Cirrhosis Support Group
Cirrhosis is a consequence of chronic liver disease, most commonly caused by alcoholism and hepatitis C. Ascites is the most common complication of cirrhosis and is associated with a poor quality of life, increased risk of infections, and a poor long term outcome. Liver damage from cirrhosis cannot be reversed, but treatment can stop or delay further progression and...
One thing is a must..........the patient has to want to help themselves because there is only so much someone else can do to remedy the situation.
You are in my prayers.......I do hope that if you give your husband a bit of "hope" that he will take the reigns and do what he needs to do to "help himself". There is a point when most of us, once hearing bad news from a doctor, want to just give up. Sometimes it all seems so hopeless and it would be easier to drink and forget it as opposed to doing the dastardly deed of changing our lifestyles to facilitate optimal health.
I hope this helps even a little bit. You may need to be the "strong" one for now........you can do much to help your husband to see that his life is vital and that he is "not alone".......and above all, there is ALWAYS hope. Prayer works wonders. Faith works miracles.......God will never leave either of you "alone in your struggles"...........Hugs and prayers...............CarolLentz
I will continue to pray for you. One thing I notice is your faith in the Lord, does your husband share this faith. The reason I ask is AA did not work for me, it took Jesus Christ to pick me up and break the chains that bound me to alcohol. Judging by the results, nausea and the seizure alone, not sure why they didn't admit him. I would ask that question, if you don't get the answers ask for another ER doctor. Is his Gastro involved if so, I would personally look for another Gastro. I had a doctor that I felt wasn't giving enough time to my medical needs. His concerns were that I was not drinking? This is important and should be first addressed but did not look at my blood levels to adjust my medicines. He left that up to my general doctor. He would run tests on schedule but my symptoms got worse. I changed doctors, and he monitors everything from tests to blood work took some time but through adjusting my medicines I am improving some each visit. Praise the Lord. I still get nausea periodically but no bleeding. Have you seen any signs of blood loss. That led to my seizure and cardiac arrest.
Now, it sounds like and I am not a doctor the cirrhosis is bad. I hate to use bad, but I don't want to give a diagnosis. Have they calculated the MELD, to determine transplant? While he would not be a candidate because he is still drinking. It would give you an idea how bad.
I wish I could help more on the medical end. I would start by addressing the doctors. I believe strongly in prayer in faith, it is still not too late, do not give up hope. Him being scared is a good thing. I know that may sound mean but maybe that will push him to put the bottle down. I will be praying earnestly for you and your husband. Don't give up hope!
God Bless you Rummi,
Steven
In the meantime, much, much, much can be done to improve his overall health as well as stabilize his liver condition. Number one and foremost is the testing to make sure of the diagnosis and to find out where he is in the disease. Many people have symptoms related to poor liver function but that does not necessarily mean that the liver is so far gone as to require transplant. That is where the diligence in care, both self and supportive. comes in. Don't waste even one day getting this started.
The thing you will have to understand is that the ER dioctors are NOT versed in care for an ongoing disease and only there to tell you what their findings are as to why the emergency visit was necessary in the first place. It is then up to you to go to a gastrointerologist or hepatologist to get the diagnosis and stage. Your family doctor will be able to direct you to a good hepatologist or gastrointerologist. Then, that doctor can oversee the testing for his status as well as follow him closely for the 6 month wait.
Unfortunately, the ER docs don't usually explain all of this to the patient. They usually just say to "follow up within so many days with your family physician." If he is like me, I was diagnosed at a time when I had no insurance and we lived on my husband's disability from polio income. Not a lot of $$$ in those days. I also have a type of muscular dystrophy for many years so I had my hands full financially speaking. My ability to work full time was non-existent yet, I could not get disability from cirrhosis nor muscular dystrophy for many years. I was one of the patients who had it really tough for a long time. Now, I am on medicare (took retirement at age 62 and now at 65 I have medicare) so things are a little easier for me financially.
Your husband needs to find out what stage he is in with the disease so he can, if warranted, apply for disability or partial disability IF the doctor rules he cannot or should not work until he is treated and brought to his optimal health. That is a whole other story. Many have easy time getting on disability due to cirrhosis (if that is the diagnosis and to this point, there has been no specific testing to determine that) and some have a difficult time. It varies.
I do wish you well and agree that you should do all you can to educate yourself as well as your husband. Again, a good family type physician (or whomever he sees for colds and minor illnesses) is vital. He/she can rely on the family physician to monitor regular visits/testings such as on going blood work and blood pressure checks. The patient has to assume responsibility for his/her own care (or the care giver has to follow up to make sure his care is optimal.) Hugs and prayers............CarolLentz