L
LoraW30
Hello,
It's been a few months since I've logged in to this wonderful site. These last few months have been pretty hectic. Last November my stepdaughter was diagnosed with Hodgkins Disease and my husband and I have been keeping the interstate hot with trips back and forth to Children's in LR.
I have been fairly stable, going to the doctor every month until December. My doctor decided it would be less stressful to me if I didn't have so many trips to LR and didn't want to see me again for 3 months.
We've both realized what a mistake that was. Last week I had what one of my docs called a hypertensive crisis. I blacked out for a couple of seconds and apparently struggled for air. I spent two days in the hospital having ekg's, echoes, x-rays, and pacemaker checks to find out what happened. Well, we think because of my LV disfunction, my pulmonary pressures are getting higher.
Now, I've been given stricked instructions not to do ANYTHING. I can't walk around, do household chores, anything that would create stress on my heart. I now have a wheelchair for shopping excursions, and have been told to carry my O2 more. I don't know what's harder, just having PPH, or watching other people clean my house.
I've really missed the companionship and support of this site and plan on logging on more in the future. I hope everyone takes care.
Lora
It's been a few months since I've logged in to this wonderful site. These last few months have been pretty hectic. Last November my stepdaughter was diagnosed with Hodgkins Disease and my husband and I have been keeping the interstate hot with trips back and forth to Children's in LR.
I have been fairly stable, going to the doctor every month until December. My doctor decided it would be less stressful to me if I didn't have so many trips to LR and didn't want to see me again for 3 months.
We've both realized what a mistake that was. Last week I had what one of my docs called a hypertensive crisis. I blacked out for a couple of seconds and apparently struggled for air. I spent two days in the hospital having ekg's, echoes, x-rays, and pacemaker checks to find out what happened. Well, we think because of my LV disfunction, my pulmonary pressures are getting higher.
Now, I've been given stricked instructions not to do ANYTHING. I can't walk around, do household chores, anything that would create stress on my heart. I now have a wheelchair for shopping excursions, and have been told to carry my O2 more. I don't know what's harder, just having PPH, or watching other people clean my house.
I've really missed the companionship and support of this site and plan on logging on more in the future. I hope everyone takes care.
Lora