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Welcome to all the new posters, like the ladies here said, it's ok to say NO, I had a hard time as well, Seeme, big hugs to you, it's hard going through the holidays, birthdays, etc.. Mom's birthday was January 13th, I know that I missed her then and miss her each and everyday. So many things I would love to share with her about this trip.

Ftarsley, Ladee is right, a glass or two of wine helps to relax you, heck, even if it just just sparkling grape juice in a champagne glass will help. the sheer act of doing something for yourself works wonders, like the other ladies here that can, I get outside in the mornings and enjoy my coffee, haven't been doing much of that during our stays at family's, but that is fixing to end as we are hitting the road again.

Ladee, tell those flowers they have to hang around till I get there, I'll buy a thermos, we can bring coffee and just go out and sit in the middle of those flowers. Chair or no chair, just don't watch me trying to get up off the ground, it isn't a pretty sight.

Watching hubby sleep (can't help it, we're in a RV) and wondering which one of us is going to be the first to require care giving.. going to be him if he doesn't start listening to me when it comes to his health. : o ) ear infections tend to go away faster if you don't wait a frigging month to go to the doctors about them.

BSO, when do you find out about the gallstones? they've come a long way in the surgery for them. But you still have to be very careful. No lifting etc.. Hope that all are having wonderful spring days and getting to be out in the sunshine for a little while.
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Well today and from now onits going to be a torture. Last night my husband got in a huge fight with two sisters that are near. For a long time I've been caring for There mother with vascular dementia n getting worse, granted theses sister only sat with her a few hours once or twice a month. NOW probably never. There very quick being judgmental and critical but yet do not experience what my husband and I experience. I don't even know what to do now because I've been having major health problems and currently waiting to see if I have gallstones or pancreatic inflammation been in pain since yesterday. I'm already burning out from the 24 hr care. Now this?
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Well, I made it through church and the building is still standing....no cracks in the road on the way home to fall in to......spoke with the priest for a few minutes. He even announced that the Mass was being said for mom and that her daughter was there to help celebrate it.............to all the other 10 people there. The Catholic school is attached to the church.......I can remember being marched to church every day when I was in school.....through 8th grade.

Sinus problems are driving me nuts. I hope everyone has a good day.......and that those on the edge of burnout get some time away..........please check into it.
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fyarsley.....welcome! Some wine is actually good for you and a couple of glasses are fine. When you begin to drink out of the bottle and are opening more than one a day....well that's when the big problems start. Do you have help coming in to take some of the care giving burden off of you? If not, you might want to consider that as it sounds like you are moving toward some burnout. We have all kinds of different ideas and suggestions so come back and visit with us....hugs to you!
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Good Morning Posse!

lildeb....your mother-in-law sounds so much like mine so I can greatly sympathize with what you are going through. When the col was still living here in her own home, we built her a small house attached to our house, she could still do a few things on her own but she was getting worse each day. Left on her own she would never bathe and would fix a Banquet frozen dinner for every meal...she remembered her morning meds because she knew she needed Nexium but wouldn't take her evening meds at all. Before I took over doing most everything for her, she wore the same diaper for 10 days, so no bath, can you imagine the smell? That was my first clue that something wasn't right. So the Alzheimer's is going to get worse....whether it's mild, moderate, or severe there are going to be different things to deal with every day. And as for holding conversations...well you will swear that your mil is only pretending to have Alzheimer's because of the normal conversations she will have. There will come a point where she is confused about the steps in bathing, feeding herself, dressing herself and you will need to step in. Remember that most son's are not comfortable doing those things for their mommas. That was what I dealt with here. Even though hubby/son is a physician there were certain boundaries he would not cross with his momma. We hired 2 women to come in 5 days a week from 10am to 4pm....I didn't do a bit of care giving during those times....but I still had that task in the evenings and every weekend and it was hard on me physically and mentally. I strongly suggest you get some help and get away from home when at all possible. The cost of help comes right out of mil's bank account. You don't have to pay for it. It is not possible to be a care giver and not have it impact you in some way and now is the time to make some changes to the routine...it will be easier on all of you.....remember that without you there is no care giving....save yourself first then you will be able to "save" everyone else. Hugs to you!

Swim ladee AKA Benny!!!!!!!! I know the feeling.....I'm beginning to quack like a duck.....weather radar looks like we might get a little more of the rain later today...looks like it's moving out of your area.

stormy....Dad's vitals sound good for his condition. The nurse has been in her job too long if she is that comfortable with her reaction.....or not long enough if she hasn't learned to hide her reaction. You might want to keep in mind that it's usually not normal to have blood coming from body openings, would bear having it checked out.

Hope everyone has a wonderful, DRY day.........hugs to all!

Happy Trails,
Jam
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Take a walk 15- 30 min..or a good hot shower..wine is good too any thing that helps to break the emotions through the day. God Bless you
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I can certainly relate...my mom live w/me too, she's 87, she doesn't have much mobility due to a stroke 12 years ago, therefore, her memory is not all there, it may be dementia not sure, she is also legally blind. I do almost everything to try & give her quality of life, however, it does get frustrating. She's been living w/me & husband for 2 yrs and for about the last 6months or so feel like I can't give anymore...classic case of burnout!!! We have a glass or 2 of wine every late afternoon, I now look forward to it as it seems to be my coping mechanism, it worries me though, but continue to have wine makes me able to cope better. Any advise or opinions...
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Ladee..glad the rain is gone..it is on its way here..
Lildeb ...you have to get some you time ..even if it is only a few hours a week. Your mil should qualify for help through your area on aging ..is there and adult day care anywhere near? My husband stays with my parents so I can get some away time..it sucks cause we aren't together but sometimes it is the only way to get such much needed away time.
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Woke up today feeling like some of you this morning, the not getting a full nights sleep, oh the memories of Ruth, calling me "Benny", her brother, thinking it was time to get up... but this time it is from coughing from the cold.... so my heart goes out to all of you who didn't get to sleep all night.... I do beleive that is the one thing that wears us out the most...then we are too tired to deal with the day to day stuff...
Hope you all have a day, if not a good one...
And Seeme, I'll be waiting for the rumbles... hugs to everyone..
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Seeme..she will be jumping for joy..I will have you in my prayers today
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Today is my mom's birthday. She would have been 84. I will attend a Catholic Mass in her honor. Hopefully there won't be any earthquakes today............never can tell...............try not to hold me responsible...................
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Sorry it was one of those days for you lildeb. we all have them... and yes sometimes we raise the roof... no perfect way to do this job....but I am going to suggest since you said you are new at this, that you educate yourself about ALZ... it will save some of your sanity..that is my job, taking care of Alz patients... right now I am stuck as a housekeeper to a grumpy old lady and her husband has ALZ.. I have seen a decline in him over the winter... He also dresses himself, takes his own shower, but can not remember where the bathroom is... I know it is hard to know when it is AlZ or when they are just being stubborn... I can get Sonny to help with chores , like folding towels, he absolutely refuses to fold Marie's panties, lol, but soon as he sets down he has forgotten what he was doing... but he is further advanced than you mil.... so we can't gauge it on the fact that he dresses himself....And routine is absolutely neccessary for Alz... and I tell Sonny everytime I leave the room what I am doing, he doesn't remember, but like if he is in the bathroom, I knock on the door and let him know the noise he is about to hear is the vacuum cleaner, so he won't be afraid while in the bathroom and hearing a strange noise... is it tiring , yes, but it helps to keep him calm, and there is a possiblity she got so irate this evening about the 'cup'( read your other post) becuase she was embarrased... not saying that is all there is to it, you live with her, we don't... and am not trying to make excuses for her... there were times Ruth would be up roaming around and getting into things... one day walked into the kitchen and she had the sugar canister down and had both hands in it... and had no idea why I as upset, becuase she had no idea why she had done what she did... so please, read as much as you can about Alz, and get that respite day, and soon.... we HAVE to have breaks, we have to... hugs to you and hope you take a little walk or a hot shower and take some deep breaths.... you are doing a good job whether it feels like it or not... come back and let us know your face hasn't turned blue from not breathing.... hugs to you...
a
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Jam, I feel ya from your top post and I do try to be optimistic with the mnl but right now I'm at my ends wit and need to just breath! Someone told me and not from here to start taking daily notes of how the mnl attitude changes and stuff she does and give it to her doctor at the clinic so he can see the true side of her. he diagnosed her with mild AZ but I really believe from the stages she is Moderate yet, she still can have a half decent conversation sometimes. I have to admit it can have an impact on our marriage as well. Right now she is not that bad to be placed in a NH for she can dress and feed herself, take a bath except I do get the water tub ready and all other necessities and clean clothes as well or she will put the dirty right back on. She can help vacuum the house when she not in one of those nasty moods or wants you to feel sorry for her and tell us that she is old and not a young chicken anymore. She is more healthier than my iss! and I'm only 47. Working on with the hubby about either give me a one day weekend to myself or get someone to come out at least once a wk. It would really be nice to have both but he is the one bringing in the most money for mine is just SSDI and the mnl is SSI and Medicare. I cannot believe that the NH has your mom taking a bath TWICE a wk. I do good if I can get once for her. I am glad that you are able to start back enjoying her company and I bet it is for your mom. My mnl was never really nice or lovey and i could never do enough right for her grown iss son. So, I don't really see her going to make any big changes. So we have our good moments and we have some bad and then we have the raise the roof off the house where she will get right in my face and that is where my limit comes. So, hubby threating to put her in a NH if she couldn't behave around me his wife for he told her that I was the one that was keeping this family together. That part I liked but not the threat her in a NH and I told him off to the side he shouldn't do that to his mom. But, we are both new at this mess as well and still learning.
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Sorry ya'll, not getting notifications, emailed admin, so hope it gets fixed soon...
We got 3 1/2 inches of rain in three hours this morning...had to detour to work from water over some of the roads... nothing bad that I've heard about, a small tornado in Medina, but a lot of lightning and thunder.... sun is out now, and it's going to be a pretty weekend, I have to move my stuff from BG's so thank goodness it will not be raining...
I forgot to tell ya'll I got to meet Marie's sister yesterday,,, I am telling you, one of them is adopted because if there were ever two people nothing alike.... and sis is in a lot worse shape than Marie, walks with a cane, and has an awesome attitude....If I could pack up Sonny and move in with Mamie (don't you love that name!) I would be in hog heaven...Her husband is 95 , has skin cancer, and is an absolute joy....If I live to a ripe old age I want to be just like them....
I was thinking today that if I am blessed to have a caregiver and not have to be warehoused in a NH, these are some things I hope I can do, if I am in my right mind...
I will appreciate who takes care of me, and I will TELL them this, I will work very hard to not take my illnesses and old age out on them, I will aplogize if I do...I will be so grateful that someone is cooking for me and scrubbing my toilet, and I will tell them this... I will not expect them to keep moving the whole time they are there, I will ask them so set down and tell me about themselves... I want to know about who is taking care of me.... and the list goes on... I know each of you may have thought about when we need care, how are we going to be different than the ones we care for now???? Just a thank you once in awhile would go a long way....a surprise day off would be so nice, with pay, or I would have made arrangements for someone else to come in for a few hours... If I am in pain, I will take my meds like I am supposed to and drink nasty prune juice so I am not bitching about being constipated...I will not nit pick the small stuff, and when I do need something done, I will try to remember how Marie is so harsh and unforgiving, and try to be just the opposite.... All of this depending on if I am still in my right mind.... by then we should have a sight for elders bitching about their caregivers..... lol... hope ya'll had a good day, more later...
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The nurse had no right to get an atitude with you-that is not her job-she is suppose to relay your worries to the doc so he can explain what something means.
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still feeling under the weather and have ti get ready to get hubby ready for his therapist appt and as for me I can hardly think with this sinus fog overriding my other senses...oh i forgot to mentioned i am like on 12th burnout round and recognize the symptoms ...bored, hardly sleeping and not interested in nothing and oh yeah hating all the fun stuff i have too...someone pls meet me in a bar and watch me get silly drunk tonight or give me a gift certificate for a spa day ...i need a VAC KAY badly but mothers do not get those easily off for now ttyl Peace N God Bless
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I told the nurse about dad coughing up the blood last month and she said did ya'll carry him to the hospital and i said no. And she said why not? I told her that sis thought that it was coming from him not wearing his humidification mask and she just looked at me like, "What, is she crazy?" The nurse told the dr about the coughing up blood, shortness of breath, and said i was wanting to ask him about the honeycombing of the lungs. Well the doc said that he thought dad might have some infection and wrote him a prescription. And about the honeycombing he said that most of the time it means end stage fibrosis, but that dads was at the bottom of the lungs and the fibrosis affects the sides of the lungs. And dads weight at the drs office was 205. His bp was 150 over 94 and his oxygen level was 92. So that was about it what the dr said. I hope all of ya'll have a good day. Love and hugs stormyyyy
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notlike, thanks for asking. My wife's hand is continuing to heal from the carpal tunnel surgery and thus is able to do more of the things she normally does. There is something wrong with her foot that the podiatrist has yet to totally figure out.
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Notlike...I would have left the room too! Haha just give her a blank look if she says anything. Hope dad had a better night with c-pap.
Ladee..so glad you are letting things roll and being yourself I know you feel better at the end of the day. Hope everyone had a decent night.
Love and prayers..
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I will let ya'll know what the dr says tomorrow. As always praying for answers that will never come... Love and hugs stormyyy
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Stormy-let us know what the doctor says. You are doing the right thing by talking. Hugs, hugs, hugs.
Cmag-how is your wife doing? I haven't been on the other thread in awhile. Hope all is well.
Ladee-be careful in the bad weather. Hooray for your attitude today with Marie! Much better way to spend the day. And my stand with Mom just keeps getting bigger...thanks to all of the support here.
I was so nervous about dinner yesterday, especially after the way Mom acted at Thanksgiving. She did put on her "good person" face and interacted with people. That helped. I ignored the snide comments on the way there and back. And when one of my SIL used a very descriptive word for a male-only body part, I just left the room! Figured it was better than getting glared at. I haven't heard any complaints yet from her, but dinner was just yesterday....
Dad's new C-pap is so small! I thought it would be alot bigger. Looks like it's pretty easy to run, too.
Goodnight, and better tomorrows.
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notlikemom, very true, I am not the same person that I was back then with all of the self-insight that I have and what I'm doing with it which is helping others and means the pain is not wasted.

ladee, true I didn't analyze and paralyze my venting :) When I first got on this site, I do remember a few times back around 2 years ago that on some threads I really jumped in there with both feet. I get so triggered by dominating, narcissistic, abusive mothers who treat their adult sons and daughters like little kids and could care less if it damages their marriage, plus blind them with F.O.G fear, obligation and guilt to keep them from seeing what is really going on. True, the anger over some things never completely goes away and neither do the flashbacks, but I think that I'm more in control of that anger now via therapy than I was before.
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Cmag, how wonderful that you vented and did not self analyze to the nth degree!!! I don't think that anger goes away about some things, I just think we learn how to channel it... Nothing you said on here was too strong, it's how you feel...
There are things that trigger me too, hearing about a child being abused, and to this day, the rage is there...If I was on a sight about child abuse, I'd vent...
Wonder, hope some answers have helped you today... all of us pretty much said the same thing... take care of you.... it's not easy after a life time of 'pleasing' others, but it can be done... even Notlike has made a little stand with her mom.... and as I said, we are works in progress, we are better, but we haven't arrived anywhere, still plugging along and learning from each other....
I walked into work today, first words out of Marie's mouth, and I'm going to do it in caps because she was not saying it softly, " THERE IS A PAN ON THE COUNTER, DO NOT USE IT UNTIL YOU SCRUB ALL THAT GREASE OFF OF IT, SO MUCH GREASE ON THERE IT WILL START A FIRE!!!!" As ASG would say, 'blink blink, ya think'.... I hadn't even put my purse down, so in my best Texas drawl, I said, ' Draaammmmaaaa Maaaammmmaaammmaaa" ie Drama Mama....
then she did the 'blink blink'... then I said, "good morning to you too Marie".... went on about my business.....even a few short weeks ago that would have sent me into a tailspin... stuffing feelings all day, being angry and hurt, but when I talked with her recently, told her then, I was going to start coming back with something... I use humor, for me, she's not a very happy camper so that is what diffuses it for me.... of course she was grumpy all day, what else is new.... I didn't feel good with my cold, so just stayed in the 'zone' and did my work.. but two things that happened and I don't consider myself passive aggressive, but I have to wonder...
I was getting ready to go out and smoke, lit the smoke in the HOUSE !!!!! I was pumping my fat ass out that front door!!!! She never said anything, so she must not have smelled it or I never would have heard the last of it... and then, I look at the clock and start fixing lunch... alrighty, making good time, noon sharp... look at the clock again and it was only 11, !!!!!! Bwhahahahahaha, and this is after she had told me NOT to cook the noodles until I was ready to put in on the table...I didn't even tell her, just heated everything up, no complaints for lunch... so I am sure I am going to get some feedback from this from ya'll, that's what happens when you are hired as a caregiver and your mind turns to mush from being a housekeeper and verbal bullet dodger.....
conclusion, Marie is feet made of clay just like me, she chooses her ways of doing and saying things, and now so do I... so taking my power back, little peices at a time.... hope everyone had a good day. Everyone that had Dr''s appt.s let us know how things went....
Bad weather coming this evening, so may not be on the computer when it hits.... but love ya'll and just keep comin' back.... headin' toward the future...
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Thanks Notlike I appreciate your input. I know it has been worrying me and along with the shortness of breath and now with him losing 11 pounds in just a little over 2 weeks. I feel that is not right either. So i think i will tell the doctor and just see what he has to say about it. I hope he has some answers as to what is going on with him. Much love and hugs to you!!!! Stormyyyy
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Stormy-TELL! No question about it. Doctors need to know what is going on. Let the doctor decide if it's important or not. Docs need the whole picture, so even little things can be important for them to know. And if it is making you concerned, it IS important. At least, the doc may be able to give you an explanation and ease your worry. Hugs.
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So many things going on with everyone in just a few days. Welcome to all the new posters and glad you found us.
Starri-safe travels when you do pull out!
Jane-the decline is one of the hardest things to watch. And it makes us have to re-evaluate and find new solutions for new problems. Hugs.
Stormy - 2 years, now. Hugs and blessings.
Jam-most everyone seems to like spring or summer, but I love fall. The cool, crisp nights, the colors, and knowing it will be time to hibernate soon! (There's a reason I collect teddy bears)
ASG2-sounds like your Aunt is having almost like night terrors. At least she is able to get back to sleep.
Vic-Sounds like you had a wonderful day of rest! Good for you. Good for hubby, too for helping. Let us know what Dad's blood tests show.
Ladee-Maybe if you gave the fire ants some drugs from the neighbors, they would mellow out and not bite. LOL
Wondering - Decide right now that you will survive this! You can, and you can make it better for yourself. There are wonderful people here on this site to help. You are not alone. It's not easy, and it can be a thankless job. Don't be afraid to vent. Many of us have been where you are now. Hugs.
Cmag-It can be so hard looking back. But the past is past. You are not the same person now that you were, and you've learned alot, especially about yourself. Your insights help the rest of us here, so as awful as it was, there is some good and a reason you went through what you did. Hugs.
We get Dad's C-Pap machine later today. Then All Quiet until Mom's radiation starts next week. Everybody, incluing M&D, went to lunch at my in-laws yesterday. Ah, the stories I could tell...
Smiling and having a good day. Hope you all are too.
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Hey everybody i hope all of you are doing well today. Dad has a drs appt today at 3 but sis is going to have to take him to that one. Its with the dr that done his throat stretch a couple of weeks ago. And sis told me today that me and brother are going to have to take dad to his drs appt with the lung dr tomorrow. I just don't know if i should say anything to the dr about dad coughing up blood last month. I don't want to make more out of it than what it is. But what if something is going on and i don't say anything about it. I just don't know what to do..... I asked brother and he said that i should tell him about him coughing up the blood. So i guess i will have to decide what to do between now and tomorrow. Love and hugs stormyyyy
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For those of us with narcissistic or borderline parents, I think we tend to not want to "upset" them, so we take their abuse as adults because we did as children. When I look back several years concerning my mother, I know why I did not act with my Durable and Medical POA sooner than I did. I did not want to upset my mother and my would my step-dad have fought me tooth and nail. She made me joint owner of all of her personal bank accounts with the right of survivorship the year of or before she gave me both POAs, but did I go online to keep an eye on things. Nope, but had I, I would have seen the IRS was garnishing her funds and had I been willing to upset her worshipfulness, she and my step-dad would have never gotten in the tax mess that they did. When she did tell me about her long term health insurance policy, I should have dug around for it then for I would have found the riders she paid for to provide her home health care and home builder care for she still wanted to stay at home instead of going to go to assisted living like her neurologist want her to. Plus, at that point with medical POA, I really should have been going with her to those appointments and interacted with that doctor sooner than I did. Had, I fought that battle, my mother and step-dad probably would have never hired that stranger who stole so much money from them. I knew something was not right about taxes at some point, but I believed the lies that everything was ok instead of boldly moving forward to make sure. I was even willing to call my mother three times every day, at one point, to see if that would keep her on her meds regularly, but that did not work either. I really should have moved for some change at that time, but I was afraid. It was easier to stand up to my MIL whom my wife had lived in fear of since childhood, than it was to stand up to my mother whom I thought that I had more freedom from but I didn't. I could hardly believe my ears when her sister told me that she knew in 2004 that my mother was behind in filing and paying taxes, but she did not think of telling on her older sister who is evidently afraid of her as well, and get this she has all three of her grown boys afraid of her abusive iron hand that controls them despite their being married with their own children, but that is another story of her abuse of her boys in itself and unlike me, they don't see it for they still bow down to their own mommy dearest. So, I can definitely see how one can be willing to take the abuse and not risk making them mad by not standing up to them when doing so is really in their best interest which they can't and don't want to see for one thing they still view us as their little child who is supposed to obey. I will add though that when she made these POAs and her living will was the same time when I went into sever depression, had to leave my work and go on disability, but still I could have done more sooner than I did. It has helped to deal with my anger, etc. concerning her in therapy and my own anger toward myself, and it is great that my wife is no longer afraid of her mommy dearest since 2005. Well, I've vented a lot this morning. I didn't know all that much anger was still inside of me. Some of the stories that I read on this site from time to time trigger some memory feelings from the past and I've learned not to write a response normally right then because I know that I will unload which is not healthy, but I think that sometimes I have come on way too strong at times on various threads on this site because of that. I hope everyone has a better day. Thanks for listening or should I say thanks for reading!
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What Jam andLadee said it so true when I made up my mind that it was not my job to make the husband happy it became easier and when I said no the first time to one of his request the sky did not fall and each baby step I took made me stronger and I was able to move forward-when he would call from I would turn down the answering machine and later just errase his ramblings.
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Good Morning Posse!

Sitting here drinking my morning coffee and waiting for the rain to move in....4 days of rain.....my pond will love it...I, on the other hand, am not looking forward to carrying the blind doggie outside to potty....it's a good thing she is old enough that she sleeps 20+ hours a day.

Wondering.....I understand and can sympathize with what you and your husband are experiencing.....my mil was getting to that point before we placed her in the NH....before dementia she was the sweetest thing and still had her moments, but she was getting more and more verbally nasty. One thing that people sometimes don't stop and think about is that there is no unwritten "rule" that says you have to care for someone in your home. Especially when that care is impacting all other relationships, like marriage. We tend to not want to "upset" them, so we take their abuse, it starts to creep into every part of our daily life, making us resentful of them, resentful of the person who put us in that situation and things just start to go downhill from there. Soon the dementia is going to overtake your mil to the point where she won't remember when or who she is angry with...but you will still feel the hurt and the sting from the words. You have some different options and there will be some different opinions offered to you here to help you through this.....I am an advocate for placing a loved one in a NH when necessary.....I took care of my mil for almost 2 years and she was becoming more and more too much to handle even with help coming in. Now she has the best of care 24/7.....three meals a day, snacks all day, bathed twice a week, meds given, PT when needed, and all I have to do is visit with her. The one thing I noticed quickly was that I started to enjoy her company again.....it's amazing how much better it was knowing that I didn't have to walk around smelling like poop or listening to her tell me what a good driver she was....:). Bottom line is that you don't have to take abuse from anyone, especially in your own home. A simple "no" is very empowering....come back and visit with us, we'll leave the lights on..........

It's the start of a new week and I hope a good week for everyone.....my thoughts and prayers are with all of you as you go about your care giving..........

Happy Trails,
Jam
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