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check out the FAQ by clicking the
link above. You may have to register
before you can post: click the register link above to proceed. To start viewing messages,
select the forum that you want to visit from the selection below.
Your Participation in this message board is strictly voluntary. Information and comments on the message board do not necessarily reflect the feelings, opinions, or positions of the Hypertrophic Cardiomyopathy Association. At no time should participants to this board substitute information within for individual medical advice. The Hypertrophic Cardiomyopathy Association shall not be liable for any information provided herein. As a good practice screen names should not be "full legal names" as we can not full assure your privacy from search engines if your FULL name appears on the messageboard
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Long week!
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About the Author
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non-obstructed hcm, AICD 11-01-02 and 10-6-05
Find out more about Toogoofy317
Mary, I'm so glad your finally getting things figured out. I'm sorry that you have to deal with the shots and all of the rest of it and I will add you to my prayer list.
Is their a possiblity that the electric company has any programs to help you? In Oregon and I'm sure in other states there are ways to get help with utilities? Also is there any family that can help with financial assistance while you go thru this? Please forgive me if you have posted about these things in the past and I have forgotten.
I have faith that things will get better. It will just take a little while. My only problem now is finacial burdens. I have not worked in about a month and for some reason down in Florida money doesn't grow on trees. Prescriptions costed 80.00 and electric is due. I had to make a choice which kinda sucked.
I would kill for a REALvacation. Unfortunatly, it will have to be next year. Thanks for listening to me whining about my life. As my cardiologist reminded me there are people a lot worse than I am and I should be thankful that my heart condition allows me to be close to normal. Easy for him to say but at 22 it does become too much sometimes.
The docs believe it was a combination of an allergy to phenrgin and an infiltration. He said it could be cleared up though which is good news. I gave Dr. Maron a call today and see what his imput is on this mess. Especially as far as the CHF is concerned. They did start me on potassium as well just like you said Lisa mine dropped dramaticaly.
Right now I am going to sleep. I think every drug I am on right now has a side effect of dizziness and sleepiness. I can barely keep my eyes open! I'll let you know how things go as far as that other hospital.
Oh yeah the weather is a high of 88 without a cloud in the sky!
How I wish I were giving out good news like everyone else. But I guess when the time is right I'll have some.
At the advice of my primary physician I went to the ER on Monday night because I was not feeling any better. Well the news wasn't so great. Yes, I was in CHF only mild but still in it. My arm, well it has a ton of blood clots. Including partial occlusion of my jugular vein. I am not happy about all of this especially having to take three times the drugs I was taking. Having to inject a blood thinner into my stomach twice a day sucks and I am on coumadin for the next three months. I am also permnantly on Lasix as well as my Isrdil being doubled. It has taken a lot out of me but i guess I should be thankful I am still here and able to get out of the hospital. I'm just trying to find a little good news right now but its not happening.
Just thought I would let everyone know how I'm doin!
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