Long time no post!

Hello Friends, To those who stuck around:)Its thursday aug 18th.Im still here at the Center.I once agian apologize for the delay as my computer had some issues and I cant very well type all that was needed to be said from my phone.I had the great blessing of going home this past weekend to see my family.It was short but sweet.I was excited to see how my body was going to respond outside and after the treatment center.All went well,Praise God!Jeremy and I decided for me to stay one more week as requested from my Dr,considering the last 7 yrs what was 4 more days?, It was worth a shot.We are still hoping and praying for a bit more improvment in the heart and the vegus nerve as the disease has done significant damage in those areas and it is becoming a bit challanging to adress and correct.I arrived back in Kansas on monday and right away met with my amazing Dr.After a few tests he told me he was happy with my progress,I was hoping for that news as every day I was feeling a bit better:)There has been a few rocky moments but thats all they are moments.The effect and or reactions are short lived.The Drs work hand n hand and step by step with you.Therefor the communication is always open meaning,as soon as you start to have a shift in your progress they ARE ON IT!!.This is something I have never been able to experience.Normally Im put on a pharmacutical drug that they hope works,while it destroys my kidneys and only masks the symptom instead of fixing the problem.SERIOUSLY the whole thing is crazy,backwords if you ask me!And when I would have a adverse reaction from that drug,GOOD LUCK getting a hold of the Way to busy Dr to tell him.And all this after paying him 400.00$ for a half hr.K,so Im not bitter just frustrated with the whole system its sad:( On a more positive note,I have had significant results here and am truely blessed to have had this opportunity. Thank you to all who have had my back and given me the support and courage to continue.My journey does not end here,I will be posting my treatments and my last days events at the HANSA CENTER tomarrow.While here,I have had the honor of meeting some of the most amazing people .I will miss them so but,I will keep their love and their stories of healing close to my heart.As stated at the begining,God is still God and worthy to be praised,He is so faithful and as promised he never left me nor did he forsake me..God Bless you all and thank you for your continued support and love.

Wednesday

Hi all,Im still very happy you are here,I will not be writing a whole lot tonight as Im having some severe ups and downs tonight.My body is responding well to treatments but, because of that the detox process has made me not feel so well.And even though I have had a minor setback Im still very happy with my progress.Dr Jernigan is an amazing Dr and Im in good hands.It has been requsted that I stay one more week which would include the weekend.I have not made my decision yet,Im praying for direction.My faith will sustain me:)I miss my family terribly and wish they were here with me.Im trying not to let my emotions get the best of me.Im greatful for all the support and hope your all well!

Happy saturday!!

Hi friends and fam,Thank you for tuning in:)I apologize for the delay.Mycomputer has something funky goin on with it.Im in need of my dear friend Denise Murphy who always bails me out of my computer flops.Im going to be working on it today,I think perhaps in setting up this blog I did something????.Any how I pray you are well and happy:)Im learning here at the HANSA CENTER how stress and unhappiness can actually have an affect on your DNA,and a huge effect on your immune system.Scientific studies have revealed this ,I did not make it up:).My days at the clinic have been going well,Agian the Drs are incredible and Im blessed to be here.The Hansa Center creates a very peaceful environment..The professional kind staff makes the expierence good.Every morn we meet with the Drs( my whole family).We discuss the previous 24 hrs and the current days therapies and The dr treats while Im in there.Brenn and Jeremy find this quite entertaining:).Thursday night I had a bit of a jolt with my central nervous system( vegus nerve).The biggest and one of the most important nerves in your body,This nerve affects your heart,stomache and your ability to swallow etc.......the things it controls seem limitless.So My Dr met me at the facility after hrs, with my family, and with treatments I had significant improvments shortly there after.Im praying I have continued improvments next week.We are spending the day togather today as a family:).Im a tad bit weak today but nothing I cant tolerate.Im hoping to go into further detail when my computer is performing at its normal pace.Thank you guys Im blessed your all with me!.Have a great day!God Bless.        P.S. Im gettin a bit home sick,I miss my babies that had to stay home!.Foxy,Whiskey and Sami ...Love u !Jeremy and Brenn leave in 2 days to go home:(I want to spend as much time with them as possible befor they go..LOVE YOUR FAMILY! And Thank God for every day of life he gives you.Its a gift!
 

Long Day today.

Hi friends and family,Agian Im so thankful for all your support and love.Im so blessed you care.Im unable to go into great detail in reguards to my treatments I under went today cause its 12:12 am here and Im beat,It was a long day.It was a successful day though.Im doing ok,which is better than I thought I would be doing at this point:).Im afraid if I try to explain my day with being this tired you will read complete Jiberish.I have some time tomarrow,so I will give more specific details on todays events then.God Bless!night.

Meeting my Drs and starting my treatments.

Hi guys,Thank you all for your support ,concern and prayers.I was awake most of the night (last night),I was so tired but my mind sure wasn't.I couldnt help but think about todays events.....Meeting my Drs,starting treatments and just the outright anxiety of sharing my story.Its very hard to describe the last 7 yrs of a very complicated disease in an hr and a half. And yep,.All that for nothing...My Drs were amazing and my body responded very well to the treatments:)Thank the Lord!.The team of Drs here are some of the best in understanding lyme and the severe complications and effects it has on your entire body.(The disease has NO boundries) They are Experts in my opinion.I was able to listen first hand to many stories of great succsess today.I was over joyed not just for myself but,for the thousands of others that suffer in silence everyday,without answers,support or the proper treatment.Im excited ,humbled and blessed to be here.Todays therapies consisted of some serious cranial adjustments.A non invasive treatment with a little discomfort while being applied.,within a few minutes I felt relief from the congestion and inflammation in my head..A symptom I have had battled with for 7 years.The inflamation in my head and brain has at times been so severe that it has caused me double and blurred vision,facial numbing and mild seizures,and pain of epic proportions.So needless to say Im stoked! I had adapted to the pain as many of us do and now I remember what it was like not to have such discomfort and pain in that area.:)Due to the amount of time spent with the Drs today I only had a few treatments.Tomarrow will most likely be different.Thank you all for your support and prayers. Words are not enough to show how much I appreciate you all being with me.. I must go to bed now we are 2 hrs ahead here and that means it is almost 12:30.More to come!

My first day

Welcome so glad your here! As you follow this journey with me pls feel free to ask any questions or post comments in response to anything I may blog about.I wish I could have followed someones blog to find out specific info before I made the decision to come here.That is why I decided to allow people to be a very close part of this experience.And of corse to keep my friends and family posted on my treatments and my progress.Pls forgive me in advance for spelling and punctuation issues or the lack there of as quite often I will be posting the days events after a long  day and many hrs in treatments.I will be posting truth not only about my progress but about the disease,so I have chosen to keep details off of Face Book:)As many of you know I have a very strong faith in God therefore during this difficult time I cling to all his promises and hold in my heart that He will NEVER leave me forsake me.He has a perfect plan for my life and even if my Disease does not respond to these treatments in a positive way,He is sill God and I will continue to thank Him for every day of life he gives me.He will perfect that which concerns me.I would not have survived the last very painful and difficult 7yrs without my Faith.Esp considering this disease causes my heart to stop ,and when It starst beating agian it has runs of V-tach that the Drs tell me some dont live through to talk about.I do not live the life of a sick person ,infact many of you would agree I dont  look sick or act sick.This has been a choice .When you have a chronic illness you have to do your absolute best to live as normal as you can and live every day to the fullest.My amazing husband and daughter deserve that.Drs told Jeremy 6 yrs ago to prepare for me NOT to survive.Agian one more reason I chose to appreciate every day of life Im blessed with.The drive to be well,even when I dont feel it stems from watching my daughter Brennley need her mommy to be normal and healthy.So I will fight everyday to be all I can,even when I cant.

My journey to health

Finally here!!Witcha Kansas that is.I just set up this blog ,Those of you that know me are saying right about now,"She set up her own blog WITHOUT help?"Well yes I did ,so bare with me as I learn:) Any suggestions would be helpful.