post viral symptoms
Posted , 7 users are following.
Hi guys,
I just wanted to ask people about their symptoms. About 5 months into this life debilitating illness I am scouring the internet for answers to my own problems with it and not finding much. So does anyone else have the feeling in their chest, that their heart is not right ? That it is being suffocated, that solely because of this you cannot do what you did before ? It's like there is this blockage around my heart energy and it's being supressed. Out of all the symptoms I have experienced this is now the most noticeable and most persistent and I absolutely hate it. Anyone else get this ? I know prior to becoming unwell I was fully vibrant and lived from the heart and life was enjoyable, now this has been taken form me and I feel like my heart has turned to stone. I'd like to know if anyone can find anyone else having a similar experience ? Is this a nervous system disorder ? Or something else ? thanks for reading.
0 likes, 12 replies
dawn97
Posted
Then get some counciling to help you come to terms with being ill ( it helps to get it straight in your head !!) it doesn't cure you but will help you in the long run
Good luck x
david59662
Posted
mike76241
Posted
panic a bit when things seem desperate,
a heart specialist had me on a treadmill
for an hr, which made my cfs/me problem considerably
worse, and took me 3 months to get over, and no heart problem
then to an allergy specialist again no result, reading all other posts
notice this dry mouth/nose/ throat is common, I used to carry a small
plastic bottle with cold water as a spray to use in summer, and winter in a central heating
environment, and ginsing to get through a long day/drive home, small benefits
but might help
susie_63109
Posted
Gizmo1963
Posted
Yes, what Suzie says is exactly what part of my symptoms have been. I had palpitations and tightness in my chest and at one point I was convinced I was having a heart attack. It turned out I was suffering from high blood pressure (up to 174/115 at one point) and high cholestrol 7.6. I am now on beta blockers to control this plus it helps me have lfewer migraines.
sue81694 david59662
Posted
david59662
Posted
I've NEVER had this prior to becoming unwell, my eyes were always big and bright and clear. Definetely eyesight is being effected, eyes are slower to react.
tori7494 david59662
Posted
david59662
Posted
Does anyone also get bloodshot eyes, it comes and goes ? Sometimes right eye sometimes left ?
bigroat david59662
Posted
This sounds very familiar to what my wife describes. All the literature on ME and CFS doesn't quite fit for her nor does fluttering heart descriptions. But this description you have given in your your initial post is spot on. She has been like this for 3 years now... very slowly getting better but for about two years it was just unbearable for her. How are you getting on 5 months along the road? Did you manage to find any solution. She hasn't yet. She used to walk faster than I could ever keep up and would dance and talk using huge arm movements but now she is trapped. Whenever she forgets and becomes her old self again she gets ill again in a bad way. Can't do anything but lie down and wait it out. On occasion something does work for her is performing the valsalva manouvre... not sure why it works... doctors insist nothing wrong with her heart... losts of tests with nothing to show.
Elle1234 david59662
Posted
Hello David,
I was wondering are you feeling better? I have been diagnosed with post-viral symptons too. I wonder if there was any light at the end of this tunnel.
Best wishes,
Elle.
david59662 Elle1234
Posted