WE ARE IN THE FINAL STRETCH

I got some good news this last trip to the Fibro & Fatigue Center.  Because of the improvement they don’t feel that any more chelation therapy is necessary for me.  I will continue on the supplements that I am taking for the rest of this year. After that I will be just on some maintains supplements to make sure my body has all the minerals it needs to work well. 

What a fantastic year this has been for me.  Going from what I was to what I am today has been a BIG change.  Even when visiting my MD she was astounded at the change in my health.  I had to see the cancer doctors and the urology doctors this last week.  They both told me that I don’t have to come back, unless there is a problem. 

SO AM I CURED???  Well I won’t say that, but my health and ability to do things has changed 95 percent this last year.  I was housebound, in a wheelchair and had not driven in over 15 years.  Now I am driving again, doing almost all I want to do (in moderation).  Do I still take a nap in the afternoon, sometimes.  But my quality of life has been so much improved that it’s hard to describe.  Will I return to the working world???  That is another good question.  I am being told to wait and see if this last for over a year, then my doctor might give me the go ahead and go back to work.  So we will see what happens.

Would I recommend that you try a natural approach to your health?  That’s a no brainer, after seeing what it has done for me, it’s hard to not tell everyone to do it. 

If you have any questions I can help with please contact me.   I will be continuing to post here monthly to let you know how I am doing…

God Bless…

FMSJerry

ANOTHER CHAPTER IN MY STORY

I had my last scheduled chelation (IV) this last week.  The doctor thinks that they have done all that they will do for me and I agree.  I have not seen a lot of improvement because of them for a couple of months.  They say now that you only normally need six chelation treatments in the beginning to get your system going.  Then the supplements will take over and continue the process. 

This will save us the cost of travel, hotels and food in restaurants when traveling, that will help a lot.  I was surprised at how much we have spent in medical travel expenses this year.  More than the medical treatment and because it’s in Las Vegas Nevada the hotels are all below $50.00 per night(where we stay).  

I just ordered all my supplements again and learned that I still have three problems.  The latest blood test came back to show that I am loosing Iron.  The doctor said that it’s unusual for a male to have his Iron content drop.  He thinks I must be bleeding either in my kidneys or in my gut.  My testosterone level is still low and he suggested I up my dosage.  Also my Aldosterone level is low, (a hormone that the adrenal glands make).  So he has put me on an additional supplement to help this. 

I will be seeing my MD at the VA this week and will request that she check me to find out where I am loosing Iron.  Also will have her increase my Testosterone by half again so that my levels will be in line. 

I am dealing with some pain from sleeping on a hard bed for two nights while in Las Vegas.  But if you’re a fibro patient you know that these usually resolve themselves in about three days.  So I should be good to go tomorrow. 

Another trip this week to Salt Lake City to see several specialist at the VA hospital.  I am having a spot checked on my back for cancer.  Also will be getting two new pair’s of glasses ordered.  I wear one to drive and normal things and the second pair has prisms to allow me to read better.  These became necessary after what can only be described as a stroke in 2008.  There is no evidence of a stroke in my MRI but the eye specialist said that is the only thing that explains my eye problems.  It was necessary to have eye surgery to correct my sight problems after this event. 

Till next time…

FMSJerry

SEE MY NEW WEBSITE DEDICATED TO HELP OTHERS WITH FIBRO/CFS START THEIR RECOVERY FROM FIBRO.

ANOTHER GREAT VISIT

Well I was back to the Fibro and Fatigue Center last week for more treatment.  To be sure I am getting the right supplements they took another 14 vials of blood.  I should have the results this next week when I go back.  Of course I had the two bags of IV meds twice while I was there.

This month has been strange, my wife is with her parents in Michigan and I am alone.  This has happened each year, but this year I don’t have an aide coming in daily, I am able to drive and I am allowed to cook food.  In the past the aides have cooked for me at least one hot meal.  My wife did make meals that could be microwaved to heat.  But I was not allowed to cook.  Just because I had brain fog and caught the kitchen on fire she band me from cooking… Go figure??  Well this year I am doing so much better, I have been out of the house everyday.  I have had some nice meals and have gone out with friends. 

I will be driving back to Las Vegas next Wednesday for treatments on Wed afternoon and Thursday morning.  Then will stay over and pick my wife up at the airport Thursday evening.  On Friday we plan to go to Bull Head City, AZ to see an electric vehicle that we are considering purchasing.  This little thing is 32” wide and will take both of us and our dog up to 30 miles.  We plan on having one when we start our travels so we can use it to get around in national parks and even RV parks that we stay at.  Because my wife had replacement knees and I am just getting my muscles back in shape we will use one of these “crickets”.  It will fit in the back of my pickup under the shell for transportation.  

Till next time…

FMSJerry

SEE MY NEW WEBSITE DEDICATED TO HELP OTHERS WITH FIBRO/CFS START THEIR RECOVERY FROM FIBRO. 

THINGS ARE CONTINUING TO LOOK UP!!

     Well another visit with my doctor.  Things are going great and I am really encouraged.  I have been able to get out and really have some fun.  I got on a 4 wheeler for the first time since 1994 and it felt great.  My remission has continued and if I don’t do stupid things I continue to enjoy not being in pain. 

     My doctor tells me that I will be off the chelation and most of the supplements by the end of this year.  I will take some supplements to help maintain my remission.  But won’t need to see the Fibro and Fatigue Center Doctor unless I have a relapse.  I will do everything in  my power to prevent a relapse.  Life is so much better when you aren’t in pain. 

     I had to see my dentist for a couple of broken teeth.  A few years ago my teeth all fell apart in about six months.  Back then we didn’t know that fibro/cfs does not allow your body to use calcium correctly.  Most of my upper teeth have been caped with porcelain caps.   Now we are starting on the bottom.  The VA pays for my teeth because they are effected by my fibro which is service connected.  This is not a fun process but one that is necessary.  I also have to have my spine checked every two years, because I have Osteoporosis from the fm. 

     Just some things to watch out for if you have FM/CFIDS.  We are closer to having a website set-up to support people medically with chronic conditions that want to get better.  We are just waiting on the final steps. 

Till next time God Bless… 

FMSJerry

P.S.:  We have not sold the house so I guess that means we will be here for a while.  But God has his timing and we will wait on him.  In the meantime I can get my teeth fixed and finish my treatments at the Fibro & Fatigue Center. 

ONE MORE TIME

     Well I went down to the clinic for another treatment… All went well and I don’t have to go back for three weeks. At that time I will see the doctor again and see if I can stretch out the visits more. We will also be talking about my starting to get of some of the supplements.

     Can you believe how much things have changed in only six months.  When I went to the clinic the first time on January 4th 2011 I was as they say a train wreck.  I was in tremendous pain, using an electric wheelchair to get around and spending most of my days in bed.  What a change in six short months.  I am  now in remission and free of pain( for the most part).  I only have muscle pain when I over do.  Course that is hard for me, I am a type “A” personality.  I want to do everything I did before the “big crash”.

     I have been able to take care of my own yard this summer, help get the house ready to sell.  I also have completed my honey do list.  I still have things I want to get done.  But I have learned with the heat that I have to take it slow.  Our heat is now in the 90’s daily and so that seems to sap my strength.   I take a nap in the afternoon most days.  I am not cured, only in remission.  I pray for a long time… But I do understand that the beast could come back… So I have not given up my disability nor have I made plans to return to work.  I would like to think that will come, but I have to be realistic. 

     For now the doctor thinks that I will be free of chelation treatments and all the supplements by the end of this year.   I am just down to a few pills that I have to take for blood pressure and my thyroid problem.  Life is so much better not having to take 29 different prescriptions.

Till next time….   

FMSJerry