Keeping Chickens When You Have Arthritis.

Pics
Welcome to the thread @ValerieLovesChickens, @Sammi_0411 and @rbnk1. Glad to have you join in and so sorry to hear that you all have joined the ranks of arthritic chicken parents.

@ronott1 I don't think there is any tips when it comes to avoiding MRSA. It's pretty rampant, or at least it was in hospitals and once you get it, you have it for life. It can be knocked back into remission with Vancomycin, or at least that was the drug of choice when I was working hospitals. But Vanco is a powerful drug with lots of nasty side effects. And like you said, a silent carrier can spread it around without ever knowing that they have it. Good hand washing, good wound care and that is about it. They were testing people beforehand to see if they were carrying MRSA before they even had surgery.

I have arthritis in my hands also, @rbnk1, both osteo and serum negative RA types. It's pretty miserable as it is throughout my body also.

I use two gallon kitty litter containers for my birds water needs. Lifting them is a bit of a job and my sweet husband helps me fill and load them into my wagon for me. Usually I can wrestle them around with two hands but I'm saving milk jugs now with the realization that the days where I can use them are now officially numbered as due to the degenerative disc disease in my neck and shoulders.

As for the fatigue, conserving energy is the goal. Sometimes I'm so weak and tired feeling that I cannot pull my wagon up the small hill to my coop without stopping and resting before proceeding on. There are days where I do my coop 'chores' in phases so I can rest between watering and feeding.

For cleaning I went from a big grain shovel to a wide spade and a 5 gallon bucket. It's easier for me to lift the smaller amount of debris with the spade, put it into the bucket/buckets and carry it out to the tractor bucket for my husband to spread on our pasture and garden. It takes longer to get the job done but it's easier on my joints

I work at it until my neck starts to tighten up then I quit and rest. The chickens don't mind if it takes me a couple of days to get the job done. Poo is Poo after all.

@Sammi_0411, like you, I got chickens to keep me moving. With them, rain or shine, I have to get up, get dressed and head out to the coop to let them out, clean, supervise and yes, build when necessary. Right now I'm waiting for the weather to settle and the ground to dry so I can build a wall in the existing shed that houses my main flock to house my bachelor roosters this winter. My spare coop is free standing and not all that pleasant to deal with in bad winter weather. The new room will serve as a rooster coop in the winter and a brooder room in the summer. I enjoy building but even that has evolved into using a table saw and power nail gun and my husband doing the heavy work.

Where there is a will there is a way and I will keep my chickens until my health makes it impossible for me to do so, till then, like everyone, I hobble/drag myself out to the coop every day and enjoy my chickens.
 
I tested positive for MRSA before my second knee replacement. After some antibiotics I was clean, and I haven't tested positive since. So out of 5 joint replacement surgeries, one being a revision I only got MRSA once. I didn't even know I had it until they swabbed me for it.
Thanks!
 
@ronott1, the Prolia pretty well is the pits. If you can take Fosamax, do it because if you cannot tolerate Fosamax (like me) your only recourse is to go to one of the sub Q, IV drugs. I pretty much have side effects from the Prolia hard for a month after my injection. Mainly fatigue, weakness, flu like symptoms etc. It has also caused me to have severe joint pain. Hard to explain that other than to say if you have it you know it isn't your regular joint pain. I was hoping to get off of it but my doc pretty much nixed that idea. When I told him that I 'still hate it' he said, yes but you only have to deal with it every six months instead of every week. That's the good news. No, I have to deal with the side effects 6 months out of every year because the drug peaks in your body in 3 months then declines so that you are clear in time for your next injection.

True I do not want a broken hip, compression fracture in my spine or a broken bone somewhere else due to everyday fall risks on a farm but is the cure worse than the risk? That is open for debate as far as I'm concerned. I recently talked the doctor into letting me have a months' reprieve in getting my next shot. Yes I had pain, which I will always deal with but I felt GREAT! Pretty frustrating.
 
@ronott1, the Prolia pretty well is the pits. If you can take Fosamax, do it because if you cannot tolerate Fosamax (like me) your only recourse is to go to one of the sub Q, IV drugs. I pretty much have side effects from the Prolia hard for a month after my injection. Mainly fatigue, weakness, flu like symptoms etc. It has also caused me to have severe joint pain. Hard to explain that other than to say if you have it you know it isn't your regular joint pain. I was hoping to get off of it but my doc pretty much nixed that idea. When I told him that I 'still hate it' he said, yes but you only have to deal with it every six months instead of every week. That's the good news. No, I have to deal with the side effects 6 months out of every year because the drug peaks in your body in 3 months then declines so that you are clear in time for your next injection.

True I do not want a broken hip, compression fracture in my spine or a broken bone somewhere else due to everyday fall risks on a farm but is the cure worse than the risk? That is open for debate as far as I'm concerned. I recently talked the doctor into letting me have a months' reprieve in getting my next shot. Yes I had pain, which I will always deal with but I felt GREAT! Pretty frustrating.
I will keep this in mind for my DW. She had osteopenia about 5 years ago related to parathyroid adenoma but her Dr.s have not checked her again to see if removing the tumor improved the condition
 
I will keep this in mind for my DW. She had osteopenia about 5 years ago related to parathyroid adenoma but her Dr.s have not checked her again to see if removing the tumor improved the condition
Pls urge her to have a Dexa Scan done. You also, Ron. I always chalked my joint pain up to having RA so when I asked the doctor to order me a DS after the rheumy diagnosed my finger joint deformity as Osteoarthritis nodes seriously believing it wouldn't show what it did. Moderate osteoporosis in one hip and lower spine was pretty much a shocker for me. I wish I had pressed earlier for the DS.

I am an extremely active 67 year young woman. I have been active my whole life, always ready to embrace the next adventure. I really thought my high activity level would protect me from OA, OP, but it didn't. Mine has, they told me, a genetic factor. No matter what I did, it didn't help it.

The earlier you get it diagnosed and get it under control the easier it will be. I've been told some women with mild bone loss look as though they have never had OA on the DS's after 2 years on Prolia. One was the nurse who gives me my shot, mother. She couldn't get Medicare to pay for continued treatment because her 2nd DS showed no bone loss.

That is something for your wife to shoot for, you too!
 
Pls urge her to have a Dexa Scan done. You also, Ron. I always chalked my joint pain up to having RA so when I asked the doctor to order me a DS after the rheumy diagnosed my finger joint deformity as Osteoarthritis nodes seriously believing it wouldn't show what it did. Moderate osteoporosis in one hip and lower spine was pretty much a shocker for me. I wish I had pressed earlier for the DS.

I am an extremely active 67 year young woman. I have been active my whole life, always ready to embrace the next adventure. I really thought my high activity level would protect me from OA, OP, but it didn't. Mine has, they told me, a genetic factor. No matter what I did, it didn't help it.

The earlier you get it diagnosed and get it under control the easier it will be. I've been told some women with mild bone loss look as though they have never had OA on the DS's after 2 years on Prolia. One was the nurse who gives me my shot, mother. She couldn't get Medicare to pay for continued treatment because her 2nd DS showed no bone loss.

That is something for your wife to shoot for, you too!
Thanks!

I will have this checked out
 

New posts New threads Active threads

Back
Top Bottom