Acceptance?

*****I actually started this post in October....just getting around to posting it now****

I have had a sort of shift in my thought process in the past few weeks. You hear about "acceptance" in the stroke world and it always carried such a negative sort of connotation for me. As if accepting any of these deficits means I've surrendered, quit, or given up....and that is NOT what I'm about. I am persistent like crazy so how could it possibly be that I am coming to place of acceptance. Perhaps it's a different kind of acceptance, my own kind...that means I only accept certain parts of this for the moment...for now. I still hope and pray I will get better but I need to be cautious to not allow my not fully recovered state to limit me. Rebecca, from Home After A Stroke blog wrote a short line that has really sat with me and helped me move more towards acceptance than ever before. "Waiting for my real life to begin." That's exactly how I have felt. Once I'm all better I could do x, y, or z. Well guess what....this is my real life...I'm not all better. I'm lucky to be here and be as good as I am. I need to move forward and stop waiting for my real life begin. Coming to that revelation was very emotional. My life is far from the way it was, I'm not sure when or if I will ever get where I want to be. It doesn't mean I'm giving up on getting better ever...it just means that I'm going to continue to live in gratitude where I'm at today. Living with my current deficits means I need to make some changes. I'm going to need to ask for help sometimes...even though I hate asking for or needing help. This fatigue is consuming at times. It's frustrating for me to want to do so much only to find my self NEEDING to sleep a few hours after I woke up. I have spent the better part of 2 years trying to find a solution...to which nothing much has helped. I remain optimistic because I am way better than I was immediately post-op, but I still have a long way to go. So far there has been no great explanation for why my fatigue is so intense. Some of the doctors have called it "post stroke fatigue" PSF and they said I could deal with this forever. I hope they are wrong. There is little research focused on PSF, although it is a very common occurrence after stroke. This is my most limiting deficit today, and yet I am comfortable accepting it and moving forward. If I was left with a leg/hand that didn't work, I would have to use an AFO or brace to help me...I need massive amounts of sleep, breaks, naps. That's just how it is and I am LUCKY! I'm not waiting for my real life to begin anymore and that makes me happy! :)

Tackling fatigue

I am now a year and a half out of deep brain surgery and stroke. Fatigue is a deficit that I can not yet escape. My recovery has been excellent except for this fatigue. I HATE it!! I am constantly reading, researching, trying to figure out how to fix it...a mostly fruitless effort. But I never give up HOPE that it will get better. When? How? I have no idea, but the following outlines my latest effort.
I saw an endocrinologist to make sure there are no other medical explanations for the crippling fatigue I deal with daily. It seemed like a good idea because after brain surgery one can never be sure that something else didn't go wrong while they were in there. I also have hypothyroid (onset 4 years ago during my pregnancy) which is often a cause of fatigue, but supposedly my thyroid has remained stable according to my PCP. My opinion is that my thyroid is at least part of my fatigue problem, but I can't be sure. So, I had a full work up with the endocrinologist and there were a few issues identified. According to the tests, my thyroid was within the "normal" range and my blood sugar is low frequently. The doctor changed my thyroid to Armour and doubled the dose despite the "normal range". What do you know? I got two more hours out of the day. Previously I was awake for 4 hours twice a day, now I'm awake about 5 hours twice a day. So I think I'm heading in the right direction. My assessment is that I need more thyroid, and I need to do something about my diet to regulate my blood sugar better. I probably need to eat more frequently. Since my surgery I am less hungry, my body just doesn't seem to send the hungry message, so now I'm trying to eat at least every few hours even when I'm not hungry.

Next, I saw a naturopath. She did an assessment and made a ton of recommendations both dietary and supplements. I went home and started to look up all the supplements and was completely freaked out. I don't like taking any mediation and supplements are even more scary to me since they are not regulated at all. There is no guarantee that what they say is in the bottle is actually in there and sometimes they don't even know the active ingredient so there is no chance of "dosing" the unknown. You can not easily look up interactions, contraindications, adverse reactions, and such like prescription medications. The research on supplements is largely anecdotal and rarely includes double blind, controlled, peer reviewed, published studies. SCARY!!! I like evidence based medicine. But I want to feel better so badly and maybe this stuff just might work, but at what risk? Oh, what to do? I did a quick look up of all the supplements she had recommended and most of them contained ingredients that had the potential to lower the seizure threshold and figuring out which could be blood thinners was close to impossible(anyone with cavernous angiomas must avoid anything that thins blood)..YIKES!! and no thank you! I'm trying to get better not worse. My risk for seizures is high since I have "persistent hemosiderin" "remnants of old blood from my bleeding angioma" (they were not able to remove all of my blood stained brain during my surgery because there was just too much.), and now I also have scar tissue that can create seizures. I am also off anticonvulsants by choice, risk known to me, which puts me at an even greater risk. So  anything that can potentate seizures is out for me. To me that is what is frightening about alternative medicine. Some people think, "It's natural...it must be safe." No way!! Supplements can be more dangerous than pharmaceuticals, even though it's pharma that gets a bad rap.

The diet recommendations were a whole other story. The purposed diet was: no dairy, no caffeine, no gluten, no corn, no beans, no white rice, no soy, no nightshades(potato, tomato, etc.), no mushrooms, no eggplant, no carrots, exchange regular sugar for stevia when possible, no soda, and no alcohol. So what's left exactly? Not much. As much as I was less than thrilled with the purposed restrictions...I thought I had to at least give it a try. For one week...I did. I lost 5 lbs that week and felt like I was starving...still completely exhausted. No different in the energy dept.

Needless to say, the whole thing was a waste of time and money. The lady did refund my money for all the scary supplements she recommended, after arguing with me(which was completely annoying to me). Especially since she told me that I was "lucky" she was not charging me for the time that she spent arguing with me on the phone. Please, I already spent $300 on the office visit that was a complete waste I think if you are in the professional business of recommending supplements you should be completely informed of the risks involved. As a nurse, it was my responsibility to make sure that each and every drug, prescription, intervention, was appropriate for my patient. Sometimes the doctors made mistakes and it was my job to make sure the drug, dose, etc. was right for the patient. If you are in healthcare it is your duty and responsibility to not cause harm at the very least. I expect the same level of responsibility and accountability from members of my healthcare team that I provided for my patients and I think it's complete crap when my expectations are not met. 

As for my fighting fatigue plan, I'm starting to run out of ideas, but I will never give up hope.

Learning to just BE

Many parts of this whole "brain thing" have been difficult...and I have faced many challenges along the way...but one thing that I have gained is priceless. Previously, I was borderline OCD....type A personality....a "perfectionist" of sorts. I was also always on the move, going, doing, busy, very busy. I held several jobs at once while in college. I was always taking a class, earning a certification, maintaining a licence, on and on. I was going in a million directions all the time. A brain problem and major fatigue is a sure way to put an end to all that chaos. It's coming up on three years since my initial diagnosis and my life is completely different. While my new attitude would likely make me "less employable" it doesn't matter today and I am finally enjoying my new found ability to just be. There are days...sometimes weeks that I don't actually do anything or go anywhere, and I'm ok with that. Doing nothing, or going no where would have made me crazy before. Prior to all this if I didn't have my car for a day, I would feel claustrophobic. I guess not being able to drive at all for almost 2 years is a sure way to fix that. I can drive now, but I rarely do. Accepting and embracing my new lifestyle was a slow process for me and quite an adjustment. I certainly shed many tears along the way, frustrated when I "couldn't" do this or that. Now, I'm completely content to just be...as long as I get a nap. ;) Even as I improve I hope to never fall back into my old ways. We recently went on a vacation to Kauai. It was a fantastic trip, and I spent most of my free time just taking it all in...from my lounge chair overlooking the ocean. I didn't need to be snorkeling, going, or doing anything. I was content just hanging out. With a very busy three year old, the opportunity to just be is far and few between, so I am glad to be able to sit back and enjoy the few fleeting moments in time when nothing is happening. I'm so thankful that I am now able to really capture the moment and I have learned how to truly savor it.
    

Cental Pain Syndrome (CPS)

While this term/diagnosis might be unfamiliar to many of you...the symptoms or complaints are possibly painfully familiar. Central pain syndrome remains a bit like a "mystery diagnosis", in that there are few doctors identifying this syndrome. There are likely greater numbers of survivors suffering in pain alone because doctors have failed to identify CPS. Even once the culprit of the pain is identified, there are few treatment options today. :( My dear friend, Patti G, is not only afflicted with multiple cavernous angiomas but she also has been afflicted with this monster and she is doing her best to "get the word out"...so that CPS will not longer be such a mystery...and hopefully some day there will be a solution to this terrible pain. Please help spread awareness by sharing the fantastic video that she put together. Watching this really puts my fatigue in perspective.  As much as I hate being tired all the time...at least I can escape it while sleeping. Pain is truly the worst deficit imaginable to me.

HOPE

I saw this on another survivor's blog. While his recovery is seemingly not a brain injury, to me the message is the same. HOPE is so powerful...don't let anyone put limits on your recovery. Your recovery is over when YOU say it is...That's it!! I love this video!
Warning: I don't know about all the falls he took...looks pretty dangerous to me, and the standing on his head...no way!!But his focus and determination are simply amazing!! 

Thanks to Barb for sharing it. She wrote an article,  http://www.communityadvocate.com/2012/06/18/i-was-just-thinking-about-disabilities ,and someone responded with the video. I had to share it and I can hardly wait to see the movie.http://www.inspiredthemovie.com

WHY? Why did I decide to have surgery?

I have been asked this question many times. Just recently a reader asked again, and I don't think I've ever spelled it out here...so here goes.

My decision to have surgery was by far the most difficult decision of my life. By no means is my explanation an endorsement of surgery or a suggestion to anyone else to have surgery. Surgery is a very personal choice and one that I think warrants much thought. When I was first diagnosed 8/31/09 with a cavernous angioma in the middle of my brain (located right insular cortex/putamen/internal capsule, basal ganglia), I was told by my the first doctor that I had better hope I never needed surgery to remove it because they will never be able to get it out without causing significant damage. The first doctor also said not to worry about it because according to her "angiomas NEVER cause problems." Well, she was wrong in almost everything she told me. I went on to get several more opinions because I had a list of questions and nobody could answer them. I didn't feel comfortable with the opinions and advise I was receiving and as a nurse I had a decent understanding that many of the MDs I saw were blowing smoke...they didn't know what they were talking about....and I wasn't buying it. Basically, I saw doctor after doctor looking for real answers. Meanwhile, I was feeling worse and worse. My choices for doctors were limited at first because I had an HMO insurance plan. Prior to this diagnosis, I was never sick, never went to the doctor, and I wanted the cheapest form of insurance I could get. When you end up with a brain problem, HMO insurance is pretty much a bad idea (I don't want just anyone poking around in my brain...only the best of the best if absolutly necessary, please)...so I eventually switched to a PPO and then I could finally see some real experts and I started to get very different answers. While the first few doctors I saw said no surgery, they also knew nothing...so how valuable were their opinions? Eventually I saw Dr. Martin at UCLA, who has an excellent reputation. First time I saw him, he said I needed more testing, "a better work-up". I saw a bunch more neurologists and went back to him with my list of remaining questions. He seemed pretty annoyed with my barrage of questions and ended up giving me a flip-flop answer to surgery...No then yes, but maintaining that I will more than likely NEED surgery because of future bleeding and resulting worsening deficits in my lifetime. I wasn't sure what to do, but I was finally getting answers. I sent all my "stuff" to Dr. Spetzler and his resident called to tell me that they recommended surgery. My heart sank. I felt sick...now what? I had a lot of knowledge at this point and was hoping he would say, "Let's wait and see." I felt that if one of the best experts told me to wait and see...then that would be it....wait and see. The resident told me that they felt my risk was much greater to leave it than to remove it. Based on my MRI's and my worsening condition I knew he was right, but I was so scared. I had an MRI every six months from diagnosis and each time my cm was bigger and showed new bleeding. One year from my initial diagnosis, my cm had doubled in size to about 4cm.  The growth and bleeding coincided with me feeling more dizzy, more frequent partial seizures, worsening vision to the point I could no longer drive, and a few occasions of not being able to walk. Not being able to walk was really scary as were the seizures. It was becoming obvious that I might become paralyzed because of the surgery, but I might also become paralyzed without the surgery. At first, I was worried that having the surgery might make me worse....but I was getting worse anyway. I began to feel like,"What am I waiting for?" Still not convinced I was making the right choice I connected with others that already had surgery and I sent my "stuff" to more experts.(While no surgery or recovery is the same, talking to others helped me tremendously.) Dr. Samson in Texas has a great reputation so I sent my stuff to him. He wouldn't give me a recommendation unless I was physically in his office and Los Angeles is a long way from Texas...so I never actually got his opinion. I also sent everything to Dr. Steinberg at Stanford, who is also considered one of the best, and he recommended surgery too. I was getting good at asking questions by then, and his nurse practitioner gave me all the same answers as Dr. Spetzler's resident...so I finally felt I was on the right track. All my questions were answered the same...finally!  Connecting with others who had been there done that was invaluable and a big reason why I put my story in this blog. There were so many wonderful people willing to share with me their ups and downs, their personal experiences...I am forever grateful to them for helping me make my best choice and for supporting me from start to finish. :)  The main criteria the doctors gave me for recommending surgery for me were: my cm was big 4cm...since it was so large, the potential for a very big bleed was increased, my cm had a history of bleeding (more than 3 times already) so chances were higher it would bleed again, my age (36 at the time) "young" according to them giving me many years of possible recurrent bleeds without surgery and younger people tend to recover better, I only had one angioma (having multiples changes everything),and they thought they could access my cm without much damage. There was also the added bonus for me, that if my surgery went well I might get to have another baby...which I would love! I believe that my first pregnancy/delivery was the trigger for my angioma to bleed and grow. I knew that I could not consider another pregnancy unless my angioma was removed, the risk of further bleeding and progressive deficits was just too high for me. While a possible future pregnancy was not my only or primary reason for having surgery, I did view it as a possible bonus. Being a mom to Jack and wife to John were my two most important goals. Would I be able to be all I wanted to be without surgery? Long term, would I be better or worse off with or without surgery? Those are the tough questions that nobody can answer. I suspected that the surgical risks they quoted me, 5% chance of all the scary stuff was probably very optimistic..but I wanted to believe I would be lucky enough to avoid all the scary things...especially death. Honestly, I think the surgeons should do a better job of explaining the reality and high risk of brain surgery, especially deep brain surgery. I guess it was their attempt to make me more comfortable with the whole thing. It didn't work...I was terrified, but ultimately I knew it was out of my hands once I decided surgery was my best option. I knew from doing tons of research that my location was terrible. It's a really tough spot to get to and it all comes down to splitting the Sylvian fissure. If that part goes well...hooray!!! If not, ut oh! The brain stem is often considered one of the most difficult locations, but I knew mine was right up there in terms of difficult access, and ultimately that's why my surgery resulted in a stroke...very uncommon for angioma surgery especially with Dr. Spetzler. My Sylvian fissure did not want to be split. There were several blood vessels in the way, so it was either they cut one vessel and take out the angioma or they stop the surgery and tell me, "Sorry, we cut your head open and started, but we can't get it out." They made the executive decision to proceed with the surgery and I am thankful for that.

Some people go into surgery with the expectation that they will not have any new deficits following surgery. To me, that is a naive and unrealistic expectation. As a nurse, I always felt that once you have brain surgery "all bets are off". You might survive but will you be you? I don't remember which book it's from but this line stuck with me, "Brains are not built for service".  Brain surgery is always a BIG deal, and I felt/feel very lucky to be alive and to still be me!!! When I woke up, I was a mess...I knew it...and I was a tiny bit scared...but I was very HAPPY!! I thought I'm alive, I am still me, we can work on everything else, and I still feel that way today.

For me, the decision to have surgery was the right one. Maybe for others, they would have been wrecked by the whole stroke complication. I knew that stroke was a possible risk...while I was hoping to avoid it, I know there were far worse things that could have happened to me. Living with the monster that was in my head and the reality of a lifetime of progressive neurological decline would have been worse for me. I wanted to be proactive about my life and not let this angioma consume me, as it had for the year prior to my surgery. My angioma was growing and bleeding actively for a year...it was horrible!! There were days prior to my surgery when I couldn't do much of anything. Jack was small and just learning how to walk. Some days I would just lay on the floor blocking him and I into a "safe area" and hope we would survive another day. I had surgery ultimately to reclaim my life that I felt was slipping away, and I am glad I did! Please feel free to ask me any questions if I left something out that you are wondering. Best wishes to anyone out there contemplating surgery. I know how hard that decision can be. My advise :get as many opinions as you need from  cavernous angioma experts and then weigh your decision carefully. 

No "wonder drug" and April updates

Of course, we all know there is no such thing as a wonder drug...but I was foolishly hoping there might be something out there to help me with this dreaded fatigue. Back in November the neuro-psychologists that I saw said I would be a good candidate for fatigue medication. I was skeptical because I HATE taking medication, so it was a complete stretch that this could be a part of my solution. I am super sensitive and usually react negatively to medications, but after reading the side effects for the first purposed fatigue medication, Amantadine,...I thought the possible listed side effects didn't seem so terrible and it was worth a try. My fatigue is so terrible that I am willing to give almost anything a try.
This past month seemed like a good time to try to tackle my remaining deficits and hope for the best. My plan was to see a few new neurologists...hoping one might be a match to work with me on my remaining issues. It turned out to be a complete disaster. The doctors were not good and the medication...oh....YUCK!! The first neurologist was actually very smart...I think...but hardly gave me any time and he just wasn't my type. He said some of my complaints were permanent, which I never want to hear, and don't agree with either. How does he know that my leg/foot muscles will never get better and my left shoe will always fall off? I don't agree and I don't want to work with a doctor like that. He also prescribed the first medication. He said there were 3 that are used commonly for post stoke fatigue, and that if the first didn't work, we could move onto the others. He suggested that I start one a tiny dose(50mg) of Amantadine and work up to a full dose(200mg) in a month's time. He said the primary side effects are GI related and are normally only seen when taking large(greater than 200mg/day) doses. I went home and looked it up right away. It's actually an old anti-viral drug that some people noticed the side effect of fatigue relief. I read several positive testimonials, and hoped this could work like magic for me. I was hoping that at the least I might get some placebo effects because I wanted it to work so badly.I took 50mg once a day for 2 days and I thought I was going to die. It was horrible. My heart was racing/pounding, anxiety like crazy, neck and shoulder pain (tension type pain),zero patience, terrible insomnia. I was still exhausted but I felt so uptight I couldn't sleep. There was nothing to be stressed out about and since I've had surgery, I am always super calm...it was obviously the drug, although nothing that I experienced was listed as a possible side effect. I felt horrible, and decided even though I was only 2 days in, I could not take any more. The next day(day 3) I had already abandoned hope that this was my answer and I didn't take it, I got the worst headache I've had in a long time. My eyes were messed up, dizzy, nauseous, excruciating pain. Like a migraine, but slightly different. The next day (day 4) it was gone...thank god!!! That's it no medications for me. I decided I need to be more patient and wait it out. I need to stick with the basics: good food, exercise, and regular sleep. There is no wonder drug to save me from this fatigue monster. I sorta feel like I wussed out only two days in. I wanted to know that I've tried everything to reclaim my life, but my experience was so horrible with the Amantadine, I just can't bring myself to mess with my head and body like that again. I just keep asking for patience. I am a doer. I want a plan and the energy to complete it. I would rather work super hard at something than stand around and wait for it to be done. "Waiting" to get better is really hard for me.

I also saw another neurologist later in the month...the WORST one yet...and that's saying a lot because I've seen my share of clowns. I left in tears because I felt like he was my last hope to work with me on my remaining deficits. I shouldn't have let it bother me, but it did at the time. Looks like I will be working on my own. He clearly didn't know anything. I could ramble about all the misinformation he gave me, but I'll spare you the details. Basically, he said all my problems were "in my head", which I always partly agree with. ;) Seizures, stroke, bleeding angioma...yes, all technically in my "head"...but fictional....oh I wish...that would be easier to fix right?!! This has been an ongoing issue for me. If you "look good", there is nothing wrong with you, no matter how much "proof"(MRI's, EEGs, etc.) you have that something is not right. I can just hardly wait to feel good again and forget all these clowns that don't have a clue.


I have one last specialist to see next month, an endocrinologist. We'll see what he comes up with, but so far the doctors have been a waste of time.


I also attended a new stroke support group this month. I have wanted to attend some sort of support group forever, but there were not any in our local community. I saw an ad  for a new group right by house. Perfect! It was great, although I always feel like I don't quite fit in. It doesn't matter...I do fit in. They just don't see it yet. Like many brain injury survivors, my deficits are not usually immediately visible.

What brain injury survivors want you to know

Here is a great article  that explains what it is like to deal with a brain injury. This article is directed at family members and loved ones but anyone can gain understanding and insight if they chose to. Thanks to Patti G. for passing it my way.
http://www.brainline.org/content/2011/07/lost-found-what-brain-injury-survivors-want-you-to-know.html

I look forward to the day when this article is no longer relevant to me personally. That day has not come as of right now. This article details a number of the "issues" those of us with brain injuries face on a near daily basis. To use my mom's phasing..."I'm not complaining...I'm explaining." Really! I am completely grateful for where I'm at today and how far I've come, but the reality is I still have a number of things I would like to see improve.
I recently attended Easter festivities with a large portion of my family. It was one of the first "family functions" that I have attended post-stroke. I have been to a few other events, but none quite the same as Easter. It was difficult. I came home basically in tears and somewhat disappointed about how hard it was for me.  While I knew it might be challenging, I wasn't entirely prepared for how hard it turned out to be. When I get upset with myself for not doing as well as I wished...I come right back to where I started. It was a bad place. I have come so far, and I am doing really great no matter what.  I am so grateful for what I can do and for the things that I can do well. Turns out, large social functions are on the list of still needing improvement. I am always hoping that these situations will just get better in time. This article acts as a reminder to be more gentle and patient with myself as I slowly try to regain all that I lost. It is certainly hard for my family to understand what I am dealing with, as I didn't even expect it to be such a challenge.

Brain injury recovery video

Another great video on recovery. Alison Shapiro also wrote an inspirational recovery book, Healing into Possibility. Even at this point in my recovery (almost a year and a half), I am still hoping to see improvements. I just keep reminding myself that it's about belief, and will. This type of video reinforces how much control we have in making our brains change to work for us. Thanks to Patti G. for sending this my way. :)

Horray for Wes!! Inspirational recovery story.

Everything is possible. It's all about will, attitude and perseverance. Enjoy!!

Meeting Angioma Alliance members

A few weeks ago, I got the opportunity to meet up with some other Angioma Alliance members that also live in the Los Angeles area and Connie (ambassador and founder of AA) with her daughter Julia. It was an awesome and also humbling experience to meet others who's lives are affected by cavernous angiomas. Several of the people in attendance have "multiples"...which to me is like a whole different deal. Having more than one means you most likely can't just have one surgery and be done. Not that one brain surgery is any walk in the park, but having more than one surgery multiplies your risk of complications, deficits, recovery, and associated stress. Also, if you have multiples, you could develop more angiomas at any time, meaning greater risk of bleeding over time, and constant uncertainty. It could also mean that there is a genetic factor involved, resulting in a 50/50 chance of any of your kids inheriting the faulty gene that creates angiomas. Point is...to have one stinks...to have many really, really stinks!! So in the group of 15 or so...I felt lucky to have only had one angioma. It also keeps what we had to deal with it in perspective. I feel like I have no right to "complain" about how hard it was. Sure it was tough, sometimes it still is tough, but really...people with multiples have to deal with what I went through plus so much more. Meeting Connie and Julia was an honor, after all, they started Angioma Alliance and they are very involved in finding a cure. Make sure you and everyone you know with a cavernous angioma signs up for  the international patient registry...even if you already had surgery www.angioma.org/registry I have said it many times, but Angioma Alliance was a tremendous resource for me from diagnosis through today, and supporting this organization is near and dear to my heart. Connie and Julia are continuing their trip cross country so check the website if you would like to meetup. www.angioma.org/roadtrip The meeting was great and left me wanting to do more to raise awareness for this unrepresented illness/condition...whatever you call it. I have been brainstorming fundraising ideas...but unfortunately my brain doesn't work all that well and so far I have no ideas. 5ks are popular, but there are so many in my area for other causes already and I'm not even a runner...it just doesn't make a lot of sense to me. I like some of the ideas that other people have done...a wine auction, dinner event...but I have no idea where to get started...so the brainstorming continues. Everything takes longer when your brain doesn't work quite right. ;) If I can ever figure out how to upload the picture we took of everyone at the meeting, I will post it. (It is at the end of almost 3,000 photos on our camera and it will only load all of them.Safe to say I am not tech savey in ANY way.)Take away:
 1. If you have not signed up for the registry...do so now...a cure depends on it.
2.    If you are able to meet Connie and Julia...do so...it is an opportunity you don't want to miss.  

Still working on recovery

It has now been about a year and two months since I had surgery and my resulting stroke. I am always completely thankful and grateful for the recovery I have had/made, how far I have progressed, and for "what is" today! While I always am thankful and grateful, I remain hopeful that I will continue to move forward. The past two months have not exactly been encouraging as I have seemingly taken several steps back rather than forward. At this point, the dreaded plateau sounds almost welcoming. I finally feel as if I am beginning to almost hold steady again. I am anxiously awaiting the next steps in moving forward again...hopefully!! In November and early December, I was doing the best I've done yet. And then I was hit hard by a new set of issues. The whole UTI/kidney infection really zapped me and continues to deliver pain daily. It became abundantly clear that I am different now. I do best when I can just go through our predictable daily routine, without any extra taxing events. I am not prepared to deal with any additional health problems, so I hope I can just stay healthy forever! Our daily life, without any extras, currently consumes ALL of my limited energy.
As we move into the next phase of recovery, the chronic phase(after one year), I have started looking at some new options. I had been hoping/praying that my fatigue would just disappear...but it hasn't. I have tried several techniques to "manage" my fatigue with little to no success. Fatigue is my worst deficit at this point, and I am hoping to beat it. Currently, my fatigue is severe and very  limiting. I  had neuro-psych testing done back in November and they provided me with a number of recommendations. One of their suggestions was to at least try some meds. for fatigue. The biggest issue with that lies in my risk for seizures, so they said medications could be a difficult balancing act. I was encouraged by the hope of eliminating this fatigue, so I began my search for a new neurologist AGAIN. Lucky #7 or 8!!! So I have 2 new neuros to try next month, I hope one of them works out and I can get back to working on my recovery with the help and support of an expert. I also had a sleep study in November which looked pretty problematic to me...but I'm not the expert. ;) The neuro-psychs also said they thought that could be a big part of my fatigue, but I needed a "good" neuro to work with me since my current neuro didn't offer any insight to address my concerns.
This coming month is jam packed with several specialist appointments and I look forward to finding answers, initiating solutions, and finally feeling better!!   

Spreading awareness about cavernous angiomas

Since being diagnosed with a cavernous angioma in September 2009, my life has changed greatly. I never really had a "cause". Many people are touched by one thing or another along their path of life and they get motivated to make that their "cause". While I had been touched by many things, no specific thing moved me like this diagnosis and all the emotional ramifications that this diagnosis created for me. In finding Angioma Alliance, I have also made dear friends that share in this dreadful diagnosis...many of them have it much harder than I do/did. I was blessed to hopefully only have one bleeding mess in my brain. Some of my friends have multiples or they have them in a location that prevents surgical treatment. For many of my friends there is no cure yet. :( I hope that will change in time, and I intend to do my part to help be a part of the cure. I have taken on trying to spread awareness about cavernous angiomas as a part of trying to better the lives of "us" afflicted with this condition.  While I...hopefully.. no longer have a cavernous angioma I will always identify with those afflicted. I have been there/done that! I understand how hard it is to live with the uncertaintly, the bleeding, the seizures, the deficits, the surgery, and the recovery.
I am not a professional writer...I was a math and science lady prior to all my brain problems. Writing has never been my thing. I didn't start writing until I found a "cause" or rather my "cause" found me. I originally wanted to be a doctor but changed my mind many years ago. My degrees and work experience are in psychology and nursing. With that said, I have been writing this blog since just prior to my surgery. I originally started it to keep friends and loved ones informed...and as a much needed source for positive feedback and encouragement during my darkest days...but it has become something very different. It now is my voice for spreading awareness about cavernous angiomas and sometimes stroke recovery. While professional writers probably cringe while reading my blog...fragments/run-ons, grammatical errors, punctuation all wrong, as well as my casual writing style...my writing is anything but professional. Proper writing aside, what I am presenting is my side to the story. My experience with cavernous angiomas, brain surgery, stroke, and stroke recovery. As part of my continuing push to spread awareness, I sent my story to a few publications...hoping they would publish it and help to raise awareness. The first place I sent my story was to Stroke Connection. It's a magazine put out by the American Heart Association. I submitted my story 9 or 10 months ago and they called a few months ago letting me know they selected my story. I am never short on words and my story was extensively edited down to a mere 500 words. The published version varies dramatically from my submitted version, but non the less here it is! Stroke connection article
While my article was edited extensively, I still perceive it as a win for my cause and I hope it is only the start of great things to come. I would love to see the day when physicians actually know something about cavernous angiomas and treatment involves something less invasive than crainiotomy. I will continue my advocacy for this condition and my dear friends afflicted with it.
   

A new year and a new set back

As we rang in the new year...we were hopeful we were leaving all of my health problems in the past. I was hoping 2012 would be filled with continued recovery and good health. Turns out...2012 has brought a minor set back so far. I was not feeling well for several days since Christmas, but had hoped it was related to "over doing it" with entertaining family during the holidays. It became alarmingly clear that there was actually something more going on when I experienced extraordinary back pain that persisted for several days. The first day, I tried to ignore it. The third day that I had the pain, I went to the ER...hoping to resolve any possible problem in 2011. Following the ER visit, I initially improved  only to experience increasing pain over the next two days. When my doctor's office finally opened on Tuesday morning after being away for the long holiday weekend, I was there waiting for her. She examined me and took a complete history of my complaints after which she explained two options. Option A: Go to the hospital, be admitted to figure out what's wrong with me, and get me treated. Or option B: do lab work, abdominal CT scan, and change the antibiotic again (4th switch)...wait for the results and then be admitted if need be. I chose option B...hoping to stay out of the hospital. My lab work and ct scan did not indicate any specific reason for my pain, although while I was in the ER my urine contained bacteria and blood, leading them to the diagnosis of kidney infection. (I had a UTI about a month ago that must have not been entirely treated although most of the original symptoms resolved.)  Normally, one can just be treated with oral antibiotics and the problem resolves. For me, finding an antibiotic that works that also does not lower the seizure threshold was proving to be a challenge. I had been on 4 different antibiotics in the past week that didn't work. My doctor finally selected Levaquin to treat my infection and it is a 10 day course. After consulting with my seizure specialist...he put me back on Keppra. :( So here I am back in a fog, not able to drive while they adjust my Keppra so that my infection can be treated outside of the hospital. There were several other antibiotics that do not increase the possibility of seizures but they are only available in IV formulations. This is just another example of how having a brain problem complicates life.
The good news is that it seems this 5th antibiotic is working. My pain has been greatly reduced and is limited to my left lower back. Additionally, I am still seizure free on day 5 on the 10 day course with the Levaquin. :)
While I do feel this whole episode has been a set back in my recovery...I am hopeful it will resolve in the next few weeks and then I will be back on track. I was advised to stay on Keppra for the length of the Levaquin course and then I will be able to wean off slowly over the next week or so. Looking forward to being "Keppra free" again soon. This stuff makes me really groggy!! And happy New Year!!!