Grief support groups, condolence advice, funeral etiquette and more
A continutaion of the "When a Spouse or Partner Dies" thread.
Latest Conversations: 10 hours ago
This might be a rough time for many of you. Do what you feel you need to do to get through it. Remember, someone is here almost all the time to talk to you.
Started by Legacy.com Dec 28, 2017.
Started by David Heggi. Last reply by David Heggi Nov 22, 2017.
Started by denise. Last reply by Marsha H Oct 25, 2017.
went with my sis Barb to a scrap booking convention this weekend , we had such a great time and only had to leave the room twice, both times when tables next to us were discussing people passing away, one table was discussing what they would do if their husbands passed away, and believe me they are totally clueless on the reality of it and it took all my willpower not to tell them that. but all in all it was great but once again sad when I got home, was the only time that I kept thinking I cant wait to tell Greg about my weekend or show him what I did, at home I talk to him all the time maybe that's why, I don't know but I do know that I think Ive finally realized hes really gone, and while its hard and I know that I have a lot of pain to still deal with at least I feel better in that one little area, does that make sense?
Steve am sending prayers your way that they get your health issues figured out soon I know it must be so frustrating to be in pain and getting the run around,
I checked out the Face book link and only found 3 groups listed so far, none were for grieving spouses.
Good to hear that you are OK.
To All my family,
I am still running in circles trying to find out exactly what is wrong with my right hand and wrist. My PCP is the one that sent me to the Orthopedic clinic which referred me to a neurologist that ordered two MRIs and a sonogram of my thyroid. Went back to my PCP and he disavowed the findings of the neurologist insisting that I have nerve damage even though the tests say otherwise. So I am in the middle and fit to be tied, when my blood work came back all I got was a phone call stating everything was good. So I started asking the nurse specific questions about the bloodwork, what the ranges were for thyroid and where my results fell. I was told that mine were within acceptable ranges. That is when I lost it and said OK,what does my PCP recommend now since he does not accept that thyroid can cause nerve disorders...and so that's how the merry go round started.
So now in two weeks they have scheduled me with a Nerve specialist in another part of NJ (about an hours drive) and they assure me he will get to the root of my problem...in the mean time, the guy that has been mowing our yard always asks how Steve is doing, Chuck relayed the story to him and he asked if Steve has been tested for Lyme Disease. His neighbor is a carpenter and he started having carpal tunnel symptoms that kept him being able to grip a saw and hammer. His PCP tested him immediately for Lyme, his results were positive, he was treated with antibiotics and has recovered after about 30 days. Tomorrow I am going to call my PCP once more and suggest I get tested. Apparently it is a widespread problem here in NJ, last year when I arrived Chuck and I worked outside a lot and even during the winter and . Lyme can stay in your system with minimal symptoms that can be misread as having a cold, flu, allergies to pollen, mild arthritis, muscle strain and the list goes on. When I googled "can lyme cause carpal tunnel symptoms", it came back yes.
I just hope that if I do have it that I can get rid of it and if not that the other doctor will find the right diagnosis.
Thanks for letting me rant, all of this has worn me down to a place where I was not so long ago and wondering what next?
Hugs to all, your brother Steve
Marsha, It is great to hear from you. I was getting a bit concerned. The group has been a bit quiet. I'm not getting all of the alerts of posts either and perhaps that is prevalent right now.
Just to clarify my earlier post. I'm not going through those emotional symptoms of grief any longer. You were always here to remind any newbies that days did get better. I can now join your chorus and echo your refrain.
I had a wonderful day yesterday. A high school classmate and her sister were visiting my area for an annual winery tour. I discovered they were here via FB Friday night and reached out to let them know they were in my neighborhood. They invited me to visit wineries with them and we had a fabulous time. Neither knew of Bob's death. One of the first comments made was to ask how I was able to get away on a Saturday. I explained that they would have no reason to know that my husband died on July 22, 2015. We had hours of fun, wine, meals, and great conversation. It was a wonderful day.
Today I return to the mundane task of cleaning my house. I do plan to add some fun in somewhere.
Are others also not receiving post alerts? I'd love to hear how everyone is doing. Debbie
Deb S ... Unfortunately dear friend this is the way grief has been going for some. Ernie passed in 2011 and although I'm energetic, volunteer, go to Bible Study and out with friends or see my family there is just that hole there that I can't seem to fill so yes, I can cry uncontrollably every so often. I eat to live, I have energetic days and other days just like you I lay on the sofa not even pondering life. Other times I feel I have some sort of future. I really fluctuates depending on what is going on in my life. Even though I go through since this it becomes less intense. What you are experiencing is very normal and each day you get through is a day you are becoming stronger.
Dear Deb ...
You are so sweet to think of me and ask how I'm doing. I'm not getting any of the posts into my 'in box' and since the forum has been so slow I thought that was just the way it was. LOL Don't know why I'm not getting a 'heads up' on new posts. Hope it's fixed soon.
Luv ya girl
Mary Jane, Something to brighten your day (I hope)
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