On the news this evening. Interesting.
http://www.ctvnews.ca/sports/canadian-m ... -1.3602745
Search found 15 matches
- Fri Sep 22, 2017 5:50 pm
- Forum: General Discussion
- Topic: Keeogo. keep on going.
- Replies: 1
- Views: 870
- Fri May 19, 2017 5:56 pm
- Forum: Ampyra (Dalfampridine)
- Topic: Modified ampyra dosage??
- Replies: 4
- Views: 4236
Re: Modified ampyra dosage??
I definitely feel a benefit started 2x a day. 1st one at 5am getting up for work. Around 11am I was dragging my arse around wishing for a nap - no energy. Started taking another dose around 1pm this enabled me to get through the rest of the work day. At 8pm I was usually exhausted and in bed. I stuc...
- Sun May 14, 2017 8:00 am
- Forum: Ampyra (Dalfampridine)
- Topic: Modified ampyra dosage??
- Replies: 4
- Views: 4236
Re: Modified ampyra dosage??
Hi
I have modified the frequency. 3x per day every 5 hours works for me. My neurologist knows I do this. I have had no issues.
I have modified the frequency. 3x per day every 5 hours works for me. My neurologist knows I do this. I have had no issues.
- Sat Apr 02, 2016 6:46 pm
- Forum: General Discussion
- Topic: Red/ ginger hair
- Replies: 5
- Views: 1832
Re: Red/ ginger hair
WhyRwehere I had a poke around regarding red hair and MS I never really thought of it before. Not much there in terms of information. I did find this https://en.wikipedia.org/wiki/Red_hair. Interesting in terms of genetics. I would consider myself fair skinned however, I might burn at first but I ev...
- Mon Mar 28, 2016 12:07 pm
- Forum: General Discussion
- Topic: Red/ ginger hair
- Replies: 5
- Views: 1832
Re: Red/ ginger hair
I have dark auburn hair. Lots of redheads in my family ranging from ginger, strawberry blonds and different shades of auburn. I've not heard of redheads producing D without the sun. Looking back on my life I have spent more time outside than inside. As kids we never wore sun screen and if you were s...
- Wed Feb 17, 2016 5:32 pm
- Forum: General Discussion
- Topic: Eating and symptom exacerbation
- Replies: 2
- Views: 1265
Re: Eating and symptom exacerbation
For me yes. I feel good have more energy and move much better when fasting. If I have an appointment or need to go out I just don't eat anything. I try to eat light or small meals. If I do have a large meal I'm like dead weight and become weak and sloppy getting around. Not sure why this is. Moragh.
- Wed Jul 01, 2015 5:29 pm
- Forum: MS Etiology and Pathogenesis
- Topic: CNS lymph vessels found. Brain is not immune-privileged
- Replies: 59
- Views: 13870
Re: CNS lymph vessels found. Brain is not immune-privileged
Many of us go searching around the internet looking to better understand the roles and responsibilities of things. (well me anyway). With this new information I started searching around as I really didn't understand what the lymphatic system did. I came across this site and found it very helpful in ...
- Wed Feb 25, 2015 5:16 pm
- Forum: Ampyra (Dalfampridine)
- Topic: Ampyra Seizures anyone?
- Replies: 4
- Views: 5435
Re: Ampyra Seizures anyone?
I have been using aminopyridine (4) for almost 6 years. I think its the same thing. like the benefits it provides. I have never had a seizure. Kidney function tested yearly so far no issues.
- Sat Sep 06, 2014 10:56 am
- Forum: General Discussion
- Topic: Sex Headaches and MS. Related?
- Replies: 11
- Views: 3226
Re: Sex Headaches and MS. Related?
God gave men both a penis and a brain, but unfortunately not enough blood supply to run both at the same time.
Robin Williams
Robin Williams
- Sat Sep 06, 2014 10:25 am
- Forum: Chronic Cerebrospinal Venous Insufficiency (CCSVI)
- Topic: new! call centers and hiccups! don't miss it!
- Replies: 10
- Views: 2454
Re: new! call centers and hiccups! don't miss it!
Hi 1eye: I used to get the hiccups (not as bad as you) but it was uncomfortable. It just stopped. Now days if ever I get a rare hiccup its only one. However, my issue now is sneezing. For no reason I just start and cant stop. The most sneezes in a row are 27. When I start the entire house starts to ...
- Wed Aug 14, 2013 1:09 pm
- Forum: Chronic Cerebrospinal Venous Insufficiency (CCSVI)
- Topic: Actress Alison Peebles and cervicals
- Replies: 3
- Views: 1854
Re: Actress Alison Peebles and cervicals
Sorry I cant attach the link. Not quite handy capable with W8 yet. Search Dr. Chongsu Lee. He outlines his treatment. You may find it interesting.
Moragh
Moragh
- Fri Mar 15, 2013 7:52 pm
- Forum: Chronic Cerebrospinal Venous Insufficiency (CCSVI)
- Topic: Vit D3>125nmol/L (50ng/ml) in blood. Goal for pwMS
- Replies: 821
- Views: 147377
Re: FIRST STEP-Vit D3 min for pwMS=125 nmol/L in blood
Hi MarkW: Trying to read through your thread. Interesting. I have been taking 20,000 IU VD daily for the past 6+ years. I don't have my levels in front of me but they are usually over 300. After I get through your thread I would like to tackle Jimmylegs files as I need to understand my other levels ...
- Fri Feb 24, 2012 12:50 pm
- Forum: General Discussion
- Topic: Weather
- Replies: 1
- Views: 1476
Re: Weather
Hi LR1234 Not from the UK. I’m in Southern Ont. Canada. Every spring (early to mid April) my eye (optic neuritis) would start to act up. Big black floaters in my left eye. I would get into a panic thinking I was starting another relapse. I would stress myself so much that my drop foot would start ac...
- Fri Feb 17, 2012 1:59 pm
- Forum: Chronic Cerebrospinal Venous Insufficiency (CCSVI)
- Topic: TAKING MATTERS INTO OUR OWN HANDS: What would you do?
- Replies: 6
- Views: 1659
Re: TAKING MATTERS INTO OUR OWN HANDS: What would you do?
For the most part Donkeys are running the country. No clue on good business sense/ decisions or understand /comprehend how to prepare & plan for the future. We are an aging population and need forward thinkers. Preventing this procedure is bad business and will only further strain an already str...
- Fri Jan 27, 2012 2:11 pm
- Forum: Introductions
- Topic: Hi Everyone @ ThisIsMS
- Replies: 0
- Views: 1590
Hi Everyone @ ThisIsMS
Thank you all for the valuable information I have found on this site. It has enabled me to investigate and make my own decisions on how I attack my MS. I’m not going down without a fight. I get discouraged here and there but I can’t let it get me. I’m in Canada so some of you know the boat with no p...