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Complaining About Complaining

August 22, 2010 in Awareness, Better, Chronic, Chronic (medicine), Complaining, Conditions and Diseases, Life Issues, Musculoskeletal Disorders, Novel Patient Posts, Support Groups, advice, balance, chronic illness, chronic pain, competition, cut, feeling, flip side, health, ill friend, loathe, mind, monopoly, pain, reminder by Novel Patient

When you're sick it can be really difficult to listen to other people's complaints - especially if they seem trivial.  Excessive complaining about physical problems especially can be really wearing for me to listen to.  I often find myself comparin Share

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Complaining About Complaining

August 22, 2010 in AComplaintFreeWorld, Awareness, Better, Chronic, Chronic (medicine), Complaining, Conditions and Diseases, Life Issues, Musculoskeletal Disorders, Novel Patient Posts, Support Groups, advice, balance, chronic illness, chronic pain, competition, cut, feeling, flip side, health, ill friend, loathe, mind, monopoly, pain, reminder by Novel Patient

When you're sick it can be really difficult to listen to other people's complaints - especially if they seem trivial.  Excessive complaining about physical problems especially can be really wearing for me to listen to.  I often find myself comparin Share

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Scrapbooking My Illness Journey

August 22, 2010 in Appointment, College, Danielle, Doctors, ER, How-To Sites, Infusion, Lauren, Life Issues, Novel Patient Posts, Recovery, WALKING, actual time, appointments, art, arts and crafts, bat mitzvah, chronic illness, college graduation, crafts, creative muscles, doctor, experience, experiences, future, glue, happy memories, help, high school graduation, hospital, illness, journey, last several years, life, life got in the way, mom, novel, obsession, passion, patient, philosophy, picture, rituxan, rituxan infusion, scrapbook, scrapbook memories, scrapbook page, scrapbooker, scrapbooking, sister, walk by Novel Patient

You have to take the good with the bad. I subscribe to this philosophy not just when it comes to my life but also when it comes to my favorite hobby – scrapbooking.

Sandwhich > Tube

I started scrapbooking almost two years ago now. My mom had made me a beautiful scrapbook for my Bat Mitzvah when I was 13. She promised my younger sister Danielle the same thing. But life got in the way and my sister’s Bat Mitzvah scrapbook turned into a middle school graduation scrapbook then a high school graduation scrapbook and finally a college graduation scrapbook.

As Danielle’s college graduation approached my mom still hadn’t started the scrapbook. But I figured maybe I could help. After all, I was home all day with nothing to do. It might even be fun, I figured. I had no idea I would end up loving it so much, that I would find a hidden talent, and a passion… well more like an obsession.

When all was said and done, my sister’s college graduation scrapbook became a three volume set encompassing her entire life up until that point. It was time to move on to other things, so I started in on my own life.

While going through my own pictures from the last several years, there were many pertaining to my illness. Hospital stays, doctors appointments, and so on. There was even a birthday I spent in the hospital.

At first I was hesitant to include these not so happy memories in my scrapbook. But I realized that these were experiences that I also wanted to remember. These bad times in my life are part of what makes me who I am. So I put them in.

The actual time I spend scrapbooking is therapeutic. It exercises my creative muscles and helps me relax for a few hours while I design and arrange, cut and glue, label and decorate.

It’s actually rather therapeutic to scrapbook memories of my illness. Once it is scrapbooked, it feel more concretely in the past. And it can help me look to the future. For instance, I did a page of my me taking my first few steps when I first started walking again. Now I am able to walk around a store! I can look back and remember it and see how far I’ve come!

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Scrapbooking My Illness Journey

August 22, 2010 in Appointment, College, Danielle, Doctors, ER, How-To Sites, Infusion, Lauren, Life Issues, Novel Patient Posts, Recovery, WALKING, actual time, appointments, art, arts and crafts, bat mitzvah, chronic illness, college graduation, crafts, creative muscles, doctor, experience, experiences, future, glue, happy memories, help, high school graduation, hospital, illness, journey, last several years, life, life got in the way, mom, novel, obsession, passion, patient, philosophy, picture, rituxan, rituxan infusion, scrapbook, scrapbook memories, scrapbook page, scrapbooker, scrapbooking, sister, walk by Novel Patient

You have to take the good with the bad. I subscribe to this philosophy not just when it comes to my life but also when it comes to my favorite hobby – scrapbooking.

Sandwhich > Tube

I started scrapbooking almost two years ago now. My mom had made me a beautiful scrapbook for my Bat Mitzvah when I was 13. She promised my younger sister Danielle the same thing. But life got in the way and my sister’s Bat Mitzvah scrapbook turned into a middle school graduation scrapbook then a high school graduation scrapbook and finally a college graduation scrapbook.

As Danielle’s college graduation approached my mom still hadn’t started the scrapbook. But I figured maybe I could help. After all, I was home all day with nothing to do. It might even be fun, I figured. I had no idea I would end up loving it so much, that I would find a hidden talent, and a passion… well more like an obsession.

When all was said and done, my sister’s college graduation scrapbook became a three volume set encompassing her entire life up until that point. It was time to move on to other things, so I started in on my own life.

While going through my own pictures from the last several years, there were many pertaining to my illness. Hospital stays, doctors appointments, and so on. There was even a birthday I spent in the hospital.

At first I was hesitant to include these not so happy memories in my scrapbook. But I realized that these were experiences that I also wanted to remember. These bad times in my life are part of what makes me who I am. So I put them in.

The actual time I spend scrapbooking is therapeutic. It exercises my creative muscles and helps me relax for a few hours while I design and arrange, cut and glue, label and decorate.

It’s actually rather therapeutic to scrapbook memories of my illness. Once it is scrapbooked, it feel more concretely in the past. And it can help me look to the future. For instance, I did a page of my me taking my first few steps when I first started walking again. Now I am able to walk around a store! I can look back and remember it and see how far I’ve come!

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  1. Definitions: More Than Just a Novel Patient There are many things that define me a Novel Patient, mainly my collection of unusual...
  2. Better Enough? I'm well on my way on the road to recovery. I've been doing more and...
  3. Keeping The Faith Through my chronic illness, I have come to realize how crucial it is to have...


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Definitions: More Than Just a Novel Patient

August 17, 2010 in Academy, Adverse effect, Appointment, Arts, Awareness, Career, Chapter, Doctors, ER, Family, Fiction, Freedom, God, Lauren, Lauren Soffer, Life Issues, News, Novel Patient Posts, Online Writing, Writing, appointments, art, brief summary, center, child, child of god, chronic illness, coming of age, creative thinking, doctor, elevator, excerpt from, feeling, first draft, flickr, grandmother, hospital, illness, illnesses, life, many things, novel, novelist, pain, patient, populace, question, scrapbooker, script, sick girl, sister, soffer, ssi, story, symptom, time, title, type, walk, walker, walkers, web designer, weight, wheelchair, writing a novel by Novel Patient

There are many things that define me a Novel Patient, mainly my collection of unusual illnesses, symptoms and side effects.  But one of them has nothing to do with being sick.  If you recall last November, I started writing a novel.  It’s working title is The Alone Elevator.  It’s a coming of age story set in a dystopian future about the pains and trials of going up and the importance of the freedom to think for yourself.  Here’s a brief summary:

Chosen to attend the prestigious Riddlebane Academy, Kylie Lockmore soon learns secrets that turn her world upside-down.  From the drug her grandmother invented to control the populace to the missing sister she never knew she had, Kylie is forced to question the truth and decide where she stands.

Wheelchair IIAs I’ve been writing this novel I’ve been thinking lately about how I define myself.  So much of my life revolves around and is affected by my illness that it can sometimes feel that that is all I am.  But that is not how I want to be defined.  I am more than a sum of doctors appointments and hospital stays, symptoms and side effects, walkers and wheelchairs.  There are so many other things that define me.  And it occurs to me how important it is that I remember that.  I am a creative thinking feeling being.  I am a graphic and web designer, a scrapbooker, a novelist.  I am a daughter, a sister, a friend, a child of God.  I am so much more than just a “Novel Patient”.

But how do others see me?  Do they see just a “sick girl” with a walker?  Or do they see the real me?  I think that the more I define myself as I want to be defined the more people will see the me I want them to see.  If I focus on being a patient that is what will define me.  But if I focus on being a Novel PERSON…  well that is what I will be and radiate to the world.

Here is an excerpt from the first draft of my novel:

The Alone Elevator Chapter 1 Excerpt

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Being Public with Chronic Illness

August 9, 2010 in ARGFest, Alternate reality game, Atlanta, Awareness, Better, Chronic, Chronic (medicine), Conditions and Diseases, Conference, Disability, Family, Life Issues, News, Novel Patient Posts, Support Groups, alternate reality games, blessing, blog, catharsis, chronic illness, difficult times, experience, flickr, friends and family, game, health, help, illness, journey, life, many blessings, quandary, right decision, sharing, speakers, ssi, story, transmedia by Novel Patient

Since I’ve been open with my chronic illness, the positives of letting the world take this journey with me have always outweighed the negatives.  But as I strive to make a career for myself, I am starting to wonder if I’ve made the right decision in being so public with my illness.

Moo cards for blogging workshop
Being so open with my illness has certainly brought me many blessings.  I’ve had so much vital support especially during difficult times from the people that read this blog.  Sometimes just reading caring comments from people left here have made the world of difference in my ability to get through the day.  My friends and family also have been better able to know what’s going on with me and stay in the loop, so that they can better understand and support me.  I’ve been able to help others by sharing my story and helping people who are going through similar situations not feel so alone.  And I’ve had an outlet for catharsis for myself.

There have also been some downsides.  Sometimes I get unkind and unwelcome comments left here.  Being so open about my illness opens me up to everyone’s opinion on the matter.  I also sometimes have to be careful of what I say because I know that a person I care about in my life will read what I write and I don’t want to hurt them.

But lately I’ve been working really hard to get myself off disability by starting a career in Transmedia.  I went to ARGFest, a conference for Transmedia and Alternate Reality Games, a few weeks ago where I networked and learned a great deal from the panels and speakers.  I had a blast and came back energized to continue pursuing this as a career.  But while I was there I discovered that a lot of people follow my blog, and I started to wonder how that might negatively effect my chances of succeeding in that industry.  Would people not hire me because they had read my blog and knew I was ill?

So that leaves me in sort of a quandary.  This blog is a big part of my life, but I don’t want to give it up, but I also don’t want to sabotage my own career.  So what do you think?  How has being open with your illness been a positive or negative experience for you?  How has it affected your career?  Please leave me a note in the comments!

Here are some photos from my trip to Atlanta, Georgia for ARGFest!


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Being Public with Chronic Illness

August 9, 2010 in ARGFest, Alternate reality game, Atlanta, Awareness, Better, Career, Chronic, Chronic (medicine), Conditions and Diseases, Conference, Disability, Family, Life Issues, News, Novel Patient Posts, Support Groups, alternate reality games, blessing, blog, catharsis, chronic illness, difficult times, experience, flickr, friends and family, game, health, help, illness, journey, life, many blessings, quandary, right decision, sharing, speakers, ssi, story, transmedia by Novel Patient

Since I’ve been open with my chronic illness, the positives of letting the world take this journey with me have always outweighed the negatives.  But as I strive to make a career for myself, I am starting to wonder if I’ve made the right decision in being so public with my illness.

Moo cards for blogging workshop
Being so open with my illness has certainly brought me many blessings.  I’ve had so much vital support especially during difficult times from the people that read this blog.  Sometimes just reading caring comments from people left here have made the world of difference in my ability to get through the day.  My friends and family also have been better able to know what’s going on with me and stay in the loop, so that they can better understand and support me.  I’ve been able to help others by sharing my story and helping people who are going through similar situations not feel so alone.  And I’ve had an outlet for catharsis for myself.

There have also been some downsides.  Sometimes I get unkind and unwelcome comments left here.  Being so open about my illness opens me up to everyone’s opinion on the matter.  I also sometimes have to be careful of what I say because I know that a person I care about in my life will read what I write and I don’t want to hurt them.

But lately I’ve been working really hard to get myself off disability by starting a career in Transmedia.  I went to ARGFest, a conference for Transmedia and Alternate Reality Games, a few weeks ago where I networked and learned a great deal from the panels and speakers.  I had a blast and came back energized to continue pursuing this as a career.  But while I was there I discovered that a lot of people follow my blog, and I started to wonder how that might negatively effect my chances of succeeding in that industry.  Would people not hire me because they had read my blog and knew I was ill?

So that leaves me in sort of a quandary.  This blog is a big part of my life, but I don’t want to give it up, but I also don’t want to sabotage my own career.  So what do you think?  How has being open with your illness been a positive or negative experience for you?  How has it affected your career?  Please leave me a note in the comments!

Here are some photos from my trip to Atlanta, Georgia for ARGFest!


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Progress!

July 11, 2010 in ARGFest, Baptized, Busy, Christianity, Chronic, Church, Conference, LDS, Latter Day Saints, Life Issues, News, Novel Patient Posts, Recovery, Religion and Spirituality, WALKING, blessing, blog, caregiver, chronic illness, church of jesus christ, church of jesus christ of latter day saints, clear liquids, energy, faith, feeding tube, games, hope, hospital, illness, jesus christ of latter day saints, life, living my life, pain, patient, picc line, walk, walker by Novel Patient

I’ve been home from the hospital for 45 days today I just realized, and I somehow managed to not blog once this whole time!  I feel terrible, and I hope I haven’t worried anyone!  But I’ve been very busy recovering and living my life.  A novel thing!

I’ve made tremendous progress the last 45 days!  I’ve gone from having a feeding tube to clear liquids to solids to totally normal food.  I started out practically confined to bed, but now I’ve been going out and walking around with my walker again.  I even got my PICC line out last week!  Things are looking up!

And since I’ve been feeling so much better, I’ve been able to enjoy a social life again for the first time in a long time.  It can be really hard to make friends when you debilitated with a chronic illness.  I’ve had very little to no social life for years.  Partly due to pain and lack of energy but also due to lack of friends.  But when I was Baptized back in March into The Church of Jesus Christ of Latter Day Saints, little did I know that I would suddenly find myself with as much social life as I had the energy to keep up with.  It’s been a great blessing!

In fact, I’m feeling so much better that I’m actually leaving to go out of town on Wednesday to ARGFest – a conference for the kind of online games I develop and play.  I will be going for 5 days, and I will be taking my caregiver with me to help me out.  I am super excited and thankful that I am well enough to go!

Now that’s what I call progress!

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Progress!

July 11, 2010 in ARGFest, Baptized, Busy, Christianity, Chronic, Church, Conference, LDS, Latter Day Saints, Life Issues, News, Novel Patient Posts, Recovery, Religion and Spirituality, WALKING, blessing, blog, caregiver, chronic illness, church of jesus christ, church of jesus christ of latter day saints, clear liquids, energy, faith, feeding tube, games, hope, hospital, illness, jesus christ of latter day saints, life, living my life, pain, patient, picc line, walk, walker by Novel Patient

I've been home from the hospital for 45 days today I just realized, and I somehow managed to not blog once this whole time!  I feel terrible, and I hope I haven't worried anyone!  But I've been very busy recovering and living my life.  A novel thi Share

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A Place For Him

May 23, 2010 in Aunt, Awareness, Demyelinating Diseases, Doctors, ER, LDS, Lauren, Lauren Soffer, Life Issues, Medication, Mental Illness, Neurological Disorders, Novel Patient Posts, Relationships, Symptoms, amber, art, blog, brain, brain stem, cause, center, chronic illness, confusion, consecutive days, count, cousins, definitive diagnosis, diagnosis, doctor, emotional moment, faith, flowers, heart, help, hospital, inflammation, life, midst, mom, moment, patient, place, poetry, relationship, script, silent scream, soffer, time, title, transition, type by Novel Patient

Things have been emotionally rough and raw lately.  Lot's of things are in transition.  Relationships in flux.  And I'm still stuck in the hospital (33 consecutive days and 39 total days in the hospital by my count).  I'm trying to think of it as Share

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