Familar Surroundings
Posted , 9 users are following.
Hi
Does anyone else get paniky and anxious when going out of their familar surroundings? After being diagnosed in November with large PE in both lungs I have been trying to go out and about a little and recently been wanting to go further than the village we live in, however once we get out of familar surroundings I can feel myself getting anxious and just wanting to get home.
1 like, 21 replies
Cocochanel2910 debby01
Posted
Hi Debbie, yes I do too, and like you I had massive clots in both lungs ! It's scary the thought of it happening again! My main problem is the breathlessness and chronic fatigue .. it's so depressing. I hope you get better with time .. mine was a year ago!!
debby01 Cocochanel2910
Posted
Hi Cocohanel2910
I get the feelings of chest heaviness, a bit breathless, rapid heartbeats and just feel horrible, it is really frustrating.
I hope you are get better too, they say it can take ages to feel 'normal!'
Cocochanel2910 debby01
Posted
I feel as though I'm going to be like this forever .. my life has changed dramatically.. it doesn't matter how much rest I get I still feel tired and out of breath even after short walks ...
debby01 Cocochanel2910
Posted
I totally understand how you feel. I used to love going out walking and cycling, now I hardly go out and feel like I am never going to get back to something how I used to be.
I have another CT scan this Friday to see if the clots have dispersed at all and I am getting pretty nervous about it, I want it to be good news but the way I feel at times makes me think otherwise.
Just have to try and keep positive
Cocochanel2910 debby01
Posted
Cocochanel2910
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hi Debbie I hope they've gone .. mine have so I can't understand why I'm like this ... fingers crossed for you and all the people like us ..
debby01 Cocochanel2910
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Hi Cocochanel
Thank you
I am so happy for you that your clots have gone, it could be because your body has gone through a major trauma and it does take time to heal both physically and emotionally. I am sure that given time you will be back to your normal self.
Take care x
Sway Cocochanel2910
Posted
debby01 Sway
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lizzie70061 debby01
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debby01 lizzie70061
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I was diagnosed in November but had ben feeling bad for about a month before and was getting worse, kept getting told it was viral or anticbacterial before finally being diagnosed.
Now I get feelings of rapid heartbeats, a little breathlessness, and generally felling horrible, this also comes on when I am at home and for no apparent reason
Sway debby01
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Windy8000 debby01
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ann55375 debby01
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My bilateral p.e's were three years ago. Been on warfarin since then but have developed anxiety too about things which didnt bother me before. I am considering apixaban as dr says i wont need inr checks. I am looking for anyone with experience.
lizzie70061 ann55375
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Windy8000 ann55375
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My rivaroxaban there are no one check ups either but I still worry because I have had bariatric surgery and don't absorb medications normally. That's why I have to take 3 vitamins a day 7calcium pills, b-12 shots, 100,000 units of vit D a week. Yet the Dr is sure the 1 20 mg pill is absorbing correctly. I don't absorb vitamins from my foods I eat just the calories. My iron is low.
Forgive me Doc if I just don't trust you.
lizzie70061 Windy8000
Posted
I agree with you. it is so hard to trust someone when your body and instinct is telling you something else. Enjoy your vacation 🌴. x
ann55375 Windy8000
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i have read a lot of bad reports about these new thinners and at present am of a mind to stay on warfarin. You are right, dont trust drs as they have messed me up too much over trying out meds and making me worse
debby01 ann55375
Posted
I am Apixaban twice a day and have been since being diagnosed in November.
It seems to be working well and I have not had any side effects.
I am suffering with anxiety too and it is difficult when your body is going through these problems and trying to cope and recover.
Take care x
ann55375 debby01
Posted