Category Archives: Physical Illness

Pain, Knee Injection, Psycho-Analysis


Due to my upcoming steroid injection in my knee on Tuesday I had to cut out any pain killer that is an NSAID. If used it could cause dangerous bleeding. So by cutting out my Meloxicam, the pain became worse.

I have spent most of the last few days in bed. Laying down is less painful than sitting. If I had a couch I could sit with my legs straight, but since I don’t have one, sitting in a 4 legged chair or my computer chair is quite painful.

My knee is not the only painful area. My back is still a problem. I still feel my spine moving and popping. My whole body is an issue.

I mentioned that I was losing my therapist and then the whole office was closing down. My last appointment was last Tuesday, well I slept right through it. In a way, I am glad, since that eliminated the emotional part. I figure since I am not in a panic, that things are good and maybe it is time to let it go for good.

I still have my psychiatric nurse who prescribes my medications for my mental issues and is willing to talk if I need it. She does therapy too, but way out of my budget.

I can’t take much more of this pain and need to lie down again. The longer I am without my NSAID the worse my arthritis pain gets. Getting there on Tuesday and then having only a local anesthetic I am going to really be in pain. I can’t be knocked out unless I go to a surgical center or the hospital due to my BMI since I am obese. I have been knocked out with no problems, but new laws won’t allow it done in a procedure center at the pain management office. If what they give me is an anesthetic I would hate to have it without. The pain is tremendous. They tell me it will just feel like a bee sting. I would like that bee to sting them. That is the worse bee sting I have ever had.

My neighbor is driving me home. I drove myself last time. It was possible, but having someone drive you is much more comfortable. My dad used to drive me before he had a stroke.

Can’t wait until it is over.

Tessa – 

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Author of a book, a work in progress on the blog, https://tessacandoit.com/government-property-a-memoir-as-a-military-wife/

Highlighted chapters are done and ready to be read.

Problems Showering With Fibromyalgia and ME/CFS


Problems Showering With Fibromyalgia and ME/CFS

I find showers exhausting. I am lucky if I can take one per week.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Why Fibromyalgia or ME/CFS May Worsen Period Pain


Why Fibromyalgia or ME/CFS May Worsen Period Pain

It has been many, many years since I had to deal with period pain so I can’t tell you if I feel it adds to my Fibromyalgia pain.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Sex With Fibromyalgia or Chronic Fatigue Syndrome


Sex With Fibromyalgia or Chronic Fatigue Syndrome

There would be times that I would find sex with Fibromyalgia to be painful. It would depend on just what I was feeling at the time. Pain comes and goes and so do the other symptoms. You would and should talk with your partner about what you are feeling emotionally and physically as well. In some cases it may not be possible depending on how bad your Fibromyalgia is and some people are certainly worse and in more pain than others. The rougher the sex the more exhausted you might end up being. Just take it slow and easy and talk your partner through it. If they’re understanding they will work with you to make the experience a good one.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Changing pain meds – JusJoJan #31


January 31, 2019 #JusJoJan Wrapup

I have been on Percocets, high dose and not much relief.

After talking to my pain management doctor we have decided to try Morphine which is supposed to be stronger. I haven’t started yet so I don’t know for sure, but hope to start tomorrow. There was an issue with the dose (smallest) not being available. After much debate from the doctor and asking me if I would be willing to cut the next dose up in half we are going to hopefully have it for tomorrow.

This is also an experiment as supposedly I was allergic to Morphine according to the ER. I told the dr and she said the IV brands are much stronger and they probably overdosed me to begin with which she did as she was going to help me for the pain in the next few hours. I hope this works as I didn’t like being allergic to the Morphine. Ambulances can only use Morphine around here and if I were to be unconscious Morphine is the pain reliever they use. Granted I wouldn’t feel it most likely if I were unconscious.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

JusJoJan – Sunday – January 27th


JusJoJan January 27th

I haven’t been reading posts so January is almost gone. I won’t be going back and trying to catch up.

Life is difficult with dad’s stroke and dementia. I had no idea what a stroke does to you. He is DNR (do not resuscitate). I wasn’t happy years ago when my parents told me their desire for this, but they legally made up living wills. When my mom passed 5 years ago I began to understand the sense it made. My mom suddenly was not responding. Even with the DNR it took about 10 days for her to finally pass. No one wanted to see her like that for who knows how long not to mention the immense expense that could arise. I am fine with my dad’s DNR. He is suffering right now and he wants to go and if assisted suicide was legal he would be all for it. Although now he is not really of sound mine most of the time so it wouldn’t be allowed anyhow I am sure. He is living in a long term care center which is just a fancy name for nursing home. He is mad at us a lot of the time because we have to sell his assets to pay for his care. This isn’t easy anyhow as his house is old, outdated and simply needs to be completely re-made over and there is an expensive retaining wall in the back yard fally down which will run from $10,000 to $20,000 to fix. We are not fixing the house up because the government is going to get whatever money we make over the reverse mortgage lien. We are waiting for Medicaid to kick in as it costs us $10,000 a month to keep him there and we, well he, is paying for that.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Chronic Pain – So tired of it!


It has been 2 months since they deadened the nerves in my back. It was supposed to take only 6, maybe 8 months til it worked. It hasn’t although it does occasionally give me a small period maybe even a day without major pain. Nothing they do seems to help me. I am so tired of this chronic pain. It doesn’t give me much of a life, but what can I do but live with it.

I am trying to do things to take my mind off of it. I joined a book club, joined overeaters anonymous and go to bingo once a week. I am also reading more besides the book I have to read for the book club.

I haven’t felt much like writing though and my blogs are just sitting here.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Strokes suck the life out of all concerned


My dad’s dementia is getting much worse. He isn’t lucid very often.

We just had to go to the hospital as he was not responding and waking up. He WAS awake, but pretending he was not conscious because he was sure the nurse’s and aides were alien monster doctors and they wanted to eat his brains. The last time he wasn’t responding there was something wrong but this time it was strictly fear. He thinks everyone in his facility is an alien and bad ones most of them. An expensive hospital visit because of his dementia. I only hope he doesn’t keep doing this one. An expense for nothing. I understand why they had to send him, but I hope he doesn’t keep doing this.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Dementia Is Horrible


Dementia increasing. Never know what he is going to say or do. We are having a family Christmas party tomorrow. Hope he is in a receptive mood.

I am finally getting some relief in my spinal area that has been so horribly painful. Finally having some times without pain, thank God!

Merry Christmas from my son and I!

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com

Opiates for Fibromyalgia


Opiates for Fibromyalgia

I take opiates for the problems with my spine more-so than Fibromyalgia and so I don’t know if they are doing anything for the Fibro or not. Right now they aren’t helping my back and spine either. Since having the 6 facet joint injections in the spine the pain has been much worse. No  help at all for the most part. I have to see if they have a higher dose and if she will prescribe it. Since I take psyche and anxiety meds they don’t like to mix them as they are more dangerous in combination.

Tessa

Advocate for mental health and invisible illnesses, also a devout Christian

Author – http://www.finallyawriter.com (this blog contains my old work mostly although occasionally I do add something new here), new work is mainly on this blog http://www.tessacandoit.com