Living with 'long Covid'

It's been a year for me... this condition is terrible! I hate living like this. I am 32, but I feel like I'm 90.

I am the same. It really is a living hell. I cry most days. I am back living in my mums and she is doing everything for me and looking after my son. I want to be my old self again 😢

I am utterly perplexed and well as angered as to why it’s taken a pandemic for medical staff to recognise that ME/CFS is a genuine medical condition. People with ME/CFS have been silenced,ignored and dismissed. All of these things have lead to a lack of funding for the condition and thus a lack of understanding. The new research for me/CFS is promising yet beyond infuriating. The funding just hasn’t been there for medical staff to fully grasp and understand ME/CFS. Patients gave therefore been denied help and been miss understood by medical staff for years and years. I hope that the pandemic funding will have a more positive outcome for those with l ME/CFS and a greater understanding from medical staff and others. I’m hoping this pandemic will allow medical staff to have more education about ME/CFS.

I've had LC now since 2019. My symptoms have gotten better. I can walk and talk and some small walks but that's it. I can't run, swim or work. I have teamed up with a doctor that treats me with IV vitimins and NAD, LDN, NAC and tons of glutathione. IM B12 really helps to for about a week. The vitamins I use are pharmaceutical grade not the ones that you obtained from your near Walmart or Kroger. The virus wreaks havoc on your mitochondria. This is the power plant for your cells and how it absorbs energy from the blood. And also wipes out your serotonin stored in your gut. I am not a doctor nor am I offering any advice I am only sharing with you what I have found to give me about 30% increase in energy. I spent 18 months bedridden until I found a doctor who was willing to take the time with me and go through painstaking trial and effort until we were able to get me out of the bed and back to doing simple task. We can only hope some better treatments arrive soon. Much love.

Pray she gets better 🙏🏽🙏🏽

Thank your highlighting Long Covid. We need to raise awareness of Long Covid in Kids so that parents can make informed decisions.

Praying much for you and your situation 🙏 continue to trust God continue to pray.

I share your pain...going through the same thing if not worse. Everyday l suffer from something...6 months now. It's crazy

Get well soon 🙏🏻

I have long term covid too 😢😢

6 months & im so depressed!

This is ME/CFS my life has been like yours for 15 years!!

😭🥺

Don't think she's been active for a few years......

N

🚨IMPORTANT🚨 try reading some of Joe Dispenza's books and courses they could be very useful in this particular situation! Wish all of you suffering from it a fast recovery

This is the new "yuppie flu".

She has PTSD she need to start dealing with her issues and get help from a therapist.

How many licence fees have you got to lose before you realise that the public see through your propaganda?

Is this a comedy?