Just in case you were wondering, I am still around. Life has just gotten busy. I think I need to put "write on blog" on my calendar because then it will get done. PT and doctors appointments have become my full time job since my last big hospitalization. During my last episode of paralysis, it turns out my bowel was damaged, so I have pelvic physical therapy once a week, pool therapy once a week and regular PT once a week. I go for my weigh-in at Ideal Protein once a week and usually see the chiropractor while I am there. I almost always have at least 1 doctors appointment each week. The week of Halloween, I have 3. Having a chronic illness is a full time job. I have to factor in a lot of drive time too since we moved out to Del Valle. All of my doctors are at least 25-30 minutes away and a few are 40 minutes away. I would really love to have a more energy efficient vehicle. Handicap vans are not the most energy efficient things. They are always big and the equipment weighs a lot. I really didn't think I would still be driving a van when I didn't need it to chauffeur kids around. I would love to be able to drive a smaller car. I am so grateful to have this van though and that we were able to inherit it from Stan's mom when she passed away. These handicap vans cost double the cost of a regular van.
Last week I had my 4th hospitalization for the year. I have broken 2 personal hospitalization records this year. Not somethings I was trying to do. First, longest hospitalization - 5 weeks. Second, most hospitalizations in 1 year -4. My previous record was 3 and all 3 of those were fairly short, like 2-3 days. This year I have spent over 8 weeks in the hospital. Now I bet you want to know why I was in the hospital. It was actually planned. I had to have my baclofen pump replaced. The battery was almost dead so we wanted it done while my deductible and out of pocket max were still met.
This surgery was much easier than the initial placement. Only had to be in the hospital over night. I was in the hospital then in rehab for 2 weeks last time. The worst part of the recovery has been unrelated to the surgery. I have a condition called autonomic dysreflexia. It developed after my 2nd paralysis episode. This means the autonomic nervous system doesn't regulate itself the way it should. The autonomic nervous system controls all of the nerves that are involuntary like in your heart, blood vessels, lungs, sweat glans, hair follicles and many other areas. This disorder is common after spinal cord injuries and can happen in things like Guillan Barre or multiple sclerosis. My paralysis episodes are very much like Guillan Barre, they just don't fit the diagnostic criteria because of some of my test results. So, after we got home from the hospital, my skin started feeling like I was sunburned everywhere. I have had this a few times but not really since I started IVIG. This is the one symptom I have a hard time dealing with. I can never get comfortable. The breeze from the ceiling fan makes my skin burn. There were some strange things with it though. I was getting goosebumps everywhere off and on. There was a lot of pain associated with the goosebumps. They are the worst on my legs. Also my legs feel like I haven't shaved in several days despite the fact that I have shaved twice since my surgery. It's like the goosebumps are pushing the hair follicles out more. If anything rubs on those stubbly areas, it hurts even more.
I have found nothing that gives me any lasting relief. Stan gave me a blessing and commanded the nerves to begin healing and the pain to ease. I have pleaded with God to take away the pain multiple times and asked him what I needed to do to get rid of the pain. I've broke down into tears a couple of times a day. Early Saturday morning I really broke down but decided I needed to approach this a bit differently. I prayed to god and told him I was going to turn this over to him. I asked him to help me have faith in the blessing Stan gave me. Then I asked him to inspire me that I would know things that would prevent the pain from getting worse. I immediately received some very clear instructions. These instructions not only kept my pain from getting worse, but I actually experience some improvement. Sleeping has been difficult for me, but I have been able to sleep on my side better than I usually can. The really strange thing is that I wake up hot but it I remove the covers, or even just the top blanket, then I get goosebumps and I am in more pain. I am really hoping my AD was just triggered by the surgery and the pain. I really don't think I could deal with this on a daily basis.
Showing posts with label pain. Show all posts
Showing posts with label pain. Show all posts
Sunday, October 21, 2018
I haven't fallen off the edge of the eath
Labels:
disablity,
home,
hospital,
IVIG,
MS,
pain,
prayer,
PT,
rehab,
spasticity,
speech,
spring break,
swallowing problems
Sunday, April 15, 2018
Where did those muscles come from?
I have been in physical therapy for the years and years, mostly for my legs, especially my right leg. It has been paralyzed multiple times. With lots of PT and IVIG, I regain my ability to walk at least some. I've had paralysis in every extremity in my body at some point over the last 10 years. The majority of the exercise I get come from PT exercises and a recombant bike at a slow pace for 20-30 minutes most days. These are not the kind of work outs that can make a person sore. This is why I was very surprised when just a day of rehab made me very, very sore. I started getting a little sore after my first 2 hours of PT/OT yesterday. We did core work almost exclusively. I took some Tylenol and felt better. This morning though, I was very sore. My back and obliques hurt a lot. It's not my normal back pain. My abs hurt too. I guess that is what happens when those muscles are paralyzed for a few days, then have to be strengthened. I feel like I did 500 sit ups. I guess the soreness is worth it is because my trunk is stronger today than it was yesterday. I can hold myself up for several minutes before I start to drift. Do you know what the worst thing about being sore is? Being in the hospital, I am limited to what the doctor orders for pain and they only ordered Tylenol every 8 hours. Who gives Tylenol every 8 hours? I need to get this changed as soon as I see Dr. Latorre in the morning.
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