After 5 Months on CBD Oil & Meneire's Disease Update

 

Update on the CBD OIL how it is working for me. I have had less events.  Any major events have not wiped me out for days or a week.   Its about a couple of hours to a day of recovery time.  Still having problems with the body temperature of overheating for no reason.   Hopefully the longer I take the CBD Oil it will help with that. 

I have had more energy.  I have been able to walk with a friend at our local park 3 times a week, able to do a little more around the house too.  Able to help in the kitchen more.  Still need breaks with all that stuff, but making good improvements.  Having to take less naps during the day.  Starting to have less brain fog.  Now the brain fog only comes on after doing stuff.  It's not always on & having to fight through it.  Just when brain gets used a lot. 

My improvements might be slow, but they are improvements.  Hoping the longer I am using the CBD Oil the more improvements I will have.  

If any of this was helpful to you or you just want to make a donation, there is a button on the side for that. 

Health Improvements with CBD Oil Updates

 

I got my test results from my doctor after using Full Spectrum CBD Oil for a few months.  My doctor was pleased with the results. My white blood counts are almost to normal range.  The count stopped climbing & came down.  My energy level is a lot higher.  The doctor told me to keep taking it & to get my husband on it.  

I started my husband on it.  My husband has had improvements. He was able to not take his pain killers & muscle relaxers for two days. Plus he had more energy.  Sad to say, he over did it & had to take the pain killers & muscle relaxer for a day.  But as he has more relief, he can build his body back up.  It will take some time.  

I had a friend visit me for a few days.  We were hanging outside a bit.  I ended up having a bigger Meneire's event.   When I was visiting with another one of my friends house, I got slammed with a migraine, nausea & ear pain.  The dizzy spell was creeping up on me. Thank God I was only 5 minutes from my house.  I got home, told my husband what was going on.  He helped me to start to get everything under control.  Ginger, ice pack for my head, tea for my ear, AC on, shades pulled, CBD Oil. With in a couple of hours, I was back to "normal".  This is a big deal!!!

Normally after a major event with Meneires I'm out for a couple of days if not a week, trying to recover.  The CBD Oil is making a big difference on recovery time with major event.  I will take it easy for the next day, just to make sure things are going in the right direction.  I didn't have to take the anti puke pills that put me in a deep sleep for a day then into a zombie.  I got to skip all that!!  

As I take the CBD Oil longer, I will do my best to keep you all posted on how things are going.  If any of this is helpful, let me know by donating. There is a button on the side. 

Meneire's & CBD Oil update

 

  Update on the CBD Oil, I ran out & had a few bigger events of Meneire's.  I'm back on it & I'm upping the dosage.  So far I have noticed more benefits for Meneire's with using the CBD Oil more.   It has helped with some of my other aches & pains also.   I have noticed more relief for the nausea with the increased dosage.  During the night, I woke up with nausea, took some of the CBD Oil & went back to bed, didn't have to use the anti barf pills.   

  With the CBD OIL helping with the nausea, that will make me be able to take less of the anti barf pills, that make me sleepy to the point of deep sleep where I sit.  Then being a "zombie" the next day. 

  With less "zombie" time, I should be able to be more active.  If my activity cause me to be dizzy & nauseousness, I can use the CBD Oil for the nausea & just sit while the dizziness slows down.   

  My "more activity" is  just more moving around the house, doing normal chores. It's not the glorified fun yet.  Hopefully I will be able to get to the more glorified fun as I get a better handle on the Meneire's.   One step at a time.  

  My husband found some vertigo pills on amazon. We order it to see if it helps too.  I'll keep ya posted if it helps or not.    

 

  If any of this is helpful & would like to give a gift, there is a link on the side for paypal.  Thank you.

Meneire's Disease part 2

   After trying different medications & receiving some relief in my ear, but still having vertigo at least twice a week, falling & near falls (family members caught me before going down) my ENT (Ear, Nose & Throat specialist) informed me that the Meneire's was not uncontrolled if I was still having vertigo twice a week.  That was a shock & a bit of a let down for me. 

  He then informed me that I am down to one more medication to try before having to move to injections into my ear & proceeded to explain it to me.  I think I turned a couple colors of white.  I hope I never come to that.

  As of now, the medication is working.  Thank God!!!!  The ringing in my ears, can not be fixed.  But the vertigo is less, still happens for time to time.  I have sprained my ankle big time & trying to recover from that.  It was sprained from rolling it, not a dizzy spell & passing out.   Now in PT for that, hoping for no surgery.


  If what I offer here is relevant to you in any way, please consider donating. As I tend to my family (disabled hubby and homeschooled kids) I write in my free time. No knitting here but I love Taco Bell now and then and your donations help keep the spicy food coming. Every donation is appreciated!!!

Donations are not tax deductible.

Started another platform for my blog posts.   Visit it & see if it works easier for you.   It should be the same information as this one.   I made some updates to this one, hopefully it is more user friendly.

 Here's a link to the other blog post:
http://unencumberedliving.home.blog

If what I offer here is relevant to you in any way, please consider donating. As I tend to my family (disabled hubby and homeschooled kids) I write in my free time. No knitting here but I love Taco Bell now and then and your donations help keep the spicy food coming. Every donation is appreciated!!!

Donations are not tax deductible.

UpDate ON Blog posts

   There will be some new changes coming in January of 2020.  I will be change where I post my Blog posts. I will keep you post on where to go to find the posts.  Sorry for any & all inconveniences this change may bring.


  Thank you for your patience & understanding.  Blessing in you & your family as the year ends & a new begins!!!  

Vertigo

  It's been awhile since I have made a post.   I have been dealing with vertigo from my last ectopic pregnancy a year ago.  As I made progress with the vertigo through physical therapy & vision therapy, I have had a set back from life events.  It was just a set back but able to move forward still.  Then an ear infection hit, which cause more dizziness & vertigo stuff.  Ear infection did not want to leave without a good fight.   Still working on healing from that.

  With having vertigo for a year straight, I have had to learn how to do normal stuff without stirring up vertigo or I had to find the limit of where vertigo would start.  It's a hit & miss.  Normal activity has became a difficult progress to do.  For example typing out this blog is taking me days to do.  I'm unable to be on the computer for to long or read for more than 20 minutes a day. After the 20 minutes I'm done & need a nap to recover.   Lots of naps have been taken in the past year.   

  Vertigo has changed my life.  I have to stop & think about if it will cause dizziness, or how long can I do it before vertigo stirs up, is it worth the energy & time to invest in, how long will recovery take after doing something.  These are only a small fraction of questions to think through when dealing with vertigo.   Then the effects of vertigo tossed in with every day life stuff.   Then if anything else is tossed in on top of that.  All can be a bit overwhelming while learning how to deal with vertigo & praying it goes away as fast as it hit.   

  Then trying to explain to people you know what is going on with ya & why you can no longer do the things you use to.  And not get depressed by what you can no longer do & not sure if you will be able to do it ever again.   Feeling like your not yourself but you still have the desires to do all of it.  Is very frustrating, overwhelming, depressing, exhausting,  angry are just to mention a few emotions to deal with.  

  Having to deal with all the emotions plus the physical of vertigo is one crazy mess.   Having people to support you & to help you through it all is life saving.  If you are dealing with vertigo I hope you have a good support system around you to help you deal with the emotional stuff & the physical stuff.   

If what I offer here is relevant to you in any way, please consider donating. As I tend to my family (disabled hubby and homeschooled kids) I write in my free time. No knitting here but I love Taco Bell now and then and your donations help keep the spicy food coming. Every donation is appreciated!!!

Donations are not tax deductible.

UPDATE

Sorry you have not heard from me in a few months. Lots has been going on.  All is good, you should be reading new posts in September 2018!!  Hope your summer was wonderful!!