Chat with M.E. Podcast

07/02/2024

ʟɪꜰᴇ ᴏꜰ ᴘɪᴘᴘᴀ
Pippa Stacey of Life of Pippa will be joining me for a chat on our show next week, focusing on life with M.E. Whilst navigating blogging, content creating and charity work
The episode will air later this month, but if you have any questions for Pippa, please leave them in the comments below or in the stories shortly

07/02/2024

I am a
World ME Day is just around the corner and we have to unite our voices as a collective to push for more research, further treatment and better support to a long-term condition that’s seriously underfunded
ME doesn’t discriminate! It affects many different people in all walks of life; it has no borders! Let’s use this ideal to advocate for ourselves and for others and combat this global crisis!

30/01/2024

𝕎𝕙𝕖𝕟 𝕓𝕣𝕒𝕚𝕟𝕗𝕠𝕘 𝕒𝕥𝕥𝕒𝕔𝕜𝕤
I told Rory she didn’t need a Hairband from upstairs as we had one in the bookshelf… was funny but she still looked so beautiful 💜🩷🩵
Yeah it was a freakin’ usb cord 😂
Maybe I’m on to something

26/01/2024

New Blog is up
>>>link in stories and bio

26/01/2024

Yeah right! Happy New Year! Firstly, I would like to wish all of you a very Happy New Year and hope you have all had a wonderful Christmas and festive period. Whether you are religious or not; or follow a different religion. It is a time where all families try to be together. So I do hope you had some quality time with your loved ones....

Yeah right! Happy New Year! Firstly, I would like to wish all of you a very Happy New Year and hope you have all had a wonderful Christmas and festive period. Whether you are religious or not; or f…

25/01/2024

𝐍𝐞𝐰 𝐘𝐞𝐚𝐫, 𝐍𝐞𝐰 𝐂𝐮𝐫𝐞!?
Sadly not… there is still no scientifically proven cure for M.E./CFS as of yet; as much as we would like otherwise
With a certain show having a section about this possibility and its misleading content - I had to lay on my soap box and have a rant… we can't allow this to derail the good work that research like are doing
>>>link🎙️in bio & stories

24/01/2024

𝕀𝕞𝕡𝕣𝕠𝕞𝕡𝕥𝕦 𝔼𝕡𝕚𝕤𝕠𝕕𝕖 𝕋𝕠𝕞𝕠𝕣𝕣𝕠𝕨…
Happy New Year 🥳
as you can tell by my picture, I’m just as shocked 😂
I’ve not been feeling well this past couple of weeks, but I felt I needed to do this episode in light of recent publicity about cures
Will go live and ready for your ears at 1am tomorrow morning
Links in bio and links will go in my stories tomorrow
!

22/12/2023

Our 2nd Questionnaire is optional but hugely helpful to aid us in gaining a deeper understanding of . Your experience matters. To read up on our 2nd Questionnaire for all registered participants, go to https://shorturl.at/dCJLX

21/12/2023

ℂ𝕙𝕣𝕚𝕤𝕥𝕞𝕒𝕤 𝕋𝕚𝕞𝕖
the latest podcast is live now, featuring from chatting all things ME/CFS around the festive period
>>>link in bio >link in story for 24hrs>all links in bio too

20/12/2023

𝔸 𝕘𝕖𝕟𝕥𝕝𝕖 𝕟𝕦𝕕𝕘𝕖
To say Merry Christmas and all the well wishes possible to all of you heading into 2024
A big thank you to all who have subscribed to my little podcast over this year
And a little reminder that the last podcast of the year recorded as a Christmas Special with from goes live at 1am tomorrow morning - talking all things ME/CFS and the holidays
>>>links for podcast and Post Exertional Malaise content in bio

17/12/2023

𝕷𝖆𝖘𝖙 𝖊𝖕𝖎𝖘𝖔𝖉𝖊 𝖔𝖋 𝖙𝖍𝖊 𝖞𝖊𝖆𝖗
I popped in to chat with from podcast to discuss what the festive period is like and tips for management for fellow ME/CFS patients and the Spoonie community as a whole
Out on Thursday - usual links in bio including PEM podcast pages