Guest guest Posted March 26, 2002 Report Share Posted March 26, 2002 Marilyn, That is such good advice for all of us. God Bless, Belinda > Noreen, > > This message is too long. I apologize before you begin. > > I like the others are very sorry that you must be with us on this list, > but I can tell you that I have learned much from this group. There are many > people here with different experiences and different opinions. I am a night > person, so I have spent many a night reading these messages. In many cases, > I have been able to see that something going on in our life was similar to > events in the lives of others on this list and be relieved to just know that > others are having similar experiences. My husband's symptoms have advanced > fairly rapidly following his diagnosis, in 1998. Infact, the only way we > can move him now is with a lift attached to the rafters of our home and a > power wheel chair. We know that he had many of the symptoms for years prior > to that diagnosis, though. > > We certainly are seeing that no two people are the same. I am sending > you info about our family, but do not take us as the gospel. Who knows > whether we are average or not. > > > My husband is the MSA patient and I am the caregiver (Well, sometimes I > wonder, if that is really true.). I am responding, because I see your need > and that of your folks from a different perspective than you might. I hope > my thoughts will be of help to you. I am 63 and my husband is to be 70 in > April. Our sons are between 36-41 who are very caring, but also have very > demanding jobs, plus wonderful families. In addition (but thank goodness) > they want to spend lots of time with their own children/wives. We want them > to do so. > > So we can see the strong " PULL " of emotions, physical needs, guidance > and so on that comes from the parents who were 'smacked in the face with > this illness' and all of the circumstances that go with it, plus the needs > of our sons with growing, but young families. Our sons will do anything for > us, but we do hate to ask them. I will say that in past few months, I am > less hesitant to ask. > > I will include some ideas that I have written previously for others. I > hope they will help you. My husband and I may be a little more/less needy > that other families, because I had major coronary problems within the year > following my husband's diagnosis (two heart attacks, angioplasty and finally > four bypasses.Now congestive heart failure) I do not think that my health > problems had anything to do with my husband's diagnosis. My problems are > genetically oriented, but my weakened health has probably made me some more > dependent upon my children than others may be. > > > I would suggest to you. Don't leave it to your parent to tell you > anything. He/she may want to but be unable emotionally/intellectually to > tell/ask. > > 1. This is the most important gift that you can ever give your parents, but > it takes time and commitment. Don't just say, " I love you " . Show them your > love. You may have to make major changes is your lives today, but remember > they made major changes in their lives when you needed them as an infant. > That may be exactly what your ill parent has become, an infant. > > 2. No matter where you live or where they live, go to your mom and dad. > Stay for a period of time. This trip leave your children at home. Neither > you nor your parents need the distraction of children. Don't just drop in > for an hour. Stay long enough to see what really is going on. Take things > in your own hands, but remember they have a routine going. It will take > time to change old habits. Some of those very things that you disliked the > most in your home when you were a child may be the very things that they > want to hold on to now. Remember it is their home, it is their life. > > 3. Make it a point to go with your parents to the doctor. It always helps > to have more than one set of ears. Doctor's offices can be very stressful. > Even though my husband and I are both of sound mind (we think), we sometimes > hear two different things when we are at the doctor's. This happens for > either one or both of us. If it is not possible for you to actually go with > them, get written permission from your parents for the doctor to meet with > you to discuss your parent's condition. > > 4. Make arrangements for you or your spouse to help your healthy parent > care for your ill parent on a regular basis. If that is impossible find > someone to help on a regular basis, whether they think they want the help or > not. Find someone to clean house, cook a few meals, sit while your well > parent runs errands, etc. Be sure it is going to happen week end and week > out. > > 5. The most important thing your healthy parent needs is your support and > love. He is already grieving for the loss of his/her ill spouse (as she has > known him), the loss of his own life (as he knew it), and many other aspects > of their life together. Your healthy parent may well be in a psychological > shock without being able to recognize it. She may need some medical care > herself. > > 6. Put all of your energies to loving your parents and showing that love to > them in actions and not just words. Do all you can to make their life > comfortable. > > 7. A young friend who was my employee prior to my retirement is dealing > with her own parents. The mother has Parkinsons. The doctor has said to the > dad that he must get away. His prescription for the spouse is to have > outside help at least 8 hours a day, one weekend a month, and one week every > two months. I¹m not sure that either my husband or I would ever be willing > to this much time away from each other, but I am seeing the need for help. > > My thoughts come from the fact that the members of this list are mostly > caretakers and patients. In most cases, we are not medical professionals. > We all care for each other, but we also see that the illness is different in > each case. > > I will be happy to discuss other issues if you like. Please know that I > care for you and your parents. My thoughts and prayers are with all of our > families each day. If you live anywhere close, I would be happy to meet > with you or your parents. > > > Best wishes to you on your journey. > > Marilyn in TN Quote Link to comment Share on other sites More sharing options...
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