Health Update – Dec 2016

3 Jan

Hello again lovely readers! I really need to start keeping better notes on how I’ve been. A full month in between is hard to keep track of. Because, right now, I’m liable to say ‘I’ve felt awful this month’. But the truth is probably a little more of ‘ I took some steps backward in health but I had some really good days and have gotten better in this or that area.’ But, without really good notes, I just don’t remember. So. Goal for this coming month is to sit and write a bi-weekly account of how I’m doing.

For a quick report from my migraine app – Migraine Buddy –   Average duration was 43 hrs. Average sleep a night was 7 hrs. 57% happened on weekdays, 43% weekends. Average pain level was 8 , high was 9 and low 6. My top Auras were fatigue/achiness, tingling near eye(s) and weakness. My top 3 triggers were neck pain, too much activity and pre cycle. Top 3 symptoms were neck pain, fatigue and jaw pain. Frequent start positions were temples, eyes and neck. Reliefs that seem to work consistently are : clonidine, oils, belladonna/pulsatilla and heat pad.

So, things have changed a little – duration has gone down a little, they are more evenly spaced during the week/weekends, average pain has gone up, and the auras/triggers/symptoms changed one item.

 

fightinglymemigraines

Overall Health: Better than November – sort of.  As of the last few days I’ve been feeling more like myself than I have all month.

Treatment: I’m still taking two Xiao Chai Hu Tang a day. I have added in one Ashwagandha a day. I started – and had to stop- taking Banderol as the the side effects (major fatigue) were just too bad. The Chaste Tree Berry daily seems to be helping my calf cramps. As I run out of vitamins/supplements, I am going to see if I notice not being on them. Excepting EHB, Ashwandha and a few others. I need to add in iron and butterbur to my regime.

Migraines:  These things have been brutal this month. BRUTAL. I’m pretty sure I told my mom I was dying last monday. That was a migraine like I haven’t had in a long while. Severe to the maximum. I don’t think they’ve gotten better since last month. they might really have taken a turn for the worse. But, the activity that naturally follows the holidays might have something to do with that.

Digestion and TMJ : While my digestion has been better than it was last month, it is still rather…touchy. I’m starting to juice again regularly – I’m going to mix it up and incorporate veggies that are high in iron ( spinach, beet, beet greens, etc) , otherwise the juice is kale, cucumber, celery, carrots, lemon, ginger and apple. Jaw pain goes away faster but is popping like nobody’s business whenever it wants to

Sleep:  The biggest change this past month is probably that I quit taking melatonin every night. I noticed I was sleeping the same length – and waking up the same amount of times –  without it. I’m glad to have one less pill every day. My app says I’m getting about 7 hrs of sleep, and I kid you not, I can predict within a half hour of when I’ll wake up in the morning from when I go to bed. Apparently my internal wake-clock works really well.

My app says I’ve been getting about 7 hours a night but I certainly don’t feel like it! I am still waking up 2-3 times a night to go to the bathroom, and sometimes can’t go back to sleep the last time. I’ve been taking a lot of long naps lately – but still am exhausted by late evening.

Memory/Brain fog:  I feel like my memory has been slipping again. Joy oh joy. I’ve added brain fog into this category because I feel like it’s something that I forget to mention – having had it so long it’s just a part of life now. The fog was heavy most days of Dec, it would lift for part of the day but it doesn’t ever lift completely- especially in a group of people, it kind of covers me like a cloak when there’s a lot of noises buzzing around me.

I did get in to my dr. for a quick acupuncture last week. I found out my results for my nutrient test that I took before Christmas. I’m low in iron, Vitamin A and Vitamin D3  (which reminds me I’m supposed to up the dosage I’ve been taking). It seems like my body is sensitive to almost everything I take to get kill the infections. Sigh. There is always going to be some herxing   but when it’s severe – it’s not fun to have to keep trying new treatments only to have to go off because of what they do to you. But, we keep on keeping on. My dream is to be as healthy as possible (for me) by the end of the year. Which also means, losing some weight. So, I’m going to start working out (in my living room) tomorrow morning. Hopefully three times a week. Combine that with eating healthy and juicing lots, I am hoping to see improvements in my joint pain/cramps, digestion and some weight loss! Here’s to renewed motivation despite chronic pain and fatigue. Lyme disease, I will kick your butt.

~Laura

p.s. that link about herxing is on a site that has a LOT of great articles about Lyme.

p.p.s. this is a great article about Inflammation and Lyme Disease 

 

 

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