Saturday, May 28, 2016

MOWING IS MY FAVORITE AND MY BEST

My favorite summertime chore is mowing the lawn. Walking, the vibration (which is said to be really good for those with Lipedema), music via headphones, singing and dancing on my lawn for all the neighbors to see (and with new neighbors that should be even more interesting this year).

I'm always reminded how grateful I am to be able to mow the lawn. I'm grateful for every step I take, and at times I still get emotional as I make my way around the lawn and realize how far I have come.

To fully understand the level of gratitude I have for being able to walk again, you must know where I started. Lipedema has a way of making you feel isolated. It starts with feeling like you don't "fit" in. From the basic and literal sense of not fitting into a chair with arms, to the more emotional and figurative sense of not fitting into society because you look differently. Add to that that you start to feel your mobility slipping away, and your legs getting heavier, and you fear how Lipedema will continue to make you feel weaker and weaker.

I was told early on in my diagnosis that Lipedema did not respond to diet and exercise and the best thing I could do was keep my legs elevated (so they didn't fill up with fluid too much (lymphedema), and stay out of the heat as much as possible to keep the inflammation down. I was also told that exercise could make my Lipedema worse. The fear of making my already progressing condition worse kept me listening to this advice for many years.

I sat with legs up and watched my world go on around me. Walking a few feet was painful, as was just standing for a few moments. My husband was like a single parent because I couldn't go to school events, I couldn't go to the fair in the summer, or trick or treating in the fall. My life was work during the week (which was a race from house to car, car to office, office to car, and finally car back to the house every day with the hope I would be able to physically be able to walk the distance between each destination) and recuperation on the weekends (which involved legs elevated and resting most of the time).

Finally I said enough. I had been listening to them say nothing you can do, I had been listening to the fear in my head of making my Lipedema worse, and my Lipedema had been progressing still the same.

It was a long, slow climb back up the mobility ladder, but the best part is that each step up was amazing. I didn't go from barely being able to stand to mowing the lawn. It was gradual, but every new step, every new ability, to stand a little longer, to walk a little further, was so amazing that it kept me going.


It is hard when your goal seems enormous, or unreachable; to plan your attack, to fight back when you feel weak or afraid. But focusing on one step (one rung) at a time can make that an easier journey. And it is not only good advice when you are just starting, when that ladder seems to go on forever, it is good advice when you are in the middle of your journey, too. Because think about it, everyone, everywhere is always somewhere in the middle of their journey.

So if you are out driving one day, and see someone mowing their lawn, with a dance in her step, realize she is in pure joy and filled with so much gratitude that she can do this activity. This "chore" is a gift she is forever grateful for. And know as I stand on the lawn mowing rung of my mobility ladder I wonder what other great rungs are ahead, and I look back often at the rungs I took to get where I am in this moment and I say thank you.

Wednesday, March 30, 2016

Lipedema Triathlon - Phase One (Swim)

The Lipedema Triathlon was created in an effort to spread awareness for Lipedema, and to keep moving and challenging ourselves, because without doing so our mobility is at stake.

June is Lipedma Awareness month, and on June 25 we will be taking on this challenge. If you would like to join us from your hometown, click here to sign up.

We wanted it to be all-inclusive, you can choose your level of involvement (do one lap, one mile, one leg of the race, or the full TRI, whatever your fitness level), and we wanted it to be virtual, so no travel was required, you can do it in your own hometown, or your own backyard or living room.

Triathlon, from the Greek words treis ("three") and athlos ("sport"), is a three sport event, typically swimming, cycling, and running.

Triathlon races vary in distance, the one we are focusing on is the Sprint: 750-meter (0.47-mile) swim, 20-kilometer (12-mile) bike, 5-kilometer (3.1-mile) run/walk. Here is a break down of what we will be doing come June 25:

Swim - The most common pool sizes built today are either 25 meters or 50 meters (Olympic size) so 750 meters will be 30 lengths in the smaller pool and 15 lengths in the Olympic.

Bike - Most bikes (road or stationary) calculate mileage, but if not , just calculate your speed (MPH) by your duration to get you to 12 miles.

Run/Walk - Most treadmills calculate mileage; or if using a standard indoor track (200 meters), you would need to do 25 laps for a 5K. If using a standard outdoor track (400 meters), you would need to do 12.5 laps.

I knew the swim and the bike were the big unknowns for me in this equation, I had not swam laps or ridden a bike since before my daughter was born over 12 years ago. I didn't even know if I could find a bike that I could use, one that would fit me and support me for a 12 mile ride. Not the average concern of a triathlete, but with Lipedema, your hips and legs can be quite a bit wider than most, and the fluid surrounding the lipedema fat cells also make our legs very heavy.

The first step was joining the YMCA, we have two branches in our town, one with a fantastic 25 meter pool.

Getting myself geared up to be seen in my swimsuit was the next step, but with the help of coach/hubby, my daughter and one of my best friends and future swimming buddy, it was easy peasy.

I opted to wear my bioflect micro massaging leggings under my suit, as I knew unlike aqua aerobics, my legs would be more near the surface and not getting the compression the water provides when standing upright in the water. I am not sure how long the bioflect will hold up in the pool, as not specifically made for that, but so far into our fourth week this Sunday, and only minor color fading is noticeable.

The first day back in the pool was exciting and scary, but I had purchased my speedo goggles and Tyr swim cap for long hair, and I was ready to go.

My friend was great, I was so thankful she was there, as she has been swimming laps for years during her lunch hour, and she had great pointers for both coach/hubby and I. While the goal was 10 laps, we did 16. More than half of the duration we would need to do for the TRI.

The second trip to the pool would be with one of my training mates, who is an Ironman (woo hoo)! She had amazing pointers, pinkies up (like when properly drinking tea) would naturally turn your hand to the correct position for cutting into the water, etc. As it turns out, the big challenge for both hubby and myself - breathing.

I started breathing every time my right arm went up and finally realized well into our hour session that I was not exhaling in the water ("you should see bubbles the entire time", she said). Mentally my body was not letting me exhale with my face in the water. So I spent time just gliding, no arms, with face in the water - when I came up they were so excited. Seems when my face is in the water, my legs  are in the perfect position at the top of the water, but when I pull my head up (you know, to breathe) the legs drop down - dragging behind me.

Breathing is the name of the game - blow bubbles the entire time the face is in the water, fully exhaling all the air out before my body turns to lift my head and take in a new breath.

After our session, which turned into about an hour and a half, my training mate, and our swim coach (Deb) informed us we did 800m (more than the triathlon).

We got changed and before leaving, Deb took me over to the treadmills, bikes, etc. and we tried a couple options. I was so excited that the SciFit recumbent bike fit me no problems - it is amazing the amount of accommodations you can make to the seat, it even turns to allow easier access for those who might need it.

I left the gym feeling fantastic! I could do the swim distance required in the triathlon, and found a bike to fit me.

On to phase two, the Bike!

Saturday, February 20, 2016

NEW YEAR, NEW GOAL: Creating The Lipedema Triathlon

Do you set New Year goals? I didn't use to, but over the past four years of reclaiming my mobility, I like to set fitness challenges for myself, I am my biggest competitor, and it gives me something to work towards during the year.

In recent years I had set and crushed my goals (flipping a 300lb tractor tire, surviving the survive the farm OCR, etc.) and as the new year approached I didn't have a goal in mind.

One of the first New Year goals I had after reclaiming my mobility, was to complete a 5K. It happened first when I accompanied my husband and daughter to her first 5K to support a cause dear to her and her school, the Ryan's Run 5K (named after Ryan Westen, who lived for only 6 months after being diagnosed with Malignant Infantile Osteopetrosis). I initially went to the race to support my family, but when I got there I did not cherish the idea of sitting around waiting for them, so I asked my husband (who is my coach) when he thought I would be ready to do a 5K. I didn't like the answer he gave me, he said if we kept training like we had been (had only been about three months) I could do it next year. 

NEXT YEAR? So I replied that I would like to see how far I could get, it would be a way to see how far I could go. It was in our local park and it had benches along the way, and if I got to a point I couldn't go on, he could come pick me up after he finished the race.

Needless to say I finished that race in May 2013 even though I was not signed up for it, and my goal was set - to do another 5K in September that year (for the Walk to FightLymphedema & Lymphatic Diseases), to be officially registered, and timed, and to see if I could improve my time over the Ryan's Run.

Best Motivator!

I chose that later 5K because I have secondary Lymphedema to my primary Lipedema, and I could not find a 5K for Lipedema. It was an amazing experience, as it was my first introduction into a virtual 5K (meaning I could do the race here in my home town, while the actual 5K event was taking place in NYC).


I had been thinking about this 5K and loved the exposure Lymphedema was getting (even Kathy Bates is a new spokesperson - woo hoo, have always loved her), and I wanted the same for Lipedema.

I decided I would create a 5K in an effort to spread awareness for Lipedema, and I would organize and take part in the race.

It would be virtual (do anywhere), incremental (can start building up your distances June 1st for the entire month if need be), and even a relay option (get a friend or two, or 30 to help you complete the race). I wanted all levels of fitness to be able to take part if they wanted to, they could do all of it or some of it, and I wanted it to be fun.

While I was talking about this race on the Lipedema Fitness facebook group, another lipedema friend was talking about the Crystal Lake open swim, that she was taking part in. Given that the pool is an excellent way for those with Lipedema to stay active, I got to thinking... all we need now is a bike component and we would have a Triathlon.

From that moment on it did not take long for the Lipedema 5K to turn into the Lipedema Triathlon, and a new goal was set. Not just a physical challenge for me, but the challenge of turning the event into a way to spread awareness for Lipedema, maybe even come up with a donation towards research; and the perfect month to do such a race is June, national Lipedema Awareness Month...

Monday, December 14, 2015

MUSCLE SORENESS, IT'S A GOOD THING

There are several different WOD (workout of the day) recovery experiences I have noticed as someone with Lipedema who does CrossFit.

  1. WOD requires a nap because I am totally drained
  2. WOD leaves my arms and legs feeling like rubber bands, but no nap required
  3. WOD leaves me feeling amazing and strong, then the next day I feel sore
  4. WOD leaves me feeling amazing and strong, and then 2 days later I feel sore
What the What? Yep, that last one is always such a shocker, but just a quick google search, and would you look at that, it even has a name...DOMS (delayed onset muscle soreness) or I guess it can even be called "muscle fever" according to good old wikipedia. Ultimately it is the pain and stiffness felt 24-72 hours post WOD.

The good news, the reason muscle soreness is a good thing, is that it lets you know you have muscles, and that what you did the day or two prior was working those muscles. It lets you know you have some control over your body. You may be sore today, but you will be stronger tomorrow!

I will never admit this to my coach, but I actually like the muscle soreness. Shh, you did NOT hear that from me. The reason I like it, is because with Lipedema it is so hard to see the results of the work. Our muscles are hidden under Lipedema fat. Abnormal fat (sometimes very painful fat) that does not respond to diet and exercise. But the soreness I feel, makes me notice all my muscles, even those hidden from the world, and even more detrimental, hidden from myself.

Our emotional health is just as important as our physical health, and feeling in control of our bodies is HUGE. This condition sure tries to take a lot of control away, so anything that can make us feel in control of some aspect of our lives is very important. Fighting to stay fit is an ongoing battle, and for me the fight helps to make me feel strong, the muscles go a long way, too. But the fight keeps me sane, I am taking action against the thing trying to slow me down.

The scary part with Lipedema, is making sure you can tell the difference between muscle soreness from a good workout, and lipedema pain.

Only you can know the pain you are feeling, and only you are the best judge of what you should or should not be doing. CrossFit trainers are amazing people, have incredible training and abilities to make MODs (modifications) to workouts for all different reasons, but Lipedema is a pretty unheard of condition in the medical field and one can imagine even more so in the workout field. So please make sure you tell any coach/trainer, etc. about your condition, the symptoms, and the fears you have.

Unfortunately I have learned over the years that we have to try something, and then notice the results. We have to become our own best resource on ourselves, because even our Lipedema friends/families may respond differently than we do to whatever efforts we are trying to battle Lipedema. From the effectiveness of supplements, to WODs, to compression, etc.

Keep fighting, you are worth it! We are making changes, even we cannot see!

To quote one of my favorite movies, Galaxy Quest...

Monday, November 9, 2015

One Body, One Life


Can you imagine the care you would take of your vehicle, if you only got one in your lifetime?

Photo by Casey Etter-Bobb #badnova 

Take a moment to really think about that, what would you do if you just got one vehicle? What would you pick as that vehicle? Something fast and fun? Something comfortable? Something that could transition through your stages of life?

We each have different attachments to our vehicles, some use them for transportation, some for fun, some even for show, like the picture above from our good friends Thomas Bobb and Casey Etter-Bobb, they were the first place I thought to seek out a photo to illustrate an amazingly well taken care of vehicle. 

The point being, that we take great care of our vehicles now, even when we trade them in every few years, and our bodies deserve at least the same level of care.

You are worth the best attention, the best love,
the best of everything you can muster!

I know some days it can seem overwhelming with the amount of time, care, and attention we put into living with Lipedema, and feeling overwhelmed is when our emotional side needs the most love. But taking the best possible care of our bodies is not just good advice for those of us with Lipedema, it is good advice for every BODY.

Keep up the good fight my friends, you are doing things now that you will continue to see the benefits of for many many years down the road. We don't get to trade our chassis in, we only get the one.

Monday, October 26, 2015

Spartan Slosh Pipe Challenge - Killington, VT

This past month (September) found me in the cheerleader role, as most of my training mates, my coach/hubby and even my daughter were signed up for the Spartan Race at Killington Mountain in VT.

The atmosphere was electric, with music pumping as the energy, nerves, and excitement filled the air. 

Parking was done well, we were close enough to walk in from the lot, but they also had shuttle buses running from the lots to the event if you were short on time or energy. 

Getting checked in takes time (the arrival suggestion they give of 1 - 1 1/2 hours early is a good one), once done we headed to bag check and then to the Starting Line (daughter's heat was at 10:00am, and everyone else at 10:15am).

It was my daughter's first Spartan Race, and she rocked it!

The only downside was the kids were coming in so fast that I missed my husband's take off. But mommy duty called, I had to get over and snap a few pictures of my girl kicking butt.

After she finished, she was hungry, so off to the lodge we went (one of my training mates and the wife/mother of a couple racers was hanging out with us). Lodge food is pricey, bring your wallets, but they do accept credit cards. 

Refueled and seeing a bunch of fun activities setup outside, off we went to check out the trampolines for her, and the Spartan Challenges for us...

The Spartan Challenges are timed events for those in waiting mode (finished racers, pending racers, or spectators like us). The one that caught my eye was the Slosh Pipe, which is a PVC pipe (I think the ladies pipe was 8 feet long, 3" wide and filled 60% full with what I assume is a couple gallons or so of water). 

The pipe is deceiving, as it doesn't weigh much (estimate about 20 or 30lbs), but the water "sloshing" from side to side, and the length of it really throws you off balance, and changes the weight you are pressing.

They gave us a chance to get a feel for it, and then you put your hands on the tape (cannot leave the tape) and ready, set, go - the timer is started and you have to get it up and do as many presses as possible in 60 seconds.

While my friend decided if she could do the challenge (her shoulder is injured), another woman came up to get a feel for it. She had great training and determination, really good form, but you could see the balance portion of the challenge got her attention. After several minutes of trying, she asked if I was ready to go, and just like that, my challenge was on.

We have been working our squats, so I was able to get low, and surprised myself when I got it into rack position pretty quickly, then I began to do my presses. You would get a couple in and the balance would go wonky, and you would need to get it stable again. I was able to get 25 presses in before time was called.



I was pleased with my performance, and stayed to watch a couple others go for it, before heading to the finish line and awaiting our friends/family to come in.  

As we were just about to leave, the woman practicing before me went. She struggled a little getting the pipe into rack position, which really ate up the time, but she was still able to get a good amount of reps in.  When she finished, she walked off the platform and gave me a high five. It was so nice to feel equal with athletes on the mountain.

That is one of the best parts of my training, feeling connected with real athletes, and seeing myself as their equal is slowly taking place within me, too. My husband pointed out that athletes are the last ones to judge, they know the work that goes into it, they respect the work and those doing it.

Fight on warriors, being larger doesn't mean we are not fit, or unable to compete and even win sometimes, too.

I say win, because I was told I had a real shot at winning the Spartan Slosh Pipe Challenge! The man running the challenge came up to me and asked to verify my email before we left. At the time the closest person to me had 15 presses to my 25. I cannot tell you the confidence builder that moment was. Win or lose, I felt amazing!

Huge congratulations to my husband, daughter and all my training mates - you guys killed it! Now off to the hardware store for slosh pipe making materials!

(Update: I did not receive the winning email from Spartan, so congratulations to the winner, I only wish I knew how many she beat me by so I could make sure next time I give her a better run for her money! Spartan HQ said they don't post the results, and they don't know the winning number of presses, the rep in Killington just sends the names and emails to HQ so they can send out the winning email - AND you get a free entrance into another race, how cool, so get yourself to Lowes/Home Depot and make a slosh pipe - so much fun, and great training, just maybe use antifreeze if like me you live in cooler climates.)

Thursday, July 16, 2015

New Goal - Time to try the High Peaks!

One of my friends (Colleen) who helped me to achieve my last goal (finishing the Survive the Farm 5K obstacle and mud run in May) is a runner and in the past couple years started making her way up the High Peaks of the Adirondacks.  There are 46 High Peaks, and they call you a 46er if you hike all of them.

Colleen's last adventure brought her up to her 15th High Peak!  How cool is that?  In my book it is pretty cool.  Her facebook post and pictures of her last hike inspired my next goal - to begin the climb.

Colleen on the summit of Upper Wolfjaw (#11 for her) in 2014

I talked to coach/hubby who said we should wait till the fall, as the heat really is a challenge all it's own in the summer months for me.  Wearing a couple layers of compression from foot to chest doesn't make that any easier.  So we have set our sites on this fall.

Part of me immediately remembered the hilly bits of the mud run and how challenging it was, and this is going to be a hike up a mountain (literally a mountain - I'm not making a mountain out of a mole hill, it is literally a mountain), I must be crazy.

Colleen's 1st peak -  8/15/2010
Coach picked Cascade Mountain (in Lake Placid, NY) as our first, and come to find out it is the first for many (according to wikipedia, Lon Pierce was the very first to make that hike up in 1872).  Not the shortest, but reportedly the easiest.  Ranked 36th in elevation, coming in at 4098 feet, and will be a 2.4 mile hike up.  Wish me luck, and thank you Colleen for the inspiration and photos below.  Turns out Cascade was Colleen's first, too, back in August of 2010...

High Peaks Wilderness Area Details

Colleen going up Cascade
Cascade Summit Marker - Woo Hoo, she did it!
Colleen's view from the top of Cascade
What goes up, must go down.