Browsed by
Tag: living with multiple sclerosis

A true dog lover

A true dog lover

There are so many things in my life I am truly grateful for and I can dedicate numerous posts to each of them. Today I want to talk about the ones that can never read my post. I actually started with cats. My first apartment didn’t allow dogs. Each fight my ex-husband and I had resulted in another cat. My dad, who always owned dogs, used to say “you’re a dog person”. I started pushing to get a dog as…

Read More Read More

Multiple sclerosis pity party

Multiple sclerosis pity party

Pity party blog today. I’m just angry today. I wrote my whole blog already was ready to post it but my hand that holds my iPad started to fatigue and my finger hit the settings button on the side panel…lost everything I just spent 30 minutes writing. What did I do wrong? I exercise six days a week. I try to eat somewhat healthy. I take my medicines. I still get worse.   I don’t know what else to do….

Read More Read More

The plant based diet and multiple sclerosis

The plant based diet and multiple sclerosis

A plant based diet is a diet based on fruits, vegetables, whole grains, and legumes; and it excludes or minimizes meat (including chicken and fish), dairy products, and eggs, as well as highly refined foods like bleached flour, refined sugar, and oil. A 2013 Nutritional Update for Physicians stated, “Healthy eating may be best achieved with a plant-based diet, which we define as a regimen that encourages whole, plant-based foods and discourages meats, dairy products, and eggs as well as…

Read More Read More

Cyber crash Monday-Happy Halloween

Cyber crash Monday-Happy Halloween

ok maybe not a cyber crash but I’m taking a crash day. I’m going to go back to bed and recharge, regroup, refuel and recoup.  I haven’t done a full day where I spend the day in bed in a long time but I think I need to today. I went to bed super early last night and I’ve been up since 2:30am. I let thoughts take over that shouldn’t be plaguing my thoughts anymore. No matter what I did…

Read More Read More

The negative friend

The negative friend

How are you feeling? I never thought I’d hate a question more. Doesn’t it seem like EVERYONE asks you that question when you have a chronic illness. I have my standard answer to people which is, “I’m good”.  I mean what else are you going to say. Truth is half the people that ask the question don’t even want to know the real answer anyway. I don’t even mean that in a mean way, it’s just people are self absorbed…

Read More Read More

Only alone if you don’t like who you’re alone with

Only alone if you don’t like who you’re alone with

I saw this quote one day and it rang true. “You’re only alone if you don’t like who you’re alone with.”  I’ve always been that person who had trouble being alone. I never really liked myself. I hated my body thought I was fat, not worthy of good things, unlovable and didn’t have any value. I also on top of it had multiple sclerosis so who would accept me.  I’ve lived my whole life with a low self esteem, no…

Read More Read More

Our Chronic illness understanding

Our Chronic illness understanding

I’m asked a lot, by my family, if I’ve learned anything since I started writing this blog. The biggest thing I’ve learned is that somehow we all understand what each other goes through. I follow a lot of people with some sort of chronic illness. I read their blogs and can totally relate to what they are saying and I get comments all the time that they relate to what I am saying. It doesn’t have to be someone just…

Read More Read More

I used to dance

I used to dance

This picture hangs above my kitchen table. It was originally a gift my sister and I bought for my dad but has been with me since the day we tried to give it to him. My dad explained art doesn’t speak the same to everyone. The picture always spoke to me. I always fantasized looking at this picture. To be that wealthy, beautiful lady dancing in the rain on the beach with someone she was completely in love with. I…

Read More Read More

Lack of sleep, fatigue and MS

Lack of sleep, fatigue and MS

It was one of those nights. I was up all night. I had a little bellyache. I ate Chinese food, I never eat Chinese food.  My belly didn’t agree with the Chinese food. Instead of going into the details of why I was going on all night let’s discuss the details of sleep. The average American sleep 6.8 hours a night. The average MS patient probably needs a good 12 hours a night.  I’m willing to bet they don’t get…

Read More Read More

High dose biotin with progressive MS a patient’s review

High dose biotin with progressive MS a patient’s review

I have finished my first bottle of high dose biotin.  I’ve been taking a 100mg pill three times a day as the clinical studies patients were taking.  My doctor felt that it was an excellent option for me to try since I am clearly progressing. She found a website www.highdosebiotin.net where you can purchase the pills without a prescription. It is slightly costly at $60 a bottle. Before I tell you my first month thoughts on it let me explain…

Read More Read More

Verified by MonsterInsights