Wednesday, April 8, 2009

Letting go to be reborn again.....

Hello All! This is Sarah writing again. I thought that I'd be on here more often but it just hasn't been the case. I have beautiful, but empty journals....I just haven't been moved to do much writing. I prefer a phone call instead, so please don't hesitate to call me....don't worry about waking me up, as I'm not sleeping during the day. I believe that all the phone calls to my mom about my condition are wearing her out...along with a certain 2 1/2 year old!!! If you could direct your inquiries directly to me, that would be much appreciated...Plus, I'd love to talk to you all myself. I'm very candid and honest about what I'm going through....I'm not afraid to tell you how much most of this sucks or to use you as a shoulder to cry on. I'll also be the first one to share with you how stoked I am to be feeling well the days I do!!!!

I have had to do a lot of letting go throughout these past two and half months. I am wise enough to know about how healing this can be...that I'm clearing space for the new, etc... However, there is a lot of grief that goes along with it. With grief there are tears....tears that are neither sad, mad, nor happy... I haven't been able to assign them an emotion as of yet...they just are. They are tears that I don't want anyone to take from me, as it would disturb their natural flow. I'm looking for people to merely witness them, honor them, bless them, and let them serve their purpose. I don't want to feel bad about having them, as I know it can make some uncomfortable. Being with someone and not trying to take their pain away is an incredible feat, being able to do this is the sign of a great healer. I know how strong I am, I'm not giving up, and I will make it through this! Don't ever doubt that, I don't! I whole heartedly believe that the most courageous individuals are the ones that show their vulnerabilities and their shadow sides freely. I'm not here to hide these parts of myself to anyone.

The treatments and procedures I'm enduring are difficult. I take them one day at a time, sometimes wishing that I wasn't going through it. The chemo makes me feel sick and just plain weird, it leaves my mouth full of sores, I feel nauseous, fatigued, and get horrible heartburn, it also tends to bring on a lot of the tears I was talking about. Most of the cancer is surrounding my heart...and I like to think the tears are caused by the cancer shrinking and leaving my body...it needs a way out somehow!

On Monday night, I had a small surgery to get a PortaCath put in. This will save my arms and veins from having to be poked anymore. I was nervous to have surgery again but am so thankful I did it, as it made getting chemo yesterday so much easier. The last time I had chemo, I had to have four IVs placed...one of the veins was so irritated from the chemo that it flared, and the IV had to be moved. I've been needing to take pain medication for it to be bearable...I can feel the vein from my wrist all the way up into my face....guess it can last weeks to months. Anyway, the surgery went well...I came home that night and felt like nothing had happened. However, I woke up at 4am writhing in pain. I'm on some new pain meds that seem to work much better...Yay!!! Today, it's feeling pretty darn manageable...a little sore, but that's all.

I'm still waiting to hear if I need to get the Neulasta shot this week. The hospital lost my blood on Monday night, so I needed to go in today to get poked one last time...I hope anyway. I would have been too sore for them to pull the blood from my port. Hopefully, next week my poor arms will get a break!! We'll keep you posted about the shot. Last week was absolutely heavenly without it!!

As many of you know, Dan and I were fortunate enough to be invited to get away for the weekend. At first we were going to take Marek with us, but ultimately decided to leave him at home with my mom. THANK YOU, THANK YOU, THANK YOU MOM!!!! (She has gone above and beyond in every way possible....doing only what a mother could do!) On Thursday morning, Dan and I headed out on our first road trip in a long time. I love road trips...I've taken many of them cross country to go to Phish shows and music festivals...I feel alive and free when on them. We drove all day and finally arrived in Palm Springs later that night. The desert has a much different energy than the ocean...the moment I stepped out of the car, I knew I was there to do some powerful work.

On Saturday, Dan, our friend Barbara, and I headed out to Joshua Tree National Park....with some clippers!! Yes, the day had finally come for me to let go of my hair...let go of my past. It has been falling out like crazy over the last month...I couldn't take it anymore! I wore a sparkly skirt, along with my very sparkly silver shoes. We took a gentle hike out to a spot known as the Vagina Vortex...this is a truly healing place...a place to give to the Mother what you don't need anymore, and a place to be reborn. We saged, gave offerings, prayers, and thanks to the Mother, walked a spiral labyrinth and performed sacred ceremony. Then I knelt down in the middle of the spiral and Dan shaved my head....well some of it anyway...our clippers ran out of juice before we could finish. That's cancer for ya, lots of bumps and uncertainty...lots of letting go!! (We have pictures of all of it that we'll post later...I not sure how to do that part!) It was freeing and extremely empowering. I love my bald head!! In fact, I've decided that I look too much like a cancer patient with hats and scarves on...I'm proudly walking around without any hair for all of the world to see! I have nothing to hide!!!!

I feel as though there is more to say, however, in my chemo haze, I have about hit my wall. This might be fragmented and I'm probably leaving some stuff out...chemo sort of has that effect on me. Maybe Dan can fill in the blank spots for you!!

I have so much gratitude for all of you! Barbara, thank you so much for the magical weekend...you were incredibly gracious and selfless. It meant the world to us. Mom, thanks again for being with Marek!! I know that he is an incredible handful right now. I look forward to you just being able to be his grandma again soon!! We love you so much!! Seems like I could spend all my days sending out thank yous...everyone has been incredibly generous with their time, thoughts, prayers, and resources. We could not make it through this without any of you!! We look forward to the day we are able to pay-it-forward!!

All of my love!!
Sarah

10 comments:

Shauna said...

Sarah-

I saw your pics online and you look radiant! Baldness really suits you- puts all the focus on your beautiful facial features.

Wow.

It is truly amazing to hear you being so strong, optimistic and willing to talk about things so candidly.

I'm glad to hear you got the portacath in- my Mom got that during her treatments and it made things a WHOLE ton easier for her to handle. I hope it has the same effect for you.

Have you thought at all about photographing that lovely head of yours?? When my Mom went through cancer (the same as yours) I was in high school and taking photography classes. I was really hoping she might let me photograph her - but unlike you, she felt more comfortable not seeing her bald head for what it was. I totally understand each perspective!

Thank you for continuing to allow us into your lives, regardless of how well you know some of us.

Take care!

Unknown said...

Ok, you don't just look beautiful, you sound beautiful too.

If you ever need a shoulder to cry on or someone to hang with who can handle the crying, feel free to call. I'm a total crier (even when things are good) so I'm totally comfortable with other people crying... ok, that's sounds a little weird,but you know what I mean.

Samantha said...

Sarah, reading how strong and forthcoming you are about your fight is very inspirational. I am in the hospital again now for my Cystic Fibrosis and it helped me to read your blog entry today. As I get older my condition deteriorates, so I am once again in the hospital to help slow that. As I get older, I also come to terms more with what is happening to me. It really helps to hear what other people are going though and how they are handling it, even though it is two very different diseases. You are a wonderful lady and beautiful friend to many. Thank you for sharing.

Samantha

Kendell said...

Sarah-
You are such a blessing. I am humbled by your awesomeness.

Nagle said...

Sarah, I am constantly amazed by your and Dan's ability to express your thoughts. You both are fantastic writers.

With having said that I hate to hear what you are going through. But with the strength and love that you guys possess, it makes a much easier thing to get through.

I am continuing to keep you all in my thoughts and can't wait to read the word that you're all better!

-Nagle

Linzi said...

I am always touched by your blogs and I check for a new one every day. Your perspective on life is amazing and it really makes me feel terrible about the things that I worry about in life. You have definitely given me a new look on life and I can't thank you enough for sharing.
I will be calling soon now that I know I won't be a bother. I give you all the credit and we love you so much.

Kristin said...

Sarah,

You are such a lovely Momma. You (and Deb) inspire me so much to live a better life. I mean not dropping my sarcasm (oh please this is me here), but to live a life that is focused on being healthy in all aspects of life.

You look amazing w/o hair and you should wear it proudly, just don't forget the sunscreen!!! You don't want to get skin cancer.

Many hugs sweetie.

Brent said...

I agree your outlook on this is so positive, it's really inspiring! Dr's and scientists alike agree that the mind is the most important thing when you're sick. It plays a much more important role in healing than the body does. You seem to have a great outlook on things, and I bet you'll recover quicker than most!

A guy on the Boston Red Sox named Jon Lester had lymphoma two years ago and is back in baseball, and was one of the best pitchers in ALL of baseball last year. I'm not sure we'll see you in a Red Sox uni anytime soon, but you're recovery will be just as quick and monumental.

Sue said...

Sarah, it is truly humbling to be on this journey with you and Dan. The courage and strength you reveal each time you write is a lesson for us all. I have no doubt that your mom is amazing in caring for Marek giving you all stability. Precious as these little ones are they do tire a person out. We regroup and she wouldn't want to be any other place. Take care
Sue

Jennipher said...

Dear Sarah, I do not know you well, but just reading your words here I feel that you have shared such a deep and inspiring part of yourself and your journey. It is very sad to think of you, so young, struggling with these challenges. But you have found a way to share your struggle with others that is incredibly moving. You are in my thoughts.
Jennipher