International Steampunk Fashions by Victoriana Lady Lisa (Jan 28, 2013)
Friday, June 22, 2012
Wednesday, June 20, 2012
Diamond Candles Coupon
Anyone ever hear of Diamond Candles?
They remind me of the Pyramid candles my sister used to get for her birthday. ♥
Decided to go ahead and grab one and see how the scent is. :3 Got the Hawaiian Coconut one. :3
If you are interested, use this link to grab $5 off your order if you decide to try them out. http://curebit.com/x/JxP69
Friday, June 15, 2012
Ben's Friends Takes the Guillain Barre Support Site Live!
Stop by and join a great community of fighters, survivors, family and friends of those hit with Guillain Barre Syndrome or CIDP.
http://www.guillainbarresupport.org/
http://www.guillainbarresupport.org/
Thursday, June 14, 2012
Amarillo Steampunk/Anime Convention Hosted by the Amarillo Public Library!
http://ama-con.amarillolibrary.org/
Saturday, July 21 – Amarillo Civic Center – Heritage Room –
11am – 10pm
I will be hosting a panel about Steampunk Inspiration and in the panel I will basically be talking about places to research design and costumes ideas when trying to develop your steamy styles. This can range from jewelry to weapons to costumes.
Things to expect at my table for vending:
Comics by Chris Ralston: Third Rail! http://www.r10creations.com/
Originally from Houston, Chris now calls Nebraska home but he will be returning to TX for Comicpalooza 2013 so grab a sneak peek of his comic Third Rail now!
Comics & Prints Chris Holm: SteamPets! http://chrisholm.deviantart.com/
Did I mention Chris is from Amarillo? While unable to make it due to schedule conflict, there is always next year. Stop by and grab some awesome comics and prints!
As far as the different types of jewelry, charms, trinkets and tokens that will be from me this list should give you an idea:
Cufflinks
Earrings - Wire, Stud & Non-pierced
Bracelets
Necklaces
Charms (Great for backpack zippers!)
Various Original Art Creations
I am very anxious to get the 3 Japanese Women Statues Modded before this event!
Some of my Austin Bats with accompany me!
I hope to complete another Steampunk Collage before the event!
Leather Cuffs
Antique Keys
Various Gear & Supplies
Pictures of recent works to be posted on the blog soon!
Tuesday, June 12, 2012
Monday, June 11, 2012
A Gift from my bout with Guillain Barre Syndrome - GBS: Occipital Neuralgia
One of the lovely things that Guillian Barre Syndrome likes to leave patients with is parting gifts; these can range from continued buggy feelings in their legs, fibromyalgia to permanent nerve damage.
In my case it is something called Occipital Neuralgia.
I wanted to post about it on the blog in the off chance that other recovering GBS patients might be sharing some of the same headache pain that I have and hopefully I can help offer suggestions to stop misdiagnosis.
I was hit with GBS in May 2009 and during my recovery at the neuro rehab facility a headache began to develop and nothing we threw at it seemed to help. Eventually it got to the point where I would just take a percocet and hope it would knock me out enough to get some rest. The next step was to move on to morphine which I really did not want to do.
Now how to describe this pain... It is as if lightening shocks radiate out from the base of my skull around where it meets my spine and the lightening branches out across the back and top of my head. Pressure on the back of my skull seems to trigger the pain so it makes for weird sleeping positions in the attempt to keep pressure off my head. At the rehab I would lay my head on the pillow and the moment pressure came down on my ear the pain would start and just continually pulse.
Eventually while at the rehab the neurologist stopped by to see how I was doing and suggested a nerve block to see if it would alleviate the pain. I received the injection and immediately passed out for the day. It felt like I finally had relief from the pain for the first time in a couple weeks. Unfortunately this relief did not last long, I had about a 3-4 day grace period before the headache returned.
With occipital nerve blocks, you are only supposed to receive 1 every 3 months. I couldn’t wait for the chance to get another to try it out again and see if it would last longer. In the meantime my recovery continued and I met with other doctors and when I mentioned the headaches they constantly referred to it as a migraine and began prescribing medicines as such to tackle it.
Finally the 3 month mark came and I was able to get another nerve block. After getting it I felt drowsy and had my husband drive me. This time I had about 1 week of relative relief. By this I mean a level 6 constant headache got knocked down to maybe a 2.
What doctors did not seem to understand and I kept trying to stress was that this was a constant headache that would gradually increase or decrease, there was no time that I did not have the headache. The easiest way to cope with the pain was buying really good light blocking curtains for the bedroom (my eyes get light sensitive and noise drives the pain up even more) and I would rest in the dark bedroom for hours on end just waiting for the pain to stop. I also found that a heating pad targeting my shoulders and skull would help take the edge off the pain.
This process went on from August 2009 until about October 2011.
The constant headache had become much worse and I went in to receive another nerve block. After receiving it and driving home the pain then began to branch down through my shoulders and back and the pain was much worse. After downing who knows what all pain pills in an attempt to find any sort of relief I was able to get back in to see the neurologist after a few days and we discussed alternatives to relieve the pain. Among the options I was given a 30mg sample of Cymbalta which while normally given out for depression has been found to stop diabetic neuropathy. I went home and began trying the Cymbalta.
Within 3 days my 2 year long headache had finally stopped.
Now I can’t say it was a cure but it has really helped me get back to where I want to be as far as going out and doing things. I still get a headache at times when I push my body too far but it at least has offered me a potential solution. When I go out and put too much constant stress on my body I usually pay for it and end up spending a week of bed rest inside my dark bedroom with all the lights out, the air conditioning at 72F and the heating pad on my shoulders and neck.
When the neurologist saw the positive response from the treatment with Cymbalta it was determined my headache is attributed to occipital neuralgia rather than a migraine. If we had figured this out earlier, a lot of pain could probably have been avoided. I now use a combination of a daily 30mg Cymbalta dose and a nerve block once every three months to manage the pain.
I do hope that if anyone else comes into a situation with similar headaches during their GBS recovery that this can help them find relief faster.
Keep driving forward!
EDIT: 9/18/2012
I am now being considered as a good candidate to try out Botox injections in my neck and shoulders. After I learn a little more about the process we may move forward on Oct 2.
EDIT: 9/26/2016
I recently went through a Ketamine Therapy Treatment and the constant 6 pain got knocked down to a 0-2 once the exhaustion of the whole process subsided. I am off Cymbalta now and have not had a nerve block for 6 months. I still take Soma and Hydrocodone at night to help keep the pain down. This is a HUGE improvement for me!!
Occipital Neuralgia Links:
http://www.webmd.com/migraines-headaches/occipital-neuralgia-symptoms-causes-treatments
http://www.hopkinsmedicine.org/neurology_neurosurgery/specialty_areas/headache/conditions/occipital_neuralgia.html
http://www.ninds.nih.gov/disorders/occipitalneuralgia/occipitalneuralgia.htm
http://en.wikipedia.org/wiki/Occipital_neuralgia
In my case it is something called Occipital Neuralgia.
I wanted to post about it on the blog in the off chance that other recovering GBS patients might be sharing some of the same headache pain that I have and hopefully I can help offer suggestions to stop misdiagnosis.
I was hit with GBS in May 2009 and during my recovery at the neuro rehab facility a headache began to develop and nothing we threw at it seemed to help. Eventually it got to the point where I would just take a percocet and hope it would knock me out enough to get some rest. The next step was to move on to morphine which I really did not want to do.
Now how to describe this pain... It is as if lightening shocks radiate out from the base of my skull around where it meets my spine and the lightening branches out across the back and top of my head. Pressure on the back of my skull seems to trigger the pain so it makes for weird sleeping positions in the attempt to keep pressure off my head. At the rehab I would lay my head on the pillow and the moment pressure came down on my ear the pain would start and just continually pulse.
Eventually while at the rehab the neurologist stopped by to see how I was doing and suggested a nerve block to see if it would alleviate the pain. I received the injection and immediately passed out for the day. It felt like I finally had relief from the pain for the first time in a couple weeks. Unfortunately this relief did not last long, I had about a 3-4 day grace period before the headache returned.
With occipital nerve blocks, you are only supposed to receive 1 every 3 months. I couldn’t wait for the chance to get another to try it out again and see if it would last longer. In the meantime my recovery continued and I met with other doctors and when I mentioned the headaches they constantly referred to it as a migraine and began prescribing medicines as such to tackle it.
Finally the 3 month mark came and I was able to get another nerve block. After getting it I felt drowsy and had my husband drive me. This time I had about 1 week of relative relief. By this I mean a level 6 constant headache got knocked down to maybe a 2.
What doctors did not seem to understand and I kept trying to stress was that this was a constant headache that would gradually increase or decrease, there was no time that I did not have the headache. The easiest way to cope with the pain was buying really good light blocking curtains for the bedroom (my eyes get light sensitive and noise drives the pain up even more) and I would rest in the dark bedroom for hours on end just waiting for the pain to stop. I also found that a heating pad targeting my shoulders and skull would help take the edge off the pain.
This process went on from August 2009 until about October 2011.
The constant headache had become much worse and I went in to receive another nerve block. After receiving it and driving home the pain then began to branch down through my shoulders and back and the pain was much worse. After downing who knows what all pain pills in an attempt to find any sort of relief I was able to get back in to see the neurologist after a few days and we discussed alternatives to relieve the pain. Among the options I was given a 30mg sample of Cymbalta which while normally given out for depression has been found to stop diabetic neuropathy. I went home and began trying the Cymbalta.
Within 3 days my 2 year long headache had finally stopped.
Now I can’t say it was a cure but it has really helped me get back to where I want to be as far as going out and doing things. I still get a headache at times when I push my body too far but it at least has offered me a potential solution. When I go out and put too much constant stress on my body I usually pay for it and end up spending a week of bed rest inside my dark bedroom with all the lights out, the air conditioning at 72F and the heating pad on my shoulders and neck.
When the neurologist saw the positive response from the treatment with Cymbalta it was determined my headache is attributed to occipital neuralgia rather than a migraine. If we had figured this out earlier, a lot of pain could probably have been avoided. I now use a combination of a daily 30mg Cymbalta dose and a nerve block once every three months to manage the pain.
I do hope that if anyone else comes into a situation with similar headaches during their GBS recovery that this can help them find relief faster.
Keep driving forward!
EDIT: 9/18/2012
I am now being considered as a good candidate to try out Botox injections in my neck and shoulders. After I learn a little more about the process we may move forward on Oct 2.
EDIT: 9/26/2016
I recently went through a Ketamine Therapy Treatment and the constant 6 pain got knocked down to a 0-2 once the exhaustion of the whole process subsided. I am off Cymbalta now and have not had a nerve block for 6 months. I still take Soma and Hydrocodone at night to help keep the pain down. This is a HUGE improvement for me!!
Occipital Neuralgia Links:
http://www.webmd.com/migraines-headaches/occipital-neuralgia-symptoms-causes-treatments
http://www.hopkinsmedicine.org/neurology_neurosurgery/specialty_areas/headache/conditions/occipital_neuralgia.html
http://www.ninds.nih.gov/disorders/occipitalneuralgia/occipitalneuralgia.htm
http://en.wikipedia.org/wiki/Occipital_neuralgia
GBS Analogy: Brownout/Blackout
This analogy came to mind yesterday. When you're recovering and you get to that point where your muscles start to fail and you can't go any further, this is like a brown out where there is too much demand on existing power lines (nerves) and your power starts to shut down. If you continue it becomes a black out situation where you collapse because there is no power left to give. If the system rests power is restored.
- Corinne Blais, member of the Guillain Barre Syndrome FB Group
https://www.facebook.com/groups/2585256706/10150838828576707=
- Corinne Blais, member of the Guillain Barre Syndrome FB Group
https://www.facebook.com/groups/2585256706/10150838828576707=
Friday, June 8, 2012
Subscribe to:
Posts (Atom)