Kathryn's Pages

The MacDonald Family Blog

Trying not to be disheartened

I want to be clear. Kathryn’s pain is not gone- it is lower.  She still has to take the same amount of pain medicine.

We are very very thankful for the improvement that we have seen so soon and we have hope that if this level of relief lasts, she can do rehab in a warm pool on a regular basis.

We are so thankful for the non-profit work and research being done by the International Research Foundation for RSD/CRPS and all the help that Kathryn has received! 

Of course we wish that her pain were gone!

We hope to be home and back to work by Wednesday.

LOVE AND THANKS TO ALL!

Leave a comment »

Kathryn has less pain!

We are so thankful!  No pictures of us celebrating, not yet- I pray and hope that will come soon.  There is more work to be done. 

Here are some things we’ve experienced in the last few days- and some surprises: 

I asked Kathryn and Dave to give me a few adjectives describing how they feel at this point- you may be surprised… drained and tired are first on the list.  Then comes thankful, hopeful and strung-out.  

Joe was the first one I called after infusion #4 was over (honestly, that was the only call I had the energy to make.)  He cried with joy, relief and hope, and in response to the loving support from VCU mentors and friends.  Perhaps we can get his thoughts onto this site soon- I love to read what he writes!    

I am so thankful that while undergoing treatments #1 and #2, we were able to stay at a room that was minutes away from Dr Kirkpatrick – Kathryn needed to “get home” quickly after each treatment. Indeed, during Ketamine treatment, Kathryn had two resounding pleas….  first on the list was “please take me home!” second was “how much longer?”

Thursday night, we thought we had the hang of things a bit so we used some points and moved to a cute little Best Western on the Gulf (it has a kitchen- YEAH, real food!!)  It is an hour away from the treatment center but we’re getting familiar with Tampa.  UNFORTUNATELY, within moments of arriving (all of us very overwhelmed with the latest treatment- Kathryn still very woozy and out of it) Kathryn turned her right ankle (her good ankle.)  Any of you familiar with CRPS are CRINGING BIG TIME right now because this is the kind of injury that can flair RSD/CRPS- BIG TIME!  Kathryn (and family) had been through too much at this point, so we considered losing it. (I’m not sure how that helps things but we had reached that point.)  Instead, WE PRAYED!  We followed Dr Kirkpatrick’s medical advice AND THEN we prayed some more!  Two days later, no complications from the sprain- praise God!

Have I mentioned previously that I am thankful for your prayers!? 🙂 

Sooo, now to what you surely want to hear the most about- Kathryn’s pain.  A huge part of CRPS pain is what’s called Allodynia pain. It can make falling rain feel like road burn or knives stabbing –a skin rash on her left side can raise Kathryn’s pain so high that she can’t concentrate to do school work.  After Ketamine treatment #3, Kathryn’s Allodynia pain was greatly decreased and after treatment #4, it has practically disappeared.  Yes it can come back, most people with CRPS have to be retreated with Ketamine.  How soon- we don’t know- but Kathryn is more relaxed and happy than I have seen her in some time!  Her left leg still has pain- how that will level out we do not know.  We see Dr Kirkpatrick for one more consultation before leaving on Monday.  Dr Kirkpatrick wants her to continue to take her pain medicine and to exercise 3 times a week in a heated pool for the next 6-12 months 

 

So this is what the Sovereign LORD says: “See, I lay a stone in Zion, a tested stone, a precious cornerstone for a sure foundation; the one who trusts will never be dismayed.”   Isaiah 28:16 

Leave a comment »

day 2

Thank you for your prayers!!

Leave a comment »

Kathryn’s thoughts after infusion #2

Hello all, and thanks so much to everyone who’s been thinking/praying/lending any mental support to me and my family the past few days because I’m sure that is truly what has helped me be most comfortable throughout this trip. The past two days (as most of you know were the first two infusions) have certainly been experiences for me that I will never be able to describe vividly with words or even dramatic hand gestures. The first day was very easy-going, and only had problems at the very end when nausea took me over momentarily, and thank God they have effective medication for this unhappy side effect that was extremely successful today. However, a big part of what made the first day so comfortable, was having my big brother Joe there. He was amazing and I miss him and am thankful for the time he could be here more than I can say. BUT, my parents were extremely supportive today and comforted me through a bit of anxiety and A LOT of the sillies. I’m hoping that tomorrow and the next day I can walk in with a clear mind and get the dosage up high enough to accomplish the overall goal of this treatment. Please continue to pray/meditate/send good thoughts my way and my parent’s way as we go through a major move in location while also dealing with the after shock of the Ketamine. We have had a few discussions with the major objective of finding out what makes me more comfortable while I’m under the influence and I must say that this experience is giving me a entirely new respect and gratefulness towards my parents and therefore is making us closer as a family.  And to add on to the good news, I have noticed a significant decrease in my alodenia pain (severe skin sensitivity) and my overall average pain level has gone from a 9 to a 6 or 7. I’m so excited to see how I feel this weekend and even if I gain no further improvement but the improvement I’m already noticing, I’m thankful for ANY relief that I am granted. Although, I’d sure love for all my pain to be taken away as well as my parents and probably everyone reading this post would rather. :p

All my love and thanks to everyone  🙂

Kathryn MacDonald

Leave a comment »

One down, three to go

The first day of Ketamine Infusion went well. Kathryn and I BOTH came back to the room and SLEPT!!  She asked afterwards, if the four hours of Infusion are boring for us.  Our answer is that Dr Kirkpatrick keeps us working too hard to get bored 🙂  And, no one but those familiar to the patient can keep the patient comfortable.  The more comfortable the patient is- the more Ketamine a patient can tolerate- the better and longer the pain reduction!  We hope to be able to help Kathryn to tolerate and deal with larger doses as the weak  goes on.  Kathryn got sick at the end, but Dr K hopes to avoid that tomorrow. 

Dave took Joe to the airport just as Dr K released Kathryn for the day- we were VERY SAD to see him go! His being here day one of infusion was invaluable!

OUR HEARTFELT THANKS TO ALL YOU GUYS- WE ARE SO THANKFUL FOR ALL PRAYERS AND COMMENTS!!!

Leave a comment »

The first Ketamine Infusion- please pray

We are finally here!Hey Guys,

  • We had an amazing storm over the weekend- we hear you are getting it today.
  • Worship and Bible Study with Pastor Vann and all the folks at Northdale Lutheran was great- but I missed my Living Hope family 🙂
  • Joe being here with us is a HUGE help- I am so thankful- Joe and Dave have taken such sweet care of Kathryn and myself.  
  • Kathryn has tried to get some school work done- we’ve learned a lot from Dr Kirkpatrick concerning why concentrating on scholastic work is, at times, near impossible for those with CRPS pain.
  • Kathryn had another evaluation with Dr K at noon today where he made a video of her “before infusion” pain levels.

Tuesday at 9:30am- Kathryn has her first Ketamine Infusion- I am so thankful for this site going out to so many- PLEASE PRAY!

We LOVE YOU and TREASURE YOU!

Leave a comment »

Kathryn’s treatment extended

Kathryn had her first evaluation with Dr Kirkpatrick today:

  • She will not have treatment Monday the 23rd as I had told many of you.
  • Monday is an additional evaluation day.
  • Her first treatment will begin Tuesday the 24th.
  • Kathryn’s CRPS has spread to her upper body- we did not realize this.
  • She requires additional Ketamine Therapy that will keep her in Tampa for three additional days. 
  • She is missing home, friends and school and is sad and concerned about such a long stay away.
  • Dave and I will call some of you to rearrange our schedules to accommodate this new information.

We learned so much from Dr K today! I am so thankful to have Kathryn here!!

Leave a comment »

WISDOM

We meet Dr Kirkpatrick today and I’m praying for Wisdom this morning, as I like to do before a doc visit – and this is a very special doc visit!

I love this Proverb about Wisdom

Proverbs 8

Wisdom’s Call

Does not wisdom call out?
   Does not understanding raise her voice?
On the heights along the way,
   where the paths meet, she takes her stand;
beside the gates leading into the city,
   at the entrances, she cries aloud:
“To you, O men, I call out;
   I raise my voice to all mankind.
You who are simple, gain prudence;
   you who are foolish, gain understanding.
Listen, for I have worthy things to say;
   I open my lips to speak what is right.
My mouth speaks what is true,
   for my lips detest wickedness.
All the words of my mouth are just;
   none of them is crooked or perverse.

To the discerning all of them are right;
   they are faultless to those who have knowledge.
Choose my instruction instead of silver,
   knowledge rather than choice gold,
for wisdom is more precious than rubies,
   and nothing you desire can compare with her.

 “I, wisdom, dwell together with prudence;
   I possess knowledge and discretion.
To fear the LORD is to hate evil;
   I hate pride and arrogance,
   evil behavior and perverse speech.
 Counsel and sound judgment are mine;
   I have understanding and power.

 

Leave a comment »

Half Way!

I feel like you are all with usTHANK YOU- THANK YOU for all the comments that you have left on this site!!! WOW- I am so moved as I read all your notes- I could not have forseen how uplifting it is to have your encouragement travel with us!!! Your love makes us stronger and gives us so much joy!

We are in Walterboro, SC- HALF WAY!  Hey Joe, the  shower head in this Best Western is high enough for you- amazing– LOL! (I’m just saying.) We are so looking forward to your joining us in Tampa on Saturday!

Kathryn is managing the trip so far with her usual grace- she says little about how she feels and wants to make sure we are ok. Much of her body has been covered in hives for days. (For those of you who do not know– doctors tell us that the hives are an allergic reaction to her pain medicine- she cannot stop taking her pain medicine- this emergency situation is what made this trip to Dr. Kirkpatrick urgent.) The hives were very bad last night. I fell asleep praying that she would be able to sleep and not feel the itching.

Dave did all the driving yesterday and took such good care of us- as always- we are so thankful to be this far- all is well.

Thank you for your prayers! We love you all!!

Leave a comment »

What I Love…Where I’m Going

I’m not a fan of talking about my pain or what I experience on a daily basis so don’t expect to read TOO much about that throughout this section. I’m a normal teenage girl in that I could spend a whole day in bed watching any movies based off of a Nicholas Sparks novel. BUT, even though I do enjoy a good chick-flick, the day in bed would not be a result of the teen-age lazies or a boyfriend break-up. It is because I can’t force my legs to get me out of bed.

Anyone with chronic pain will tell you that pain is something that takes over your world, as it has definitely tried to do to mine. However, early on in this experience I found that distraction helped me to ignore the pain’s growing hold over my body and mind. So because of the need for distraction, school and socializing have always been something I wanted to do. However, like many kids with CRPS, I had to have home-bound instruction at times and I hated it. I had great teachers and I loved them, but I need to be at school, even when it’s very hard to be up and moving.

Music has had an amazing influence on my life and has also played the role of distractor from pain. I have been playing guitar for 9 years and have been studying classical guitar for 5 years, and I think that the actual language of music will always amaze me and make perfect sense. My favorite bands are Fleet Foxes, Grizzly Bear and Radiohead. Certain intervals and genres of music emote different chemical reactions in our brains and cause us to feel certain ways, and I believe EVERYONE should find the sound that causes a chemical reaction they like the most, aka (what I call) “finding your groove”. I use “my groove” to help me feel better on a daily basis. And most importantly the person that has inspired me the most in music and has definitely helped me realize the healing powers of music is my big brother Joe. He’s my best friend in the entire world and without him, his literacy in music, and his loving, protective, and amazing personality. He’s the one person that I barely ever disagree with and I am more than lucky to have him as my mentor, and more importantly as my big brother.

I’d also like to give a quick shout out to the friend that has changed his life and daily routine to help me through everything I’ve been going through in the past few years and has been as much of a dependable distraction as a 17 year old boy could be 🙂 Derryk, you have been a Godsend to my family and especially me.. I love having you as my daily distraction and I hope that after this trip, you’ll be able to be less of a distraction from my pain and more of my bestfriend that I can have fun with, please always be my best friend even though we argue about the silliest things. My family and (especially) I, love you like you are our family, heck we already consider you a part of the family. Thank you so much for everything you’ve done for my family and for me.

Also, I want to thank everyone that has helped me and my family in the past few years and especially everyone who is visiting this site, leaving extremely supportive comments and praying for me. It is overwhelming to see how many people truly do care about me and my family and how many of you are thinking about me. However, part of the reason I wanted to share my story is to raise awareness of this awful disorder. So many physicians have NO idea what this is and I want to put an end to that. I want people to know what this is and look for symptoms, because not getting treated right away can turn into years and years of pain that I would not/could not wish upon anyone else. So yes, thank you so much for thinking about me and getting to know my story, but use my story to educate yourself and others. I am hoping to do the same by 1.Sharing my story and 2. Going to MCV to (hopefully) become a pain management specialist, because no matter what type of disease, how it happened or the patient themselves, I know how pain can effect your family, your work/school, and especially yourself and psyche.

 

Leave a comment »