Discussions: Living with an LVAD

Has anyone out there in LVAD land been successful in changing their own driveline dressings and if so, please pass along how you do it. I can only get so far before I have to let my wife finish the job. I currently do a sterile dressing change but am having a hard time lining up the tagaderm and...

If a LVAD recipient is doing some heavy physical activity like running, gyming or playing any sport, how does LVAD, which runs at constant speed, going to match the demand of blood supply. If it doesn't able to fulfill the requirement how does it going the affect the recipient? how dangerous it...

My name is Larrie and I’m Story Producer for a show called Life on Batteries, as well as an LVAD patient myself. I was hoping you could help me with research for an upcoming episode by sharing your experiences around emergency controller changes. This also may be a good discussion topic in itself,...

Lets get to it. The worst thing that can happen to an LVAD user is a drive line infection. It can put you in the hospital many times over and cures with the various antibiotics may or may not work for you. It can lead to extra surgeries for debridement and in some cases make it worse. In my case I...

My husband got his Lvad in September, 2019. Everything was going great without any problems until June, 2019. He came down with a slight fever and was not feeling well. He was still doing his exercises and everyday activities, but sleeping more and a sluggish. His driveline looked good so we knew it...

My husband received his LVAD Oct 2016 and although there’s been lots of highs and lows - we are grateful for the time he’s gained and still gaining ! However he has a lot of phlegm (sorry) and respiratory secretions that are getting worse . Has anybody else experienced these symptoms, he’s kind of...

Hello everyone, To have a great website like this can give hope and happiness for alot of people. My husband had his lvad 2 months back. And he have a C-rtd too. Still trying to adjust with his new life style. I have one question, i tried to google it but i couldnt find an answer for it, hopefully...

We seem to have issues with the anchors staying attached to the skin. Yes we clean with alcohol, let it dry, apply the skin barrier, let that dry and it still comes off. We have also tried with it with out the skin barrier after cleaning the skin with alcohol, and they still come off.

Has anyone figured out a comfortable way to get back behind the wheel? There has to be a better way than wearing the batteries on your hips. And how do I change from prospective patient to recipient?

Hi Everyone, I am new to this community but was wondering if anyone had tips about how to stay active while having an LVAD. I am currently looking for helpful advice on how to live a healthy and active lifestyle while managing an LVAD. Thanks!

Hi everyone! My name is Sophie and I am an industrial design student at the University of Cincinnati. I have recently been made aware from a close friend how difficult it is to live a healthy active lifestyle with a LVAD, and am passionate about using my education and resources to help alleviate...

My wife and I first got initiated to our lvad and heart transplant program at Oregon Health Sciences University by meeting the various teams who eventually would be treating me for the end stage of my 17 year battle with heart failure. We live about 100 miles from Portland, where the hospital is, so...

Now at age 70, living in the USA, I have to let my ten-year level term insurance expire because the rates were set to climb rapidly anyway. I have to search for a new company, maybe with much less coverage to keep my monthly or quarterly fees affordable, but I don't know if any company would take me...

Hello, My dad just got his HeartMate 3 six days ago. He obviously has a long road ahead of him, but I am trying to gather as much info and get things as ready as I can before he comes to live with me. My dad is a jack of all trades - he was a cop, a machinist, pilot, can build anything etc. My...

Something that I've been considering doing is getting a embroidered patch made so that my go bag is clearly marked as medical equipment. I feel that this is important since I actually use a LowePro Camera bag with padded compartments and dual shoulder straps for carrying my spare batteries,...

I have recently 'celebrated' 10 years of living with a Ventrassist LVAD here in the UK The machine's performance has been exemplary' I have heart failure again now so life is not at all easy Only difficulties haves been with obtaining batteries, medication and the weight of the machine itself...

Hello everyone. I am just now beginning to discuss the option on an LVAD with my cardiologist. I have had Dilated Cardiomyopathy for 15 years. Life was a breeze, cruising along at 35% EF, up from 20% at dx. However, the last year has been tough. My EF is now back to 20% and I've been hospitalized...

hi, I’ve had my lvad for 8months, had the surgery in Canada, then I’ve recently moved back to the u.k. I’ve not really met anyone with the lvad, it would be nice to swap stories, tips and chat about living with the device would be nice.

Hi Everyone, I am a RN Care Advisor that does case management for some patients with LVADs and I am trying to learn if anyone started having an increase in fatigue and SOB around year 4-5 with the LVAD and if there were any discussions/treatments/medications etc that improved it? Thanks again and I...

I am preparing for my LVAD surgery next month. Other than clothing, what types of supplies will I likely need to purchase for myself (not covered by insurance)? Are there additional products that people have made your life with a VAD easier that were not mentioned by your medical team?