HCM with no options for medication for relief of symptoms
I have HCM (without blockage) and I am not a candidate for the new medication (Camzyoz?) and no other medications relieve my symptoms (channel/beta blockers or Lasix). I’m wondering how others manage the symptoms of fatigue, shortness of breath, and chest pain. Sometimes I can’t even make it to my mailbox without having to sit down. Other times, it’s ok. Sometimes my heart rate goes up to 120 bpm just due to getting dressed for work. It’s all very scary. I find myself becoming more anxious and definitely depressed.
Can anyone relate?
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I’m fairly certain I have had a few bouts with afib. I just don’t know how bad it is supposed to get before I go to hospital or address it with my doctor. My Apple Watch keeps up with it. I have 4% afib in some days, so perhaps that isn’t severe enough? It is so incredibly unpredictable
Great you’re feeling better. What medications are you currently on?
I am taking dofetilide (tikosyn) and so far so good. I know antiarrhythmic drugs often stop working, but am hoping this doesn't happen. Am also taking Eliquis as is a must for Afib, especially with hcm and aneurysm.
I have started taking my blood pressure and it’s rather low at times. I’m wondering if I have hypotension? Also wondering why Lasix is ineffective at removing the suspected fluid around my lungs. Anyone have this experience?
My Doc had me on Bisoprolol 5mg 2x, Amlodipine 5mg, Rythmodan 100mg up to 3, Mestinom 100mg. These are the Meds I was put on to control my pain before Camzyos.
I don't see that anyone has answered your specific question. I am sorry you are not a candidate for Camzyos since it really has helped me so much with all the symptoms you describe. I am so sorry you experience these symptoms and don't have any answers. I am concerned about your chest pain specifically and hope you tell your doctor about your chest pain. I also wonder if you ever go to ER for an ekg when you are feeling this way. Thinking of you and hoping you find answers.
I have heard good things about Aficamten. I am asking my cardio team about it too.
My situation sounds similar to yours no concerning obstruction gradient, EF “normal” and I too am inquiring about Aficamten. Have you had a cardiac MRI? This is newer diagnostic tool that is correlating extent of fibrosis with symptoms/prognosis which was eye-opening but makes a lot of sense in my case. I had a ”primary prevention” ICD for years with minimal symptoms. Last few years I’ve become way more symptomatic and more often which like others have shared significantly impacts QOL. I feel like I have lost so much of my life and dreams bcz of this so I’m inquiring about septal myectomy which I would onmy do at Mayo or see about Aficamten
Hi,
I’ve become more symptomatic as well and my doctor has prescribed a stronger diuretic (Torsemide) for water retention. I just finished the clinical trial screening for Aficamten and waiting to see if I qualify. It’s a double blind study with a 50% chance of being placed on a placebo.
Where do you live and who is your provider? I’m in Atlanta and use Emory, but the study is being conducted at sites all over the country and they are actively enrolling.
Are you taking metropolol? My heart was scooped out by Dr. D'allesandro at Mass General. I was lucky. They found mine very early.