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Showing posts with label medical system. Show all posts
Showing posts with label medical system. Show all posts

Sunday, 13 April 2008

OUCH! OWIE! OH PAIN!



Have you ever felt like this duck ?




I am not writing this to upset anyone or to get sympathy. My lupus group asked me to post my progress, good or bad, through this medical abuse situation I am going through, so medical
people can understand pain better.



Can't write much, too much pain, but wanted people to know that God is helping me. This will take a few hours for me to get my thoughts out. God speaks to us through "the still, small voice inside", and right now my pain is "louder" than that voice, so I don't get as much comfort when the pain is worst, but before the pain got too bad, I was inspired to look for a "patient advocate" to help me get a new Dr. In the USA there is 1 in every hospital, but when I researched it here 2 days ago, I learned that when you sign papers to be admitted to a Canadian hospital, you are signing something that says that you CAN NOT have a patient advocate help you! Then what is a patient advocate for?
Medical system could do so much if it
was not so corrupt.


Tomorrow I will try to start to make calls to get help. There is no way I can even get out of bed long enough to go visit up to 20 doctors to find one that will accept me. I tried 17 before. Was insulted, abused, accused, neglected, and I don't have strength to bear all of that now when I am curled in a ball in pain. God has always helped me find answers before, He will help me again. I almost lost hope because I was "leaning on my own understanding", but God knows answers that I don't know, and He will help me find the solution again.



I understand now more than ever why trigeminal neuralgia is called the suicide disease, but I also have pain throughout my whole body to try to bear with the trigeminal neuralgia. It gets worse as the day goes on, and by evening I can't think anything except to silently pray, and a few times I even prayed that if this was not going to get better, or if I could not get help, if God would just take me. I can barely remember my own name when it gets that bad. It makes chest pain like when this pain made my heart stop before, so I wonder if I will have another NDE. (Near death experience.) Since He did not take me, that means He WILL find some way for the pain to get less...whether its a natural way, through His healing, or through the medical world.

It's ironic that I go unconscious from diabetes when I don't have bad pain, yet when I am in this horrid pain, I can't pass out to escape the pain. I am amazed a person can hurt this much and not pass out.

I want medical people who read this to understand that things are worse than death, to learn that much chronic pain is worse than anything a cancer patient would feel, yet we get called "drug seekers" and get denied any help. Cancer patients' pain will go away. Either they will die, or they will be cured. Lupus and and other diseases do not go away. People with these diseases will live for 40 years+ in pain, being expected to keep up with everyone else and to keep living a high paced, high stress life.

This article took 6 hours! (lots of resting between writing)
I know that Heavenly Father is helping me through this,
and I am SO grateful!I know He will help me get better so that I can finish my purpose for coming to earth. (His plan for my life).
Blessings! I'm praying for all of you that have become my online friends!
Bluebirdy

Saturday, 8 March 2008

WE ARE BLESSED! and THANKYOU ALL!

The only reason Mom is still alive is due to our Heavenly Father. She should have died in 3 days without her heart medicine or insulin or sleep meds. She does not sleep at all without sleep meds. That Dr. and the hospital will be reported. They let my mom call for help while her excrement got dried on her.
We are blessed. My brother and I are SOOO weak from the whole ordeal, but Mom bounced right back and came home to clean house etc. because she doesn't remember that she was delirious and didn't feel the fear that we felt for our lives and futures that we I felt, she didn't feel the suffering of watching someone we love suffer....and the drain of going her telling us everything she was seeing and hearing, which no human being should have to see, and the exhaustion of fighting for her rights and being her nurse. Now she's forgotten about it, but it has made my brother and I really weak.
We are drained, but of course I did have to walk about 4 miles a day and go to the E.R. for myself and I picked up some kind of bug from that hospital. Chest infection I guess. My regular temp is only 97.6 instead of 98.6 cuz my thyroid is messed up, but now it's 102. This hospital is dangerous unless you have an advocate or witness with you at all times.
Gosh SO much stress...over and over and over...Then I get so mad at myself for not being able to function at full strength.
Well thanks for letting me vent. This is great therapy, and I really don't say too much to people in my life. I just share it on paper or now on this blog.
I am thanking God and Jesus and Holy Ghost and angels and anyone else who was involved in helping us get through that ordeal. I did learn that I do pretty well during a crisis, but then I pay for it afterwards, badly. Some friends have said "It's over now. You should be fine." ...but Some panic DURING the crisis, some collapse after. It would have been SO much worse if I did not have faith that the Lord loved us and knew our problem and would be our strength and that there is a reason for everything.
It turned out that she had salmonella poisoning and lost so much fluid in just hours, that it messed up her electrolytes and brain and body fluids.
Still, I am SOOOO grateful, and tell the Lord so whenever I think of it. It could have been such a bad ordeal if she stayed in those hallucinations. I don't think we thank the Lord enough! So go count your blessings, and thank the Lord for all that you have, even those things you are not aware of!
Blessings,
Bluebirdy



THANK YOU!!!!
Hi My precious family and God-given dear friends!
Just a note to say THANK YOU SO MUCH for your miraculous prayers. I got so many wonderful loving letters that I want to reply to individually but I just don't have the strength, so forgive my "group" thank you.
My brother and I are DRAINED. So many things went wrong, as if Satan was trying to make it as difficult as possible on us, but Mom's hallucinations were temporary, due to severe case of dehydration after food poisoning. She is only alive today because of our Father in Heaven. What a blessing to know Him and His loving Son.
The power of prayer is such a precious gift. We could have had a very selfish God who put us here and left us alone, but He didn't. He made communication with Him as easy as possible...and yet most people in the world still don't think of praying. I am soooo grateful to Him, even if I'm sooo tired. I picked up a lung infection at the hospital so maybe this is why I am not bouncing back.
THANK YOU AGAIN!
Blessings, Bluebirdy


Friday, 18 January 2008

BRAIN SCANS--PROOF OF REAL DISEASE IN FIBROMYALGIA AND CFS (CHRONIC FATIGUE SYNDROME)

>>means "new paragraph starts here". I still don't know how to make my posts separate into paragraphs if I type them at the blog website. It will only separate into paragraphs if I send it from my email program.

>>The captions in the above picture:
>>Below the first set of brains, it says "Scans of a normal brain and the brain of a fibromyalgia patient"
>>Below the second set of brains it says "Scans of a normal brain and the brain of a CFS (chronic fatigue syndrome) brain.
>>The colored areas represent areas of the brain that are active and helping the body and brain to function at full potential. In the diseased brains, there is less activity, so our bodies do not function as well, they do not do what we want them to do, and this really accounts for the brain fog, or fibro fog, where we get forgetful and can't concentrate on anything very well and make a lot of mistakes.

>>If you want to look at that picture more closely, left click on the picture and it will enlarge.

>>See? There is a DEFINITE disease, a DEFINITE difference between a healthy functioning body, and a the way our brain makes us function if we have fibro or CFS. This test alone should prove there is a common denominator, a place to start with the research to treat this disease. It also proves it is NOT just a person complaining too much, as the New York Times insinuated today (see next post below)

>>I got it from a site that no longer exists, the website address is at the top of the picture, but it is no longer a used website. I got it more than 12 years ago, whent the internet first started, so if the medical world had information about these conditions, I wonder why it was not publicized more and why more has not been done. I know that in Canada its almost impossible to find a Dr. with enough time or compassion to research or treat difficult cases. They are even telling us which diseases or conditions they refuse to treat, and its so difficult to get another Dr, the patients can't complain. So if my Dr. refuses to treat rashes or kidney problems, then if I develop those problems, I am on my own, because I can't find another Dr. One lady told me she thinks even Mexico has better treatment in the hospitals than what I have been experiencing here.

>>I, like many or most lupus patients, have fibromyalgia on top of lupus, (and 7 other serious conditions which lupus caused) and I have been studying about it so much that I feel like I could teach the researchers a lot!! It affects the nerves, muscles, connective tissue, the parathyroid, which controls every chemical in your body and brain,and all "cycles" of your body such as when you wake and sleep, get hungry or not, run out of energy or get invigorated. Everything in our body goes in cycles, and the parathyroid helps regulate those cycles. Certain chemicals are released at certain times during the day to digest food, other chemicals to make you sleepy or stimulated, others to make you relieve yourself in the bathroom at certain times, and all those things are affected in fibromyalgia. Its not just sore muscles. Its a horrid epidemic of a disease. The medical world likes to blame the patient when they can't find the answer. They forget that even diabetes used to be classed as a form of insanity before they found the cause and test for it! There is definitely something wrong, they just have not found the test or the done enough research. It takes the average of 11 years for a person to be diagnosed with these "invisible illnesses" such as lupus, CFS or fibro. Before diagnosis, people are thought of as fakers, lazy, hypochondriacs, neurotic, anything the Dr. can blame on the patient. The patient's family and even the patient can start to doubt themselves and wonder what they are doing to themselves. I suggest a book I call my "Fibro bible". Its a book written by a Dr. who has fibro. Its called "Fibromyalgia and Myofascial Pain Syndrome" by Devin Starlanyl. She names every possible symptom and why it happens, and has chapters about how to manage almost every part of your life while living with this disease. I bought mine used online because its expensive, because its almost like a textbook. You can buy it used at http://www.half.com/, http://www.ebay.com/, http://www.alibris.com/, http://www.amazon.com/ , and I'm sure there are other used bookstores online as well.

Blessings,

Bluebirdy

Please help change people's opinion of Fibro!


 
Hi gang;
   I get the newsletter from  the American Pain Foundation. Just now I got an alert that they need everyone's help that has fibro. It seems that some big wig Dr. wrote an article in the New York times saying that people with fibro are just complainers who won't deal with the aches and pains everyone has (which is also exactly what my rheumatologist told me...I almost kicked him so he could feel my pain)lol... and the article goes on to say....well I'm getting ahead of myself here. I am just going to copy the letter, and I ask you to use the sources below to write your own short note to New York Times to try to undo the damage that Dr. may have done, and to teach others about fibro and what it really is like to live with it. The colored sentences are clickable links so you can see the actual article and instructions on how to contact the editor or New York Times, which goes world wide! Here's the alert I got:
Blessings
Bluebirdy
 

Media Alert 

Dear APF Advocates,

This week, there has been much controversial media coverage on fibromyalgia and chronic pain. The New York Times published an article, Drug Approved. Is Disease Real?, which questioned the validity of fibromyalgia and chronic pain itself. The article suggested that the pain of fibromyalgia is a case of people who "obsess over aches that other people simply tolerate," and that the pain is just a "physical response to stress, depression, and economic and social anxiety." This is an extreme and harmful mischaracterization of the reality of pain.

See Background Information and Additional Media Coverage 

The public and the media need to hear from you! whether you are a person with pain or someone who cares for or treats people with pain. APF is dedicated to raising awareness of fibromyalgia and other painful conditions and the fact that people in pain have a right to timely, appropriate pain care.

Please Take Action NOW: Write a Letter to the Editor of The New York Times.

Thank you for advocating for people with pain.  Together, we will make a difference!

Best regards,
The American Pain Foundation

Thursday, 10 January 2008

WE GOT ANOTHER MIRACLE!!!

Hello all!
THANKYOU FOR YOUR PRAYERS!

~WE GOT ANOTHER MIRACLE!! We went to the hospital and instead of admitting Mom, they sent her to the outpatient clinic first, where they kept us for 7 hours, the nurse acted like she was on drugs, kept carrying messages from Mom back to the Dr. who was doing scopes on people, then we would get his opinion back that way, and she kept messing up the messages, didn't understand anything we said, we repeated things up to 6 times, I finally went unconscious from my blood sugar going too low from lack of food or water and all the stress, so they some glucose to bring me around. (And mom was the one there to be treated. Gosh...what a joke, me trying to care for HER.) She is able to do some shopping and clean house a bit (do a LOT more than me), and she can get medical care anytime so she's less apt to die than me. Anyway we got so tired and in pain and frustrated after 7 hours of this carrying messages back and forth and no Dr. seeing mom, no admitting to hospital like she was told was supposed to happen, no test, nothing...so we walked out.
It was a tough day but WORTH IT cuz mom won't be having surgery soon!
Today we start over again and I take her out of town AGAIN (did this day before yesterday) to the Dr. and hospital there...BUT THIS MEANS THE SURGERY WILL BE DELAYED!!!---Which means she will be alive for a while which means I won't be homeless. They don't do surgery in this little town I take her to see her Dr. at
Now if she can delay this surgery until my husband gets home, he can earn enough that we can continue renting the house we are in now, if anything happens to Mom. Or if the Lord can delay the surgery until other living arrangements are made for me (in case my husband doesn't come back from the war zone), that would be a wonderful gift from the lord too.
Got to drag my painful body to put all mom's luggage in the car again. (Why am I doing this when she can do it and is healthier than me and doesn't use a walker and doesn't have any muscle pain at all?) ---yeah...cuz I'm the obedient daughter that is grateful for all the years she cared for me. My brothers and sister have all told me they are really worried that I will die before Mom, because she has been served and waited on for 30 years, and I have served and waited on my first hubby and now mom until my body is falling apart.
In July when that Dr. told me I would only live for 1 year...on days like yesterday, I sure feel like its true, but I won't believe any human. God decides when I go, not man, and I have things to do yet. I hope to be here for the second coming. lol.
Now I have to start looking into getting help for myself, like some cyber-friends have been urging me to do, (been trhying for 10 years but got to keep trying)...to go to the top if I have to...but have not had enough strength for that either. I can only do a little bit of functioning each day. I wish I could afford to hire a secretary for all my taxes, the legal work to get my hubby home, and now to get help for myself. I have not even had a minute or the strength to get gifts mailed out yet. grrrrrrrr!
Wow, such a faith building experience. Now if I could just keep remembering that he is taking care of us and will even make miracles for us! It is hard for me to believe that everything will be OK, because even though I put everything into God's hands, he HAS let some very awful things happen, because that's what life is all about...so even though in my heart I know God is in control...I am always afraid of how hard the next "test" is going to be and if I am up to the challenge.
See? I told you that whenever myu cyber friends pray for me, I feel it, and THINGS HAPPEN! I know the Lord hears the prayers of this group. I have never found so many sincerely faith filled people in one place. THANKYOU THANKYOU THANKYOU for your prayers!
Love you all! Bluebirdy

P.S. Though I cried and prayed half the night from the pain, hurting too much to even get up to get my medicine, hurting too much to get back to the hospital (where they wouldn't do much anyway), TODAY I DON'T HAVE MUCH PAIN! I am ready to help Mom again!!! Usually it takes me a few days to be functional after 2 days of running around like I just had. Yeah I will be hurting when I get back from out of town again, but that's ok if God helps me recover quickly like this time! Oh Lord please help me remember that you love me and are helping me and will continue to help me!

Tuesday, 8 January 2008

Like A Lamb To The Slaughter?

    Oh help. Just weeks after Dad's death, and all I have had time to do is to take mom to the Dr, and E.R. and hospital and stay with her at the hospital, then in between I collapse in pain. I have not even had a chance to get my family's Christmas boxes sent out!
  I took mom out of town to the Dr. today. I still feel so alone in these crisises. I know God is here but I need PHYSICAL help. My brother who lives here has his own physical/mental problems and is not able to help, other brother and sister live hundreds of miles away and that brother works too much to come even to the funerals.
    Mom will be admitted to the hospital in the morning before 9 a.m.  In about 3 days she will have the surgery that the doctors kept warning her she will not live through. I feel like I am carrying my mom into the place of her murder. It feels like she has accepted the surgery as a way to go be with Dad and that way it won't be considered suicide.  If she dies, I will be homeless. I have tried for years to get into cheaper housing that is sponsored by the government.My disability will not cover the price of moving or the price of an apartment. If she lives, I do not have the strength to take care of a surgery patient, or we will both be in the hospital within a day. What a messy crisis.
    I also saw a Dr. today that was on call for my Dr. who is gone for 6 months. No Dr. will take responsibility for me while my Dr. is away, (they say I'm too 'complicated') so mom is getting medical care, but no matter how bad I get physically or emotionally as I try to care for her or if she dies, I don't get any help. Feels like I will die of pain/lupus and other problems before Mom dies, because she CAN get all the medical help she needs. Maybe in July the Dr. that told me I only had a year to live knew something more than I do.
   Thanks for caring, you friends who do care and have been so supportive. Please pray for strength for my brother and I to bear our illnesses, mom's illness and surgery and maybe death, and the period after of taking care of her estate and trying to find a place to live so I won't be homeless.
Blessings,
Bluebirdy
  

Sunday, 9 December 2007

I thought my heart problem was cured, but...

I  guess it's not. I had to get a blood test a few days ago, an arterial blood gas. Its quite a painful test because they have to find an artery instead of a vein by feeling your pulse, and the arteries are usually wrapped in nerves, so when they poke it with  a needle, it just makes you hold your breath in pain. Anyway it took them quite a while to find a good artery, because my pulse was so erratic (irregular), which is what the problem was when I started this blog. My oxygen is still low, but I don't use the oxygen as much as I used to. I should have worn it today when I went out. Its freezing cold out, yet I was sweating from weakness. The problem is, the oxygen tank is in a shoulder pack, and if I barely have the strength to walk around without it, it is much harder to walk around carrying that heavy thing.
     Still they won't even offer me any medication that others with arrhythmia get, as if they are hoping I will die sooner. VERY SCARY to think that "the system" might have the power to let me die soon, ruining the lives of those who love me.
      I still don't think the Dr. knows when I will die. God will decide...but the more stress that happens, the closer I will move towards dying. I don't fear death at all, but knowing the pain that we are all feeling with Dad's death, I  don't want to cause anyone that kind of pain.
      I worry that hubby will get killed over there in the war zone, or that he will be delayed so long that I will not be much of a wife by the time we get together. I am doing everything in my power to get healthier and stronger, but maybe God has other plans.
     There is still the possibility that Mom could die soon. I thought since God found me a husband, that He found me a companion to be with me through these most traumatic times. I guess not. It does make me wonder about being a wife at all, if I  will not be getting any help, and I will be doing all the giving, like in my first marriage. I don't yet have the strength to even live a half way normal life or take care of my basic needs, nevermind trying to take care of someone else's needs who is going to be somewhat helpless for a while and might have PTSD (post traumatic stress disorder) on top of everything else.
     Ok here I go with my bad habit again. I am "what if"ing myself to death. We can't see the future. Its crazy to make yourself sick worrying about all that COULD happen. We need to hope for the best, envision the best, plan and work for the best, and live one day, one hour at a time, enjoying the moment. I used to worry so much about the future that I forgot to enjoy the present. Trying to kick that habit.
     I have really done a good job of taking in every moment and really feeling all of it, which makes life so much richer. Took a lot of reading and studying to change how I think. Hopefully I will continue improving with the way I think about life. It hard enough without adding more worries that are unnecessary.
     We have no interest or energy to decorate for Christmas this year. I think we need the joy that the decorations will bring, but we don't have the strength. The gifts that I am sending to children and grandchildren will be late, which doesn't make me happy, but I'm doing my best.
Blessings to you all,
Bluebirdy

Saturday, 8 December 2007

Interesting Experience since Funeral


        I had a weird experience yesterday. There have only been 3 times that I have cried uncontrollably since Dad died. First was when he died, second was after the funeral, third was last night about 8:00. I couldn't figure out why I was so upset and why I couldn't stop myself from crying, and I cried until about 10:30, then I realized that 7:45 two weeks ago is when Dad died. It seems like my body stored that traumatic hour in my body, and somehow, the alarm in my body went off at the same time he died. Strange.
      I noticed that with my divorce, too. Even after many years when I had forgotten the dates that some events happened, I would get into the most solemn, quiet, sad mood, and not understand why, then later it would come to me that it was that hour, day, month, etc. that he told me he was leaving, or that he did something else traumatic in our relationship.
     Just this month I have read a bit about memories being stored in your DNA, and sometimes are even passed down to the next generation. Maybe this experience has some tie to that theory? I don't know. So many mysteries that I will be so excited to learn after we are resurrected and can learn for eternity.
    I am sleeping about 1 hour every 2 days. Stress makes fibro/lupus worse, fibro/lupus flare makes stress worse, so its a vicious cycle.
    It is wonderful to feel the peace that passes all understanding, and to feel the Lord carrying us, and to have the knowledge that our family will soon be together again, and we know where he is and that he is happy and probably has even gotten to meet the Lord by now. What a comfort faith is.
     Gosh its nasty cold  here too. about -12. Its supposed to be the coldest winter in 15 years, and I believe it from the way its starting out! I'll have to go to Salvation army and get more layers of clothes to put under my coat, and a warm hat and scarf and hopefully some snow boots. I hear the snow boots are about $100 new, because the retail stores know that we have not needed them for so many years, that there are none in the used clothing stores, so if we want some, we have to pay whatever they want to charge us.
     Here is something else interesting. When Dad went into the nursing home 2 years ago, Mom, my brother and I suddenly hated food. It was like a constant nausea or knot in our stomach. We didn't even like the smell or sight of food, so we lived on very little food. This is one of the reasons I gained so much weight. My body thought it was starving, so it would not burn any fat. Now that the knot is out of our stomach, because we know that Dad is not suffering anymore, we are eating more (because there is so much food here left over from the funeral), and I lost 5 pounds in 5 days (2.5 kilos) from eating MORE! Dieting ruins your metabolism. Most large people have dieted themselves all the way to obesity. People are now learning that there are no magic pills or diets or tricks to staying thin. Only eating good food in portions that are not too big, and keep moving around as much as possible. So much has to do with genetics, also.  I AM THANKING GOD for helping me lose even 5 pounds because there is no way I can exercise enough to lose a lot of weight. Too much pain. I have found a few ways to exercise without pain, but do it many times a day, so that it will burn calories.  I hope soon I will be strong enough for my favorite activity, swimming, and to go on long walks so I can be strong enough to travel. I used to get awards in sports at school. Hard to look at my body now and believe that. lol. I just want to get stronger so I can enjoy life and help others more.

Sunday, 2 December 2007

One reason why the Elderly must suffer.

    We are finished with Dad's funeral now, and it has just occurred to me that if I had to let him go if he was healthy, it would have been unbearable; but because he was suffering so badly, we just wanted him to stop suffering, even if it meant we would miss him terribly. We cry because we miss him, but then we start to think of how happy he is and that he is not suffering anymore, and it is worth letting him go. Maybe that's one reason for all the suffering in the nursing homes. Another reason, is that someone is not willing to let them go. Mom and my brother and I all prayed on the same night "If it is your will Father, please let him stop suffering. Its getting worse and the nursing care is so bad now, its almost abusive, and it's hurting us ALL so much that we can't do much to ease his suffering, that we all think we will soon fall apart. He doesn't deserve this, please ease his suffering." It was a couple of days later that we all told each other that on the same night we had said almost exact prayers.
     I know that we had not fully been able to "let him go" before that, even though he was suffering and knew he would die soon, but as soon as we were completely able to release him, he soon went. I have seen this happen a couple of other times too, that the person stayed alive until one specific family member was ready to let him/her go, and when they do, they pass quickly. I love you Dad. You were one of the  most honorable/respectable/loveable men there could be. The church was full of people who loved you and had smiles on their faces with all the joy you brought to them with your sense of humor. I hope I can be more like you. Bye Dad. *sob* save a place for us.
Love, your adoring daughter.

Wednesday, 21 November 2007

Both parents in hospital

The day after my parents 59th anniversary was the Queen of England's 60th anniversary. I thought that was interesting, because my wedding was 1 year and 1 day from Princess Diana's, and my kids birthdays were the same months as the prince's.
   At 3 in the morning, the nursing home called and said Dad will be taken to the hospital by ambulance. I went upstairs to tell Mom and she said "I need one too." So I called another, and we live next door to the nursing home, so one ambulance followed the other, and I was ahead of them both in my car. I called my brother to tell him and he said he had woken up for some unknown reason, he never wakes up at that time! So he came over to the hospital and we spent the day going back and forth helping answer questions and get them settled in and make sure they get immediate treatment.
  So my miracle was timed perfectly so that I could help with this crisis. I walked 4 miles a day the past 2 days. I wear my pedometer to measure....but today, I can't walk and struggling to even roll over. I have tried since Monday to get my Dr. to refill my medicine over the phone, but he insists that I come out there. So I will have to go without my diabetes medicine and muscle relaxant, which is not going to make this any easier.
    I am now in unbearable pain again, massaging legs, crawling to the bathroom, takes 5 minutes to roll over. Unhappy that I have to go back on my morphine but thanking God that there is such a thing, so that when it kicks in, I can go back and care for my parents.
   My dear husband said that the list of things I am going through now (about 12 things I have not told anyone about) is worse than the war he is going through right now. He is so calm and patient and strong and full of faith. I'm so proud of him...my life is almost always 10 crisises at once, so if my life is harder than the war he is going through, do I want to bring him to this stressful life? Oh well, its not really my decision anyway. Its up to God, who will influence the court.
    I thought God gave me a husband so we could love and support each other through these most difficult times. I could sure use a shoulder to lean on after I physically and emotionally take care of mom, dad and my brother...but I just come home and fall apart, and do paperwork until the pain eases up enough to sleep.
     I am still so very grateful for my 1 week miracle and I hope God will give me the words to write an article about it.
Blessings to you all, HAPPY TURKEY DAY TOMORROW TO THE AMERICANS. Remember to give thanks that things are not worse, because they always could be worse.
Bluebirdy

Wednesday, 26 September 2007

Looking for the Dawn after the Darkness


There is a local church that has been calling me weekly to pray for me, and what's interesting, is the prayers seem very powerful, and shockingly, something very personal and unusual is mentioned in every prayer, that no one else knows about me. Yesterday a lady called to ask if she could pray for me, and I told her what was going on in a summarized version. She asked about home care, I told her what I wrote below about home care. She asked about meals on wheels. I told her its about $14 a day. She thought it was free. She told me she used to work for the medical system, and that there IS a corrupt way of treating people in Canada. Those who get the fastest, best, most expensive care, are those who are rich and who can afford the few private hospitals and clinics that are a very rare and new occurrence in Canada. Second level of care is still excellent care but a bit slower, those who have insurance from their employer and are working. Third level, not as fast care and not quite as expensive, are those who have Alberta health care only but still are employed. The 4th level of care of care are those who are elderly or on disability, and the last level is called "Tagged" which my mom is on, where they have spent 1 million dollars of care for the person over a lifetime, and/or they are elderly. Mom is elderly, and her Dr. who has also been her friend since childhood has told her she is tagged. They just offer the minimal of comfort care if the person goes to the emergency room, and never admit them for care, and often consider "Do not resuscitate", and for sure do not consider expensive tests and treatments and surgeries. At this point, care becomes dangerous. They will give drugs she is allergic to, and will fight with her when she tells them she is. They will negect her if she doesn't have someone with her.
OK back to this phone call yesterday. This lady told me she had worked for the medical system, and there are different levels, and after I told her the tests I had and the symptoms I had and the forecast I was given, I told her that today I have an appointment to get the results of the latest tests. She said she thought it was only fair to warn me that I will probably not be told exactly what is wrong, because if they tell me what is wrong, they will be obligated to treat me. This is why I did not even get a Dr. to listen to my chest for 10 years or do a physical on me, because if they find something, they have to treat it, so they bypass that by not testing. I go to the Dr. every 2 or 3 months, and never got even blood pressure or chest listened to until this year when I changed doctors to one in another town. I was getting weaker and weaker and kept praying studying hoping for a way to get feeling better so I could take care of my family and my husband, and finally when I couldn't walk 10 steps without my heart rate going to 120+, I took my mom into the office with me. This was the first time a Dr. took me seriously and referred me to a specialist. The visit before that, the Dr. kept trying to tell me that what was bothering me was a hiatal hernia, not my heart. Then when mom came in the office with me, he suddenly took me seriously and the testing started.
So after that phone call yesterday, the depression set it horribly. I realized that I would not hear the truth at the appointment today, and I would not get any treatment, and there are hundreds of people praying for me in different religions, praying HARD, doing whatever little ceremonies their belief system condones, energetic healing, I am doing 2 types of homeopathic treatments now, meant to heal everything in my body, and all my meds are natural, but yesterday it hit me that after all that, it was probably not God's will that I get well, or I would have been healed by now. So now I am trying to learn everything possible about bringing into my life those things that I want, attracting good energy and abundance, learning positive thinking and joy, doing and learning everything I can to get well, but that is not bringing forth any changes yet either.
They say its always darkest before the dawn, and I have found that in my life too, when its darkest and unbearable, if I hang on for just a little while longer, God will send me something inspirational to read or learn or an encouraging friend, etc.
I went to the Dr. today, and the person who called yesterday was right. He even denied all the bad things he said in the past! Now I am completely healthy! He said it might be due to lupus, but he couldn't help me. So a few weeks ago I had a year to live if I didn't get treatment, my blood oxygen was 86% instead of 100% and I had arrhythmias that could make me drop dead any minute. There IS treatment for that. They use pacemakers and defibrillators. I asked him why does my heart rate go to 120+ when I walk 10 steps? Why can't I walk without a walker, why does the oxygen help, could it be a blood problem? He gave me the name of a lupus specialist in town and said that was all he could do for me. The appointment was about 3 minutes. The lupus Dr. will have the same set of rules fro,m Canadian health care. I can't bear more abuse and tests and insults and corruption. I already now they can't do anything more for me and that I can't lean on the arm of men. The person I talked to yesterday was right. I was not told what was wrong or offered a treatment. When my Dad got water in his lungs last week, he was given the water pills and heart meds to take care of that. When I got water in my lungs a month or so ago, I was not offered anything, as if they were hoping I would die. I came home and slept with the head of my bed raised, barely able to breathe or talk. It took a lot longer to go away than Dad's did. I am glad Dad's problem passed, instead of HIM passing.
Then after the Dr. visit, I got a letter from immigration needing papers from my husband so fast that I don't think it will be possible to get that paperwork to the court in time. If we don't, that means him and I are through. Part of me wants to delay it so I don't have to make him suffer by coming to live with me, and I feel too sick to live with anyone and be married to anyone, so I don't know whether to give up on all the work and money and emotional turmoil we have suffered all these years and just drop immigration, or if I should see it through to the end and be miserable with him being miserable with me. I don't want anyone's life to be difficult due to me, and for sure it will be MORE than difficult with us. The helpless trying to help the helpless. Love does not cure all. We don't even have enough money to get him here. Part of me says "NEVER GIVE UP!" the other half of me says "I don't see how I will even get through one day with him since I can't help him adjust to a new culture and feed him 3 times a day. I will probably do my best and then trust God for whatever happens in the end.
As for "the dawn coming after the darkness", in the mail today, a book came that is considered 1 of the 10 best books ever written, "Man's search for meaning" by Viktor Frankl. He survived the Jewish concentration camps, and found meaning then, and likens illness to being in a prison. So again, with perfect timing, the dawn came after the darkest night, and I am hoping that book will help me create the whole new, different life I have been trying to create. I have many books to read about changing my life but have had too much nausea to read and very poor retention of what I read. Oh my loving, precious Heavenly Father, it seems you want me to stay sick, and that it will be 100 times harder if I have to take care of a helpless husband when I can't even do the things I need to do for myself. I'm overwhelmed, lost, damned if I do get hubby here, damned if I don't. Please change me, change my way of thinking, my spirit and body. Give me the strength I need to take care of my family. I want to help people in this world. I want to be a light and encourager. I want to be part of my children's and grandchildren's lives. I want to travel. I don't know if you plan for me to live or die, but PLEASE constantly tell me what I should do and give me the strength to do it. I pray this in the name of your gracious son, Jesus Christ, Amen.
Thinking on the brighter side...this depression has overwhelmed me because I can't get out, can't go to a store or to a park or even get enough to eat, which messes up body chemistry. Maybe with my hubby here, I could be distracted from the illness and experience some joy. Trust in the Lord WITH ALL THINE HEART and lean not onto your own understanding!!!"
Bluebirdy

Wednesday, 12 September 2007

Bad stress day---still jealous of cancer!

In response to the letter below asking for prayer, a friend wrote:

"Dear BB,I don't know how yet, but tonight's and tomorrow'sprayers will be longer, stronger and more fervent thanany before. Bless you, my friend.Love, CD "


I replied:

"Thanks CD
Words can't express my appreciation. I'm so worn out. I got called for instructions for prepping for the test, and it was a nightmare. The nurses started fighting with me about what the Dr. had written down that I could take my morphine before the test, (he said I could, the nurses said I couldn't take it for 24 hours before the test.) I disagreed because if you go off, it would really mess up your heartbeat due to pain and withdrawal. The stupid nurse (just a receptionist I'm sure) accused me of taking street drugs, because "morphine is only given to cancer patients", and then hung up on me, then another one called me and told me I couldn't take my nitroglycerine for chest pain either, so I asked if I should go to the E.R. if I have heart pain or what, and she said "They won't treat you in the E.R,. if you have that test tomorrow! You can't have any drugs in your system.!" I said "You mean if I were having a heart attack, they would rather let me die than give me medicine because I'm having a test tomorrow? Wouldn't it be better to reschedule the test than to not treat a heart attack?" She hung up on me. Nurse (receptionist #3) calls... She asks why I can't go off my morphine. I tell her I can't even sit up or roll over without it, so I couldn't get in to take the test. She said "Well that's YOUR choice if you don't want the test, and it WAS your choice to start taking drugs!" I told her its a prescription, not street drugs and said "no, you don't understand. I need the test but I also need to be able to get to the hospital to have the test." She said well I guess you should 'jusscontinue' the nitro". I didn't quite catch what she said. I said "sorry, did you say I should "just" continue the nitro, or discontinue the nitro?" she said I'll have the Dr. call you about this, Sheila! You are obviously having problems that we can't deal with, and as for your fibro, there is no such disease. Its a neurotic's disease." She hung up. Then the Dr. called me and said that the nurses were wrong, that the original instructions he gave me are right, that he will give them a strict talking to about them not understanding that many people take morphine that don't have cancer, and yes, Fibromyalgia is a real and disabling disease." I was crying by then, because ONCE AGAIN, I was being accused of using drugs, seeking drugs, and for lying about my pain, and again got called a neurotic because fibro USED to be considered a neurotic disease. Now there is PROOF that its real.


PLEASE don't be offended by this, CD...or anyone who has dealt with cancer, but right now I am jealous that all terminal illnesses are not treated like people with cancer are treated. I can't get 1/100th of the resources available for cancer patients, they do not get insulted for using strong pain meds, they do not get their pain denied, their friends do not desert them, they get help coming out of every corner and every agency in the community, and they know it will end! Either they will pass away from it, or they will be cured. I don't have that guarantee. I could live a total of 50 years in unbearable pain, with no support from society and no physical help. Lost my husband and children due to this...the social part of this is harder than the physical part. I need a support system. You are all great, and the best support system I have, but I am so T-I-R-E-D and can't even defend myself, and shouldn't have to when I can barely even breathe and I'm on oxygen. In the local hospital you almost always need someone with you to be your advocate, and I was looking forward to my husband coming, for 1 reason, to be my advocate when I need it.
Ok I apologize. That's enough of that. I'll write when I feel more "Pollyanna-ish".
Thanks again CD for the prayers and support, SO much. I am hoping the test tomorrow is the beginning of a better life.
Blessings,
Bluebirdy"

Friday, 31 August 2007

Back to the Beginning





Readers: Forgive me if things are repeated. This oxygen makes me an airhead. lol. Also fibro causes a REAL, scientifically proven problem called fibro fog, and pain and medication cause painfog. A lot of these posts are from letters that I wrote to others, so I tell more than one person the same thing, so it will be repeated.

July 30/07 (Day I found out I might not live a year)
Finally got into the heart Dr. today. I waited 6 weeks for this. When I first went to see my family Dr. 6 weeks ago, he said it was quite serious and wanted to admit me but he doesn't have hospital privileges. He called this Dr. to see if he would admit me. He said no, not until he sees me in an appointment in 6 weeks. He said "I am telling you I have a young woman here who could die at any moment and you are telling me she has to wait 6 weeks? What if she goes to the E.R.?" The heart Dr said they would stabilize me and send me home but still HE wouldn't see me until the 6 week appointment. He didn't even tell my family Dr. that HE doesn't have hospital privileges either! Now I am being referred to a heart Dr. WITH hospital privileges which will take 8 more weeks. If my family Dr. would have known this first heart specialist didn't have hospital privileges, he would have sought out one WITH hospital privileges to begin with! Now I will be wasting 8 more weeks! This heart Dr. said if this amount of heart damage continues every 6 weeks, I might not make it until treatment, because in Canada it could take 6 to 12 months! In the USA you can get treatment within 24 hours of finding out you need it.
So many doctors will not deal with the local hospital! THEY ARE DISGUSTED by the politics that go on there. I have seen many leave town, GOOD ONES, and others just do not deal with the hospital at all, just home care. Anyway, 6 weeks ago my EKG looked almost normal. Yesterday's EKG showed "a significant amount of damage to happen in just 6 weeks". He wants me to have another test to see if angioplasty would be any help, but that will take another 8 weeks, and if I have the same amount of heart damage in the next 6 weeks as I have had in the last 6 weeks, I will be even closer to dying. Then if I AM edible for angioplasty, I will have to wait 6 months or more. By then my heart will be too damaged to do the surgery. So I am dying because of Canada health care delay??? Makes me want to go to another country to get this test and treatment.
The biggest new travel industry is medical tourism. Its hugely popular to go to other countries for state of the art medical care, which is much cheaper and faster and they put you up in a 5 star hotel with doctors on staff at the hotel, to heal for $25 a day!
I don't know whether to ask our politician to hurry my husband's immigration so I can get well, because I do think I will get healthier if he is here, or to just leave it as it is and I will get worse. I don't want him to come here if he will just end up being a widower. I don't want to put anyone through the hell of living with a dying wife in a strange country where he couldn't even get his meals taken care of.
I am working full time calling agency after agency trying to find someone to talk to, and getting passed around and put on hold and told they won't talk to me, which is just making me more and more frustrated every time I pick up the phone.
Why does God want me to be so alone? Yes, HE is with me, but at a time like this, we need a human being to talk to and more than one to help my family with day to day living.
On the first day that I spent so many hours trying to call agencies and getting pushed away by them all, it just reinforced the idea that for some reason God wants me to do this completely alone. Even the distress line put me on hold (sounds like a skit from a Saturday Night Live Skit, doesn't it?lol) and an agency that advertises that they are there to refer people to other agencies that could help them, and their motto is "THAT'S WHAT WE DO"...said they had no idea where to refer me, that she was closing up in 15 minutes and didn't want to turn her computer back on, and other excuses, and I called the hospice. I asked if there was a counselor there or someone I could talk to after just hearing this news. They told me I could not even talk to them until I got a referral from my Dr, but that the Dr won't refer me until he is SURE I only have 6 months left, and if I live past that 6 month time, I am taken off the program, no matter how sick I am, and put at the bottom of the waiting list again, so they don't refer people unless they are ABSOLUTELY sure it is shorter than 6 months so the people don't have to go through the hell of being removed from the program while they are at their worst. I don't think I will even be referred there, because as some here said, doctors can't give a specific time line. That is up to God to decide. I have had my heart stop many times, but they resuscitated me and I'm still here! I was able to find an online hospice support group yesterday, and so far they are very kind, but they are all hospice workers, or family members of people who died, none in there who went through this themselves. If I could live longer I'd write a book for people who have just been told they are dying. There is obviously nothing out there for us now. Someone suggested to make lists, like a list of things people could help me with, a list of things I WANT to do if I get the strength and money, a list of things that need to be done, but its overwhelming because I barely have the strength to think of the lists, and certainly don't have the strength to do all the things on the lists. One friend suggested to just write my will and maybe plan my funeral and then just relax and enjoy life. Everything I own (it all fits into one room) can be sold to someone who buys estates. So many things that were on my "to do " list last week, I look at now, and think "if I'm not going to be here, why bother with that? If I have limited time and energy, I want to use it on things that I want." I am a newlywed and was in the process of getting all my cards changed over to my married name, but now wonder if the hassle is worth it. My husband is overseas waiting for immigration and it has been delayed time and time again. now I see why. It would be horribly miserable if he came to a new country to live with a dying woman and could not even get 3 meals a day because he doesn't cook and neither can I at the moment. hmmm...I think I am repeating myself. Forgive me if that's the case. Too many thoughts swimming in my head all at once. I have even thought of trying to get a loan to do something I have always wanted to do, or even to go to another country to get FASTER treatment so that I might live! I am not well enough to travel, and it will take so long for me to get a passport, that I don't know if that is practical. Just thinking of every possible option. Now if I had money, someone to help me get to another place, and a bit more energy, I would have a bit of fun before I go! I thought of selling almost everything I own so I could do that, but at the moment I don't even have the strength for a garage sale or to take all my items to the local place that sells it on ebay. I sold on ebay by myself for a year, but didn't have the strength for the picture taking, documenting, taking 20 boxes to the post office every week, dealing with honry customers, etc. Oh well, I have faith. I have HOPE. HOPE is the only thing that keeps us sane and keeps us going...so I have to hope that some people will be sent to help me. In our house with 4 terminally ill people, we tried for 10 years to get home care, but were always turned down because unless we need someone to feed us, or bath us, or give us meds, we don't get help. I don't need any of that...and if that's all they offer, why have them come?

Aug 11/07

Ha! I won a nice 2 disk CD today! So this week I won 2 hamburgers, $10, a pop and a CD. I think I'd better buy a ticket of some kind for something big, since I'm on a roll! Maybe one of those tickets that the money goes towards helping charity, and the raffle prize is a car or house or something. lol. Are raffles gambling? Wow isn't it awesome how sometimes God drops little gifts from heaven to make up for the hard times? Sometimes material, but more often spiritual or emotional, in the way of friends who say just the right thing at the right time, or you flip open the Bible to the verse that you needed right then, or are led to read a certain book that helps you get through another day...God is good.
About an hour ago we had a real faith promoting experience that I will put into my journal.
First, some background that led up to the experience. I live with mom, who has been semi-conscious since I got home from the Dr. and told her only part of the news, but she put 2 and 2 together, and the stress caused her blood sugar to raise so high that she went into a really deep sleep, one step before diabetic coma. Also right when I got home from the doc, an email was waiting for me telling me that a friends 18 day old baby just died...so my head was just spinning with dealing with my own bad news, the friend's baby, and trying to decide whether to call 911 for mom or not. I didn't know whether she had accidentally taken too much medicine, and that's why she was so unresponsive, or if it was high blood sugar, or some other reason. I prayed about it and got a calm feeling that she would be ok if I just kept trying to wake her and as long as she could respond and I could keep getting fluids into her, she would be ok. It happens quite often to me also, but I don't have anyone to check on me or to help me the way I was able to help mom. Anyway for all Monday afternoon, all Tuesday, and Wednesday most of the day,she was in this sleep.
I should not have told her anything about the Dr. appointment I guess. Then she would not have stressed out so much that her blood sugar raised so high. Anyway, without telling me, Mom got up out of her semi-conscious stupor, gets dressed, gets in the car (she should not have been driving) and went and got groceries...more than I have seen her get in about 6 months. That was another sign that she was still not quite thinking clearly. We have this folding cart with wheels on it to carry groceries from the car to the house, and she put some in there, and came to the house, and I lifted the cart up all the stairs to the kitchen, (which I shouldn't have, I paid for that physically)... then she went back out for load #2. I was unpacking groceries in the kitchen, and heard a crash. I looked outside and mom had fallen down the stairs with the cart on top of her. I ran out and pulled off all the groceries and tried to pull her up. Half of her was hanging off the edge of the stairs. AT THAT VERY MOMENT....GOD'S PERFECT TIMING...my brother came to the house, ran to us and helped me lift mom up and see if she had a broken hip or shoulder or whatever. Dad was just put into a nursing home last March, which has completely turned our lives upside down, and now thoughts of mom being in a nursing home was running through our minds too. I got mom settled down and examined while my brother put away the groceries for the first time in years, and when we determined she just had a scrape and a bruise, we thanked the Lord that it was not worse, and we realized that it was a very visual sign that the Lord was protecting us! By then, my heart was going a mile a minute and causing pain , so I collapsed on my bed, and again, perfect timing, my husband from overseas called me! its 3:45 in the morning for him. It felt good to know that we still have that kind of connection. So I told him what happened and that it was a sign that God was watching out for all of us, etc. and he was very happy that he could hear the whispering of the Holy Spirit loud enough to obey and call me at that perfect moment. I love the Lord's perfect timing!!!
What is even a greater blessing, is that my brother, who has suicidal depression, and he was attacked by a dog 2 weeks ago, and 2 days ago really spilled his guts about how frustrated he is with religion etc, just called me tonight he told me that he KNOWS that was PERFECT timing and the fact that Mom didn't get hurt absolutely is a visible sign of God protecting us! She's 75 years old and has many illnesses and osteoporosis and that fall should have broken a hip and a shoulder!
I pray and pray and pray to know what to say to my brother or what to do to help him see life differently, then today I prayed, saying that I don't know what to say or do, and asked that the Lord would do something, point him in the direction of things he could read, or something people say to him, to let the light bulb go on and help him start thinking better, to have a better life, and this seemed a bit dramatic, but it was needed, something to shock him, something VERY obvious that God is protecting us. I hope he remembers this visible sign that God is protecting us. It was a valuable lesson for Mom and I too, at this time when our family's lives seem to be such a delicate balancing act, it was reassuring to see the Lord in action, protecting us.
Just thought it would be good to share a good experience with you for a change.
Blessings, Bluebirdy

Aug 20/07
I found thousands of books and websites about grieving for someone who is dying or has passed away, but NOTHING about people who have been told they are dying. I also found that people dying of Cancer are very pampered by the medical system and by society in general, but if you are dying with any other disease, you are pretty much on your own, even though we go through all the same things as those people with cancer. With cancer, there is a chance to recover. People with other diseases, by the time they have been told they are going to die, probably will not recover, yet they are not taken care of like Cancer victims are. I am happy that Cancer victims get that type of care, but I am hoping that the medical world will wake up and realize that people dying of other diseases need the same type of care, hospice, pain control, counseling, clubs and groups of family members trying to deal with it, etc.
I am a very private person. I have not even told my family that I have been told that I could die. I write in a journal, but never thought of a blog. I hope I live long enough to write a book about dying from the dying person’s perspective. Its sure needed. I don’t even pray out loud, for fear that any negative spirits around might hear it and might arrange things to look like the answer is from God, but really it turns out the answer is from the wrong source…and I am desperately scared of doing this, because I don’t have the strength to handle people’s rude or insulting comments, and once you go public, you will get that, because there are all kinds of people out there.

I am so grateful for the internet. I have a cartoon .jpg I wish I could put here of a man hugging his computer that says “I love my computer, all my friends live in it!” That’s my lifeline to the outside world.

The day I discovered how Oxygen helps:
I got so desperate with this heart failure that I used my mom's oxygen, and the difference was like night and day! The muscle spasms went away, the fibrofog went away, the sweating so bad that I looked like I was in the rain went away, the ability to stand and walk went from 10 seconds to about 5 minutes! It reminds me that we must have opposition in all things. Darkness and light; hot and cold; happy and sad; healthy and sick; because how can we appreciate the good without experiencing the bad, and how can we discern something that might be bad or untrue or dark without experiencing the light, the truth, the peace of the information from the right source?

Aug 21/07

I was feeling alone for the first time in my life. I actually enjoyed my solitude because of the pain and weakness, then getting the horrible news, all of a sudden I didn't want to be alone anymore, but I have kind of liked my solitude up to that point.
The Lord has been doing things to make my life better, little blessings here and there to show me that He knows my problems and He cares and He is with me.
All my life I have had lupus and fibro, which makes you seldom get positive medical tests, so you get told you should go home and leave the doctors alone, because its just stress or that you are neurotic or seeking attention or a list of whatever they can insult us with because something doesn't show up on a test. It seems weird to be happy that something shows up, but it means that I will be given some treatment, and that there might be something they can do for me. With lupus, chronic fatigue, fibro, and various other diseases that they don't know much about yet, we don't have those comforts. I was actually happy when I developed another health problem about 12 years ago that required stronger pain medicine, because that pain medicine could help with the lupus pain, too, so its weird to think of a painful condition as a blessing.
Though my heart test not showing good news is not a good thing, it IS a blessing to actually get looked at with respect and treated kindly because something actually does show up as being wrong. My Dr. last week told me to go to the E.R. to get my blood oxygen tested when I was having a hard time with sweating and inability to breathe and muscle spasms and not able to think and chest pain, so I was ready to go yesterday, but thought I would call my Dr. first to ask a question about it. The nurse said "You can't get a prescription for oxygen from the E.R! First you have to make another appointment with the Dr...he's not available for 3 weeks, then he has to order a special 24 hour oxygen test, which will take another 3 weeks, then you have to wait for the results which will take another week." I said "I have been in there 3 times already about this! It takes everything I've got to get in there! I don't have any help, and why didn't he order this test the last 3 times? It seems your office really likes the $46 fee for each appointment, so you deliberately put off something I need so I have to come back!" I never talked like that to a nurse before but I was in pain, I could not breathe well, I was ready for the E.R., and now she was telling me that I would be flat in bed unable to breathe or even get myself something to eat for another 7 weeks?
I called the oxygen company to re-order Mom's oxygen, because I had used it all, and asked them if there wasn't an easier way to get oxygen. He told me that he would set up a blood test for Tuesday and I would get the results immediately and get the oxygen the same day. So, there ARE ways to get things done faster in Canada, you just have to know the right people, or bribe the right people, or be someone famous, or something! So now I am going to pray to find someone who can get my 6-8 hour cardiolite test done before 6 weeks, and if it shows I need angioplasty, some way to get that done ASAP instead of the 6 months to a year that I was warned about. In the USA they do angioplasty 24 hours after the test shows that you need it. In fact in most developed countries they do it that way, but not Canada.
So, for those that don't know, 100% oxygen is what we should have in our blood. If you get down to 90% is when they give you oxygen. They took the first test, and it was 77%. The nurse took it into the other room and the supervisor said "That can't be right or she would be unconscious." They took it again, and it was 86%, so I qualify for oxygen. I got it brought to my house. Now I can get back into life, and it sounds weird to be thankful to be up for 5 minutes at a time, but I can clean, 5 minutes at a time, then rest in between. I can cook, 5 minutes at a time, go for walks, resting every 5 minutes on the walker or my seat cane, so shopping for the first time in 8 years or so, go to the park...boohoo. So this energy is what I have been missing? This is what "normal" people feel like ? Now I feel this energy but still not allowed to do a lot of activity until the heart surgery because after only 10 steps my heart rate was 145...but now I have HOPE! I don't think the Dr. is right about me dying in 1 year. Only God decides that, and I am not finished what I came here to do and to learn. I want to enjoy life before I go. I never got much of a chance to enjoy it yet. What little blessings I do get, I am grateful for, but I want to have more experiences and do more in life.
How ironic that when things get worse, they can seem better, because you appreciate the small things more, and every little blessing is a JOY! Every little improvement in health makes you appreciate what you have because you did not have that much health earlier.
Being grateful seems to bring more and more blessings. Maybe because so few remember to thank the Lord for anything.
Blessings, Bluebirdy

My living circumstances
I am 47, RE-married, but my husband is still trying to immigrate. My children are grown and married with kids but I have only seen them and my grandchildren for 3 hours in 10 years. I live with my mom who is also in the last stages of lupus. My father lived with us until March when he could no longer stand so he is in a nursing home. We could take care of him despite the Alzheimer's, heart failure, diabetes and cancer until he could no longer stand. Now we have to go feed him twice a day. Mom and I are too sick, so my sick brother who has Parkinson's disease takes care of him. He lived with us and cooked every night until Dad went to the nursing home, then he got an apartment of his own and feeding Dad is all he has strength for each day, so none of us is eating well. Just 4 months ago I got so weak that I can't stand for more than 10 seconds to even make a sandwich or a meal, so we are living on things you can grab, like cereal, ensure nutrition drink, yogurt, pudding, fruit. I get a few dollars from disability but not enough to live on my own. I was able to earn more a few months ago by doing freelance proofreading online and worked with my husband’s translation company. I have not been well enough to do that for months.

HOSPICE IS NO HELPAs for hospice...seems like cancer victims get pampered,especially if a Dr. can give an estimated time left,like 1 year orwhatever. Listen to the rules of my local hospice and see if itseems weird. My doctor MUST certify that I have less than 6 months.He says he can't do that, because only God knows when I will go, noperson does. Until I get a "time" of 6 months, they won't even talkto me on the phone. When you are enrolled, if you live longer thanthe 6 months, you will be taken off the program. So even if I amonly 10 days away from dying at that stage, too bad, I went overtheir limit. I am then on my own to die alone at the worst time. Isthat how most of them work? I think its barbaric to leave a person,walk out of their house with the equipment, meds and staff and justleave a person alone at their worst time, closest to death.I think when a person leaves this life, they have learned allthey needed to, so they have "graduated" from this school of lifeand they get to go home. She just learned faster than the rest ofus. Some of us don't have as much to learn as others. Some religionsbelieve that our souls lived with God before we came here, andlearned different amounts there, so that made us have to learndifferent amounts when we got to earth. some religions believe thatbabies who die were so intelligent and wise, that all they had to dowas to get a body for the resurrection. They didn't need to learnall that we have to learn. Also that same religion believes thatpeople who are born with mental limitations, like Down's syndrome,etc. didn't need to learn much, but that we need to learn from them.So now I am stuck in planning my funeral. I NEVER imagined Iwould be so alone at the last stage of my life. I moved to a newcity and was too sick to go out and meet anyone, so there would beno one to come to my funeral. All the years I was sick, I did haveideas of what I wanted, and now I'm a bit heartbroken to know itwon't happen, because I planned on sticking around (in spirit) tosee it, and to see who cared enough to come. I did see a movie where a lady had her funeral BEFORE she left, so she could see who would come etc. but then the lived longer than the Dr. said, so people got mad at her instead of happy for her. People are strange sometimes. I hope to hear from someone soon.
How do I tell, who do I tell? When do I tell? I have not even told my family or anything. I don't think I could bear their sadness, and couldn't bear their grief. It would "break my heart" even more. I told a few friends, but 2 decided never to speak to me again. One was onlineand I didn't know how much he cared about me, and he almost had astroke. Had to lay his head down on his desk for a long time, andwhen he recovered a bit I told him to go get a wet paper towel toput on the back of his neck and cold water over his wrists to drawthe high blood pressure from his head to the wrists.The other friend is just too sad about me dying, and doesn'tknow what to say to me anymore. I told her to just forget that I amdying, because if I have it my way I am NOT dying yet, and just talkabout everyday topics like we usually do, but she can't do it. Shewont even take my emails or phone calls anymore...so this REALLYmakes me feel alone. I don't want to cause anyone else to suffer.Has anyone else been through this or had a family member go throughall these things that happen when they get told they are dying?Blessings,Sheila
There are some books for people that are dying: One Year to Live by Stephen LevineOn Death and Dying by Elisabeth Kubler-RossDying WellHandbook for MortalsThe Grace in Dying : How We Are Transformed Spiritually as We Die Sacred Dying: Creating Rituals for Embracing the End of LifeAfterShock – What to do next when you or someone you love gets devastating news

I will live as fully as I can as long as I am alive, and I will just make my final arrangements and leave it at that. After all, we are all going to die and don't know when.
Actually my heart has stopped more than a dozen times and they have brought me back, then tell me I can't live more than 2 years, and I tell them "So? my heart will stop, I'll get sent back, and I'll still be alive" but this time when the tests looked so much more serious, it felt much more real when he told me I might not make it through a year...but I think I have things left to do on earth, and since my heart kept stopping, and I would have driven everyone in Hell crazy, and Heaven won't take me until I learn what I was sent here to learn and to do, so I'm stuck here on earth for a while. lol. Its just quite hard to be so sick and so alone, so support groups are GREAT.
There are THOUSANDS of groups for people who are grieving for others, very few for those who are trying to deal with the emotions of dealing with their own demise. Some say my family will never forgive me if I don't tell them I am dying, so they can say what they want to say to me, finish things with me, but how is that different than what happened to your daughter? No one had a chance to say goodbye to her either or say last words of love to her either, but you can still say those things even after the person has passed, and the message will get through to them. They KNOW we love them, and often they try to get through to us that they love us too, and that they are fine, so that we will stop grieving and keep living.

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