The Show by Lenka
Tuesday, June 9, 2009
Tuesday, June 2, 2009
Tuesday, May 26, 2009
Tuesday, May 19, 2009
Friday, May 15, 2009
Fun with Traffic Sources~
My friend posted a blog where she listed all of the keywords people use to find her website/blog. I got such a kick out this and decided to copy her idea (thanks Kay). I have Google analytics set-up with my blog, so the following are the keywords that people search to land on my blog:
1. Shit on my face
2. Kay Hanley and the homophobic homo
3. merelyme
4. Boston’s homophobic homo
5. but you don’t look gay
6. Harvey Milk speech
7. Matt Nathnason gay
8. smaaart ms
9. BMW pain
10. Brandi Carile gay
11. John and Marlena montages
12. shit in my face
13. Judy Shepard
14. 1199 rally
15. a fine frenzy + gay
16. BMW cancer
17. Copaxone auto injector order
18. did Michelle Obama’s dad have ms
19. Dropkick Murphy BMW
20. Frozen Copaxone
21. gay and shit my face
22. gay multiple sclerosis
23. gay Spanish song
24. is Kara DioGuardi gay
25. Letters to Cleo homos
26. Michelle Obama talks about her father
27. people say I look gay
28. retriever skinny bmw
29. side airbag no reason GMC
30. shit on my face and give me shit to eat/pictures
31. the homophobic homo blog
32. this is MS
33. the married homophobic homo
34. the homo with MS
Hilarious! As you can see there a bunch of musicians listed in the keywords and that’s because of my Musical Tuesday videos. The others are just interesting.
1. Shit on my face
2. Kay Hanley and the homophobic homo
3. merelyme
4. Boston’s homophobic homo
5. but you don’t look gay
6. Harvey Milk speech
7. Matt Nathnason gay
8. smaaart ms
9. BMW pain
10. Brandi Carile gay
11. John and Marlena montages
12. shit in my face
13. Judy Shepard
14. 1199 rally
15. a fine frenzy + gay
16. BMW cancer
17. Copaxone auto injector order
18. did Michelle Obama’s dad have ms
19. Dropkick Murphy BMW
20. Frozen Copaxone
21. gay and shit my face
22. gay multiple sclerosis
23. gay Spanish song
24. is Kara DioGuardi gay
25. Letters to Cleo homos
26. Michelle Obama talks about her father
27. people say I look gay
28. retriever skinny bmw
29. side airbag no reason GMC
30. shit on my face and give me shit to eat/pictures
31. the homophobic homo blog
32. this is MS
33. the married homophobic homo
34. the homo with MS
Hilarious! As you can see there a bunch of musicians listed in the keywords and that’s because of my Musical Tuesday videos. The others are just interesting.
"Don't piss on my leg and tell me it's raining!"
I have been neglecting my blog for some time now, but I’m making a goal to give it 100% from now on! I have been posting videos here and there, but now I’m ready to get back into writing more…so let’s go!
So many things have happened since the beginning of 2009. I have been on Copaxone for over a year now and it seems to suit me well. I no longer need to have my MRI’s every six months which is nice. There was an “unimpressive” new lesion on my last MRI, but my neurologist wasn’t concerned about it. I feel great and just participated in another MS Lifelines Walk in Boston. It’s been 18 months since my official MS diagnosis and things get better daily.
During my appointment with my Neurologist we discussed my first year of the diagnosis. The first year was insane because I was hit with symptom after symptom. In the matter of six months I had: Optic Neuritis, right side numbness, both legs numb and numerous infusions. Then things kinda just settled down. I was hit hard in the first months and then the Copaxone starting kicking in and I’ve never felt better. Physically and emotionally I feel amazing. Everything from yoga to Reiki and taking better care of myself has really improved me all around. Also, the support from my family, friends, MSers and most important my Chaz!!! I’m truly blessed and feel the love. I would have been lost without my Carnival of MS Bloggers who gave me advice and a platform to vent. Lisa E. you rock!!!
Ok, enough about MS for now. I have so many stories to blog about. I’m back!!!
So many things have happened since the beginning of 2009. I have been on Copaxone for over a year now and it seems to suit me well. I no longer need to have my MRI’s every six months which is nice. There was an “unimpressive” new lesion on my last MRI, but my neurologist wasn’t concerned about it. I feel great and just participated in another MS Lifelines Walk in Boston. It’s been 18 months since my official MS diagnosis and things get better daily.
During my appointment with my Neurologist we discussed my first year of the diagnosis. The first year was insane because I was hit with symptom after symptom. In the matter of six months I had: Optic Neuritis, right side numbness, both legs numb and numerous infusions. Then things kinda just settled down. I was hit hard in the first months and then the Copaxone starting kicking in and I’ve never felt better. Physically and emotionally I feel amazing. Everything from yoga to Reiki and taking better care of myself has really improved me all around. Also, the support from my family, friends, MSers and most important my Chaz!!! I’m truly blessed and feel the love. I would have been lost without my Carnival of MS Bloggers who gave me advice and a platform to vent. Lisa E. you rock!!!
Ok, enough about MS for now. I have so many stories to blog about. I’m back!!!
Tuesday, April 21, 2009
Friday, April 10, 2009
Saturday, April 4, 2009
Friday, March 27, 2009
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