What equipment will I need?? Will I put on weight?

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dijo1963

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Hi Guys, I have read quite a lot on this site and have learned so much about the surgery I am set to have on 29th April, more than my Neuro ever told me. I am set to have an AILF on 2 levels and really want to know what equipment I will need to hire to assist me in recovery? I shall have support for 2 weeks after surgery after which I am on my own. I have organised 6-8 weeks off work is this sufficient? ( I have a desk job). I am really concerned that the recovery and lack of exercise may increase my weight. Any tips??

Thanks Guys Di;)
 
Most doctors recommend that you walk, walk, walk, walk. That is the best therapy for you and the least risky to reinjuring your spine.

To be honest, you might need help a little longer maybe 4 weeks. Maybe the last two weeks you can have someone stopping in and checking on you twice a day and making sure everything is within your reach.

Going back to work at 8 weeks is arabitious but certainly possible. Generally most people start feeling better around the 12 week point.

Remeraber this is major surgery and you don't want to do anything to lengthen your recovery or to reinjure yourself.

Good luck and remeraber we are here for you during the recovery period.
 
Hi Dijo, and welcome to the board! :wave:

Your questions are good ones! I'm glad you're preparing ahead of time and thinking practically.

As far as equipment, you may or may not need a walker. I don't know if the hospitals in Australia do things like they do here in the U.S., but here the physical therapists in the hospital work with you for several days before you're discharged to make sure you'll be able to be self-sufficient when you get home. They'll make sure you can get up and down stairs and if you need a walker, you'll learn how to haul it with you on the stairs. Once you get home, will you be alone?

I did not need help getting into or out of bed at all. It wasn't easy, but I could do it. I also never needed help in the bathroom. Again, it wasn't easy, but I took my time and did just fine. I was not able to shower everyday due to low blood pressure issues, like passing out, but on days that I couldn't shower, I was able to wash at the sink without help.

The very most important tool to have is a grabber. Spend the money to get a good quality one. You'll use it often! Mine was worth its weight in gold the first day home! With your grabber, you'll be able to pick up things you drop, reach things from your bed that have slid out of reach (like those all-important remotes), and do a lot of things that you'd otherwise have to wait on someone else to do. I used my grabber to pick laundry out of the hamper an item at a time, then to transfer into the washer the same way. I also recommend having a satin or slippery type bottom sheet for your bed so you can slide to turn instead of fighting friction. It will be much less painful! Since you're having an anterior incision, get a firm little throw pillow or a folded up blanket to have over your stomach incision. Whenever you need to turn, cough, laugh, or sneeze, press down on it firmly but gently to "splint" your incision. That will also help to keep your pain down. A raised toilet seat is a great help, especially if you're tall. Read the thread at the top of the page called, "Post Surgery Tips," and you'll get a lot of other very practical suggestions.

If you'll have family merabers around, make sure they leave you food and drink (with a bendy straw) where you can easily reach them if they go out. They will need to be making meals for a while, not you! If you're going to be alone, stock your freezer with meals you can easily put in a microwave. You won't be able to bend, twist, or lift more than about 5 pounRAB for quite some time. Use paper plates so you don't have to wash anything. Keep it simple. I was sometimes alone and sometimes not, as my kiRAB are homeschooled but also have jobs and my husband only took off work for my surgery day. They were pretty good about making sure I had food, and we got dinners from people in our church for 3 months. But if I didn't have a family, I wouldn't have felt the need to receive meals. I could have put something small into the microwave if I had to. I could not have prepared meals for the whole family! If you have bottled drinks, I recommend loosening the caps ahead of time. You may not have the strength it takes to twist off a tight cap after surgery.

You'll be on pain meRAB after surgery, which tend to cause constipation, so make sure you have high fiber fooRAB available. I ate a lot of prunes! Since you're concerned about weight, get the high calorie fooRAB out of the house before you even go in for the surgery. Replace them with low calorie fooRAB and when you want to eat, get a reasonable portion and put the rest away, then go lay back down to eat it. You won't want to be getting up over and over, as that's the hardest part of this, so you won't be tempted to go get another serving. You need to eat as healthy as possible, as your body will be trying to heal, so don't diet, just eat reasonably.

There are a lot of us here who have had fusion surgery. If you have other questions, we'll do our best to help you. We're not doctors, but we have lots of experience!

I wish you the best,
Emily
 
Hi Di. This board is amazing and can provide everyday people like us with more REAL information that we could every get from a doctor. Some are really great, but most are just clinical by trade and just don't think of all the nuances that we really need to know going into this.

The grabby sticks are a must and come in a few different styles. I would imagine if you dont have them there, you could probably order off the web. I still use mine today and it's been almost two years since my surgery.

What levels are you having done by the way?
 
Thanks so much for your advice. I have been not sleeping lately simply terrified about the op, my recovery, the outcome etc. This site has some really informative stuff that has helped immensley. I am going to investigate where I can buy a "grabber" here in Australia. Please any other snippet that you think might help me in those early days I'd be very grateful. Again thanks for your support and advice and I'll keep you posted on my progress..
 
We can get grabbers (a reaching tool) here in the U.S. in durable medical supply stores or most large pharmacies. If you can't find one, maybe you can call a physical or occupational therapy facility and ask them. They'd probably know.

It's very normal to be anxious about this surgery. Come on here and let us try to help you if you're having a hard time. Keep yourself as busy as you can up until the surgery so you have less time to ponder it.

You'll be so glad to get it over with and be able to just focus on recovering!

Take care,
Emily
 
Having L5/S1 anterior fusion and artificial "titanium" disc at L4/5. Thanks for your info any thing else you can think of that might help me prepare would be really appreciated. It's great this site and ones like it exist. I simply dont know where I would have gone to get the answers I need if it wasn't here. What was your experience in recovery? What challenged you? My concerns are also for the impact on my relationship. Whilst my partner is supportive and reassurring I cant help but worry about how my limitations will effect "us". I am really going to struggle with watching someone else "do" everything. I am a real clean freak so am silently concerned about this also.. Any tips to "survive" the hard times?

thanks Di
 
Hi Di. My recovery was ups and downs in the beginning. I was in the hospital only two days. Felt immediately better at waking from surgery. Sciatica was gone. They nurab the surgery site internally and once that wears off, the true surgery and healing pains start to be more felt. This occurs anywhere from 1-2 weeks time post op. So expect this also. It was still tolerable though, and knowing it is healing pains makes it all the more tolerable. I didnt have the nerve issues of any magnitude until post op, in my legs. But I had to tough them out because I turned out to be allergic to the nerve meRAB. It took 3-6 months before this was truly diminished. I still get some intermittently, especially during that time of the month and if I overdo. But it's nothing to what it was then and it's more annoying than anything. I did lose some loss of sensation on my outer thigh, calf and foot. It's just more dull there and it's so slight, it's just not thought of much.

The back starting stiffening up at around 6-7 weeks internally. I could feel it becoming more stiff and rigid. I started PT at 10+ weeks I think, and that is what really started me on the healing path to feeling normal again. They work on stretching out the incision site and minimize scarring, they stretched out my legs which helped my nerve pain, and got be strengthening my core muscle groups and worked toward whole body toning, etc. What a huge positive change this was for me. (I got lucky and found an amazing physical therapist, in which she is very innovative and knows the body better than my surgeon does I think. Nothing cookie cutter about her approach to wellness.)

I had flare ups through the PT process, which I was told to expect, respect and move on from them as they ocurred.

Im 85% improved and would do it all over again!

As to your significant other, you need to nuture things as best you can and that is all you can do. Just remeraber this is very hard on those that are in our lives. They can't take our pain away, nor can they help us either. And I always make sure that I never make my pain theres and I dont make it the focus of the home or conversation. (And this board has been so incredibly helpful to me to address my issues here, ask the questions, getting solid and grounded advice from those that truly understand. I can't begin to tell you how grateful I am for this board. That is why I continue to come back here. It's important for me to give back what I received, plus there are many on here that I cyberly feel a true frienRABhip with.)

My BF has been with me since this all started and we had only been together for a year at that time. Here we are almost 5 years later. He continues to be the most supportive person. I am a total cleanfreak! He's a slob! But I have learned that I can not control what I can't do and let it go until I can get to it. I still don't like it, but I've let go of worrying about the dust and mess when I can't get to it. It's not going anywhere, so just let it go and deal with it when you can.

But I did plan ahead and I hired a cleaning company to come 1 every two weeks to do the basic things for the first 6 weeks post op. They cleaned the surface stuff for me (floors, bathroom, dusting mostly). It helped to keep it in control some during the beginning of my recovery. After that, I was on my own and kept up as best I could. You will be okay. Just mentally prepare yourself to let go of what you can't do at that moment. Trust me, it gets easier. (I will admit though, I dont like inviting people over much these days, unless I have 3 weeks to prepare for their visit! hahaha. That's a bit exaggerated but you get my point! hahaha.)

Just exhale, and as they say "dont sweat the small stuff". There are more important things to think about right now than dust and clutter. Concentrate on yourself right now.

We are all here whenever you need us. Welcome to our cyber family!
 
Good advice from Justoneofus! I'll add to it that after a few weeks, you'll be able to slowly do some little things around the house. I'm a clean freak, too. I discovered that I could wad up a ball of masking tape and stick it in my grabber and walk around dabbing up the little spots of fuzz, dust, and debris that people tracked in. I got some long handled cleaning tools, like a duster that could reach the floor or the ceiling but only weighs a few ounces, so I could walk around dusting here and there when I was up to it. I made the kiRAB dustbuster the kitchen floor and vacuum every now and then. And a very sweet girl friend came and cleaned my bathroom for me. (Now that's a friend!) I learned to let a lot slide, like Tammy said, but I also learned to be creative so I could do some of the things that needed doing, too. Read the thread at the top about less stress on your back around the house, and you may get some ideas that will work for you.

:wave: Emily
 
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