Multiple Sclerosis (MS) Support Group
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Off topic but would appreciate information
Hi everyone. I've had MS for 30 years but a new concern has emerged. I had an ultrasound for a lump on the back of my hand and the untra-sound report said they could not rule out malignancy. So now in six days I'm to have an MRI which might tell me what sort of animal it is. If the MRI result comes back positive, then I think I would be diagosed with sarcoma. And then what treatments/tests might I expect? It's the not knowing that's keeping me awake.
And if anyone out there lives in Alberta, can I expect a long wait, given the pandemic? Thanks to anyone who can tell me anything reasonably concrete. My GP is on my side. I was first offered an MRI in June of 2022 but she got back to whoever sets up the appointments and got the date moved back by six months. Lorraine
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Usually I get a daily influx of emails on health topics. An article from Dr. Mercola really stood out recently though because it mentioned that fat cells have their own mitochondria. Not only was this the first I'd heard of this, he also mentioned that fat serves a purpose in our metabolism. Another new factoid for me. The bottom line for me was to appreciate that even our fat cells play a...
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I just do not feel well and I really think that it's because I cried yesterday on my way to work about my Aunt who is in the hospital. I don't think that we will have her much longer. She is very frail. Now she needs help eating. So, this is the third time in a year that I felt this way after crying. I think crying releases toxins into my body. I also worked up a sweat at the gym...

I dont know but would also guess a small biopsy of the lump would give insight as to whether or not it actually is malignant.
I am not in Alberta, and i hope there is not a long wait. When it comes to tumors i would want to remove it and its threat as soon as possible!
Good luck
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