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Born2lbfat

My life with Lipedema & Lymphedema...destined to be fat.

Lipedema Awareness: Just Keep Talking

November 20, 2013 by Sarah Bramblette 2 Comments

As Dorie the Fish would say “Just Keep Swimming”, in my case in order to spread awareness about Lipedema, I’ll “Just Keep Talking”, sharing my experiences and stories. Today yet another opportunity was presented to me, it was quite a whirlwind afternoon. At about 11:30 this morning I received an e-mail from James at the Obesity Action Coalition asking if I’d be interested in participating in a BBC show looking for people to share their story of living with obesity at 1:30 PM. I immediately replied, “Yes”…then I inquired about some details like “what’s the actual topic of the show?”, “who else was participating?”. Within minutes a staff member from BBC called me to give me more details, and to ask more information about me and my experiences with obesity. Oh and he asked if I had access to Skype, sure I do!

The show was BBC World Have Your Say and the segment was in regards to the story of Kevin Chenais, 22-year-old man from France who was stranded in Chicago because British Airways said that at 500lbs he was too fat to fly. Virgin Atlantic stepped up and flew Chenais to London, where he then encountered another travel issue. I was very familiar with the story, and relieved to hear he was finally getting help to get home.

There I sat in my bed, in my nightshirt, hair in ponytail, glasses on.

Skype means video, right? Ugh, I can’t talk about obesity from BED…what would people think? Probably nothing worse than they already think, but anyway I quickly got dressed, brushed my hair, and put some make-up on. Then another BBC staffer contacted me via Skype to test my connection and I found out it was going to be a radio show. Whew.

image

I was instructed that the host would start the conversation but that they wanted the participants to just keeping talking in reply to each other, no waiting on the host to call on me for my opinion just chime right in with my comments. “Is that something you’d be comfortable doing?” That’s something I do all the time!

So I had the pleasure of chatting with two new friends, Becky and Misty, both bloggers who, like me, embrace the word FAT.

Here is the link to our conversation on World Have Your Say: (our segment begins At 31:20)

http://downloads.bbc.co.uk/…/whys/whys_20131120-1910a.mp3

 

Filed Under: Advocacy, Blog Post Tagged With: advocacy, discrimination, healthcare, lipedema, lipoedema, lymphedema, morbid obesity, obesity action coalition, super morbid obesity, weight bias, weight bias in the workplace

Treat the Patient, Not the Obesity

November 18, 2013 by Sarah Bramblette 3 Comments

scale

As part of ObesityWeek 2013 new guidelines for the treatment of obesity were released. The media has stated the guidelines are encouraging doctors to “get tough”, “be aggressive”, “take serious action” when treating obese patients. The actual guidelines do not use such harsh language, and it is bothersome that the media puts the “let’s get tough on the fatties” spin to the stories. As a patient who is obese, I believe the guidelines leave out two very important pieces to the treatment of obesity: identifying the cause of the patients’ excess weight and ensuring healthcare offices can adequately access and monitor obese patients. 

Focus on the patient, not their weight.

I have always been frustrated by doctors who blamed my medical issues on my weight, yet never offered real options for losing weight. So the suggestions that doctors get serious about a patients weight and go beyond the obvious “you need to lose weight” and actually offer and prescribe nutritional counseling and activity for how to lose weight will be helpful to many patients. However, I believe dietary changes and exercise should be recommendations to ALL patients with heart disease, diabetes, high cholesterol, and high blood pressure. While excess weight can increase risk for these conditions, they are not exclusive to individuals with a high BMI.

What causes obesity?

Diagnose before offering treatment. There are many conditions and medications that can cause excess weight, doctors need to thoroughly examine the patient and address the actual cause of the obesity.

Yes, this is where I get on my Lipedema and Lymphedema soapbox. Both conditions are noticeable to the trained eye, the problem is there are not enough physicians who are trained to make a proper diagnosis. Instead, many patients, such as myself, are told to lose weight and when we do not lose weight as expected we are deemed non-compliant. And that label affects the way we are treated for all health issues. All my health vitals are normal, and should indicate that I live a somewhat healthy lifestyle, however there is still a focus my weight. For years, my weight increased while the actual cause of my weight, Lipedema, was not diagnosed and progressed to a stage further complicated by the development of Lymphedema. While the my health vitals, were normal, the Lipedema and Lymphedema was very much affecting my overall health. I developed severe cellulitis, and often required hospitalization for IV antibiotics and eventually needed a medi-port. During the hospital stays I contracted MRSA in the medi-port, that goes directly to my HEART. This greatly affected my mental and emotional health, as did the limitations on my mobility the conditions caused and the frustration of not getting any other explanation for what was happening with my legs than “it’s your weight”.

Accuracy is VITAL

As much as I was told the issues with my legs were because of my weight, the fact was my weight was unknown. The doctor’s office did not have a scale that could weigh me, nor did she attempt to locate a scale that could. On my own, I went to a local junk yard to weigh myself. No patient should have to make the effort to get their own vital health statistic. While that was ten years ago, I find today’s doctors offices are not any better equipped to care for patients with high BMIs.

In order for doctors to take obesity more seriously, they will need to have an accurate weight for patients. Currently, none of my doctors have scales to weigh me, yet, they all document the known incorrect weight. One office’s scale has a 300lbs limit, but it does at least register 328ish when I step on it. So the nurse documents that as my weight, even though I tell her that is not correct, and verbally give her my weight from my home scale. Again, this isn’t an issue in just ONE office, I encounter this problem is probably every doctors office I visit, expect for the bariatric surgeons office.

After the game of guess my weight, comes the torture of having my BP checked. Yet, another VITAL health statistic that is often not correctly taken nor monitored in obese patients. If the BP isn’t taken correctly, it is not an accurate reading, and thus monitoring inaccurate data serves no purpose. The blood pressure cuff needs to properly fit the patient’s arm. Cuffs that are too tight will give inaccurately high readings. Doctors’ offices need to have large cuffs, even thigh cuffs available, and staff need to know the where the cuffs are kept so patients can have their BP taken correctly.

Also, stop relying on BP machines, they are not accurate, especially on FAT arms. Every time my blood pressure is taken with a machine, it has to inflate twice then reads high. Again, I will let the nurse know the information is not correct, yet it gets documented in my medical record. My last employer’s wellness program was told I had high BP and I was put on a “plan” to reduce it”, which thankfully I did rather quickly by having my regular doctor submit my REAL blood pressure, which she gets by manually taking my BP using a thigh cuff. In addition, staff should be trained on how to take a blood pressure reading on the lower part of the arm, in case no cuff is available to fit the upper arm. Also, wrist blood pressure cuffs should be utilized.

Better scales and larger BP cuffs are not expensive items for doctor offices to purchase, and yet are very important tools to properly diagnosing, monitoring and treating patients.

Does your primary care doctor have a scale to weigh you? Share with me your experiences in the comments.

Filed Under: Advocacy, Blog Post, Obesity Tagged With: advocacy, lipedema, lymphedema, morbid obesity, obesity, obesity treatment, obesity week, super morbid obesity

My Story in Psychology Today

November 11, 2013 by Sarah Bramblette 6 Comments

psychtoday

My story is profiled in the current issue of Psychology Today (December 2013), as part of the article Do I Make You Uncomfortable?

This is the article for which I had My Abnormal Photo Shoot. In late August, I replied to a Facebook notice shared by the Obesity Action Coalition. Being a member of the OAC has provided many opportunities to share my story, and thus spread awareness about lipedema and lymphedema.

Does my fat make you uncomfortable?

According to the article that is YOUR issue, not mine. I knew this already, but I admit I misunderstood the article concept as originally told to me: “story about the experiences of those with physical differences—and how, on both a societal and individual level, we can overcome negative or prejudiced responses.” I thought the article was going to focus on those of us on the receiving end of the negative and prejudiced responses. Through my own sessions with a psychologist, I learned I cannot change other people’s behaviors, I can only control my own reaction. To my pleasant surprise the article’s focus is on the response people have when they see a person with a physical difference. It is a refreshing change for the discussion to address why some people have such adverse reactions to ME, since it is usually just accepted that it’s normal for people to act in such ways towards people who are abnormal. And yet, it’s not normal. Not everyone who sees me has a negative or prejudiced response, if that was the case I would not have so many supportive friends. So what does prompt the negative response?

psychtodayjeff

Protective Prejudice

The theory discussed in the article is that people’s negative and prejudices reactions towards physical difference is rooted in an immune response and survival instinct protecting against disease. Interesting idea for sure! And does go along with the idea that people project their own insecurities towards me. The personal stories shared tell of instances for which we have experiences negative reactions based on our appears, mine included the now famous “check out them cankles” incident. It is inspiring that the other individual profiled in the story have the same positive attitude and outlook as I do and the hope that by sharing our stories we can help others.

Research suggesting that prejudice is a flexible trait abounds — and simply being aware that it’s not fixed can significantly reduce discriminatory behavior. Accepting that we all hold negative associates and becoming aware of the one we automatically make are also critical steps in the process of counteracting our biases. So, too, is encouraging people to talk about their negative perceptions.

My abnormal appearance is beneficial in life, it serves as a screening process. If people do not want to get to know me because of my looks, their loss. Now sure, it hurt when I experienced weight bias in the workplace but obviously that was not a company whose values align with mine.

Leave me a comment:

Have you read the full article? Share your thoughts.

Does my appearance make you uncomfortable?

Have you ever experienced a negative or prejudiced reaction to your appearance?

Filed Under: Advocacy, Blog Post, Lipedema and Lymphedema, Obesity Tagged With: advocacy, awareness, bbw, discrimination, fat, health, lipedema, lymphedema, morbid obesity, obesity, obesity action coalition, Psychology Today, self confidence, self esteem, super morbid obesity, weight bias in the workplace

The Bias Among Us – Success?

November 5, 2013 by Sarah Bramblette 8 Comments

This blog topic is LONG overdue, and actually I have so much to say on the topic I feel the need to make it a series of posts. A couple months  ago I wrote about the fat shaming I’ve experienced from strangers, however even more troubling is the weight bias I have experienced within the weight loss surgery community. Let me reiterate I’m not calling any person biased, I’m labeling the actions and comments as biased. I know intentions are often to “help others” but as the person on the receiving end of the comments and actions, I feel it’s my duty to let you know they hurt far more often than help.

The picture of SUCCESS!

redcarpet

Last month I attended the ObesityHelp #OH2013 Conference in Anaheim, CA, I was a member of the event staff and as so I posted this picture to the ObesityHelp Facebook wall in order to promote the evening’s event. Under the picture I posted “Sarahlicious is warming up the Red Carpet! Are you ready to celebrate your success?” The theme of that evening’s party was “Celebrate Your Success”, I never actually called myself a success, I asked if others were ready to celebrate THEIR SUCCESS. A fellow WLS (weight loss surgery) patient commented on my picture with “success????????????????????????”.

This picture represents MY SUCCESS in several ways. “What? How? You’re still fat????”

  • I am a success because I am alive after surviving a deep vein thrombosis, mini-stroke, and patent foraman ovale (hole in my heart).
  • I am a success because I have maintained 100lbs weight loss for 10 years, was it more, sure…did I regain, yes! But 100lbs loss is still a success in my book!
  • I am a success because I have completed two bachelor degrees and I’m pursing my Masters in Health Law.
  • I am a success because I no longer have sleep apnea or high blood pressure, all other health vital are and have been normal.
  • I am a success because I love myself, and others love me for who I am.
  • I am a success because I share my story to advocate for and help others.
  • I am a success because I stand up against weight stigma and bias.
  • I am a success because I am winning the battle against disfiguring lymphedema and lipedema.

Success is a personal accomplishment, and since pictures are more powerful than words…

legsbefore

legsafter

However, I should not have to list my accomplishments or pull out my phone to show others pictures to PROVE I am a success. As a community we need to stop judging ourselves and others based on the scale. We need to stop judging, PERIOD.

 

Filed Under: Blog Post, Weight Loss Surgery Tagged With: advocacy, breaking, discrimination, fat, fat shaming, featured, gastric bypass, headline, health, lipedema, lymphedema, morbid obesity, obesity, obesityhelp, rny, super morbid obesity, top, weight bias, weight loss surgery, wls

Big Wheels Keep On Turning

November 4, 2013 by Sarah Bramblette Leave a Comment

day4

National Health Blog Post Month Day 4 – Training Wheels

Write about a time your health condition forced you to grow up and take the training wheels off (so to speak).

My training wheel moment involves health insurance, of course! It was very much like learning to ride a bike, I even had someone there guiding me, holding the bike seat to make sure I didn’t tip over.

When I was initially diagnosed with lymphedema I was on Medicaid. While it took a couple months for my initial treatment and compression pump to be approved, I never encountered a coverage issue or claim denial. I received unlimited physical therapy sessions, and was in the process of being fitted for compression garments when I got my first REAL JOB with REAL INSURANCE. And then came my first coverage issue and the experience that started me on my journey to advocacy.

bigwheel

Due to the size and shape of my legs I needed custom fitted compression garments, as it is important that the compression is correctly distributed over the limb. Jobst, the manufacturer of the garments my doctor and therapist recommended requires vendors and fitters (those who would take the measurements) be trained and certified to be sure the garments are fitted and ordered correctly. The average price for a pair of garments is $300 so it is very important they are made correctly, and since I needed two pair (one to wear, as the other is washed/dry) it was important that insurance helped cover the expense. After all, by wearing compression garments I was saving the insurance company the expense of physical therapy and hospitalization due to cellulitis. I was unable to find a DME (durable medical equipment) provider in my insurance network who was certified to handle my garment order but thankfully the vendor I did find guided me through the process to request network gap coverage.

I wish I could remember the employee’s name at Luna Medical, as I owe her a huge THANK YOU! She very easily could have just told me I would have to pay out of network for my garments. I would have known no different, as do most patients. Instead, she explained that since there was no in-network provider within a 50 mile radius of my home my insurance company had to cover an out-of-network vendor at in-network coverage level. She coached me on what to ask for and what to say when I spoke to my insurance company. To prove there was no vendor in network, I called every DME provider within 50 miles and documented whether they sold compression garments, and if they did I would document who I spoke with and verify they were not a custom Jobst certified vendor. It took several phone calls, and finally the insurance company said they needed to speak with my physician. I happened to have an appointment with her the next day so I asked her if she would call them. Knowing there would probably be hold time with any insurance call, my doctor told her staff to take me into her office to call the insurance and once there was a representative on the phone to get her. To my surprise, after reviewing the information I had already provided the supervisor only asked ME a few questions and then approved my request. She said she didn’t need to speak to my physician at all, she already had her signed prescription stating medical necessity.

The training wheels were OFF…and I never looked back!

I followed the same process with the next 3 insurance companies I had and successfully obtained approval for my compression garments. I transferred those skills into reading coverage documents, researching vendors and providers and overall navigating health insurance. I often help friends and family with their coverage questions.  The experience managing my own health insurance coverage  led me to a new career. I earned my BS in Health Services Administration and I am currently pursing a Masters of Science in Health Law.

Although I have been successful in obtaining coverage for most of my lymphedema and lipedema treatment needs, there are still obstacles that block patients from getting the care they need and deserve. That is why I share my story to advocate for the passage of the Lymphedema Treatment Act.

 

Filed Under: Advocacy, Blog Post, Health Insurance Tagged With: advocacy, breaking, compression garments, DME, durable medical equipment, featured, headline, health, health insurance, jobst, lipedema, lymphedema, lymphedema treatment act, National Health Blog Post Month, network gap coverage, nhpbm, obesity, super morbid obesity, top, Wego Health

NHBPM Day 2: My Big Caboose – Little Engine Remix

November 2, 2013 by Sarah Bramblette 2 Comments

healthblogpostday2

Day 2 of National Health Blog Post Month and today’s prompt is “The Little Engine” taken from the children’s story, The Little Engine that Could:

Write 3 lines that start with “I think I can…”

Then write 3 lines that start with “I know I can…”

I had to laugh when I thought of the train analogy and my medical condition because my caboose is a much more prominent and powerful train car in my journey. Do trains still have cabooses? For a few years during my childhood I lived near train tracks and I would always love waiting for the end of the train to come by so I could wave to “Mr. Caboose Man”. My caboose (butt) is big because of Lipedema. But that size and weight does not hold me back, instead it is the real source of my power and strength. Living with Lipedema has made me strong, resilient, resourceful, and compassionate.

sassy

With that said…here is my Big Caboose – Little Engine Remix

I think I can be a catalyst for change.

I think I can encourage others to be their own advocates.

I think I can change society’s perception of obesity by sharing my story.

I know I can be myself.

I know I can survive.

I know I can win most battles with health insurance companies.

What do you THINK and KNOW you CAN do? What is your source of power and strength?

Filed Under: Advocacy, Blog Post Tagged With: advocacy, breaking, featured, headline, health, health insurance, lipedema, lymphedema, morbid obesity, National Health Blog Post Month, NHBPM, obesity, self confidence, self esteem, super morbid obesity, top, Wego Health

Kids do not need a letter to know they are fat on Halloween

October 31, 2013 by Sarah Bramblette Leave a Comment

fat letter

There is a woman in North Dakota who feels it’s her duty to save obese children from themselves this Halloween. She has decided to hand out “fat letters” to children to whom she deems are obese while giving candy to the other kids. I am left to wonder if she is doing any diabetes or dental checks on the normal sized kids. After all, the reality is that candy is not “good” for anyone.

But it’s Halloween, it’s the time of year kids to get to dress up as their favorite character and go walk about the neighborhood with their friends. That is unless you are the FAT kid. Then finding a costume, especially of a favorite character, is most likely not going to happen. Definitely, NOT going to fit into a store bought costume. So maybe you’re creative and have the means to create an awesome DIY costume, which I was THAT fat kid a few times. Yes, I wanted to be an alarm clock! What kid doesn’t want to be an alarm clock? No, I wouldn’t have rather been Rainbow Brite or Jem. (of course I would have) But my sister and I were GENIUS and cut out a round piece of cardboard, put some numbers on it, and tethered it around my neck.  I was an alarm clock! Let’s go get some candy!

Trick or Treating was by far the most intense workout I got as a kid. I walked to school every day, but that roundtrip was nothing compared to the Trick or Treat challenge, cover the neighborhood in 1.5 hours. Yes, where I grew up Trick or Treat was scheduled. My friend’s mom led a small group of us around and kept us on task. We only went to houses where people were outside on their porches (wasted no time knocking on doors), we zigzagged across the street, then circled around to the next block. I really should stop and calculate the number of blocks we covered. The entire time it was “go, go, go”, we walked up steps, and up hills. And trust me, every huff n puff moment as trudged along as a clock I knew I was FAT. I didn’t need any well meaning neighbor giving me letter of notification!

But like most other things in my life, I wasn’t going to let my weight stop me from participating. I was not going to let being FAT keep me from enjoying the night out with my friends, trying to accomplish our mission of getting to every house on our route in the allotted time. Honestly, Halloween was NEVER about the candy. There was candy at home, the GOOD candy that my mom bought to pass out for Trick or Treat. If all I wanted was to stuff my face with candy, I could have sat at home and just ate what I wanted. No, Halloween like other holidays is about the experience.

Honey Boo Boo

The experience is same the reason I am excited about participating in Halloween as an adult. As a fat adult the costumes can still be a challenge, but my creativity and DIY abilities have served me well. Yes, I wanted to be Honey Boo Boo…I actually WON a costume contest as Honey Boo Boo! As for Trick or Treat, this year will be the first time in many years I will actually be at home, and live in a neighborhood where there will be Trick or Treaters. I do not have kids and I do not know many of my neighbors. I could easily turn off my porch light and stay inside.  Instead I am excited that I can participate in Halloween, and I ordered toys to pass out.  No candy. I admit I fear being seen as the “fat lady” handing out candy. I also know taste vary so much I could never possibly please all the kids with my choices. Then there are kids with food allergies.  Choking hazards, we used to buy safety suckers to give the toddlers. Also, I just LOVE toys, and I picked out some really awesome toys. I also asked my parent friends on Facebook if they would be upset if their child was given a noise maker? As you can already read I’m putting way too much thought and effort into this….just buy some candy already.

IMG_1421

Perhaps I’m too considerate of other people; perhaps the woman in ND should take a lesson from me. If her concern is really for the well-being of children then there are many better options she could do instead of fat shaming kids. How does a letter telling a parent their kid is fat help reduce childhood obesity? Yet she is STILL handing out candy to other kids, does their health not matter? Also health is not just physical, it is emotional too. Fat shaming kids on a day that is supposed to be FUN, is just mean and will hurt kids not help them. She could donate money to help local parks and recreation center, volunteer for local Halloween carnivals, or organize a Halloween themed fun run/walk for her community.

 

Filed Under: Advocacy, Articles, Blog Post, Obesity Tagged With: advocacy, breaking, bullying, childhood obesity, discrimination, fat, fat letter, fat shaming, featured, halloween, headline, morbid obesity, self esteem, super morbid obesity, top, trick or treat, weight bias

My Abnormal Photo Shoot

October 9, 2013 by Sarah Bramblette 6 Comments

selfie-abnormalphotoshoot

For me, not smiling for a picture is definitely not normal. But the real abnormality of the photo shoot was ME. I replied to a post looking for individuals with abnormal appearances for a magazine article. Due to lipedema my arms and legs are abnormally disproportional to the rest of my body. While most people try to hide or cover up the parts of their body that do not meet a certain societal level of acceptance, that is not an option for me so I choose to just be comfortable in my own skin, all 400lbs of it.

Trust me being comfortable in my own skin is much easier said than done. There is no physical comfort living with lipedema. Every inch of my arms and legs are sensitive, and the slightest touch results in bruising. In addition, the excess weight makes simple movements much more tiring.  Imagine having to do your normal daily tasks with 5lb sacks of flour attached to each arm, and a toddler clutched to each leg? Then when you need to stop and rest, people think you’re just “being lazy.” Standing for any period of time is exhausting, sitting is a bit better but gravity still affects the pooling of lymph fluid in my legs causing painful swelling, so laying down must provide the only real relief, right? Not exactly, it’s hard to be comfortable laying down because the abnormal size and shape of my hips and legs makes finding a restful position difficult.

However, rarely do I complain, because the abnormality of  lipedema has become my new normal. I have no control over the physical aspect of my disease. So I choose to make the most of what I can control, and that is the mental aspect. Which is the focus of the magazine article. Psychology Today is featuring a “story about the experiences of those with physical differences—and how, on both a societal and individual level, we can overcome negative or prejudiced responses.”

So back to the photo shoot. I realized that I had not had professional portraits taken since my high school senior pictures. I asked if there were any guidelines for what type of clothes to wear and was told nothing specific. So I did what probably few other females would do, I picked a nearly three year old dress out of my closet to wear. The dress looks nice on me and shows my arms and legs. The morning of the shoot I woke up, fixed my own hair and did my own make-up. I kept thinking how most people with bodies the size of mine hide from the camera, and when they are in a few pictures they delete any shot they think is unflattering. Here I was volunteering to have my pictures in a  national magazine and I’m wearing an old dress and doing my own hair and make-up.

The photographer arrived, moved some living room furniture around and set up his equipment. I was ready for the my close up! Then came the shocker and most difficult part of the photo shoot…I was told not to smile. WHAT? Me. Not. Smile. That’s just soooo abnormal??? And it’s even harder not to smile when you’re trying to NOT SMILE. And of course the photographer and I struck up a conversation and well since I’m so amusing, I smile and laugh a lot during conversations. I will not know which poses were selected for  until the article comes out in the November edition, but I know the real Sarah shines through as always. Although my normal persona is fun, happy Sarah, anyone who knows the real me knows my strong and confident side…and smile or no smile…I’m still Sarah.

*Update* See the final picture in My Story in Psychology Today

Filed Under: Advocacy Tagged With: abnormal appearances, breaking, headline, lipedema, lymphedema, morbid obesity, obesity, physical differences, Psychology Today, self confidence, self esteem, super morbid obesity, top

All EARS for #OH2013 in Anaheim

September 21, 2013 by Sarah Bramblette Leave a Comment

Ready for #OH2013

Ready for #OH2013

Getting ready for more education, friends, and fun at the ObesityHelp 2013 National Conference in Anaheim, CA, October 4th & 5th.

Looking forward to hearing Dr. Ayra Sharma speak, and spending more time with my pal Eggface!

photofun

I’m also hoping to have time to visit with my college mentor who now lives and works in California, the man truly changed and saved my life!

There is still time to join me in Anaheim! This will be my 8th ObesityHelp Event!

I like to stay active with ObesityHelp and the weight loss surgery community because I’ve met many fellow Lipedema and Lymphedema patients who have had or are considering weight loss surgery and it is great to meet others with similar experiences.

Filed Under: Blog Post, Weight Loss Surgery Tagged With: bbw, breaking, featured, gastric bypass, headline, health insurance, lipedema, lymphedema, morbid obesity, obesity, rny, rny gastric bypass, sbbw, super morbid obesity, weight loss surgery, wls

Dancing for Dollars! Support me in the Walk from Obesity!

August 9, 2013 by Sarah Bramblette Leave a Comment

 No tutu until I reach my fundraising goal of $1000!

 

 

If I reach my goal of $1000 in donations by the morning of the walk, August 18th! I will WALK IN MY SWIMSUIT (and tutu).

Filed Under: Advocacy, Blog Post, Health Insurance, Obesity Tagged With: advocacy, asmbs, bbw, beauty, breaking, discrimination, featured, gastric bypass, headline, lipedema, lymphedema, morbid obesity, oac, obesity, obesity action coalition, rny, sbbw, self confidence, self esteem, super morbid obesity, swimsuit, top, walk from obesity, weight lose surgery

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