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  on the group landing page.Â
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.
Thanks for the response. I am planning on having my teeth looked at by my dentist in the next week or so (if he can squeeze me in) as I was scheduled for July- which is too soon after the surgery. Think I will invest in a recliner. Thanks
They do this all the time. Grrrrrrr.
I want to bring up the real facts on teeth cleaning, and having a colonoscopy. I am 14 weeks out, and was under the impression that I could get my teeth cleaned after 3 months. Especially after spending thousand dollars and more on periodontal disease before the surgery. It was quit the fiasco going back and forth with the dentist office, and finally getting to the real reason and truth behind the reasoning. I was told that they don t want you to have anytjing done for 6 months. Not to risk any infection. The same goes for a colonoscopy. I am contacting Mayos patient advisery people to hopefully put it in the guides, for after surgery.
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. 🙂