I Am Reeling, Again 😪
Warning: this is a woe is me pity party post, so if you don't want to read my complaints you can stop now. If you want to hop on my pity bus, here we go... 🚌
My husband has had dysphagia (swallowing issues, common with dementia) for several months. His Doc referred him for a swallow study, and we waited 7 months for that appointment (we live in a small town and the hospital only does 2 tests/day, thus the long wait). Meanwhile he was coughing and gagging all the time till we got to see a speech and language pathologist finally last week.
So, this has thrown another wrench in the works and I pivot, again.
There are now tons of things he can't eat (not even bread unless it's made with specially modified ingredients), not quite to the puree stage but nearly. I even need to add a thickening agent to his drinks because thin liquids are problematic. He coughs when he drinks water or coffee, which I don't add the thickener to.
This past week has done me in! Modified foods and beverages, special textures required, slow pace of eating and drinking, and very small bites required. He also has to be monitored while he eats and drinks. I have had an educational week learning all of these new things. Because of his lack of impulse control, he had been eating VERY fast, huge bites and eating mindlessly (and yes, gaining weight). Now I have to sit next to him, cut up his food into tiny bites (because he won't), and physically keep him from shoveling too much food too fast into his mouth. I have started saying 'spoon or fork down' after each bite, or 'stop' if his bite is too big (he doesn't always listen so he gets a lecture about food safety).
This is like having a baby again. More of my precious time is now dedicated to meal prep and planning and sitting with him every time he wants to eat or drink.
Another time suck is that we have to do 8 sets of swallowing and muscle strengthening exercises daily; he can strengthen his swallowing muscle.
Meanwhile all this stress has made me feel sick.
Also very sad, at the end of the month we both celebrate our birthdays and our 40th anniversary. I made hotel reservations in a town we like about 3 hours from here, because every year we celebrate our 'big blowout' week in a special way.
I just canceled our reservation and our trip, because I don't know how I'd manage all the food and beverage modifications on the road. I am sad because I really wanted us to go out for a special meal to celebrate, and I had nightmares regarding what this process would be like sitting in a restaurant (too embarrassing).
Sometimes this is just too much to bear, so I write to unload on all of you who are also carrying big loads, sorry.
Thanks for reading if you made it through all this mess. I want Calgon to take me away. 😔
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@mm180
Thanks, some great suggestions.
I have been thinking about a care person, but since there would be several hours between meals at this point it's more feasible to take him to respite care when I feel the need for a break (it's happening tomorrow). His respite care facility offers Rock Steady Boxing designed for Parkinsons patients. He doesn't have Parkinsons, however the exercises and strength and balance moves are great for any senior.
Thanks for your message. 😊
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1 Reaction@2me
Humor is most welcome in this situation, so good pun! 😆
@marilynt
Hi Marilyn:
I like the tablecloth and candles idea. We live in a rural area, so no Door Dash or other delivery services would come out here (if they even exist in our small town). I will work to make a special meal for us, although his will have to be modified to accommodate his dysphagia.
Thanks so much, and I am accepting all the virtual hugs I can get and looking forward to the real ones. 🫂
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2 Reactions@carolreid
All the virtual hugs are adding up nicely. 🌞
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1 ReactionJudi and all caregivers
I must say, the outpouring of love and support you received in response to your heartfelt post has brought such joy to this tired, sad caregiver's heart. It's reassuring to know so many others understand.
Trish
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3 Reactions