Bedridden Today but Still Thankful
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- Опубликовано: 27 май 2019
- I am sick after a fun weekend, but I am still good.
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I'm a SAHM of 4 boys, living with a chronic illness. I also have a special needs child who suffers with ADHD, anxiety and High Functioning Autism.
My name is Meredith (aka Meri) and I'm a stay at home mom of 4 boys (including twins). I also suffer from an autoimmune disease called Sjogren's Syndrome, which makes each day a little more challenging. I am also the mom of an ADHD ODD, Asperger's child.
Like most of you out there, I'm just a regular (crazy) chic trying to survive as a mom. I'm far from perfect, but I do my best to get through each day while keeping everyone alive. I also share what works for me for managing the day to day madness of being a family of 6.
Please feel free to leave me feedback. I love to hear from everyone!
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I agree with you! Since I am sick, I appreciate much more all the little thing. And I really appreciate the fact that I have a roof and a bed to rest in when I am not feeling good. Take care!
I'm very thankful you've made these. I always appreciate them. I am currently in a flare and it's nice to be able to go back to your old videos and feel some comfort. Of course I don't wish you were sick but it's nice to not feel so alone.
"Never too late to be a better version of yourself." Everyone should say that to themselves every day. Thank you!
Thanks for this video. I try to keep my mind occupied with good thoughts. Its not easy, especially when im in pain and a flare. Its more depressing when i have to cancel and disappoint anyone
When i can, i do what i can. Im trying not to stress myself out.
It's hard trying to get others to understand what you are going through and the frustration you feel because you can't function like them. Yes you do appreciate things and life more. I was diagnosed with Sjorgens, fibromyalgia, arthritis, and degenerative disc disease. God bless you.
What a wonderful video! It´s so true! Thanks!
You´re right: It´s never to late to change!
And best regards from Germany
Milka
Those people are not dying they are living with what they have. 🙂 That is how my cousin who died one moth before her 45th birthday used to say. As Mary and Peter Frey of The Frey Life say Do what you think you can’t do. You are doing the best you can with the cards you have been dealt. 🙂
I feel the same way as you Meri - I hope today will be a better day, but if not, hang in there because tomorrow might be...hope you are feeling better soon and have that good day :)
You are Soo strong. And yet I feel sooo weak. Everytime I see you continue on and with 4 children as I....I feel like I'm useless. Why can't I feel strong like others? I feel helpelss... and...alone
You are such an inspiration...I am in bed with the same illness as you and feeling so down.
Hope you feel better!!
Prayers and thank you because I can relate your not alone in this
We miss you 😔
be strong darling we are a fighters🤜🤛
So true
Btw...you still look Beautiful Our Lady. Keep caring on
I watch shows like that too.
I was almost same way and then found out it was from Biotoxin illness from toxic black mold and lyme disease. It has caused C.I.R.S. in me and also causes autoimmunity. Do you currently live in a water damaged building?
I watch the same show too so I get it!....💕💕💕
Too tired to think but here are some 💜💜💜
I have sjogrens and low dose naltrexone has helped me. Chk it out
How long have you been on LDN?
Horolen Restrepo I’m sorry to hear this. I started at 1.5 and had. Felt worse when increased it. Now my body is allowing a new small increase and it helps all symptoms a little bit. Less fatigue a lot less pain etc. I still am not well but just started a few months ago. Make sure u get it compounded at a really good place. And experiment with different doses. I’m not on any other drugs yet I’m gonna see how it goes although I’m approved for ivig and may add that. Also important with LDN do not eat dairy and grains basically need to on an autoimmune paleo diet and take vit d. I hope that helps. Also investigate transcutaneous vagus nerve stim. I’ll be trying that soon. Study has been done on sjogrens and many more on RA and autoimmunity. Google dr Nemechek
@@monkeybearmax Hi thx for the feedback. I'll check that out. I was on LDN for 3yrs didn't help me much. Went thru different levels & eventually stopped it. Had a combination of daily pills it was crazy. Was told to take that along with Dr Chia's "Equilibrant" for Immune Health helped a little with fatigue but it got pricey after a while, Inosine supplement to help build muscle DNA, Vitamin D yes, B12, Fish Oil. That regime has changed for me over the years. I'm in Gabapentin (nerve pain) 800mg Ibuprofen only so much I can take. My Sjogren's levels are apparently to low for infusions so I'm stuck!