This is the headline I read yesterday on Twitter: Lawyers for Jennifer Esposito are trying to negotiate a deal with CBS to get her back on “Blue Bloods.” She was written off the show after recently collapsing on the set due to celiac disease, an auto-immune disorder caused by a reaction to gluten. The axing prompted her to criticize the network’s “shameful behavior” and accuse the higher ups of “implying I was not truly ill” on Twitter.
On Saturday, CBS released a statement saying the actress, who plays Det. Jackie Curatola on the Friday night Blue Bloods, “informed us that she is only available to work on a very limited part-time schedule. As a result, she’s unable to perform the demands of her role and we regretfully had to put her character on a leave of absence.”
Esposito, who has been very public about her battle with Celiac Disease, quickly shot back on Twitter that “CBS put me on unpaid leave and has blocked me from working anywhere else after my doctor said you needed a reduced schedule due to Celiac. CBS didn’t listen to my doc and I collapsed on set. Which everyone saw! After a week off my doc said I could return to work but CBS implied that I was not truly ill and this was a scheme to get a raise! It’s been almost two months without bringing me back to work + keeping Me from working anywhere else!… Absolutely shameful behavior.”
Why this is personal for me…
When I was in the throes of poor health issues and working with every doctor I could find to try to understand what was wrong, and being tested for everything from Lupus to Cancer, I was thrilled to learn of the diagnosis. I assumed that I could simply cut out the allergic foods, take some thyroid medicine, add in some supplements to address some dangerously low vitamin and hormone levels, and I would be fine. Little did I realize what the true implications of an auto-immune condition would be, nor did I realize that I might not get the support and encouragement from friends that I had expected.
To be honest, I’m still working through what it means to have an auto-immune condition, and how to make sure I make smart health choices to protect myself. And while there’s a lot more to come on this subject, today I raise the issue to plant a seed of thought.
If you’re not familiar with what an auto-immune condition is, or what it means to deal with one, here’s a basic definition pulled from pubmed:
Autoimmune disease: An illness that occurs when the body tissues are attacked by its own immune system. The immune system is a complex organization within the body that is designed normally to “seek and destroy” invaders of the body, including infectious agents. Patients with autoimmune diseases frequently have unusual antibodies circulating in their blood that target their own body tissues. Examples of autoimmune diseases include systemic lupus erythematosus, Sjogren syndrome, Hashimoto thyroiditis, rheumatoid arthritis, juvenile (type 1) diabetes, polymyositis, scleroderma, Addison disease, vitiligo, pernicious anemia, glomerulonephritis, and pulmonary fibrosis.
I’ve written quote a bit about Celiac disease and my own auto-immune condition (Hashimoto thyroiditis) and what it means to my personal health journey, but one thing I rarely bring up here is what it means in regards to the support of friends and family members. One of the biggest challenges we face is that Auto-immune patients often appear healthy on the outside. Perhaps they are under or overweight slightly, suffer from irritability and/or fatigue, but so do many Americans (more on our typical American grain and dairy-ful diets and how they contribute to poor health to come in later posts). So because we don’t appear to be outwardly ill, it’s common to be met with judgments and criticisms about how our mental state may have more to do with it than an actual physical condition. In other words, I was told I was burnt out, depressed, suffering from PTSD, anxiety, etc. Very few people wanted to get to the root of what was truly wrong with me; including my Docotor who literally threw her hands up in the air after exhausting every test she could think of, telling me “there’s just nothing else I know of to do for you.”
Some of you might know exactly how I felt at that moment; alone, scared, confused and totally unsure of what I was supposed to do next. I mean, if a Doctor couldn’t help me, after a year and a half of running tests, then who could? In fact, the Doctors visits had actually been going on since I was 10, and had progressively grown more frequent with age. And when I could no longer perform my high stress, Executive level job anymore, I was offered a resignation package. That was 2 years ago, and while I wouldn’t trade any of the knowledge, clarity, healing or personal health journey aspects of my life today, it’s still sometimes hurts to know there are some who still think it’s as simple as changing my diet.
In fact, it wasn’t long ago that I was told that a family member still thinks that it’s just as simple as cutting out a certain food, stating that they know plenty of people who are gluten-free and do just fine. That might be true, but it brings up the very reason I’m writing this today, after seeing the Twitter comment about Jennifer Esposito. No matter how healthy we appear on the outside, those of us with an auto-immune condition dance a very fine line between health and sickness. Our fragile immune systems are in a constant state of teetering on an immune attack, and it’s decisions like reducing stress, changing our diet and taking an abundance of natural supplements that help us stay healthy and safe. Yes, I say ‘safe’ because ultimately if you continue living in a state of immune attacks, your body will eventually have destoyed its organs, and you will be weakened to the point of a degenerative disease.
As I often state, I’m not a Doctor. Hell, I’m not a nutritional expert at all. I’m just a girl who got really sick, and healed herself with dietary and lifestyle changes. I created Inspired Eats to help those of you like me out there who can’t get access to the medical help you need to heal. For the millions who suffer from a food allergy, sensitivity and/or auto-immune condition and have more questions than answers. The reality is, this is a project of love because it certainly doesn’t provide an income for us that would even cover one night out to eat. But what it does give is an outlet for me to share my journey in the hopes that it will help you along yours too.
I have a vision for the site that will allow me to connect you with healing providers to help answer your questions, and who can guide you to the right resources to help you start your healing path. To offer help in going gluten-free, grain free, dairy free, etc thanks to an abundance of recipes and meal plans. To offer you product samples to try before you buy them, so you can be sure to know you love them before investing in them. And most importantly, I have a vision that this will become a community where you can all share your thoughts, struggles, successes, recipes, and detail your allergy-free journeys with each other.
So for those of you suffering along your poor health path; feeling like crap and unsure of what to do, I hope it helps to know that I’m here. And I’ve met some pretty amazing people along the way that want to help you too. And for those of you who know someone suffering, please try to love without judgement, and help them to heal by guiding them to the answers they seek. Help them find resources to help with the hundreds of questions they have, and work through the very real fears they have that they will never feel better. It took my 5 year old son standing by my bedside, tears in his eyes, asking me when I was going to stop feeling sick for me to drag my sick, exhausted butt out of bed, call a nutritionist and start my healing journey.
I would love to hear from you in the comments section below – it’s the best we’ve got for now as far as a community, so start connecting by sharing your journey with us. I hope you have your moment now and hope I have been of help!
Live inspired,
Jen
#Celiac Actress #JenniferEsposito collapses, and why this is personal. http://t.co/HK4HWBdG
Thank you for this – it’s great to hear what it’s like for someone dealing with the disease directly and how you cope. I’d love to hear more about your personal journey and how loved ones can be more supportive. I guess it’s sometimes hard for those of us who don’t deal with it personally to really understand how to be supportive.
Thanks for your comments Cindy! You’ve made me think about how important it is to write from both perspectives, and help everyone cope and heal together…
Well said.
This is a wonderful explanation of how it feels to always be teetering on the edge of illness/fatigue! Thank you for putting it into words, and doing such a great job. I’m forwarding your post to friends and family members.
Thanks Louise!
Thank you for sharing!!!! It’s so true that our disease is truly not understood by people. I thank god everyday that I figured it out early before I got diabetes however everyday is a struggle feeling like crap on a gf diet. I now feel the same ad a year ago and have no idea why. Love this site and look forward to following you! It’s great to know others understand and truly care!
Hi Lisa,
When I was finally diagnosed with everything, I was pre-diabetic and had high CRP inflammatory markers, meaning I was well on my way to life-threatening conditions. I would definitely encourage you to try the Paleo diet if you’re still not feeling better on a GF diet. It’s a complicated condition and most of us react negatively to dairy and grains in general. You might like this post too: http://inspiredeats.net/some-quinoa-varieties-may-be-unsuitable-for-strict-gluten-free-diets-study-suggests/ or this one: http://inspiredeats.net/food-allergies/glutenfreedom/gluten-and-cross-reactive-foods/
I hope these help!
Disappointed in CBS.
ME too! That is just so not right! Shame on them!
Give cbs some feedback. http://www.cbs.com/info/user_services/fb_global_form.php
Thanks for sharing this link Liza! I have a feeling CBS is getting an earful today 🙂 I have to say I’m totally disappointed in them – I love the show and have mixed feelings about watching it now. It’s just such a complicated and fragile issue…
Sent feedback.
I don't know what the law is when it comes to jobs like acting. But the decent and right thing to do is work with her and her situation. Instead they have created more stress for her, which is the last thing she needs while she is trying to heal her body!
She needs to get rid of all grains. Grass fed beef and fruits and veggies. I should thing that would help a lot.
Absolutely agree Candace; though I don’t know what type of diet she’s on, that’s the diet that has helped me the most.
Tell CBS what you think! http://www.cbs.com/info/user_services/fb_global_form.php
Celiac Actress Jennifer Esposito collapses, http://t.co/bwag2IGn
@CBS I won’t watch Blue Bloods til Jackie is back! @JennifersWayJE
My husband was diagnosed with Celiac disease three years ago, and the only reason we discovered it was because a friend had been diagnosed. We began comparing symptoms and realized so many were the same. I won’t bore you with the varying “diagnoses” he received over the years, but suffice it to say that after going gluten free, his life has changed in MANY ways. It got us thinking about our daughter, who has had stomach problems from the day she came home from the hospital. She went gluten free, and lo and behold, the problems stopped! Being a “know-it-all” teen (LOL!) plus, of course, wanting to eat pizza and other foods her friends were eating, she decided one night that maybe it was all in her head and ate some pizza after months of gluten free eating. Well, after a volcano erupted from both ends for hours with pain and misery, she has never gone back.
This led to us telling my husband’s family members, many of whom have auto-immune diseases (including an uncle who, like you, has Hashimoto, though it wasn’t until my husband got his diagnosis that he considered gluten as the culprit!) My husband’s brother also gave up gluten after many health problems and showed vast improvement. He has not been tested for Celiac.
What I was NOT prepared for was how insensitive and misinformed some people can be! I went to a lunch with a group of women, and there was someone there I had never met. The subject of Celiac came up, and this woman launched into a tirade about how gluten-free eating was nothing more than a fad and a gimmicky weight loss program. I tried to explain the severe reactions my husband and daughter have, but I got the “it’s all in their head” lecture. I was so furious, I told her she should really do her research before shooting her mouth off. I probably came off as an ass, but I was MAD! Needless to say I haven’t been to lunch with those women again. Then there are those who think just “cutting out bread” is enough. I try to forgive that because if you haven’t had to deal with completely removing gluten from your diet, you have no idea the unbelievable things that contain it (Twizzlers, for example!)
So far, my husband has not had to deal with what Jennifer Esposito is going through, but it infuriates me that something like this could happen. If CBS doesn’t want to put her on a reduced schedule, at least let her out of her contract so she can pursue other roles! Unbelievable!
Sorry for my long comment. I was just infuriated by this whole story, especially the implication that Jennifer was “faking” her collapse for a raise! Of all the things to “pretend” to be, having an auto-immune disease is a real stretch. I heard her on a show talking about how one of her teeth actually fell out on a set before she was diagnosed. Man, that Jennifer Esposito really goes the extra mile for a raise, huh? BAH!
Hi Rene,
LOVE your comment – thank you so much for sharing!
It’s funny you mention about Jennifer’s teeth, because I’ve had issues with mine too, and have a couple which are capped as they literally chipped right off. Again, I just assumed I had weak enamel since I was always diligent about dentist appts, teeth brushing, etc. There are so many health conditions I just simply wrote off as “bad luck” until I was properly diagnosed.
I’m sorry you dealt with such ignorance at the lunch you mentioned, and that’s absolutely a very real issue. I hear that often as well – can’t you just cut our gluten and be fine? Ahhh, if only it were that simple! Appreciate you taking the time to share 🙂
RT @JennifersWayJE: Beautifully put, thank you and No negotiation to return http://t.co/9ZzzdGcU
My sister had the exact thing happen to her. Turns out her Breast Cancer had returned and it has been growing over the past 8 years unknown by her. She got sick suddenly and over a year and a half of tests they determined it was Celiac Desease. But by the time they diagnosed the problem the cancer has made it's way into her spine, hips, and brain. The tumors are now increasing in size in her liver. So they misdiagnosed her contition. Over the last 8 years she has been told she is cancer free. But, what I do know is she still can't eat gluten products, and this makes it hard for her to gain the strengeh she needs to fight off the tumors. Celiac desease could very well be the sign of something else happening in your body. It is a serious desease, and I'm glad you are having all the tests, very important. Don't take anything for granted. Good luck Jennifer, I hope CBS sees the error in their decisions. They should be ashamed of how they have handled your illness. And good luck with your medical condition. I will add you to my prayers to get well.
I’m sorry to hear about your sister! Thank you for sharing in regards to the seriousness of the disease; I hope for a day when Doctors will test for food related diseases and allergies as common practice. xx for your sister and your family along this journey…
she [and everyone else] can benefit from completely eliminating gluten (and most other grains in fact) from her diet… they have no place in a diet that promotes health, especially gut health… the same could also be said (though not quite as strongly) for nightshades/fodmaps if you have severe gut health issues.
Please look into paleo / auto-immune paleo / GAPS diet, there are very good reasons for avoiding grains/vegetable+seed oils for everyone but in particular gut-health problems. 🙂 helped me sort out all my gut health issues, anxiety/adrenal fatigue and lose approx 100lbs
she [and everyone else] can benefit from completely eliminating gluten (and most other grains in fact) from her diet… they have no place in a diet that promotes health, especially gut health… the same could also be said (though not quite as strongly) for nightshades/fodmaps if you have severe gut health issues.
Please look into paleo / auto-immune paleo / GAPS diet, there are very good reasons for avoiding grains/vegetable+seed oils for everyone but in particular gut-health problems. 🙂 helped me sort out all my gut health issues, anxiety/adrenal fatigue and lose approx 100lbs
Thank you Petros. She cannot eat any products with gluten at all. She get's extremely sick if she does. So her diet has been reduced to eating like a bird. The toxic cancer drugs have ravished her body. She went from 154 lbs. to 112 lbs. over the last 3 years. She has no insolaton whatsoever on her skeleton. On days that she may have a bit more of an appetite (like eating 3-4 more bites than usual) she gets diarria, or throws up. It's one extreme or the other. But I will call her today and ask her if she has heard of this paleo/auto-immune/GAPS diet, at this point I have a feeling she has. She has tried everything the doctors tell her to do. Thank you for letting me know, that was awfully kind of you. I welcome your information and she will too. Thanks again.
hope she does find some use in the research too.. there is a hell of a lot of good data for eating ketogenic (lowish protein, extremely high fat [saturated animal fats preferentially] and vlow carb) in some cancer situations… not sure if it's applicable here but robb wolf has talked about it many times on his podcast (www.robbwolf.com, search for cancer / ketosis or something and see what podcast numbers come up)
I'd also encourage looking into cannabis (through food or vaporiser to eliminate any carcinogenic possibilities) to reduce/stop the nausea and give appetite back;- seems to be quite a bit of "alternative" knowledge/anecdotal stories on the power of orally supplementing hemp oil (the non-THC male version of the plant) providing full remission for very severe cancers.. so may be worth a look in to too (i believe there is a guy who provides it for free to people since its illegal to sell being hemp, and he made a documentary called "run from the cure", very interesting stuff)
ie: http://robbwolf.com/?s=cancer < amazing free podcast 🙂
“#Celiac Actress Jennifer Esposito Collapses, and why this is personal” – Great post by J. Mansfield (@MyInspiredeats)
http://t.co/B4TuoGVU
RT @JennifersWayJE: Beautifully put, thank you and No negotiation to return http://t.co/9ZzzdGcU
RT @JennifersWayJE: Beautifully put, thank you and No negotiation to return http://t.co/9ZzzdGcU
I like Jennifer on blue bloods she was a good actress on blue bloods.I love her a Danny Reagan partner.
Thank you SO much for this article.
Glad you liked it!
First of all CBS not understanding in this matter. Thank you for this article it reaffirms the seriousness of Celiac and auto-immune diseases. Appreciated the information you have provided. It is indeed helpful.
Hi Heather,
Glad you liked it!
Please encourage your readers and other to sign the Change.org petition started for Jennifer Esposito http://www.change.org/petitions/cbs-television-get-jennifer-esposito-back-to-work-or-release-her-from-her-contract#.
Shared on FB – thanks Jennifer!
I do not leave a response, but I browsed a few responses here Celiac Actress Jennifer Esposito collapses, CBS fires her | Inspired Eats
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