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Experiences with
Arrhythmogenic right ventricular cardiomyopathy (ARVC)
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Guilty pleasures
I have had chronic pain for years so I have an electric bed, sauna with monochromatic light therapy and hot tub. All awesome ways to treat whole body. The lighting also a good source of vitamin D. I agree with electric blanket as well. I get chills from low grade temps.
I have had chronic pain for years so I have an electric bed, sauna with monochromatic light therapy and hot tub. All awesome ways to treat whole body. The lighting also a good source of vitamin D. I agree with electric blanket as well. I get chills from low grade temps.
Damaged
in
NRAS
8 years ago
Hormones?
Hello I asked a month or so back for some advice re my daughter and her post lap treatment options - she was advised to have the hormone injection but we have resisted due to her young age (19) and she was put on the pill she has not been getting on with it or the painkillers she was prescribed. We
Hello I asked a month or so back for some advice re my daughter and her post lap treatment options - she was advised to have the hormone injection but we have resisted due to her young age (19) and she was put on the pill she has not been getting on with it or the painkillers she was prescribed. We
Andrea67
in
Endometriosis UK
8 years ago
Waking up with ectopics
Hi everyone. So unfortunately I've been having quite a bit of ectopic activity today. It was quite different this time because I awoke with the ectopic beats, whereas normally they don't come on until much later in the day. Still having them now (quite sporadic) and I'very noticed that I'm having bigemyny
Hi everyone. So unfortunately I've been having quite a bit of ectopic activity today. It was quite different this time because I awoke with the ectopic beats, whereas normally they don't come on until much later in the day. Still having them now (quite sporadic) and I'very noticed that I'm having bigemyny
micwal93
in
AF Association
8 years ago
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Alternative therapies
Just a little update. I'm starting to taper to 5 mg prednisone, continue to benefit from low intensity light therapy offered by a physiotherapist, plus my good diet (low refined carbs, high whole foods) and varied exercise regimen. I also actively avoid stressful situations. This is a taper using
Just a little update. I'm starting to taper to 5 mg prednisone, continue to benefit from low intensity light therapy offered by a physiotherapist, plus my good diet (low refined carbs, high whole foods) and varied exercise regimen. I also actively avoid stressful situations. This is a taper using
HeronNS
in
PMRGCAuk
8 years ago
Progress report from alternative treatment front
Just a little update for those who have been following my guinea pig treatments with low level light therapy for PMR. I appear to have successfully tapered to 6 mg prednisone and am now starting a taper to 5.5. As before, depending how things go, I may try to cheat the system halfway through the taper
Just a little update for those who have been following my guinea pig treatments with low level light therapy for PMR. I appear to have successfully tapered to 6 mg prednisone and am now starting a taper to 5.5. As before, depending how things go, I may try to cheat the system halfway through the taper
HeronNS
in
PMRGCAuk
8 years ago
My flecinide experience
I have been on flec for a few years now. O had PVC's in the thousands on a three week halter monitor. Couldn't control them on a variety of meds. Went to a different cardiologist, he put me on flec 50 mg twice a day. Ineffective. Increased to 100 mg twice a day. Huge improvement. Recently went to
I have been on flec for a few years now. O had PVC's in the thousands on a three week halter monitor. Couldn't control them on a variety of meds. Went to a different cardiologist, he put me on flec 50 mg twice a day. Ineffective. Increased to 100 mg twice a day. Huge improvement. Recently went to
william66
in
AF Association
8 years ago
A little light therapy info
I keep trying to find information about low intensity light therapy and polymyalgia, and here, at last, is something: http://www.chewvalleylaserclinic.co.uk/clinic_team.htm
I keep trying to find information about low intensity light therapy and polymyalgia, and here, at last, is something: http://www.chewvalleylaserclinic.co.uk/clinic_team.htm
HeronNS
in
PMRGCAuk
9 years ago
Autoimmune Diseases
The Immune System Before looking into autoimmune diseases themselves, it’s important to have an understanding of the system that it affects. The immune system is a combination of the organs, tissues, cells and associated process that provide resistance and protect the body from pathogens that can otherwise
The Immune System Before looking into autoimmune diseases themselves, it’s important to have an understanding of the system that it affects. The immune system is a combination of the organs, tissues, cells and associated process that provide resistance and protect the body from pathogens that can otherwise
Maria-Light
in
Women's Health
9 years ago
Light therapy update
So, as some reading this will already know I've been getting low level light therapy as an experiment to help reduce inflammation. It had seemed helpful as I reduced from 8 to 7 mg, but no way really to know if the LLLT was helping or if I would have been okay anyway. Over Christmas there was a bit
So, as some reading this will already know I've been getting low level light therapy as an experiment to help reduce inflammation. It had seemed helpful as I reduced from 8 to 7 mg, but no way really to know if the LLLT was helping or if I would have been okay anyway. Over Christmas there was a bit
HeronNS
in
PMRGCAuk
9 years ago
Chest pain 😟
Well this started 2weeks ago and I think I have had maybe 4days out of the two weeks I have felt normal. "Meanin no chest pain" they tell me they are PVCs but they hurt. I am going in for my first stress test tomorrow so wish me luck. I hope they find out what's wrong. This is very uncomfortable and
Well this started 2weeks ago and I think I have had maybe 4days out of the two weeks I have felt normal. "Meanin no chest pain" they tell me they are PVCs but they hurt. I am going in for my first stress test tomorrow so wish me luck. I hope they find out what's wrong. This is very uncomfortable and
NeffBritPerez
in
AF Association
9 years ago
complications :-(
Evidently when they had problems removing the sheaths from my groin they created some bruising and trauma in that area. Had problems walking and constant pain in my right leg after I got home. Went to see the EP on Friday concerning an issue with the bleeding but didn't feel the leg was worth mentioning
Evidently when they had problems removing the sheaths from my groin they created some bruising and trauma in that area. Had problems walking and constant pain in my right leg after I got home. Went to see the EP on Friday concerning an issue with the bleeding but didn't feel the leg was worth mentioning
paulh1
in
AF Association
9 years ago
PVC'S?
About 2 weeks I starting getting a very bad pinching feeling in my chest and I couldn't breath to well. I went to the ER and they said I was having PVC'S. Is there anything that cause PVC to just start? I'm scared cause it hurts and they have not told me why I am having them or if they will hurt me.
About 2 weeks I starting getting a very bad pinching feeling in my chest and I couldn't breath to well. I went to the ER and they said I was having PVC'S. Is there anything that cause PVC to just start? I'm scared cause it hurts and they have not told me why I am having them or if they will hurt me.
NeffBritPerez
in
AF Association
9 years ago
Associated symptoms of PVCs
Does anyone with these suffer from nausea, lightheadedness and frequent bouts of pins and needles in hands and feet? Looks as though I have PVCs from my last Alivecor reading . Saw doc last week who thought some of these symptom is the excessive wax in my ears. Waiting for results of Holtor monitor
Does anyone with these suffer from nausea, lightheadedness and frequent bouts of pins and needles in hands and feet? Looks as though I have PVCs from my last Alivecor reading . Saw doc last week who thought some of these symptom is the excessive wax in my ears. Waiting for results of Holtor monitor
Stephanietee
in
AF Association
9 years ago
Paroxysmal Atrial Fibrillation on Eliquis
Background: Some where around 20 years ago I was told that I had benign PVC's and was given Metoprolol 25mg twice a day. Eight years ago I had a coronary angiogram done and everything looked good and was told I had good heart function. Recently I started having lightheartedness, low energy and something
Background: Some where around 20 years ago I was told that I had benign PVC's and was given Metoprolol 25mg twice a day. Eight years ago I had a coronary angiogram done and everything looked good and was told I had good heart function. Recently I started having lightheartedness, low energy and something
AAB13X2L
in
AF Association
9 years ago
light therapy. does it help?
just purchased a light therapy box and started using it. Been having trouble sleeping for months and I would really like to get some rest at night. Has anyone used one before and does it help? thanks
just purchased a light therapy box and started using it. Been having trouble sleeping for months and I would really like to get some rest at night. Has anyone used one before and does it help? thanks
Kainan
in
Mental Health Support
9 years ago
Ectopic beats and oxygen levels
Hey all, new to the forum and have read a couple of the threads so know what your all going through but I do have a couple of questions. I'm getting these ectopic beats what feels like more frequently then I blink, they are highly annoying and uncomfortable. I don't know if it's PVC or PAC and don't
Hey all, new to the forum and have read a couple of the threads so know what your all going through but I do have a couple of questions. I'm getting these ectopic beats what feels like more frequently then I blink, they are highly annoying and uncomfortable. I don't know if it's PVC or PAC and don't
Nikos1985
in
Arrhythmia Alliance
9 years ago
Skins on fire
Hi everyone, Ive recently reduced and stopped the prednisalone I was on for 11 months as I have an autoimmune disease (Wegners) WG. My skin has gone ballistic, my whole body has erupted with psoriasis , forgot to say I've had psoriasis for 35 yrs, its usually pretty well controlled but now its horrendous
Hi everyone, Ive recently reduced and stopped the prednisalone I was on for 11 months as I have an autoimmune disease (Wegners) WG. My skin has gone ballistic, my whole body has erupted with psoriasis , forgot to say I've had psoriasis for 35 yrs, its usually pretty well controlled but now its horrendous
Llinos
in
Beyond Psoriasis
9 years ago
Report from the alternative treatments frontline
I have been getting low intensity light therapy about two times a week for several weeks. This morning I woke up with a sore back and after thinking about yesterday's activities decided it was a short trip into the library with an unexpectedly heavy box of books I was donating that had triggered the
I have been getting low intensity light therapy about two times a week for several weeks. This morning I woke up with a sore back and after thinking about yesterday's activities decided it was a short trip into the library with an unexpectedly heavy box of books I was donating that had triggered the
HeronNS
in
PMRGCAuk
9 years ago
Low level light therapy - report from a guinea pig
I have now had two low level light therapy treatments. The first one was just over twenty minutes with LED light applied to my lower spine. I felt pretty well after that and noticed an unexpected effect - I've long had a tender area where my two vertebrae are that are affected by OA , and that area
I have now had two low level light therapy treatments. The first one was just over twenty minutes with LED light applied to my lower spine. I felt pretty well after that and noticed an unexpected effect - I've long had a tender area where my two vertebrae are that are affected by OA , and that area
HeronNS
in
PMRGCAuk
9 years ago
Can any one help me?
Hello ,I will try to make this as short as posible(!?) .. I have multiple autoimune issues ,SLE,Hashi's ,Sjogrens,APS ,fibro,+++++and multiple allergies and intolerances to meds and foods .I am dairy free .gluten free ( no grains at all) yeast free and I don't cheat as I can become very ill.it's not
Hello ,I will try to make this as short as posible(!?) .. I have multiple autoimune issues ,SLE,Hashi's ,Sjogrens,APS ,fibro,+++++and multiple allergies and intolerances to meds and foods .I am dairy free .gluten free ( no grains at all) yeast free and I don't cheat as I can become very ill.it's not
Mrsoverall
in
Pernicious Anaemia Society
9 years ago
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