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How To Look And Feel Beautiful With Autoimmune Disease

Autoimmune Disease Beauty

Posted: 11/28/11 08:30 AM ET

By Angelica Catalano for YouBeauty.com

"But -- you look so good!" your friend says with a confused look, after hearing that you're sick.

One of the ironies of certain illnesses is that even when you're feeling cruddy, you can appear just fine. But imagine that you didn't feel your best most of the time ... would you still try to look it?

For those who suffer from autoimmune diseases, looking good means masking a civil war going on inside: Your immune system attacks healthy cells in your body as if they were enemies. Over time, tissues become inflamed and cause pain in the war zone, which differs based on the affliction. In the case of Rheumatoid Arthritis (RA) the battle zone is your joints; your intestines with Crohn's Disease and for Multiple Scleroris, the brain and spinal cord.

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There are more than 80 types of autoimmune diseases, some of which may have genetic components. The environment can also make things worse by prolonging or exacerbating symptoms. For example, stress and infections can kick up symptoms by activating genes that trigger an autoimmune response.

While some people experience chronic, debilitating symptoms, others have the occasional flareup. It's unpredictable, and it takes effort to maintain a strong sense of personal style and inner beauty.

"You could feel fabulous today and horrible tomorrow," YouBeauty reader Jane says about RA. When a bad day strikes, she'll stay in bed. But most of the time, she puts her best face forward, even if she's swollen and in pain. "I make a point of looking my the best," she says. "I always feel better when I put on my red lipstick."

Integrative Health Expert Jim Nicolai, M.D. agrees -- you could lift your spirits with something as small as finding a really good set of cosmetics. "If there's something you feel really good about and it makes you feel good, I promote it as a health strategy," Dr. Nicolai says about working with patients at the Dr. Andrew Weil Integrative Wellness Program at the Miraval Spa in Tuscon, Arizona.

Jane has been cultivating her style for years, looking polished even during the early hours of preschool drop-off. "It's just a trick. I put sunglasses on, a pair of gold hoops and a long trenchcoat on top of my pajamas," Jane would tell mothers who asked how she always looked so put together.

She's stayed true to her style through her RA diagnosis, sometimes looking so good that people don't understand she isn't feeling well. She attributes it to her signature scarlet lips, which keep her looking like herself, even when steroids cause face bloating and other side effects.

But when you look so good that no one knows you're not feeling it, does it help or hurt?

"There are times when someone has a chronic illness, that they relish in normal interaction with other people. If you're not showing lots of visible signs, you have more of a chance to feel normal," says YouBeauty Psychology Advisor Art Markman, Ph.D., a professor of psychology at The University of Texas.

This appears to be a boon for our wellbeing, though it can backfire on days where you're with people who can't see the disconnect between how you feel and how you look.

YouBeauty reader Maria has trouble interacting with others during a Multiple Sclerosis flare-up. "Sometimes I need support and if people think you look good, then they are not understanding. If you had a neck brace on people would know something was wrong," Maria says. "On the other hand I don't want sympathy either, so it's complicated."

Dr. Markman suggests that when you really aren't feeling well "You have to learn to say, 'I'm having a tough day,' if you're not showing it on the outside," he says.

This is exactly what Chef Seamus Mullen does when he experiences RA symptoms. "I think it's most important to speak openly about it." He's straightforward on a bad day, telling his restaurant staff at Tertulia what he can and cannot do. That way, when he's stubbornly trying to lug something into the kitchen with achy hands, someone will lend a hand.

Even on the ugly days, there are ways to try syncing your body and mind, so you start feeling as good as you look.

Enhancing Mindfulness: Conditions can flare up in response to emotional ups and downs. One component of an integrative medicine perspective is psychoneuroimmunology -- the study of the link between psychology, the nervous system and immunity, based on the idea that our bodies respond to the way we process information mentally and emotionally.

Both Jane and Maria use guided meditations, which help them reframe stressful situations and avoid exacerbating their symptoms. Maria puts aside 20 minutes to meditate with a Healing Meditation by Kelly Howell. "It gives an overall focus on the strengths of your body and how you can incorporate those strengths into feeling better," she says. Other times, if she is experiencing a significant amount of stress, she visits a placid place to reflect.

"I go to the convent; it's really quiet. You hear the cloister nuns chant. It's an environment that's really conducive to going within, and being grateful for your blessings. I feel lighter, stronger and supported. Everyone there is focusing on mindfulness," Maria says.

Jane wishes she were more spiritual, but admits that she's not very. She finds other ways that bolster her emotional wellbeing. Jane's doctor recommends that she continues her hobbies as usual. "I have a homework assignment to go to my studio and paint," Jane says of her last doctor's appointment. In the quiet space of her studio, she produces abstract portraits of woman in vivid colors, so alive, they appear to jump off the canvas. Painting is one of many hobbies that people get immersed in, that can greatly benefit physical and emotional health. Called "flow," regularly getting lost in such an activity can enhance concentration, self-esteem and self-reported health.

Finding a Personal Exercise Routine: "Keep regular exercise, not just because it keeps weight down, but it makes you feel better," Dr. Nicolai says. He adds that mild to moderate exercise is best for boosting your mood without overtaxing your body.

With arthritis or pain-related problems he recommends activities like water aerobics or Zumba. "After doing that you're going to have a better physical response than if you sat for three to four hours at a time," he says. "Changing the way we move can change the way we feel."

Jane has done water aerobics. "They have a dedicated class for people with arthritis and they keep the pool at 86 degrees, so it is very nice. I did find it beneficial," Jane says. "I find, however, if I am in really bad shape, I don't want to go and usually don't. Look at it this way: if you had the flu, would you go out and do anything? That's kind of how it is," she adds.

Feeling well enough to muster up the energy to exercise class is often the biggest hurdle.

Maria splurges on private Pilates lessons because she feels it forces her to make exercise part of her Multiple Sclerosis treatment. "It's a private setting so I can't blow it off, I have to commit to it," she says. Setting small goals for yourself can give you the push you need, even on the bad days.

Not Giving "It" Power: While it's beneficial to talk about what's on your mind, talking too much about the negative aspects of your disease may drag you down. "I don't want people to be in support groups that focus on symptoms and nastiness," Dr. Nicolai says. He encourages patients to rise above a hopeless, negative attitude, so they can still feel beautiful.

If your diagnosis isn't definitive, Dr. Nicolai even suggests not naming your problem. "A lot of people's autoimmune symptoms are nebulous or grey. The lab tests say you have one marker for lupus, and another test says Sjogren's syndrome." In this case, he suggests focusing more on treatment than naming the problem. Let's keep it gray, see how it's manifesting itself.

Being Beautiful, Inside and Out

"Rheumatoid Arthritis is my reality, I can't deny it and run away from it. I have to acknowledge it," Chef Seamus Mullens says. This mentality not only helps him, but will help many more people -- his anti-inflammatory diet cookbook, "Seamus Mullen's Hero Food," is set to come out this spring.

Hone in on the things you know will boost your mood and beauty. Surround yourself with people who lift your spirits and understand your situation.

Even on those days when you feel your body is complete chaos, you can maintain your personal style and inner calm.

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By Angelica Catalano for YouBeauty.com "But -- you look so good!" your friend says with a confused look, after hearing that you're sick. One of the ironies of certain illnesses is that even when...
By Angelica Catalano for YouBeauty.com "But -- you look so good!" your friend says with a confused look, after hearing that you're sick. One of the ironies of certain illnesses is that even when...
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01:13 PM on 07/19/2012
Positive thinking is a great thing to employ but that doesn't change the fact that RA is a life threatening (and yes I said life threatening-put RA and Cardiac issues in Google and you'll see what I mean) that can leave people totally disabled. What you see on the TV drug commercials isn't the norm for sufferers. Just as an FYI, the battle zone isn't just your joints. Your entire body is it's playground.
01:05 PM on 01/01/2012
Autoimmune is a increasing scourge on our society, but this solution is not simple.
Taking care of ourselves is a large part of the answer, from yoga to eating right
to sleeping and not feeling guilty. Sharing our experiences is another part of the answer,
as autoimmune disease is so heterogeneous that one man's solution is another woman's
poison. Talking out our tribulations and triumphs will help guide us towards a solution
for every one of us.

http://questorganic.com/categories/autoimmune
01:26 PM on 07/19/2012
Taking care of yourself is important but the only things proven to have an effect on the progression of RA itself is trying to keep your body in motion as much as possible (without injuring yourself) and pray that a biologic works for you. No diet has been proven to keep it at bay or cause it flair up. You also should monitor your healing process closely from any illness or surgery and to follow doctor recommendations for heart health.
05:44 PM on 12/13/2011
Lipstick? Seriously?

As someone coping with two autoimmune diseases, I'm sick to death of hearing this kind of shallow advice. Yes, I'm as active as I can be and I make a concerted effort to be positive. However, this article negates the fact that we're talking about systemic illnesses, folks. Wicked, destructive, diseases.This article is all over the place - lipstick, lying in bed all day, meditation, Zumba... if you're out of your league, don't write about it. Your words just might do more harm than good.
04:21 PM on 01/06/2012
Hello,

Like you, I too suffer from two autoimmune diseases. I know the realities of having to literally "push through pain" to perform at my full time job, have a personal life and still be the primary manager of my healthcare... I wish you the best.
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HUFFPOST COMMUNITY MODERATOR
ConfuciusSay-
Aglets: their purpose is sinister.
08:54 PM on 11/30/2011
If you are taking Prednisone for your illness, you can consider asking your doctor about Deflazacort. It's less potent, and has less side effects. Sold under trade name Calcort here. I use it on patients with remissions, and less severe times with their illnesses.
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HUFFPOST SUPER USER
Sharon Hanson
Skeptical of the *pseudo-skeptics*
10:32 PM on 11/29/2011
I should also say that I am so tired of hearing the medical profession say "we don't know what causes it" that I want to gag. Why don't they know? Is it because someone might be liable for your illness? Is it because they don't want to cure you, only treat your symptoms? Why do we let them get away with saying they don't know. When I was working if I said that I would of gotton fired and my field was very complex with limitless variables.
01:31 PM on 07/19/2012
They actually DON'T know what causes it. There is a lot of research going on to try and answer that question. The first thing they need to do however is looking for a lifestyle cause for this disorder because they aren't going to find one. There is too much evidence to suggest that this is all about your genetics and what it does to your immune system.
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HUFFPOST SUPER USER
Sharon Hanson
Skeptical of the *pseudo-skeptics*
10:29 PM on 11/29/2011
I'm going on my forth autoimmune autoimmune disease maybe five. The difference from other posts is that I KNOW what is causing mine. I think something enters our body that shouldn't be there and we start attacking it. For me that something is gadolinium from contrasting agents used for MRIs. I want to say try and find the cause. Right now I'm very sick but I know what I need to do as gadolinium is a toxic heavy metal and to get rid of it I am using chelation therapy.
08:01 PM on 11/28/2011
Love your perspective on beauty...the secret of inner beauty!

I have had Rheumatoid Arthritis for 26 years. I spent 15 years on medication and the last 6 using my inner guide and natural healing. On my journey, I have been led to the healing powers of inner beauty and sexuality. My internet radio show, "Living an Organic and Orgasmic Life" is one manifestation of what I have learned.

Thank you for this article and all your great work with kindness. Would you be interested in being a guest on my show? www.coachbettylive.com
07:57 PM on 11/28/2011
Looking good, feeling good...so very connected and sometimes getting out the door is hard enough, let alone getting out the door looking cute. I struggled for a long time with finding the right balance. When I get gluttened I balloon up, looking full-term preggers, yet yoga pants aren't de rigueur for an office setting. In my biz outfits, I'd get plenty of compliments around the office but on the inside I'd be in such pain and misery it hurt to sit/stand/kneel at my desk. A celiac disease diagnosis, a new eating routine and meal plan, and really cute shoes (those always fit!) have gone a long way to making everyday cute again.
07:51 PM on 11/28/2011
I suffered from Chronic Fatigue Syndrome for 15 years - another 'hidden' condition, so I can relate to all your stories. I tried everything (and spent a fortune) trying to get well - finally I did, and quite fast, by learning how to change my body chemistry using self-hypnosis. There is so much science out there now proving this is possible (psychoneuroimmunology) so there is hope! I've seen the same process work for people with things like MS and hyperthyroidism too. www.timeforachange.biz
06:37 PM on 11/28/2011
Great article. I've got chronic nonspecific neuropathic pelvic pain, after 8 years of endometriosis and adenomyosis, followed by a hysterectomy at the ripe old age of 35. It's been really hard lately to keep from being buried by feelings of hopelessness as well as the endless pain. This article gave me some good ideas on how to get myself to feeling better.

I think that "feeling beautiful" has less to do with using cosmetics (I almost never do--personal preference) than with deciding that I Am Beautiful(tm) on an emotional level. Like many of you, I can't afford exercise classes. That doesn't mean I can't meditate--I often do it in bed as I'm going to sleep. I've done it on planes, in cars, in train stations...meditation is about finding a quiet space inside you, not outside. If you've got nowhere else to do it, try meditating in your desk chair at work. You can stretch there too, and even exercise to build muscle tone. Seriously.

I need to make my life better, and I have the power to do that if I want to badly enough. I've just got to make good choices every single day. That's super-hard, but the results can be more than worth it.
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HUFFPOST SUPER USER
gemmax
09:54 AM on 11/29/2011
I've been ill with two autoimmune illnesses for 19 years. My muscles are now inflamed almost all of the time, preventing any repetitive exercise, so that I am limited to stretching. Even though this is the case and my life is quite limited, I find that the stretching helps me, and I surround my space where I rest with all of the beauty that I can. I keep my hair in great shape and I always have pretty PJs or sweats. I keep books and a sketch pad and journal handy. Music and candles and flowers and the coziest blankets. I pamper myself. I believe that it is very important to love yourself. Rest when you need to with feeling that you need to make excuses, stay home when you don't feel well enough to attend certain events. Take care of you.
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HUFFPOST SUPER USER
gemmax
09:58 AM on 11/29/2011
sorry, with feeling = without feeling
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HUFFPOST COMMUNITY MODERATOR
ConfuciusSay-
Aglets: their purpose is sinister.
08:50 PM on 11/30/2011
Sorry to hear about this, gemmax.

Your suggestions are spot on - feeling bad about not being able to do things isn't helpful. I take care of someone with a similar illness, and often have to encourage her to sleep more, limit her activity to something manageable, and supply things like a cushion for the iPad when she's reading. Wish I could do something for you too.

Our oldest dog will lie on her tummy and hug her food bowl, and eat very comfortably with little effort. It's a great example for us humans.
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04:57 PM on 11/28/2011
The best way to live with Autoimmune Disease is to continue living and building your life. Since tomorrow maybe not a great day, make today remarkable and start doing meaningful to add-on to your life. Don't wait for the perfect day to dance, to sing, to write that novel, to ask that person out, or to do whatever it is you desire that can enhance your inner sunshine and happiness. Your days will pass you by if you wait. Don't wait! "It's never too late to be what you might have been" Do it today!
05:23 PM on 11/28/2011
I totally agree with your statement. You may have to modify your lifestyle a little, but that doesn't mean you can't try new things. Since being diagnosed with CVID (common variable immune deficiency) I took on a challenging position with a legal firm for a 2 1/2 years, met and married a wonderful, caring man and moved twice. It's not always easy, but life never is, whether or not you are healthy.

Manage your condition, treat yourself right, do the best you can and smile. Even when I have my monthly IV/IG treatment, for 10 1/2 hours, I still manage to smile at all the other patients coming and going through the day and chat with the ones who are willing. My motto, I wake up, it's a good day!
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10:41 PM on 11/28/2011
Good for you. Life is worth living in spite of the disease. Keep up the good work. Wishing you all the best.
03:43 PM on 11/28/2011
No advice on lupus and all the skin troubles that go with it?
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HUFFPOST SUPER USER
tiemposdepaz
08:11 PM on 11/28/2011
They are addressing all different types of autoimmune diseases, not just lupus. As for the skin troubles with lupus, I have to say that i have a prescription to protopic, which helped with my bald patches and malar rash. It cleared up both within a week.
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HUFFPOST SUPER USER
gemmax
10:02 AM on 11/29/2011
I don't know much about all of the skin conditions that go with lupus, although my illness is what is called a lupus-like illness. My daughter suggested trying nipple cream for my face. Its a bit difficult to use, being a very firm substance. You have to warm it up between your hands to use it. You might ask your doctor about using it. Just a thought. It has improved my skin so much.
02:13 PM on 11/28/2011
You've probably been told that it’s in your genes… please consider…I once read a book about a Chinese American medical doctor (forgot the title) who had moved to America when he was a little boy and developed this dreaded disease...he eventually became bedridden.

At this point, he reviewed his family history and found that no one had had this condition. Upon further reflection he noted that the diet of his ancestors was very different from the American diet he had entirely embraced. The differences were that they ate a lot of dark greens, very little meat, very little fruit, no dairy and whole grains i.e., brown rice. He switched to this diet and within a month he was able to get out of bed and his health continued to get better from there.

I strongly recommend that you look into this. It might not be genes, but instead bad lifestyle habits passed down from one generation to another and perhaps more so in this s generation. Don’t manage this condition…I encourage you to do research and find a way to heal it; go beyond the conventional medical community.
02:37 AM on 12/15/2011
Like most patients who get a devastating illness, I bought the alternative books and tried several 'miracle cures' including diets, exercises, etcetera. I was exceptionally healthy when this hit, and doctors don't know why anyone gets it. I am still looking for my cure, and have found doctors willing to try some alternative ideas, but I accept now that it may not be as simple as diet change. I know you mean well, but a lot of people have heard of 'someone' who was cured of every illness, and if it were as simple as changing bad habits most of us would be healthy by now.
08:44 AM on 12/24/2011
I was recently diagnosed with Diabetes type 2, AIC 16.5 - 502 average over 120 day period (below 7 is considered nondiabetic). My eye sight was going blurry, etc. I was prescribed Metformin 500 2 2xs a day; I went to urgent care and not to my regular doctor. My doctor wanted me to come in for a check up, primarily because she felt that this was not enough medication. Ordinarily she'd be right, per research it appears that Metformin affects a change of approx. 1 - 2 points.

I told her that instead, I wanted to wait 120 days and to implement Dr. Neal Barnard book on Reversing Diabetes. I didn't go completely Vegan, but dramatically changed how much fat and simple carbs in my diet. 120 days later I re-tested at 6.3 (145 average). My doctor acknowledged this as a "signinficant" reduction.

I think that when you research, keeping on looking up info from different sides, until you reach a number of good legitimate sources saying the same thing. Then try it for a long period of time...natural ways heal, but take time to do so.
01:59 PM on 11/28/2011
Thank you so much for this article. I'm 22 and was recently diagnosed with Lichen Sclerosus. It's really difficult to not be overwhelmed but it, especially since I'm so young. It is, however, amazing to find an article like this. Not because it's necessarily new information (I've had severe depression for years and people tend to tell you the same thing) but because I know others are out there, just like me, trying to live one day at a time.