Does anyone have a practical solution when needing to turn (re-position) an elderly parent during the night on a regular basis?

Waking up every couple of hours for extended periods you Do Not want to do!
Do you have a husband that could take a turn--in the turning?lol
I would go for the bed/mattress/whatever is automatic--to eliminate you physically having to get up-- that will assist in relieving the pressure. You may need someone to come in 2 over nights a week--midnight to 5 am-- at least you could sleep from 10pm to 5 am. I did that after awhile when my Mother was waking every 2 hours--or just yelling all night. It is not good for the caregiver. Please be proactive about this. I'm sure someone else will have a better idea, but this was my experience:) Take Care, xo

I don't have a clue about how to help you, but I send sympathy and best wishes.

I've worked some conferences about those hospital beds & they have pretty impressive statistics for preventing bedsores. I don't think they are hard to get out of (otherwise they wouldn't work for hospitals or nursing facilities either). They aren't "squishy". Don't think that the most expensive is necessary, either. They have air that pulses through them so that it shifts pressure gradually, & keeps the pressure sores from developing. I know there are mattress overlays with pumps that do something similar, so that might be an option too. Maybe rent one? I don't think Medicare covers them, but maybe insurance might? As odd as it sounds, maybe look on Craigslist to see if someone has a used one. Much better all around if you can find something that will prevent the sores and still let you sleep at night.

My mom was bedridden for about 10 years. In all these years, we have never changed her position at night every 2 or 4 hours. It's impractical. Father watches her in the daytime, and I take over after work. We both need our sleeps and even then, we are always exhausted. The only time mom got the bedsore that never went away after it dugged down her left butt muscle - was from stayng in the hospital for a month. She returned home with a hole in her butt - you could see the "meat" inside. Very gross. Father and I aggressively attacked it. We were able to finally get the hole closed (spending over $200 on duroderm pads which was $10 per one small square pad). Her upper skin never closed over her secondary skin.

In the 10 years of caring for mom, we turned her every 4 hours in the daytime. At nights, we took turns -one night she will sleep on her left side, the next night her right, then left, then right. We don't put her on her back at nights because she chokes on her phlegm and she can die if we both slept too deeply to hear her choking and suction it up. So, nights - she slept on her sides.

From the beginning, we had the air mattress. It inflates and then deflates. Mom's latest air mattress had very hard a bubbles that it left round red dark marks on her body. So, we used a pin to puncture a hole on the mattress so that some air comes out as it inflates and the bubble is not so hard...even with the inflation on the lowest level possible.

Also very important to avoid bedsores - I ordered one of those triangle pillows for the foot. It will cradle the feet and ankle so that she doesn't have pressure sores on her bony feet.

When she's on her back, to help relieve pressure on her legs, we would put a pillow right beneath her knees. On her sides, a pillow between her legs. As for her arms, she sweats when her arms touches her body. So we use those mini pillows (for babies) to put between her upper arm and the body, or a slightly longer pillow to put between her hand resting on her stomach.

Pressure sores also come from not moving much. So father had made it a point to mover her legs and arms - exercises. Get the blood moving. Hope this helps.

The air mattress is covered by Medicare. For us it was 80% coverage. We pay the 20%. Doctor has to prescribe it and you need to find a Home care supplier who accepts Medicare. In the end, I just bought the air mattresses instead of the hassle of taking mom to the clinic to get a prescription. Here - it cost about $200.00.

So, it's a combination of things that helps to prevent pressure sores.

I forgot to mention this. Since I take over after work, father is usually knocked out by 8pm. I come home around 6:30-7:00pm. Eat dinner, etc.. By the time I change her pampers at 9pm, clean her trache, etc...it's about 10:30-11:00pm. So, by this time, I will put mom to her side to sleep (but night time is her awake time, and sleeps in the daytime). I wake up at 6am to change both their pampers. So, mom is turned on her back by 630am. So, in reality, mom was on her side for about 7 hours. I'm mentioning this because I've read from several caregivers that their parent wakes up much later. Mom has no choice. I have to be at work by 8:30am,and father cannot change her pampers. So, we change her pamper - whether she sleeps thru it or wakes up from it.

Thanks very much, you guys. ChristinaW, I appreciate your perspective and agree that I need to be proactive in finding a solution. No, there is no one else who can take turns turning. We may eventually need to do the 12-5A caregiver shift you suggested at least once or twice a week. Thanks for that. I am also going to discuss this with my dad's dermatologist this week and get her thoughts on practical solutions. Horserider and Bookluvr, I appreciate your insights and will look at some of the pressure-relief overlays, keeping in mind Bookluvr's mom's experience with the dark marks from a hard type of bubble. I will also look into the triangle foot pillow you mentioned, Bookluvr, and thank you for the helpful detail you sent. Where do you find the time with so much going on at home? Bless your heart. Jinx4740, thank you for your kind post.

The caring support and practical wisdom from folks on this site is awesome. Take care and very best wishes to each of you and your families.

Jola, Thank you for letting us know what helps and please keep in touch! All the best:) xo

Just happened by and thought to share about a way to position. I use a pull sheet. Just a sheet laid across the bed under the person from the butucks to the shoulders, with sheet to hold onto at the sides. When you roll the person from one side to the other all you do is roll the sheet for a little gripping action and pull. Be sure to suck in your gut on count of one, tighten your butucks on the count of two and flip on the count of three. This protects the strain on your back and gives you a work out to.

Charliegirl, those lifter sheets are sooo practical, isn't it?! I used it all the time when mom was alive. She tends to slide down the hospital bed. So, I go to the head, put a pillow between my body and the wooden panel, lean over, grab the sheet where her shoulders are, count to 3 and pull one time. Sometimes I do it wrong it and get this severe back pain. I now have arthritis on my upper shoulders and neck due to the constant repetitive pulling/pushing strain on my body all these years...and I'm only age 47. Don't want to know what I will be suffering further down the road....I still have father who weighs much more than me....I never thought about clenching the buttocks.

My mom just got an alternating air mattress that actually inflates and deflates in such a manner that she is being constantly repositioned yet not disturbed in any way and I don't have to do a thing to help. The mattress does it all.

It is called an Apex Neo-Turn 5300 and Medicare is covering it because mom developed a couple of pressure ulcers because of after now becoming bed bound from two broken hips (couldn't walk after the last one) and then broke her arm a few weeks ago (forgot she couldn't walk!) and even though she's always had great circulation and avoided breakdown before, I had her so doped up on Lortab for the pain and was busier than a one-armed paper hanger, I totally forgot to check her heels and they got bad. They are healing up as soon as I got the pressure off them, which I did as soon as it was brought to my attention (but at that moment I wanted to just die! I couldn't believe I had let that happen!).

But those ulcers were a blessing in disguise because my mom doesn't like to lay any way except on her back and anytime I tried to turn her on her side, she cried until I relented. She's good. ;-)

So getting this bed was the best thing so far that we've gotten to improve both of our qualities of life...she stays on her back and the bed gently turns her from side to side but the cells under her head are static so she doesn't feel sea-sick or anything like that. And there are cells on either side at the edge that stay inflated so that she doesn't roll into the rails on the bed. When we need to do something that does require manually positioning her in bed, there is a button I push and it makes the bed flat and static (but still inflated) while we do what we gotta do. I can adjust the time cycle for different increments, I think it is every 4 mins, 8 mins, 15 mins, and 60 mins.
The mattress costs something like $5000 but with a Dr.'s order that includes the proper diagnosis (one of which is bedsores and I don't know if there are any other qualifying dx such as immobility) Medicare covers 80% and the supplement gets the rest. They rent it for 13 months and if we are still using it then, it becomes ours and Medicare doesn't have to pay anymore. Kind of like medical-rent-to-own.

Look into it and see if you can get one or something similar to help your situation! Especially since your dad's circulation isn't optimum, judging from what you said about the healing time of the darkened area he developed...he's going to be very susceptible to pressure ulcers and if he gets one, it will require even more diligence to heal (or improve as they say) than you might be able to muster.

I think you could talk with his Dr. and figure out how to get it Medicare approved, considering your situation. In any case, I suggest you give it a try! You can't go on indefinitely doing this as you are...and I know that from personal experience.

Good luck!

I'd vote for the alternating air mattress and gradually reduce repositioning to just once a night as skin tolerance permits.

EVERYTHING HERE HAS BEEN A BLESSING! my brother and I have been moving our dad back and forth for almost 22 months in our homes due to him being 24/7 care...just yesterday, my brother says he quit. so because I DO NOT want to throw my dad in a nursing home, ive been trying frantically to find out if these beds will allow you to sleep and then the rest of the day will be do able. before ive spent every month hes here getting up at 12,3, and then 6. then your day begins...VERY HARD on my wellbeing physical and mental...I am recooping and also stressing wondering how I will accomplish this alone. I am going to GET ONE OF THESE BEDS. GOD BLESS YOU

Thanks much to all who have posted. Here's an updated summary of what we tried over the last few months and the solution that has worked.

- As mentioned, the ROHO cushion on Dad's recliner/wheelchair we got improved his skin condition somewhat. But in the weeks that followed we saw no additional improvement--it seemed to level off.

- I continued repositioning overnight, but it eventually caught up with me and I no longer felt with it during the day. Sometimes I had trouble remembering this and that as I went about my daily tasks. This concerned me, both for my own health and because I need to stay on top of things for my parents.

- I eventually purchased a ROHO overlay for Dad's mattress (big, static air pockets). This appeared to help relieve pressure overnight. When Dad would get up in the morning, I noticed the area tended to look better than the night before. When I tried lying on the overlay myself, I hated getting back up--it was kinda like lying on air!

- I then asked Dad's dermatologist to look at the area on his buttocks. She told us that we needed to handle this pressure situation more aggressively to avoid it turning into a bedsore. She recommended turning overnight, but I explained that with the ROHO overlay in place it wasn't even physically possible for me to reposition Dad in bed. (I had tried this when we first got the ROHO overlay, but no luck.) She then suggested focusing on a better solution during the day and said if we got that part resolved, maybe repositioning at night wouldn't be necessary.

- I then started researching online the alternating-air cushions for wheelchairs/recliners There weren't all that many advertised online and none on Amazon. The prices were pretty ugly. I was also concerned because some of the customer reviews were negative in terms of reliability, ability to reach the sellers for resolution of a problem, etc. Eventually I chose a product from the Ease Cushion website. It had the most consistent, positive customer reviews I had found and extensive technical details about their product. They had me talk with their engineer about Dad's particular needs first and he recommended for Dad the Ease Cushion Stage 1 Overlay with Answer Pump. I chose the waterproof version. (The Stage 1 Overlay is actually one of their lower-priced models. Some of the alternating-air cushions on various websites run as high as two or three thousand dollars--or more.) Their engineer had me go to another of their websites to view its product details; he felt we'd be happier with their Answer Pump because it's portable and doesn't have to be plugged into a wall socket while in use.) Dad uses it about 12 hours a day and it sits on top of a regular foam cushion. The battery stays charged for about a week. It's nice because we can take it to doctor visits, restaurants, etc. and not have to worry anymore that Dad is sitting too long in one place.

- After a week or so of using the Ease Cushion Stage 1 Overlay, we started noticing improvement in Dad's skin tone. Occasionally I'd see flesh colored skin where there was previously red, even after he'd been sitting for long periods of time like an hour or so. This continued to improve so that there was eventually only a very small area of purple surrounded by flesh-colored skin.

- Yesterday we saw Dad's dermatologist again for a different skin issue. While he was being seen, I asked her to look at Dad's buttocks. She said the skin is back to normal now--no remaining pressure issue. Hurray!

I am so grateful we eventually found something that worked to resolve this skin issue--and works good enough during the day that I don't need to reposition overnight anymore. I've seen photos of what pressure sores look like and how bad they can get and have had friends tell me about the horrors of their loved one's pressure sore, and I sure didn't want that to happen to my dad.

We found a Med-Air adjustable/alternating bubble topper through amazon for under $80. It's been a lifesaver for overnights. Our greater challenge is for daytime in her recliner. So far, nothing we've tried works, except changing her position (which is, in the long run, ok .. since getting her active and moving during the day is a good thing).

Update for dad and I...my dad is bedridden mostly due to declining health, so I did want to mention We purchased one of those rotating alternating pressure mattresses. I am so grateful. During the day I manually turn him (by choice)while the bed stays mostly flat position, and at night, thankfully, I can turn on the rotation feature and his skin looks great. this has been 5 months of use and has been a real blessing for me, as now, I do not have to get up at night anymore... well Im here to tell you they are worth the money ....WORTH IT.

yay!!!

There exists a special air mattress that has pockets of air, with a motor that hangs on the end of a hospital bed. Throughout the night, the motor fills and deflates areas of the pockets, effectively and gently repositioning your loved one. I've seen it work with 2 end of life loved ones of my own.

The alternating air mattresses are good and you have been given a good link and explanation. What about putting a timer on it so that it goes during the night but is turned off and deflates when you are getting the person up and out of bed, Its very important that you get a decent sleep yourself, I feel for all those caring for their parent. I personally don't have a house that my Ma could even get into and its not safe for her in her demented state to be in. So yes she is in a dementia unit.
so its very important that you do care for the carer.