In 2010, to celebrate my tenth year of a wonderful life on dialysis I sort of got in shape and canoed 225 miles with the Grand River Expedition 2010. It was an incredible journey that couldn't have happened without my family and many dear friends.

I have been on dialysis since 2001 and have used every form of dialysis currently available in search of the best outcome and the best life. I have done in-center hemodialysis, at home hemodialysis with a traditional dialysis machine, peritoneal dialysis and finally, NxStage's System One home hemodialysis machine. I have had two kidney transplants, one from my beautiful wife and another because a thoughtful motorcyclist had checked the donate organs line on his license. For me, the technology for a successful transplant does not exist for my disease. I remain open and optimistic about wearable and implantable artificial kidneys.

Since I started my first blog, Tasty Kidney Pie, in 2001, I have tried to, and hope to continue to, inspire dialysis patients and others living with chronic illnesses to get outdoors and live an active and fruitful life.

Since 2001, The Riverdudes, my National Kidney Foundation of Michigan Walk Team has raised $78,000.

I currently spend my time writing, raising my children, snuggling with my wife, getting outside and staying active, and hopefully inspiring others along the way.

Thank you

With your help we can exceed this year's goal of $5,000 for the National Kidney Foundation of Michigan. Thank you very much for your continued support. Erich



Thursday, December 8, 2011

Providers - Do not underestimate the value of your Social Worker

I was surprised when I attended my November Clinic visit at Henry Ford to find that my social worker was relocated to other facilities.  Also, I was surprised at the transition to my new social worker.

The dialysis social worker is a very interesting position on the kidney care team.  The position doesn't scream vital like the physician, dietitian and nurse, yet it is still critically important to a patient's well being and ability to embrace life after dialysis.  With my eleven years of experience on dialysis, I find that the SW provides a subtle, humanizing aspect to the medical machinery that we rely on for life.  The effectiveness of a SW is based on a trusting relationship which is forged over time.  At times the SW is critical as when s/he helps a patient to work through important paperwork to ensure dialysis reimbursement or access to medicine.  Other times s/he is assisting on the important aspect of helping a patient to find a way back to work or to enjoy aspects of a life they thought they lost forever, such as traveling or intimacy.  For me, dialysis social workers have provided a kind smile and check on things that do not require a blood pressure cuff or a poke.

Rather than just informing me that my social worker was gone and that there is a social worker at in-center dialysis that can be made available, it would have been nice for the new social worker to stop by and introduce him or herself.  Personal touch is the hallmark of social working.  Without being introduced to my social worker and getting to know them I will be reluctant to call for him/her when needed.


Wednesday, November 16, 2011

Celebrating organ donation this Sunday at All Saints Episcopal Church East Lansing

She is nervous. Sitting in the waiting room she tries not to think about it. Everyone chats around her - mom, husband, and friend. The beach, focus on the beach she reminds herself. The warm sun, emerald waters and her son giddy with excitement when he scoops a handful of sand and water appears. Focus on your favorite place they told her. Don’t get up and run that would be childish, see the waves. The vision is interrupted when the attendant states her name and says that it is time.


Laying on the gurney, all that she can think of is that they need to put the IV in so that she can get the relaxing medicine. They promised her relaxing medicine. But the IV is going to hurt. I’m voluntarily subjecting myself to pain. Remember, they said you can change your mind at any time. This is crazy. It’s in, and her eyes close for a second; that is all that is needed for her little boy’s smile to reappear. As he digs his hole a pair of larger hands is helping. She opens them and sees her husband at her side whispering words of encouragement. She draws courage from deep inside. She is still scared but she knows that donating her kidney is what she must do.

Tuesday, October 4, 2011

Sticking the needle for the first time - first published in 2006 on Tasty Kidney Pie

The first time I had to stick, I held the surgically sharp tip with my right hand just above the bulging vein in my left bicep. I just held it there. After some time I tried to imagine my hand moving forward at the correct angle. I tried not to think about the razor sharp metal slicing layers of skin until I felt a “pop,” the feeling described to me when the needle bursts through the vein wall allowing blood to flash into the connected tubing. I was instructed that at that point I would know when to stop pushing. “But, how would I know?” “What would keep me from continuing right on through the opposite wall skewering the Triceps brachii like some tender piece of marinated tenderloin?” The answer given was that I would just know, which was comforting, not!

After a few more very long seconds of what on the outside must have looked like a Zen meditation trance but on the inside I knew what was really going on - panic and a mental image of me throwing the needle out of my hand and lifting my butt of the seat and hauling it on out of there. Instead, I took my leap of faith. I thrusted my extended fingers forward while my left big toe searched for a table leg to wrap around to calm itself all the while I silently screamed, “I do not like this “Sam I am.” I do not like big needles in my ham.” But before I could butcher any more Seuss it was over. Some magical force stopped my forward motion leaving the needle right in the middle of my vein. I sighed. My arterial bloodline was secured. After a few moments of quiet celebration I reached for another needle to secure my venous bloodline. When both lines were set and the machine was on, I leaned back into my chair exhausted but smiling. . . I had scaled the Mountain and found that my life was better for it. Six out of seven days I scale that same mountain but each day the slope flattens just a bit.”

Wednesday, September 7, 2011

Sweet dreams my dear


At the first crack of thunder, she leaps out of her princess carriage bed, skitters out of her room and around the corner and pounces on to our bed.  She slips her feet beneath the sheet quickly pulling it up over her head, hoping to be established as a permanent fixture before I came out of the bathroom.  I scan the room as I enter whispering to myself, “I thought I heard a commotion out here?”  I scratch my head and quizzically squish my face and say, “I guess it was my imagination.”  This elicits a giggle.  “What was that?” I ask myself as I reach for the closet door, swinging it open with an “Ah hah!” to find nobody there while hearing more bursts of giggles from across the room. After checking another closet, a couple of drawers and under the bed I quietly step to the side of the bed where a lump has appeared.  I imagined my daughter holding her breath, trying to silently sink deeper into the mattress, struggling not to laugh as her eyes follow my silhouette through the light blue sheet.  Her anticipation heightens with each step closer I take knowing that her father’s hand will soon reach down, grab the sheet and unveil her with a cheerful, “Gotcha.”  
Tonight I take my time with the day’s last dance.  I step closer to the bed, my silhouette looming largely through the sheet but then quietly retreat to my rocking chair.  I spread out my protective pads on the tray table and start to unwrap my supplies.  The only sound in the room is the swoosh of the saline circulating through the machine and the hum of its pump.  I sense the sheet being carefully pulled down across my daughter’s forehead, exposing her espresso eyes.  I quickly turn from my task to look her way only to see a fold of sheet melt into the pillow.  As I turn back to continue my set up, a loud “beep, beep, beep,” sounds, startling my daughter out of her ruse.  “It is o.k. Sweetie, it is just the machine.”  She knows but it still surprises her.  Now sitting up she watches as I come toward the bed where the machine is inches away.  As I sit down on the bed I simultaneously reach for her with my left hand as I press a button to mute the alarm with my right.  I pull her close with a hug and say, “How did you get her?  I thought you were sound asleep in your bed.”  “Dad you knew,” she says with her all knowing smile.  “I did not,” I respond unconvincingly.  “You can lay here until it is time for me to hook up.  Close your eyes and try to fall asleep, Sweetie,” I urge while bending over to give her a kiss.  Playfully she jerks her head and shakes it slowly with a tight lipped smile, “No kissey, Daddy.”  “O.k.” I say and get up and return to the tray table.
I open the 30 cc syringe and the two 10 cc syringes and put the needles on.  Then I unsheathe the large fifteen gauge needles which have long tubes attached.  I place the band aides on the table and start unrolling lengths of silk tape, securing them to the table.  As I do this, from behind my gaze my daughter watches.  Having completed my set up, I get up from the rocker and head back to the machine.  My daughter’s beautiful brown face is bathed in red light from numbers illuminated on the machine.  I sit down next to her and say, “Please close you eyes my dear.  You need to go to sleep.”  I grab the tubes attached to my machine and start snapping them to remove the air bubbles.  
“Daddy when will you stop doing dialysis?” Antonia asks a matter-of-fact.   I let go of the tubes, turn to her and put my freckled hand on her soft cheek and say, “I’m going to do dialysis for a long time.  Long enough for you to get much older, go to college, have a career and get married and have children so that I can be a Grandaddy.”  After a moment, with sleep getting closer, she asks “Then will you stop dialyisis?”  Trying to seem unfazed by the depth of the questioning of my seven year old daughter, I respond, “I will be on dialysis until I go with God.”  Her lids now heavy across her eyes, she silently mouths, “o.k.”  I lean over, kiss her on the forehead and return to the rocking chair. 
I switch on the radio and with Handel’s Water Music, Suite No 2 playing softly in the background I swipe the line on my left bicep with alcohol.  After it dries I swipe it again, this time with beta-dine.  I trace the burnt red line with my right finger tips feeling the outline of the graft just below my skin.  The narrow graft connects a vein and artery enabling the blood to easily leave my body and return after a quick trip through the tubing and artificial kidney supported by the machine.  As my daughter sleeps soundly I pick up one of the fifteen gauge needles, take aim, wince and push it cautiously into my arm.  The blood immediately rushes into the tube, relieving my anxiety.  It is disconcerting when I miss.  After placing the other needle I walk over to the door and turn off the overhead lights.  I walk back to the bed and push Antonia to the middle with my right hand.  I connect the tubes in my arm to the tubes on the machine and press “go.”  The blood comes out of my arm and pushes the saline through the machine and into my arm through the return needle.  I make some adjustments to the machine and turn on the heparin pump.  I grab my Kindle, turn off the bedside lamp, turn on my reading lamp, lay my head down and take a last look at the machine.  The tubes run garnet, everything is secure and I am ready for eight hours of cleansing and sleeping.  Antonia lies peacefully at my side, her mom will move her to her room when she comes upstairs.  I listen to the rain falling and my daughter breathing.  The lightening and thunder are now miles past to the East.  I flick on the Kindle and settle into Hiaasen and Montabalno’s A Death in China.  

Thursday, April 21, 2011

Please help me raise $5,000 to help beat Kidney Disease



Dear Friend:

Last year was a hoot and together we raised $17,000 as we walked and then paddled the length of the Grand River.  It was an incredible journey both in raising the amount that we did and in getting the word out that life begins a new on dialysis and that one can be active despite one's chronic illness.  Thank you for all the support last year.

This year we have a new goal of $5,000.  With our support to the National Kidney Foundation of Michigan we will be helping the organization reach out to everyone in Michigan, including our friends and families, about the importance of maintaining a healthy weight and blood pressure, both if out of control can lead to the loss of one's kidneys.  And let me tell you, while everyday I try to live a great life with the help of dialysis, it would be a whole lot easier if I didn't have to do it.

I want to share a short story from my blog http://paddlingondialysisforkidneyhealth.blogspot.com/


My daughter and I are driving and she notices a couple of children running on the sidewalk and turns to me and says, "I wish you weren't fat.  I wish your were skinny."

 I take a Twix like pause to give my good daddy side of my brain time to kick start and them timidly ask, "Why?"

"Because then we could run together," she innocently responds.  

Apparently all the physical benefits of my 235 mile canoe odyssey last year have disappeared.  This year's goal will be to run with my daughter.  

There are three ways that you can get involved:

1. Make a donation through this secure website right now. http://donate.kidney.org/site/TR/Walk/Michigan?px=1006841&pg=personal&fr_id=3391

2. Join The Riverdudes and The Hubbard Law Firm Walk Team and collect funds to help us reach our goal. We will be walking down town starting at Cooley Law School Stadium (an no they don't fight attorney gladiators there) on Sunday, June 12. Let me know and I will happily sign you up or you can sign up on the Team Webpage http://donate.kidney.org/site/TR/Walk/Michigan?team_id=85711&pg=team&fr_id=3391

3. Become a virtual member of my crew.  Join the Walk Team but because of timing or distance, just help raise money.  If you can't walk with us, you can still be a part of the Team.  Use the Team Page link above.

The money you donate to NKFM is used for research into cures and better treatments, sending kids on dialysis and with transplants to camp, making medicines more affordable to patients, and educating at risk populations about how to reduce their risk to kidney disease.

Please donate $100, $50, or what you can to day. If you would rather, you can send a check made out to the National Kidney Foundation of Michigan and mail it to me at:

Erich Ditschman

Together we can help many others through supporting the NKFM.
Dialyze for the Prize!  And, have a wonderful day.
Erich 




"I wish you weren't fat."

My daughter and I are driving and she notices a couple of children running on the sidewalk and turns to me and says, "I wish you weren't fat.  I wish your were skinny."

I take a Twix like pause to give my good daddy side of my brain time to kick start and them timidly ask, "Why?"

"Because then we can run together," she innocently responds.  

Apparently all the physical benefits of my 235 mile canoe odyssey last year have disappeared.  This year's goal will be to run with my daughter.  

After I told this story to Andria, she mentioned that I could have said, "At least I'm not dead."  

To which I responded, "Honey, I don't live in a world of attorneys.  I have to assume innocence first and anyways, sarcasm only works with Jacob."

Monday, February 28, 2011

A message to a friend

Hi:


I understand things are going very well for you at FSU.  It is because you are a very smart and confident young woman.  This is a wonderful time in your life and I am very excited for you.


I've heard that you are wrestling with whether to pursue a Ph.D. Perhaps you have already decided, but in case you haven't I want to share briefly my experience on pursuing a Ph.D.  O.k., I'm sure you are thinking what could a 45 year old due that you just met a few years ago possible share that has any value?  I know I would be if I were in your shoes.  But,  I wholly believe that it "Takes a Village," so here it goes.


Andria and I were high school sweethearts who miraculously waited until we graduated from college to get married.  When she graduated I had just started on my MS at MSU.  I had a well funded Assistantship which pretty much covered my end of our shared financial obligations and Andria worked full-time.  As I came closer to finishing my program I started working close to full-time at MSU and Andria started law school at Wayne State.  We lived in Farmington Hills and she commuted to Detroit and I to East Lansing.


I graduated and moved into a full time position in Rochester Hills at a not for profit organization (means low pay but meaningful work) and Andria continued at WSU.  A couple years into my position I started a PhD program at MSU.  Andria graduated and took a position in Port Huron.  For a while she commuted to Port Huron and I to East Lansing in the evenings for classes.  Eventually we moved to PH and I commuted to Rochester Hills then to EL and back to PH.  I really wanted the Ph.D.  I saw myself sometime in the future as a professor who did part time consulting.  I knew some professors who did that and it seemed like a pretty good gig.


Eventually I moved from my not-for-profit job to the private sector.  The money got better.  Here is an important point - as the money got better so did our lifestyle - from Ramen to actual cuts of meat as well as futons to to solid furniture and ten year old cars to  new cars.  


So, I'm into my new position, enjoying developing the work I was doing, making new clients, doing things with the Partners and along comes a three-year full ride Water Science Fellowship.  The Fellowship is designed to pay for my classes, give a decent stipend (in graduate school terms) and significant opportunity for professional growth.  It was a sweet deal.  You see I was still commuting to EL now from PH to Bloomfield Hills to EL and back to PH.  This Fellowship is like a gift from the heavens, right?


The problem is that there is no way we could take such a big cut in our combined household income to live on that stipend, even with Andria working full-time.  So I passed on the Fellowship.


I still was not daunted in continuing to pursue my Ph.D.  It just took a tremendous about of time and discipline and wear and tear on our cars.  


During this time Andria experienced a number of miscarriages and we also experienced issues with fertility.  As we sought fertility treatments, I realized it wasn't fair for Andria to have to administer her shots by herself and to not have me by her side as we worked through this very emotionally difficult time in our lives, so I walked my last walk at MSU and decided I would stop pursing the Ph.D.  


A year or two later I was able to continue to pursue my program until we started having difficulties with the adoption process.  And again, I took what I thought were my last steps along the Red Cedar River so that I could be where I was needed most.


A few years later I take a new job in Lansing and we buy our house which is blocks away from the University.  I again restart my program.  In fact, this becomes the third time I take the same Ag Economics Course with the same professor.  I proudly tell him, this time I'm going to finish his course.  And darn if a month in, my feet swell and it turns out I'm losing the use of kidneys.  I don't complete his course and instead go on dialysis.


That was ten years ago.  Last year I found out that I timed out of the system and would have to take most of the course work again not to mention that I would have to re-apply to the program that I spent ten years in.  I had nearly finished my course work and was starting my dissertation research.


My dreams have changed and I have lost the desire to pursue the Ph.D.  I spend a significant amount of time with Antonia and Jacob and of course Andria and I can't conceive of having to be away from them right now to sit in a classroom or be holed up in a library.


One of my regrets is how much time away from Andria I spent over the many years I pursued my Ph.D.  She was always supportive of my pursuit but it just wasn't fair to be away from my love for so long.  In retrospect, had I taken the Fellowship, the program would have been done in three-years and I wouldn't have missed all that time with Andria.  We would have just had to eat Ramen more frequently and make a few other economic adjustments.


While this might sound like a sad story it isn't.  Life is a crazy ride.  Thankfully each of us are very resilient.  If not, we'd be a miserable lot.  Instead, we have the ability to rebound from the many difficult hurdles that come our way.  I have learned to become an incredible Rebounder.  I think Izzo could use someone like me right now.


You are such an incredible young lady that I know that whatever decision you make will be right for you.


I am lucky to know you.


Take care, Erich

Monday, February 7, 2011

A cool picture published in Our Grand Journey: discovering the river we thought we knew.

This photo is on page 108-109 of Our Grand Journey: Discovering the river we thought we knew -http://vintagegrandrapids.com/



Removing my fistula and inserting a Graft

The following are recent posts to my Paddling on Dialysis for Kidney Health Facebook Page.

January 16, 2011
Tomorrow I say goodbye to my fistula, what Jake and Antonia affectionately call my snake. We have had a great ten year run. It is the access that keeps me alive and keeps me paddling...


I struggle posting this type of post. For many it is too much information. However, occasionally I hear from someone who has happened on something I write, rarely mind you, but it happens, and they tell me thank you for posting. So it is with that thought- that perhaps what I write may help someone else dealing with kidney disease or crisis, that I post too much information. Thanks for reading.


For more information on what a fistula is see http://kidney.niddk.nih.gov/kudiseases/pubs/vascularaccess/



Jaunary 17, 2011


I'm posting this because I have had some questions. Always Fistula First!. A fistula is the best access to avoid infection and blood clots. No one likes needles but you eventually grow to tolerate them. After numerous sticks scar tissue develops and it becomes less painful. Of course the best to combat pain is to develop button holes, a technique that allows you to pick off a scab and place the needles through a tunnel similar to how pierced ears work (without the scab of course). My first fistulagram was after eight years of use of the fistula and my first angio was last week. My skin became very tight and was not longer able to make button holes, then it became difficult for the skin to heal. But, it wasn't until my fistulagram last week that it was determined that the walls were too thin and that there was a real risk of rupture. Please keep the questions coming.





(these are Xrays of my fistula showing the 
large pseudoaneurysms that eventually were incised 
after the vectra graft was placed)

Does this mean that you will need a new fistula made...

Eventually. But I'd like to gain as much time as I can from the graft. Because it will be more difficult sticking my right arm with my left hand after a new fistula is placed there. Also, once the right arm is used up we have to move to a leg and that doesn't sound at all appealing. But waking up with Andria at my side and coming home to big but cautious hugs from Jacob and Antonia make it all worthwhile.


So fistulas can go wrong? Do you mean the vessel part or the actual fistula tubing? In the hospital they told me they were for life which clearly isant the case! So where do they go when your arms and legs are all used up? 
:-(

They can go wrong but they are the least likely to, especially if the are being followed by a good vascular surgeon. Some people have used their fistulas for over 35 years. Every patient is different. Remember a fistula is you - nothing artificial. The blood vessel is the fistula. The artery is rerouted to a vein. The vein which is a low pressure system back to the heart enlarges when it receives the high pressure from the artery. This is how it gets large enough to use as an access. I absolutely love to swim and canoe and kayak as do my children which are 6 and 11. The fistula allows me to continue to do these things. Also, I love the fact that I don't have anything hanging on like a catheter. Home Dialysis Central has a great tutorial about establishing button holes athttp://www.homedialysis.org/learn/buttonhole/

February 7, 2011
After a couple of weeks of recovery I had the thirty staples removed from arm. As the pain of the surgery and and the swelling both subsided, I started to poke my new graft.  I am now happy to report that Dialysis Dad and graft are both doing fine.


Friday, February 4, 2011

Phi Sigma Sigma Golf Outing in Mt.Pleasant to benefit National Kidney Foundation

If you are in the Mount Pleasant area on April 16th check this out http://www.wix.com/holla4jm/phisigmasigma-golfouting
The sisters of Phi Sigma Sigma are hosting a golf outing to benefit the National Kidney Foundation. I just found out my cuz is a sister - small world.


I plan to attend.  I  hope you can join me.

Paddling upstream

After last summer's excitement of the Grand River Expedition my rapids spilled into quiet waters.  The camaraderie, active schedule, renewal of old friendships and the creation of new ones and the daily sense of accomplishment I received paddling with sixty other river enthusiasts created a palpable kinetic energy.  Even though I was tired at the end of each day and had to dialyze, I felt a sense of renewal, of purpose and of who I once was.  My first job at the Clinton River Watershed Council was to canoe its length and observe its condition from the headwaters in Waterford to its confluence with Lake St. Clair.  I was young, excited, and on the water getting paid - pretty much a riverdude's dream job.  As with all good gigs, the Expedition ended.

The Grand River's rhythm established a beachhead on my soul.  From enjoying limited excursions the year before,  I now craved the feeling of sitting in a boat and paddling upstream with Buffett's Far Side of the World cruising from my Blackberry to my brainstem and down to the peripheral nerves in my toes.  Upon reaching the upstream point where I had to turn around in order to finish in time to get my children, I maneuvered the kayak downstream and let the current bring me slowly back to reality enjoying the eddying of the current as I slipped over the rocks.

While I continued to enjoy the Grand River on my own, I changed the social dynamics of my life.  Since Jacob was now a Boy Scout I no longer was a Cub Scout Den Leader.  I chose not to continue in my role as Marble's Yearbook coordinator and since Andria was no longer the Parent Council President I no longer was its number one go to volunteer.  I resigned as a Board Member ofDialysis Patient Citizens.  While I believe it is a good organization with a dynamic staff I just wasn't feeling a connection with my fellow Board Members.  Also, while I loved the trips to D.C. - roaming the halls of the Cannon Building in search of Mike Roger's office, sitting in John Dingell's Rayburn Building Office and watching him take a meeting with IBM representatives as his handlers handed us over to a policy aide, strolling past the Capitol en route to the Hart Senate Office Building to talk to Debbie Stabenow - which sparked life in this aging political science major, I tired of becoming entrenched in the dialysis industrial complex.  I believe that true recovery from kidney disease is when one has restored the passions enjoyed before the onset.  I didn't want kidney disease prevention to become my new identity.  However, I found that without the structure of these volunteer endeavors I was rather rudderless in my pursuit of happiness.

Each day I thought about sitting down and writing but by the end of the day a home improvement project, grocery shopping, children shuttling, or dinner making had absorbed my time.  So while one close friend landed a new job and another found his way back on Broadway I just lived day by day.  Living in the moment is not easy for someone who has been a planner all his life.  To ease my frustration as I lay in bed connected to my dialysis machine, I recalled that my major goal in life that I set in high school was to wake up with Andria in my arms.  With that in mind, I suppose anything else is gravy.

As Christmas drew near, interesting things began to happen.  A carpenter who was working on our basement noticed my Fresenius boxes and asked me about dialysis.  His wife was on dialysis and not doing so well in center while using the catheter in her chest.  Apparently she just cancelled a meeting with a surgeon that day to discuss putting in a fistula.  I showed him my fistula and we discussed home hemodialysis.  Later in the week I found out that his wife had rescheduled and attended her consultation.  She was now planning on getting her fistula.  I then received a call from a fellow All Saints parishioner.  She was concerned that a local surgeon had botched her son's graft placement and inquired whether I knew about Michigan Vascular Access Center (little did I know at the time that I would soon be a patient there).  We talked at length about the situation and about connections I had at U of M.  While it wasn't much, I was there for her and her son and I think she found solace in our call.  A short while later, my regular postal carrier knocked on our door and handed me a $50.00 bill for the National Kidney Foundation of Michigan.  He said that he and his wife were touched by my efforts and wanted to make a contribution.  I was floored by his kindness.  Talk about out of the blue.

My wife and I attended the Christmas Party at her law firm.  At one point during the dinner I presented the president of the firm with a copy of Our Grand Journey:  Discovering the river we thought we knew with an inscription thanking the firm for their generous contribution and support for the last ten years.  Later that night during the white elephant gift giving the president and his wife, who own's Yesterday's Toys in Laingsburg, donated a couple of toy ping pong ball guns which were spontaneously raffled and raised $80.00 for the NKFM.  Over the holidays a couple of more donations from friends came in the mail.  Just recently I received a check for $115 from the employees of Spectra Laboratories, the place I send my monthly blood samples.  Spectra was already a corporate donor to Paddling on Dialysis for Kidney Health but to find out that their employees raised money on their own was surprising and delightful.  While I may have removed myself from actively lobbying policy makers and separated from the dialysis industrial complex, I am still able to make a difference on a more personal scale which is very gratifying.

I recently found an editor for my book.   I'm hoping this will add some current for my rudder to take hold.  Perhaps a good "hard to starboard" will help me regain the helm and set a course to finish Amos.  As I write, I will continue to grocery shop, make dinner and shuttle Jacob and Antonia because that is my true dream job.  I will also be there for those that I can help as we each make the most out of living with kidney disease.  And, as soon as my new graft that I received from the good doctors at the Michigan Vascular Access Center heals and the temperature rises a good bit above the current ten degrees I'll put a boat in the Grand and paddle upstream.