis

Meds: Prednisone 20mg daily, starting Methotrexate injections 10ml once a week 12/11/2009, Prenisone eye drops daily.

 
 


susan1
Regular Member


Date Joined Dec 2009
Total Posts : 80
   Posted 12/22/2009 4:05 PM (GMT -6)   
My Mom was on it for a very long time with her Rhuematoid Arthritis (high doses too) and she never got a moon face and she actually lost weight too.

Hugs

christine_rightbrain_writesjunk
New Member


Date Joined May 2009
Total Posts : 17
   Posted 12/31/2009 6:57 PM (GMT -6)   
Hello..this is an interesting and long thread. :) I think it started in 2007~~ I don't take prednisone anymore bc it makes me completely out of my mind with anxiety!! But this is only because Plaqunil and Methotrexate have worked as an alternative so far. It is funny, my husband did not notice a moon face or what I was talking about. However, my Realtor at the time came in the house and said "look at your moon face, I can tell you are on steroids!" (LOL) I also gained weight, but all of this was after a few months at a high dose. I was lowered to 20mg..but after 8 months on it..the side effects stuck (especially the very high level of anxiety). I have been off of it for about a year and my angular face has just about totally "un mooned".... There are unpleasant side effects with every med. I look at it as whatever trade off is worth experience the good moments of life ....love to you all on this New Year
CTDU/Probable SLE- Peripheral Neuropathy, Partial Complex Seizures, Severe and chronic joint pain/fatigue, Sun sensitivity, butterfly rash, vitamin D deficiency, skin rash in sun, Skin rashes, mouth, lip, nose sores, Hair loss, head sores, some muscle pain, Muscle cramps, Vascular: Raynoids syndrome, Hx of Pericarditis x 4, Severe Dry mouth, persistent, Thyroid Disease, hx of moderate asthma, lung inflammation at onset of illness, hx elevated RF, recent protein serum elevated. No positive ANA yet


Methotrexate, 2.5 mg (4tabs 1x a week) Folic Acid (1mg daily), Plaqunil 600mg day, Topomax 200mg day (neurapathy), Ultram 100mg (prn) pain, flexaral, pm for feet cramps, Synthroid .50 micro, estrogen patch, lexapro 5mg, (mild anxiety),

~nothing is impossible~


happyman
New Member


Date Joined Jan 2010
Total Posts : 1
   Posted 1/14/2010 5:27 PM (GMT -6)   
hi there...ive joined to post about the whole prednisone moon face thing from a personal perspective.

im now 39 and was on prednisone for about 2 years - my dosage varied dependent on need but averaged out at around 15mg a day. now that wouldnt be seen as excessive.....

i never really thought i looked any different 6 months, a year, even 18 months after starting the drug. my weight stayed under control due to excercise and strict dieting. so i though all was well, and that i wasnt succumbing to the 'moon face'.

but just as you cant see changes in a close relative or friends appearance when you see them on a daily basis - only when you look at old/new photos - this works in the same sinister way.

fortunately i was able to wean myself completely off pred last summer. now the bad bit. i took a snap of myself in december to test out a new cameraphone i had...and found an old photo from a year earlier, in exactly the same type of shot - when i was in the middle of my 'moderate' pred dosage. i was shocked. the differences...oh i nearly cried...i hadnt noticed the horrible fat deposits around my eyes that almost reduced them to slit when i smiled, the swelling and bloating of my chin, the loss of jawline definition, and a whole yellowing of my skin cry i have a naturally long face, but even this took on a different look.

it looks like ive had plastic surgery in my new pic, it looks so much like a facelift with my features back to normal, the fat out of my face and skin tone losing the jaundiced look. not saying im anything special to look at, but 10x better without the pred-effects, and hopefully the pics clearly highlight the physical changes that this drug induced.

so just to advise people that you may not notice whats happening to you - maybe your friends or family wont as they see you on a daily basis - but be careful....you can see for yourself what i mean - with the pred photo 1st then my recent pred-free one.

after 18 months on average of 15mg day of pred


4 months after stopping pred entirely



at least the ending is happy, and i hope everyone concerned about possible effects can see from my ghastly photo the sort of changes that it can cause to you - and that it goes away then dose is removed. :-)

Post Edited (happyman) : 1/14/2010 3:39:33 PM (GMT-7)


Lynnwood
Forum Moderator


Date Joined May 2005
Total Posts : 5706
   Posted 1/14/2010 6:29 PM (GMT -6)   
Just a note -- any reduction in prednisone *must* be done under a Drs guidance as it can cause very serious consequences, such as your heart stopping!

Thanks for the photo illustration, I've seen similar results as my pred usage has gone from 15 down to 4mg over the course of a 1.5 yrs.
Lynnwood, Lupus & Sjogren's Moderator
"Life is far too important to be taken seriously" - Oscar Wilde

New Topic Post Reply Printable Version
46 posts in this thread.
Viewing Page :
 1  2 
Forum Information
Currently it is Wednesday, October 01, 2014 1:17 PM (GMT -6)
There are a total of 2,231,198 posts in 248,269 threads.
View Active Threads


Who's Online
This forum has 156839 registered members. Please welcome our newest member, poojag.
441 Guest(s), 26 Registered Member(s) are currently online.  Details
Celeste15, JungRulz, pictureofhealth, MustangSally52, irenie, Cardamon, melodee, annieoak, Scaredy Cat, Girlie, Merrida, getting by, Judy2, Fronton, lesweet1971, Dreadsteel, Happychick, bakomom, deltaforce, Azgram, electracat, Momtogigiandquinn, Tembo, Sunny13, (Seashell), iPoop


Follow HealingWell.com on Facebook  Follow HealingWell.com on Twitter  Follow HealingWell.com on Pinterest  Follow HealingWell.com on YouTube
Advertisement
Advertisement

©1996-2014 HealingWell.com LLC  All rights reserved.

Advertise | Privacy Policy & Disclaimer