Losing me!
We do so much, give so much, care so much and as a result we lose who we are, who we were! Please I miss me! I miss my belly laughs, I miss my glass full, I miss my friends, family, life, laughter, that joy of each day! How do we reclaim the “me”? I won’t give up on DH nor will I give up on me, but how do I reclaim that person in me that made me me? I miss me!
Comments
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As they say on airplanes, you need to adjust your own oxygen mask before helping somebody else with theirs. Seeing to your own mental and physical health will also benefit your DH in the long run. Are you able to leave him alone for short periods or is there somebody who would be willing to sit with him for a short time? The joy of going to the grocery store alone or meeting a friend for a quick lunch always leaves me feeling better. I also highly recommend an in-person caregiver support group if there is one available near you. While this site is amazing, human interaction is irreplaceable as our social circles dwindle.
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Tks so much! Needed some affirmation and hope! 😘
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@JC5 thank you for posting this. I sometimes feel guilty for continuing to maintain my sense of “me”. I have a 2 - 3 hour weekly get together with 4 friends. In scheduling my husband’s numerous doctor appointments my Tuesday friends day is non negotiable. So far I’ve always been able to schedule around Tuesdays. My time with these friends helps keep me “me”.
Keep looking for ways to hold onto “you”, you absolutely deserve it. It makes a world of difference for me in caring for my husband.
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This is so important. We all have had those thoughts about losing ourselves, and there should be no guilt involved. Being a long term caregiver is harder than anyone can ever imagine and if you lose yourself in the process, you may not be the best you can be for your LO. The only way I found to get back some of me was to bring in some help when he couldn’t be left alone. Even just a few hours a week is a help - it will be better for both of you.
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I had my daughter provide me with some respite for only one hour today so I could run some errands. That one hour was so enjoyable! I didn't have any worries. I felt free. I felt like myself again. You need to find relief for yourself so you can have some down time. Look at in-home care if you can afford it.
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JC5, I could have written your post. I felt I was losing my strong, independent, funny, witty, optimistic self. Caregiving wears you down and can skew your view of life. For far too long I didn't realize the importance of prioritizing time for me. I was miserable, short tempered with my DH, ate too much and drank too much to numb my unhappiness. I finally decided my husband is sick but I am not. This disease will take him, I can't change that but I refuse to let it take me too! He is not at the point yet that he can't be left alone. I walk for 30 min most mornings and make sure I get out one afternoon a week for about 3 hours. Today I went to the movies alone and it was a wonderful escape. I highly encourage you to plan time every week out of the house. If your spouse can't be left alone safely, hire someone. I realize it is expensive but losing your health, yourself, your sanity or your life is a far greater cost. You deserve to live and also have some peace and happiness. Hoping you find the strength to save yourself. 🫂 and 🙏
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From my experience, you really have to commit to fighting for you, however that looks for you. I hate to fight my guilt at leaving my DW with a caregiver, but I finally got a couple of caregivers so I could walk on the beach by myself and run errand for 3-4 hours 4 days a week. I still nearly crumpled with the stress of it all at the end of my DWs battle with this mean disease, but it's the only reason why I feel like I am able to feel gratitude, laugh and feel a commitment to honor the joy, kindness and love my DW spread each day of her life. I know it's also the only reason I know I'll find my way through my grief at her loss now that she's gone.
Please find a way to get some respite. You're worth it!
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Just throwing this out there for people that may not know, if your person is a veteran you should qualify for respite care or a caregiver. I'm fortunate to have this and our daughter and son are very good about staying with their dad when I need some time away. Do I feel guilty? Yes! But I'm so much better for myself and my DH once I've had that mental time off. Good luck and take care of yourself.
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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