LVAD... Left Ventricular Assist Device

THIS BLOG POWERED BY THE THORATEC HEARTMATE II LVAD:















PARTIAL HEART PUMP = LEFT VENTRICULAR ASSIST DEVICE = LVAD = THE HEARTMATE II



THE LVAD ALLOWED ME to go HOME and conquer my normal and newest tasks once again.



Thank you Columbia-Presbyterian... Dr Naka and his Surgery Team, LVAD Nation, Dr Bijou & Dr Bonoan, Dr Mascitelli and Dr Shulman-Marcus!!!



AND TO THE SCORES OF PHYSICIANS, NURSES, PROFESSIONALS AND PEOPLE THAT PUSHED ME ALONG THE WAY... FORWARD.



Thank You God For I Am Blessed!







If I Was An LVAD-NASCAR Race CAR

If I Was An LVAD-NASCAR Race CAR
I would look like this :-)

FROM THE BOTTOM OF MY LVAD DAILY NEWS AND INFO FEED

Showing posts with label Dr Naka. Show all posts
Showing posts with label Dr Naka. Show all posts

14 February 2012

The Most Important LVAD SweetHeart: YOUR OWN HEART! LOVE IT! RESPECT IT! Walk It!


As Valentines Day is here, i would like to emphasize my Love for my Wife and for my Family on Valentines Day 2012.  However MORE importantly is the fact that our BIGGEST SWEETHEART should be our own hearts and those with heart failure... what remains of our functioning heart should be treated well. Loved! Respected! TREATED to healthiest diets possible. And last but not least our Hearts should be walked and if possible... exercised to Healthier and stronger limits.

I have an LVAD which means my Left Ventricle is in dire need of assistance from my Ventricular Device... The LVAD.  I am so blessed to be in the age of the implanted LVAD and to live another day to make a difference.

I OWE IT TO THE  RIGHT SIDE OF MY HEART TO KEEP IT AS HEALTHY AS POSSIBLE as my HeartMate II is taking care of the Left side chores... :-)

Happy Valentines Day to My Wife,Mom,
Daughter,Son-in-law,grandson1,grandson2,Son1,Son2,Sisters and Families, My Extended Family, Friends, My LVAD FAMILY, Dr B and his Family, Columbia New York Presbyterian Hospital Family and to my Thoratec Family.

23 December 2011

Dear Wife,Mom,Family,Friends,Columbia New York Presbyterian and Thoratec... THANK YOU!!!




Thank You for Fighting The Good Fight and saving lives with your gifts, dicipline and passion. I will never run out of ways to thank you. Not a Single Day goes by that I dont wake up and I Thank you!




And The Good Saga Continues...

02 December 2011

AND THE GOOD (LVAD) SAGA CONTINUES IN AARP MAGAZINE By Peter Jaret

X
The Morris' pictured here in front of Yankee Stadium, are enjoying 'extra innings' in life.

Photo by Gina Levay


Below is a Direct link to the article. However here are some excepts from the AARP article by Peter Jaret...


When damage to the heart is irreversible, as in most cases of congestive heart failure, the pump can buy time until a donor organ is available for a heart transplant. Before he suffered a heart attack at age 47, Michael-Joshua Morris, of New York City, was exceptionally active. After his heart attack, he couldn't walk more than 10 steps without gasping for breath and leaning on his wife, Anne Marie. Two years ago he had the device implanted. "What the heart attack took away from me, the LVAD gave back to me," says Morris, who still hopes to undergo a heart transplant.


But most recipients shrug off the inconveniences. "Sure, you've got a wire coming out of your gut, and batteries to worry about, and all that," says Morris. "I'm a Yankees fan, and someone once asked me if I felt as if my life was at the bottom of the ninth inning, two outs, bases loaded. The way I put it, my life is in extra innings. If I'd had my heart attack eight years ago, I wouldn't be alive. What can I be but grateful?"





AND THE GOOD SAGA CONTINUES...

25 November 2011

HEARTMATES TOO WITH THE HEARTMATE II / "LIVING THE NEW NORM HAPPILY!"

WHO HAS THE LVAD?

Look carefully, the ugly one in the grey hat has the LVAD :-)... Me! My driveline exits my body, yet for a moment, my wife gives me a break wearing my batteries and controller. My whole family plays a roll in living the NEW NORM with me ! My wife and family and my LVAD... Living the new norm happily :-)



AND THE GOOD SAGA CONTINUES...

23 November 2011

My Second Year Anniversary With The LVAD... Has Me Thinking NASCAR. Unlimited Thanks To ALL My Supporters And Sponsors :-)


For the Past 2 years, countless people, institutions and companies have made me what I am today... A THANKFUL, productive and Loving citizen within society... as time goes on... i will add to this post with stories of the folks who have restored my life for me and my Family!!! THANK YOU Thank you thank you!!!


HAPPY THANKSGIVING!!!


AND THE GOOD SAGA CONTINUES...

17 November 2011

ANOTHER NEW NORM! WHAT CAN I SAY? I AM BLESSED BY MY TRUST IN GOD, Columbia NY Presbyterian Hospital And Thoratec.

The Noble person who had my life and heart in his hands.

Dr Naka The Selfless Surgeon

(Great Name For A TV SHOW)





This is My Wife, Me and My Mom just 8 hours after pump swap. I already was off the Vent, sitting up in a chair for 3hours and back in bed.




DISCHARGED 7 days after pump swap and heading home :-)





7 days after my LVAD Pump Swap I headed home Happier than before. Stronger than Ive ever been. I have alot of folks to thank but must start with 3 people. My Wife, Mother and Dr Naka who has had my heart in his hands twice.



2 years ago I had the Heartmate II implant. However I always knew I would be back in the hospital... for a Heart Transplant and or perhaps a pump replacement as i am blood type O negative which is the rarest blood type and longest wait for a heart.



Anyway with this mindset from 2 years back, i was always somewhat prepared to return for surgery. Like a Samarai Warrior, i envisioned myself going through different types of scenerios. Good ones and Bad ones... in an effort to always be prepared.

I like to constantly remind myself of the variables and possiblities surrounding me at any given time. I am not trying to be a hero but more a realist so that if something arises I AM THE STRONGEST I CAN BE... mentally or physically. To Me 90% of any battle is mental.

Today is the first day where i do not feel as exhausted as yesterday. :-) so for me this is DAY 1. I will be posting my experience and findings on my pump failure and swap. How it felt when the pump stopped and my native heart took over.

I will also discuss the folks involved in my surgery and recovery... but for now i leave a photo of me upon discharge... in the back seat of my truck as my wife is driving and my mom riding shotgun. One of me and my Caregivers and Dr Naka the most gifted man that has saved/restored/restarted my life TWICE!!!





AND THE GOOD SAGA CONTINUES...

28 October 2011

22 June 2011

The 1st LVAD Interview I Granted after turning down TV/RADIO And Other Print Interviews: Read and see why...

It is probably better if you travel to the direct link as it has photos... AND the CircuitSurfers.com site is one of my favorites as it is very innovative:

http://circuitsurfers.com/2011/06/22/the-joshua-story-ii/



The Joshua Interview:

Editors Note: Josh is a HeartMate II recipient and is awaiting a heart transplant. Please click here if you are unfamiliar with his story and would like to see how we got to the point of doing this interview.

On 06/09/2011, Teutonic 13 wrote:
Hello Joshua, this is Frank from Circuit Surfers.

Wasn’t “Joshua” the name of the computer in “War games”? It was something like that.

Anyway let’s begin the interview:

You contacted me via twitter regarding CircuitSurfers- and mentioned it was very innovative and that you liked it.

I saw your handle LVADone and assumed you to be a perfusionist, never actually considering to read your name and understand what it implied.

There is a lot of your biographical history on the fantastic blog that you write. What was it that made you reach out and decide to blog your HeartMate II experience?

(When you get this- just reply to it- and we’ll do the interview that way- if your ok with it. Please ask questions as well- or offer your opinions of the situation, me- the blog whatever-… keep it raw and keep it real…)

Frank

On o6/15/2011, Joshua wrote:


Frank, big apologies for the delay…

My wife flew to take care of her Dad and last night i got back 230am after spending 7 hours discussing Thoratec’s future products.

Anyway my response to Q1 is as follows:

Initially my blog started off as a Journal for my family and friends.

When I came home from my implant I had many calls throughout the day asking how I was. At some point I was ” tired” of sounding redundant so I told everyone to check out my blog posts for my health updates.

After a month or so i noticed that my blog was receiving recognition from interested parties from across the nation and around the world.

So I thought that I would share what I could about the LVAD for those looking to learn.

When I first started blogging about the LVAD there wasn’t any real “patients perspective” on the LVAD. It was all Clinical info.

I then began to microblog, using twitter to obtain and pass information about the LVAD as well as my blog.

On o6/17/2011, Teutonic 13 wrote:
I’ve had a chance to actually read your blog and learn more about you Joshua…


I am fascinated by your bluntness and the immense spirit you show to others less fortunate, or as is the case recently, a fellow LVAD recipient.

So the next few questions are centered on your “drive”.

Q 2: Were you always as outgoing and generous with your empathy as you seem to be now? I know you are a New Yorker- or at least a Yankees fan, but were you always this kind, or was the reality of walking on the edge of continuity- a spiritual paradigm shift for you?

Josh



I might be less outgoing and generous now as I do have restrictions because of the LVAD.

I was raised to be selfless… Altruistic, A humanitarian at heart. It runs in the family.
Walking on the edge didn’t bring a paradigm shift, but a battle cry to help others get through what I had already experienced.

My approach is that I am further up on the hill then them and I am just calling down to them to watch out for this obstacle or that obstacle.

Q3: It is obvious that you are “eternally grateful” to the immediate family of clinicians that were your custodians so to speak as you went through this experience, but it truly was their vocation to do so, just as it is mine to deliver a safe bypass run during open heart operations.

So it seems that the line was crossed at some point, where you stopped being “patient X with the VAD” and became a source of inspiration, accomplishment, and siphon for emotional commitments from seasoned individuals who rarely allow themselves the gift of that sort of intimacy. A departure from their emotional walls. When did that happen? At what point did it become obvious you weren’t just an exercise?

Josh



Wow, your observations are keen, spot on! Ive learned from a young age to assess people on WHO they are and NOT what they are. I ran into a doctor who had a messiah-complex and was arrogant to me and my family. Although i was so ill at the time, i did verbally put him in his place. Afterwards each nurse in ICU came in to thank me for straightening him out till this day, 19 months later he is behaving

However from the moment I entered the hospital for treatment of THE heart attack, I made sure I wasn’t going to be Patient X or PtX w/LVAD My wife is always amazed how strangers, Professionals… Warm up to me quickly. I can never be wrong by being Me.

Q4: Sometimes those who need the most, get the least and end up offering up to others what they themselves need. Is that subconsciously a driving factor for the raw nature of your drive to support and educate others?

Josh



I don’t believe so. I never expect much, so being this way I am rarely disappointed or feel slighted. I just realized when my Blog was being noticed by others and the questions began to pour in, i realized there was a place for me to steer folks in the right direction. Connecting the dots.

When I was seven years old, My Father was one of the first Home-Dialysis patients in NY, this was in the early to mid 1970s. So at the age of 7 I assisted my mom placing my Father on and of Dialysis, 3x per week/6 hour sessions. So as you can see, from a young aged I’ve been shaped for this.

On o6/18/2011, Teutonic 13 wrote:
As you and I know, you are at the tip of the spear regarding the human equation.

Your outcome shall be the tether for future efforts to sustain life and defeat our greatest limiting factor – death.

(That concept may be totally skewed as the concept of “an end” may be what propels us to solve the problem).

Q5: Obviously life and death are side bites in most people’s lives. To be afraid to die is to cancel the check on living. So how does that play?

Josh



Tomorrow is not promised to anyone. I have always believed that fear of death or not wanting to grow or look old are selfish traits. Fear of death causes midlife crissis et al !? No? It Causes folks to be addicted to substances that allows them to get lost in their lives avoiding the inevitable. However, one day the same folks awaken because death is before them.

Q6: Is your blog an extrapolation of your will to survive?



Quite the opposite… As it started as a journal for my friends and family to review, it is also something for the future that my children and grandchildren will show to their kids and hopefully twill say ” wow he was a good guy”

Q7: Where does the concept of experiment begin and end? Do you feel that you are… an experiment? Or do you trust the next evolution of technology to take you further? And if so- where does it take you?

Josh



I take 1 day at a time, but keep my eye on the industry’s progression. As i told one of my surgeons, Dr Takayama ” I am so grateful to have an extension upon my life, knowing my children’s generation will benefit by this.”

We LVADers are “test pilots”, some crash and burn some live on and exceed expectations. we are still in the new frontier of battling heart disease and I don’t mind being an experiment.

If humanity does not experiment we will never achieve new and great things. It won’t happen in my lifetime but I would like to see the artificial Heart replace heart transplantation as there isn’t a rejection factor with titanium

But this opens up a whole new can of worms… Will mechanical hearts allow people to live to 150?

This is a deep issue. Deep.

Q8: I like to think of your story as a bottom of the 5th inning getting a string of hits- and tying the ball game- when you were down a few runs. At this point is it a tie game for you? There’s a lot of game left and the 7th inning stretch.

Josh



Nice analogy… But perhaps I am in the bottom of the 5th,tie game and with 2 outs/full count I hammered out a homerun to take the lead (LVAD IMPLANT). Now we are in a rain delay… Still in the lead.

Q9: Is a new heart the relief pitcher?

Josh


No, more like extra innings




I’m thinking that the guy above is going to slam it home…

On o6/18/2011, Joshua wrote:
Josh



Frank, have you always lived in Texas ?

You mentioned your Dad being in France…

Its the obvious passion you possess, drive to juggle numerous tasks and callings while maintaining your profession that doesn’t make you “normal” And this is why you can’t write “normal” stuff . normal is average…. Some are born/wired not to be “just average” and it intrigues me… I am certainly not normal or average.

It’s apparent that you are on a mission (that only a few can compete with and complete). To share what you know and selflessly build upon it with others. Folks will be inspired by and or envy/jealous of you i.e.: that email you sent out of a colleague who unethically dislikes your website/blog and it’s theme.

IMHO I say ignore the distractors. Do not delegate time to launch rebuttals etc, as they want the attention. “speak to the hand” approach will leave you less stressed to do what you do best.

Will send complete answers to your questions by tomorrow, the latest. Been alone last few days (by choice) since my wife flew to care for her dad. Feels good to be totally autonomous even for a brief shining moment. However I promised my wife, I will allow family members to sleep over and babysit me. :-)

Josh

On o6/19/2011, Teutonic wrote:
Nah. I just moved to Texas 3.5 years ago. Was doing alot of Locums work, falling behind on everything, away from my family so much it was ridiculous.

Finding a job in perfusion with the amount of experience I have is hard to do. People either think there is something wrong with you, or they feel they are going to insult you with a lower salary offer. It sucks.

I got a break from two really decent guys out of Dallas, Loyd Yancy, and Steve Sutton. They trusted me, and I am grateful to them for that.

I did the blog thing initially because I wanted to write it down. I wanted to write something that was perfusion and the human equation part of it.

It started out as a directory for perfusion related topics. Very dry stuff- but important information to people that may not have the resources or professional affiliations to get that info quickly.

I’m talking about our other perfusion friends in smaller countries around the world (have had 116 countries come to visit).

Then it morphed into something else. What that something else is- I do not know. But for some reason it just feels right.

I don’t know where that conviction comes from, but it just seems like my gut instinct on writing this stuff is that it’s there to serve a greater purpose. Who knows what that truly means, but I trust my instincts.

The fact that it’s not for profit is exhilarating in terms of the freedom it confers on the blog.

I can handle the flack, but don’t like embarrassing myself- and I may have in terms of my response to the event you referred to.

So a couple of thoughts to close out this interview:
Q 10: What do you know of perfusionists? Have you met any, and what if anything would you like to say to us as a profession?

Josh



Pre-LVAD I thought Perfusionists to be Those who control blood flow to a patient under the knife in open heart surgery.

Since my own implant… I grew to know more. Minutes prior TO ME JOINING THE “zipper scar club”

I met everyone on the cardio-surgery team except the Perfusionist.

It was not until a month or so after surgery I participated in the only perfusion test/controlled blood perfusion to the brain. The model they created from the study is the only in the world. It will help future LVAD patients as well as Stroke patients. Here I met neurologists psychologists surgeons and my Perfusionist.

He introduced himself and I explained what he had done. This was the first time I knew my own heart was stopped as part of the procedure.

I now look at Perfusionists as “our” first Caregivers, so to speak prior to the LVAD taking completely over.

The test yielded info that was able to map my brain function while my pump speed was reduced by 1,000 rpm increments until pump was spinning at minimum

I was tested for my brain activity as well as 2 or 3 six minute walks. The study was monthly for 12 months. I believe it was called the SOCC study? I posted this info on my blog.

Q 11: Do you have any questions regarding us? Anything you want to know about what we do- see- or feel?

Josh



I know a sense of confidence along with a clear and disciplined head dictates your work ethic and performance. However, we are all human; we are all mortal.

On days that you may feel under the weather, mentally and or physically… finding yourself in your scrubs ready to jump into the theater of life saving…

Do you compartmentalize your distractions and proceed to surgery? Or is it more akin to an athlete who psyches him or herself into “The Zone”?

Teutonic13




I think we are reminded of our human fallibility (the potential to err is in all of us) every day we pump a case. With so many steps and moving parts in the equation, the goal is to choreograph out a perfect “10″ every single time.

Of course that doesn’t always happen, as unforseen circumstances may come up, equipment may fail, and the totally unexpected “never thought that was going to happen” moment rears it’s head.

So the “10″ ends up being- not the perfect pump run, as much as it represents, the perfect recovery from an adverse situation.

That’s truly when we are “perfusionists”. The ability to adapt to rapid change, think through a previously unencountered problem, and still keep your heart in your chest- is what makes us all so special. Anybody that’s been in the field for a period of time has been in the zone. That’s a cool place to be. But ALL of us, have hovered outside of it as well.

Eventually it boils down to consistency and “showing up” every day. You have to love this profession or you might as well leave it. I am proud of the field, and very proud of the friends and colleagues I have met doing the same job.

On o6/22/2011, Teutonic wrote:
Well Josh that wraps it up. The interview is done, but it feels like a beginning in terms of having gotten to know you, and seeing the kind of person you are.

I have learned a lot , and I thank you for your time, effort, and your contribution to all of us who pray for you, but but can’t be you.



Safe Journey to You & Yours …

Sincerely,

Frank Aprile, BBA, LP, CCP

AND THE GOOD SAGA CONTINUES...

14 November 2010

EVERYDAY LVAD and Dr. Naka / Dr Deng's Book

My Life With The LVAD is not any different than those featured in the book or those in the future that will need this modern day miracle. An everyday miracle that folks like Dr Oz, Dr Naka, Dr Deng, Dr Takayama and all LVAD/Transplant surgeons strive to perfect even further. Thank You

AND THE GOOD SAGA CONTINUES...
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18 October 2010

TO SUBWAY PLATFORM My LVAD HAD TO CLIMB 2 STEEP FLIGHTS OF STEPS

2 flights like pictured, one right after another and not outta breath!

And The Good Saga Continues...
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29 September 2010

The General's General, The One You Want Leading The Good Fight For Your Cause.


Margaret Flannery was the first from "LVAD Nation" to meet with me and my wife. With patience Margaret explained in depth about the LVAD implant, the peripheral procedures and testings involved in order to become eligible.

Her confidence, professionalism and approachable demeanor made my decision to trust Columbia Presbyterian Hospital to perform the open heart surgery/LVAD implant very easy. A short time later Margaret made my decision even easier by bringing in Dr Naka, the surgeon who would perform the surgery. Both Dr Naka and Margaret showed me a replica of the HeartMate II LVAD. I was able to hold it and realized that this device would bring back most of the stamina that I had lost. I felt that the 2 of them were the Best of the Best Columbia had to offer.

10 months later, LVAD in place, from the bottom of my LVAD I am thankful that folks like Margaret and Dr Naka are affiliated with Columbia Presbyterian hospital.

And the good saga continues...

27 September 2010

2nd LVAD LUNCH AND LEARN


2nd LVAD LUNCH and LEARN... They are great as it focuses on the
LVAD recipient/patient/care-givers/Families ONLY!

The last one pulled in over 20 LVAD recipients. I am hoping more of us is there.

And the good saga continues...

26 September 2010

Large LVAD Community Cheering Vice President Cheney

After attending the HeartMate II Ambassador Summit in Pleasanton, California, I was constantly asked how VP Cheney is faring. I only know as much as the rest. My knowledge of VP Cheney's recovery is as good as what's being released in the media. In an earlier post, I cited remarks made by his daughter, Liz Cheney and linked a radio interview that she made, where she stated that her Dad is doing well.

I would just like to express that there will be a day, maybe now, that Former Vice President Dick Cheney will become an LVAD Recipient, rather than an LVAD Patient. That threshold is realistic and obtainable. It is a point in that person's life that he or she says, "Yes, this LVAD has restored my life and stamina to where it was years ago. I do have restrictions however it is a wonderful trade-off to feel this good.

So again from the bottom of our LVADs, the LVAD community wishes Vice President Cheney a happy recovery.

And the good saga continues...

24 September 2010

“What can we do to make THORATEC better?” My answer was “ Build ALOT more LVADs. Save more lives”

Every since the LVAD was implanted in me, I have adopted the phrase “And the good saga continues…”. So all along my “good saga”, THORATEC has proven time and again that it is an organization that is sincerely committed to their visionary mission of saving lives. They are manufacturing a product whose “end users” are in different stages of heart failure, in which mine is End-Stage Heart Failure.


In more ways than THORATEC may ever know, their product, the HeartMate II is a gift… a gift of life, and life is the most precious commodity anyone can have.

THORATEC has proven to me that they are always looking to improve an already well-run organization. They go to extreme and tedious lengths to reinforce quality control at all levels in creating the components of the HeartMate II.

The participants of the Summit were treated to a tour of THORATEC’s manufacturing plant where I found employee morale to be comprised of pride and accountability. The participants of the summit were also engaged in a round of discussions to assist THORATEC in their future decisions and directions.




And I can say from the bottom of my LVAD that each summit participant took pride in answering any questions THORATEC posed as we all knew that sharing our experiences, giving our opinions and ideas will better the quality of life of future LVAD patients and their families.

One of the easiest questions asked of me was “What can we do to make THORATEC better?” My answer was “ Build ALOT more LVADs. Save more lives” ;-)

Being a participant at THORATEC's HeartMate II Ambassador Summit has been a phenomenal experience I will never forget.

Thank you THORATEC… from the bottom of my LVAD… each and every employee.

18 September 2010

I am who I am TODAY because of a lot people and their passion. Let's start here...



This Wednesday at 5am, My Wife, Rosie and I are flying off to California.

We are attending Thoratec's HeartMate2 Patient Ambassador Summit 2010. We are honored and looking forward to sharing what we will learn once we come back.

Posted in the photo is part of LVAD NATION from Columbia Presbyterian Hospital in Manhattan... I am who I am now because of them and would like to thank the ENTIRE staff there.

Not pictured are Margaret, Donna and the many doctors & nurses that saw me through surgery and recovery. L to R Rosie, Jennifer, Anne Marie, me and Khristine... pictures of Margaret and Donna soon to follow.

And The Good Saga Continues...

24 August 2010

Palimed.org Adresses The LVAD

I only knew the Left Ventricular Assist Device (LVAD) existed just one week prior to my LVAD implant / surgery. 11 days later... I was home with my LVAD in front of my computer looking up the Who, What, When, Where, and Why of the LVAD.
One of my first interesting finds about LVAD usage was from http://www.pallimed.org/
This website is run by a group of passionate Medical Professionals who happen to be practicing physicians within The Hospice/Palliative Care field. The Pallimed's website offers ideas, debate and methodologies of their work within... allowing seriously ill people to live with dignity, control and freedom of choice; all in an effort to offer Quality Of Life... throughout their serious illnesses at the end stages of life.

Having an LVAD and experiencing a healthy existence, again, I can only imagine that the LVAD will prolong many lives that otherwise would have expired just a few years ago.

However, it does not stop there. The same Doctors and Medical professionals that run PalliMed's website and Blog are also spearheading Hospice and Palliative issues via Social Media/Networking. They can be found on Facebook, twitter...
Below are direct links to Pallimed's
articles mentioning the LVAD :
Pallimed: A Hospice & Palliative Medicine Blog: Destination LVADsNov 12, 2008 ... We see a LOT of LVADs at my hospital. They truly can be a bridge to better things--but often they are a "bridge to nowhere". ...
http://www.pallimed.org/2008/11/destination-lvads.html

Pallimed: Case Conferences: November 2008Nov 13, 2008 ... Most recently, she went to the OR to have her current LVAD replaced with a ... Patients on LVADS or BIVADS are physically restricted... http://www.pallimed.org/2008_11_01_archive.html

Pallimed: A Hospice & Palliative Medicine Blog: Heart failure ...Aug 27, 2007 ... LVADs, in the simplest terms, are implantable devices which augment the pumping ... Full-sized LVAD image (& further discussion) at WebMD, ...
http://www.pallimed.org/2007/08/heart-failure-devices.html

Pallimed: A Hospice & Palliative Medicine Blog: Rise of the MachinesDec 10, 2009 ... For those of you unfamiliar with LVADs, essentially they are .... Personally, I'd take the LVAD, at least at a younger age (and if you are ...
http://www.pallimed.org/2009/12/rise-of-machines.html

Pallimed: A Hospice & Palliative Medicine Blog: Holiday HeartAug 15, 2010 ... At the time, LVADs were used only as a bridge to heart transplant. ... The number of patients receiving a LVAD as a bridge to transplant or ...
http://www.pallimed.org/2010/08/holiday-heart.html

Pallimed: A Hospice & Palliative Medicine Blog: Pall-PourriDec 3, 2008 ... Many of the cases submitted this year for the Annual Assembly case conferences were on LVAD's. We ended up selecting one. December 08, 2008 ...
http://www.pallimed.org/2008/12/pall-pourri.html

Pallimed: A Hospice & Palliative Medicine Blog: 09_12Dec 1, 2009 ... For those of you unfamiliar with LVADs, essentially they are implanted pumps which are inserted directed into the heart and major vessels ...
http://www.pallimed.org/2009_12_01_archive.html

Pallimed: A Hospice & Palliative Medicine Blog: 07_08Aug 3, 2007 ... Journal of the American College of Cardiology has a trial looking at left-ventricular assist devices (LVADs) as destination therapy in ...
http://www.pallimed.org/2007_08_01_archive.html

Pallimed: A Hospice & Palliative Medicine Blog: NYT Sunday ...Jun 20, 2010 ... I come across these situations fairly often working at a large hospital where the heart transplant and LVAD services are quite aggressive. ...
http://www.pallimed.org/2010/06/nyt-sunday-magazine-turning-off.html

Pallimed: A Hospice & Palliative Medicine Blog: 08_12Dec 3, 2008 ... JAMA has a paper looking at some aspects of the 'natural history' of LVADs (see recent post). The paper adds some further detail to the ...
http://www.pallimed.org/2008_12_01_archive.html

Pallimed: A Hospice & Palliative Medicine Blog: Quality vs ...Aug 15, 2008 ... LVAD, improved symptoms and survival, lots of care burdens, lingering death). The basis of this seems to be several trials of oral inotropes ...
http://www.pallimed.org/2008/08/quality-vs-quantity-of-life-in-chf.html

Pallimed: A Hospice & Palliative Medicine Blog: 07_01LVAD anyone? The other talk that looks pretty interesting to me is the one on Pain Research, although I hope it does not get to bogged down in discussions ...
http://www.pallimed.org/2007_01_01_archive.html
And the good saga continues...

AS THE LVAD SPINS... The LVAD Links Its Recipients Into A Special Community



Since i started this blog, folks come to me with questions about the LVAD. By no means am i an expert, nor medical professional. I am a very lucky man with an LVAD implant and it is grafted to my heart. The LVAD, Heartmate 2, has given back to me what the Heart Attack took away!


Ever since the NEWS broke about VP Cheney receiving an LVAD as well, my email inbox and phone messages are SWARMED by the question HOW IS VP DICK CHENEY?


I wish some words or signals came out of his camp. But i do understand his need for privacy... as I do enjoy my privacy as well. I can only guess that he is doing well and following the course set for him and his condition by his team of Doctors... We hope and pray he is well, but am comfortable in knowing he is in great medical hands... no doubt!

Again The LVAD community sends its BEST wishes and Prayers out to Vice President Dick Cheney! Keep Strong in body and mind!!!

And the good saga continues...

11 August 2010

One Spin At A Time, A Day In The Life Of A Lucky LVAD Recipient. No Rodeo Yet!

With The LVAD, we must listen to our Doctors and Nurses and KNOW our own limitations and safety concerns while keeping active. Common Sense ABOVE ALL!

Here I am riding an old gentle horse name Delores. I mounted her via a concrete platform with steps, like a loading dock. i did not climb up on her as I would have normally done without the LVAD. On my ride, I was joined by a guide, my wife and daughter.

Everyday I am finding new reasons to love and respect my Heartmate2 LVAD!


Me, Myself and My LVAD, getting to ride Delores on a slow and easy run. No Rodeos yet!

Take Note: The LVAD battery wire (gray) exiting the controller :-)

And the good saga continues...