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Dearest Friend,
Everyone has pretty much summed up what I believe as well.. I just wanted to offer my support in whatever way I can. You know, there are perfectly healthy women out there who would not be able to handle raising teenagers, caring for an ill spouse, helping adult kids when needed, and working. None of us are super human. Take the time to care for yourself, and all else will work itself out. :hug: and best wishes! |
Decision to Reduce Work Load
I have decided to work just half time starting with the next school year. :( I have already worked it out with my district. They are very supportive... I am very lucky in that way. I was considering retiring completely, but just can't close the door that tightly yet.
You folks have helped me work through this MORE than you can ever realize. :grouphug: The decision was SO huge for me. It's hard not to feel like a failure. :o But I now realize that it's just me feeling that way, not the rest of the world. This has been a big step for me. It's hard to let go of the person I thought I was. I'm starting to look at myself as someone a little different, not lesser, just different! This is such a huge revelation for me.... it bring tears to my eyes as I share this with you... It's bittersweet. My hubby, feels I probably should retire full time. He is the one who sees what I look like every day when I get home. But he is being very supportive of me not being ready to give it up completely. I'm not completely confident of if I can make it even half-time. But I have to try it that way. Thank you so much for your kind words. I have done just as I said and pulled them up several times to read them for strength. :hug: I love you all. |
I won't complicate it with more words.
Just a big Moose hug for you. ((((Friend)))):hug: |
Hey Moose~
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I will have you know that I WAS (IN BIG CAPITAL LETTERS) was the QUEEN of multi-tasking. :cool: You were so right....over-rated big time!!! I am now SINGLE TASKING! Still the 'queen' ...ha!...but slowed down big time! (Can't give up everything!) :p Tapering off is the name of my game now! Thanks for the advice! :hug: |
Hello dear,
I am sorry I missed your original post but glad to read today how you are changing and adjusting. I too had a disabled husband and a very challening marriage as a result. Not his fault, as he had short term memory damage and I had very intrusive in- laws. I fought for him, advocated for him until the end. He was so toxic from his medications, 2 brain operations, etc that he died, suddenly and unexpectedly. I am glad for him that his suffering is over after 46 years of meds and seizures. I never knew what a toll taking care of him and putting him first played on my health until now. He also was upset I think that he could not truly care for me a I did for him. His parents played that up and as a result he would live with them and not me. STRESS can and will kill, slowly or quickly. We must take that seriously. Prioritizing, and delegating is so important. AND to re-think your goals and calling in this world..amazing!! What a learning experience!!! Keep us informed and let us know how you are doing, the good and the not so good. Warmly, Jan |
Dear Jan,
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Thank you so much for sharing with me. I am truly sorry for what you have been through and can certainly relate to most of it. It can all be so very stressful. My hubby does feel so bad that he can't be the one to take care of me. I try to let him do little things for me when he offers, even if I don't really need the help. We are just doing the best we know how to do... taking it one day at a time. Luckily, we have God in our lives... We are still human, however, but having our faith gets us through a lot.:) I wish you the best. Yes, I will keep you updated. I have gotten so much good from everyone here at NT. This website is truly a blessing. You take care! :hug: ~Friend |
In addition to drugs for fatigue, I'd suggest getting ahold of the local MS society for help. There are local support groups that you can join and these groups will be a life saver for you, trust me. You need to hear what others are going through and you need to tell what's happening to you to others who have been there and gone through it.
Don't delay make the call and go visit them. That is why so many people walk for ms. Quote:
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Michael,
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I had kinda "forgotten" about a local MS society, though at one time I did know about it. That is a good idea. I live about 60 miles away from the city where it is, but when I go back to town, I am going to check it out. Thank you so much for the advice! Take care! |
Hi Friend...
Hi Friend,
It sounds like you are truly taking care of yourself by deciding to reduce your work load...though I understand the feelings associated with that :( I'm sorry you are having to go thru this. As for MS Society stuff - they offer lots of support in addition to in-person stuff. I recently completed a TELEPHONE support group for newly diagnosed individuals (I think we ranged from 1 month dx - me - to people dx a year or so). Anyhow, every Wednesday night for 8 weeks we would meet on the phone together. It was run by a therapist. I know it might sound weird - and at moments it was - but it was also really good and helpful to me. They also have a program called "Knowledge is Power" where they mail and email stuff to you. You should check out what they have to offer you: 1-800-FIGHT-MS. Good luck, ~Keri |
Thanks Keri!
I appreciate the phone number and will give them a call. I "think" / "hope" the shock of it all is sorta wearing off. Maybe going into having summer break in a couple of months, I can kinda settle in and get better oriented. The last few months have just been a whirlwind. :Doh: I am trying very hard to be realistic and starting to make some gradual changes that will be beneficial. Thanks for the help. You are all great! :hug:
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