HCM-ers: Introduce yourself or just say hi
Welcome to the Hypertrophic Cardiomyopathy (HCM) group on Mayo Clinic Connect - a place where you can connect with others, learn about living HCM, share experiences and exchange useful information.
I invite you to follow the group. Simply click the follow icon
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I'm Colleen, and I'm the moderator of this group, and Community Director of Connect. I look forwarding to welcoming you and introducing you to other members.
Why not start by introducing yourself here?
Interested in more discussions like this? Go to the Hypertrophic Cardiomyopathy (HCM) Support Group.
Connect

I was a HAPPY camper in my recliner. Just shows what works for one, and not the other. A day short of 14 weeks out of my myectomy.
Hi @ataylor8668 - Sorry you have to have surgery, but glad you are going to a great place.
I did buy myself a recliner for after surgery, and honestly, I found I didn't need it. I slept better propped up with pillows and sleeping partially on my side on the couch. In fact, at Mayo I had a suite and found the sofa more comfortable for sleeping than the bed.
I wrote a blog about my myectomy experience at Mayo which you may find interesting, though it has been quite a few years ago now:
http://www.cynthiassummeradventure.blogspot.com
I have started a new blog that is generally about HCM which has a page of resources about preparing for myectomy which you also may find interesting:
https://hcmbeat.com/resources/resources-for-patients-about-myectomy/
Wishing you all the best as you go forward. Let us know how we can help advise you further.
Welcome to Connect HCM, @ataylor8668.
You've come to the right place to get your questions answered about your upcoming HCM surgery at Mayo Clinic. You'll notice that I moved your message to the introductions thread so you can meet other members like. Allow me to introduce you to a few others who have had surgery at Mayo. Please meet @cynaburst @lynnkay1956 @PatMattos @janicepike @ronaldpetrovich @mbcube
@lisa7 @vivian88 and so many others. They can help answer your recovery questions.
You may also wish to read this discussion thread: "What is the recovery like following septal myectomy?" http://mayocl.in/2fdCxHz
Good question about the CPAP machine and surgery. @dawn_giacabazi might have something to add about that in particular. You can also find additional discussions about CPAP in the Sleep Health group: http://mayocl.in/2kSSYM6
Good afternoon all. I am a 45 yr old male who was diagnosed about 2 years ago with HCM. Things have progressed to the point that I am having/need the surgery. Have to admit I am a bit terrified, but know I am in Great hands at Mayo. I have also had a couple major surgeries for some unrelated issues, so I have a general sense of the hospital experience.
I have had a history of back problems, and from reading this board, seems like this is a common struggle post surgery. I am thinking I need to go out and buy a recliner to sleep in when I return home....any advice from those who have gone through the recovery process? I have sleep apnea, and do use a CPAP, but have never been able to sleep flat on my back, so I am trying to get something worked out before the procedure.
This all became real this past week, so I am reeling a bit and sure will have additional questions....so thanks in advance for your help.
Cheers
I've had the loop for about 1 year 5 mouths... it has shown af, tackiecardia and bradycardia, eptopic beats,. (sorry for spelling). I fill my heart 24hours a day, more at nite when I'm in bed... when I got the loop fitted it only took them 10 mins... so much better then wearing a monitor... I tell my docter every thing.. but I'm not sure he hears what I say... (but I may be wrong)
Yes. I've been gene tested.. I'll check that page out now.. many thanks. 🙂
I do not have an obstruction, I had to go on line to find a docter. But I found one,and he's only 2 hours way so not to bad... thanks. 🙂
@traceysmith Well put! Thanks for sharing about your loop recorder. Not to worry about spellings - we all understand what you are saying! Teresa
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2 ReactionsHello, and welcome, Tracey. I was misdiagnosed for 23 years, so I can relate. I agree, if you can find one of the HCM specialists in the UK, that is where you should be. You can check out http://www.4hcm.org and they can help you find someone. This disease is quite the challenge for those of us who have it, that's for sure. It is so easily misdiagnosed and we, particularly women, get patted on the head and sent home. Been there, done that.
I presume you were gene tested and they found one of the HCM genes, correct?
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1 ReactionWelcome Tracey, welcome to the site. I think you'll find the site can help you relate to others who are going through similar experiences. I'm 56 , was diagnosed with HCM two years ago and also had a septal myectomy at Mayo Clinic. The surgery changed my life. (full disclosure, I work at Mayo in Communications) It worked and I feel better than I have in years. I never blacked out but had shortness of breath and extreme fatigue and always felt like my heart was working way too hard.
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