Month Check Up – Good News

Good news.  The medication seems to be working.  I took my notes to see the doctor.  He was very pleased with my progress and has reduced the prednisone considerably.  I had already asked two weeks ago to have it reduced because it was starting to over charge me.  Insomnia city!

The following was decided:

  • No more advair until completely off prednisone.  No need for double steroid use
  • Continue with labs every four weeks to keep track of blood counts
  • add anti-bacterial medication for next three months, three times a week.
  • Keep walking four times a week and try to increase distance beyond 5 blocks
  • Sjogren’s syndrome has been officially added as part of diagnosis.  He still thinks that I may have more than one auto immune condition.
  • Prognosis is good.
  • Special sleep test, bone density test and full pulmonology tests are to be done before return visit in June.  Depending upon those tests, I may be able to get rid of night-time oxygen, singulair and other allergy medications.

Now, let’s talk about this from a long hindsight back to my childhood.  We briefly discussed how I have always responded well to steroids.   I told him that my mother and sister’s both stated how I had a dent in my butt as a child from all the steroid shots.  Supposedly I was born having an asthma attack (according to the stories from mom).  Asthma was just being treated by new drugs at that time (mid 1960’s).  Who knows the side effects of those drugs that I took as a child.  You can barely find a trace of them on the internet.  In fact, one I remember clearly is not found anywhere except as a brief mention when I searched  for another medication.  Airayne.  It was a capsule that had a special inhaler that punched holes in it and then you sucked it in like today’s version of advair.

Doc said that my auto immune condition has over ridden the asthma.  That made me think back to my childhood.  Maybe all those “asthma” and pneumonias I had may have been an auto immune condition all along.  Yes, the asthma meds worked.  Or did they mask the real problem all these years?  It has me wondering and I will be doing more research as I go along.

I did tell the doctor about how all my rashes, itchy skin and open sores have just gone away.  My skin has never been so soft.  My allergy eyes and post nasal drip have completely gone.  He did say that I still have crackles in my lungs.  That is the scar tissue.  He said the skin clearing up is the cellcept working.

I am also grounding.  He didn’t quite know what to say to that.  He said he had no information, but did put it in my chart.  It is supposed to help with inflammation.  I am sure it is helping the medication to do its job more effectively.

I mentioned about my hip hurting again as I reduced the prednisone last week.  He said for me to continue to track what symptoms return as the steroid is reduced over the next 12 weeks.  If anything unusual happens, to please email him.  I also said that I was not as slimy as before.  He gave me a questioned look.  I told him that the post nasal drip has stopped, I wasn’t coughing up clear goo anymore and that overall I felt less slimy.  He attributed that to the cellcept also.

So, Even though I have over $300 in doctor visits and several sets of trips to the vampire (Quest) over the next several weeks (and months).  Not sure if insurance will cover sleep test or bone density test, it is okay.  Somehow God will make sure it gets all done, the money will be there, and I will be moving forward to being more comfortable.

I did complain that the exhaustion factor has not really changed.  He said that since I have gone so long with minimal exercise, it will be while before I regain my strength.  He said that depending upon the lab results in June, he will refer me to pulmonary rehab to help with it.  In the mean time, keep walking the dog.

Personally, I think it is God blessing me.  Yes, He is using medicine as a tool.  I know that I have team of women, men and leaders praying for me on a regular basis for health and endurance.   Things all turned around when a group of godly men gathered around me at church and prayed sincere fervent prayers for me and my family in February.

There are still bad days.  But now the hope I had in my heart is being felt as hopefulness.  I look forward tomorrow’s promise of a new day.  May it be a great day.

 

 

Two Week Update

It has been a little over two weeks since starting the cellcept and the prednisone.  I have seen another doctor and wow, did he inform me of a lot.  It has been over 11 days since my fingers have turned blue.  Amazing how something like that I can count.  I just never really understood how bad I had gotten.

But, getting back to the medical stuff….Endocrinologist who has been treating me for GERD and fatigue was glad to hear I am no longer terminal.  He sort of agreed with the treatment plan, but was extremely concerned with the amount of steroids I am on.  I informed him that the doctor was going to wean me off at my next visit.  I explained to him about some of the side affects I am experiencing.  He stated it was normal with the prednisone.  But, he did recommend some tricks to override the stimulation of it so I can sleep.  He is trying to get the insurance to pay for a baseline bone density test since heavy use of steroids causes osteoporosis.  Let’s see if that happens.  Also, he upped my GERD medicine since it isn’t making it through the night anymore because of the steroids.  I am okay with that.  The B-12 will remain the same.  My depletion will not get better with steroids or without.  So be it.

In the mean time, he stated that he cellcept will induce menopause.  I was on the way there anyway with reduced oxygen.  So, he wants to watch my calcium even more closely.  We discussed that since I have GERD I am unable to take the pill form.  I have a calcium powder that I may start sprinkling on my food instead.  He said that way is less intrusive to my stomach and will help fight the osteoporosis with the steroids.  I am going to wait for next week’s labs to see what the results are.  I am trying to eat a yogurt every other day for the probiotics and calcium.

I know – eat my greens. They have it also.

Overall.  I am feeling so much better.  The hard part is trying to balance out what I used to do, with what I can do and what I want to do.  I keep over doing it on Saturday because I feel so good.  Then I end up exhausted on Sunday and Monday.   So, on Saturdays I am allotting 10 minutes for one chore.  Whatever that may be (sweeping, mopping, scrubbing tub, etc.).  After that, no more.  Still walk Daisy on Saturday morning the 5 block trip we do.  I am not ready to expand the walk yet.  I am still a little winded after the 5 blocks.  But, I have been able to up her walks during the week by two-three times.  She is happy about that.

I have a lot of labs and doctor visits next week.  Along with some fun planned with Groupons for Spring Break.  My college work won’t stop.  But, I can at least have a small outing each day to be with a friend.  Follow-up after Easter.

He is RISEN.

Two Weeks of Change and Grounding

It has been officially two weeks being on the new medications.  I feel so hopeful again.  I never really lost hope, I was just so used to trudging through the day struggling that I didn’t realize how much I was NOT enjoying.

My fingers haven’t turned blue in a week and a half.  My face and lips no longer have a blue tinge to them.  I can breathe without feeling like there is an elephant on my chest.  He still has a foot holding me down, but I can deal with that.  The coughing has almost completely stopped.

I have been able to take Daisy for a walk three times a week again.  Going to get a hair cut or to the store after work doesn’t seem like a herculean adventure anymore.  I wasn’t even totally exhausted after working the food pantry last week.

I realize that these results are due to the prednisone and that once the doctor starts weaning me off the high dose, some of the previous symptoms may return.  That is okay.  I am able to do basic things in the house without having to plan my whole day around a 20 minute chore.  I have found myself overdoing it because I am so excited I can do these things without thinking if I am ready to do them.

I did start something extra that I will discuss with the Dr. about in two weeks when I return.  My sister has sent me some grounding information, sheet and cuffs.  The help has been dramatic.  The puffiness in my legs have gone down and my skin is softer.  The arthritis in my hands are better also.  Could that be the prednisone?  Maybe.  I want to attribute it to the grounding.  I bought grounding shoes and have worn them three days now.  My ankles have stayed the same and my feet were not as tired at the end of the day.   I am logging all my changes and observations with the medications and grounding.  I have shared this information with a friend who is in the science field.  She is so intrigued she is getting a sheet for her and her husband to see if it will help them with their issues.