I unfortunately don't have any experience to offer, but I would think that it would be a good time for pretty aggressive pain management, whether that be opioids, stellate ganglion blocks, ketamine infusions, or whatever. Personally, I would encourage you to look into a ketamine infusion, but that's just because it is the only thing that has been helpful for my daughter. Just like any treatment, they don't work for anyone, and it can be challenging to find someone who will do them. But I would think you would want to double down on any treatments you have access to to avoid a flare.

Yes. Your doctor should watch you like a hawk and maybe even before and after the cast extra treatments can be given, just to be sure you don't flare-up the CRPS.

Hi Abigailsophie,

Preventing further contracture and resulting problems is a worthy cause. So many additional discomforts can come from being out of alignment. I really like the idea of the casts/splints being soft and removable. Depending on how often you go to PT it may be helpful to take them off more often to do passive range of motion on those joints if you can tolerate it. Tendons and ligaments tighten up so quickly and routine movement of them can be very helpful. I had both casts and splints as part of my journey (not for the same reasons as you) and I remember being surprised by the atrophy and stiffness that resulted. Being able to do passive movement could make a big difference and minimize losses in range.

I remember too how awful the bandaging felt against my skin when I developed CRPS after my last operation. Find the softest material you can that causes the least aggravation and use it as a liner. Topical cream may help. I use one with ketamine and gabapentin in it that I find helpful. Avoid opiates when and if possible. They certainly have their place but can contribute to hypersensitivity.

Good luck on this. I hope you find relief with it. I am two years out and still wear a brace at night to keep my foot from contracting. I can definitely tell when I don't use it.

I feel that medication is a very personal thing and something between you personally and your doctor. No two people are the same or react the same to the same things.

That cream? What is it called? I've never heard of ketamine/gabapentin cream, ever.

Sorry for any confusion. I could've been more clear about compounded topicals. I have not been on much lately and skimped on details. My topical is made by a compounding pharmacy for my particular needs.

It has 10% ketoprofen, 4% ketamine and 6% gabapentin in a creamy base. DMSO was added to help absorption. This was prescribed by my Doctor. We could have added lidocaine but I opted to buy it separately over the counter. I tried another topical formulation that did not help nearly so much. We are indeed all different.

I absolutely agree that medications are highly personal and between a patient and Doctor. That said, we can pool tremendous resources of experience by making suggestions from our own toolboxes. I am sure Abigailsophie understands I was offering something that "may" help and was helpful for me. We must all follow our own wisdom on what is best for us based on our knowledge of ourselves and the advice of practitioners we trust.

Best to you Abigailsophie on whatever treatment you pursue.

That's great to hear. Thank you for clarifying.

I have never heard of such a cream/compound. Hmm, interesting! I have heard of full DMSO cream, but that you can't leave on your leg and have to remove within a certain amount of time, or else it burns the leg.

I firmly believe casting caused my RSD. Mine started in 2006 after a bad fall down the stairs. I went to the urgent care the following day because my foot looked broken. They didn't find anything on Xray but assumed a break because of how it looked and did an aircast. The RSD set in 3 weeks later. I had it manageable, which isn't saying a lot, but I could walk a year later with much pain.

The pain still seemed to be both RSD and bone so they did an MRI and bone scan and found that there were indeed 5 fractures in my 3rd and 4th metatarsals - great, I thought it was the 1st metatarsal that was broken. In any case, we cast it in a plaster cast because after a year they didn't know how else to heal it. It took a week and the RSD was flared worse than ever and I wouldn't walk for months. The only thing that allowed me to walk again was pushing through insane pain. The RSD in the cast caused my leg to swell around the cast and I had to have the cast removed immediately. When they cut the cast off, they also burned or cut my skin and that was the worst pain I have ever felt to have a cast saw burn my skin with RSD.

I worked for years to be able to walk and be active. Now if I'm down for any reason - if I have a cold or if I am recovering from something or if I don't walk a few miles in a day (granted still in pain) the RSD flares. The immobility seems to be a major trigger and a cast is straight out for me.

Since they are talking about removable casts for you - with a strict physical therapy plan I could see it being okay, but you probably need to be able to move and work on things. For me now, I still have the broken bones in my foot and I broke another bone in the other foot a few years back. Broken bone pain isn't as bad as RSD so I know which one I take. Good luck in whatever you end up doing -- but please ask about doing PT or any exercises if you opt for the cast!