Skip to main content

MS

Diet and exercise


As I have an interest in both diet and exercise, this was a no-brainer as a first choice; I live and love both!

Diet:

Tracey Harrison was the presenter (a stand in, due to a sad bereavement) for the diet element – not ignoring exercise links it must be added; Manolis Sfakianakis to do / did the exercise part after Tracey.

Health food selection on a plateTracey brought a lot of energy with her interacting well with us all giving brilliant ‘diet data’ and how they relate, or can relate, to MS and other conditions using the presentation superbly.



I scribbled down:

·             ‘Diet: Conflicting views’
o   in that there are SO many different ideas as to what is good for what and when; right and wrong; should shouldn’t; amounts; tried tested… I was listening, enjoying and focused best I could; so I have (of course) forgotten a bit!
o   Offers a sense of control
§  it’s your diet, your choice
o   Key to self management
§  Promoting good general health and wellbeing
·             ‘5-a-day, vitamin D, foods’
o   More I knew/know of and practice best I can. Aye, some say should be 10-a-day. Let them say!
·           ‘Exclusion diets’ (“The majority of these diets are ‘exclusion’ diets. Exclusion diets suggest that you stop eating one food or several groups of foods. Other diets suggest that some foods are only eaten at certain times and not combined with other foods.”), eg -SWANK; -best bet; -overcoming MS
·             ‘Hydration, obvious’
o   It – water as the base – is what we cannot do without, but it is easy’ish to try and do without/less in potential of not going to the bog as often. However that’s a ‘nil effect’ if anything the opposite as can open doors for UTIs etc. So do hydrate! Says umm, Dr Cook!(which I’m not, ha) As a decaf drinker I escape the effects caffeine can have, thankfully (it - decaf tea & coffee - taste ok)
·             ‘diet discussion’.
o   Talks about e.g. diary, gluten, low carb, paleo, & group discussion ‘what works for you’ etc.



At the end we opened to talk about and share our thoughts on what we thought and do. Lovely way to finish and then to thank Tracey leading directly onto Exercise! Really enjoyed the session!

To exercise…


Fit woman sitting holding a barbell and food


Hopefully this may've given an insight and more about MS diets.

For more of my Living with MS Edinburgh blog :-)

Comments

Popular posts from this blog

MS

Living with MS Edinburgh *This is my bit blog and therefore my thoughts/options * on Living with MS Edinburgh being an information day for anyone affected by MS that I happily attended, and will be more about the day than the travel to and from it ! This event was held in the Sheraton Hotel which was beautifully laid out, in a spacious floor in the hotel with many orange-clad volunteers supporting the 150 attendees. MS Scotland The area in the hotel had been planned well, wasn’t too big or small offering fine accessibility and had plenty of MS stuff throughout! So what was the order of the day, what happened? It began with a welcome from the chair, Mary Douglas from the MS Society Scotland (9:45 – 10:00) welcoming us and touching on what was ahead. Breaking Boundaries in MS Research , was started straight after ( ~ 10:00) by Becky Driscoll. A fairly generic(ish) overview (IMO!) of MS initially, presented very well. The content was detailed and shows/sh...

Is what it is

Is what it is IT IT IT! There is no “It” in the title. Well, apart from actually making up the word “tITtle”! Not a mistake. When chatting about whatever, and #MS comes up as pretty usual when at an MS Social, that phrase is an acknowledgement of acceptance (canny phrase itself!). By saying it, we know that we do know what we/it mean/s. Good repeatability there! For myself, even by voicing it with another understanding MSer, it’s like a ‘mutual respectful recognition’ sharing. Acceptance. Here’s a tangent. I have recently started with Ocrevus as my DMD . So far (literally a couple of months as of typing) so good. It is doing it’s thing. I’m no better, and much more importantly no worse. Yes, I have had questions about my Ocrevus, due to the lowering of one’s immune system, and feeling terrible for a while. But! This time of year everybody seems to pick up a ‘bug’ or 2. Even some bloody COVID – I didn’t – phew. SAD. That’s S.A.D. “Seasonal affective disorder (SAD) is...

PIP reflection 2024

  PIP reflection 2024 Over the last few months, it’s safe to say (metaphorically) that my head had been somewhat up my arse; with anxiety. All due to my friend P I flipping P. Yes. Personal Independence Payment ( PIP ). Having received the renewal form LAST year (that’s 2023 as of typing), I anxiously stressed to get what legitimate proof I could get to assist my honest form answers. Big kudos to the Citizens Advice Bureau for help with said form ‘completion’. I was struggling. And without ANY surprise, I still live with MS ! Multiple Sclerosis the chronic Central Nervous System disease. Has it improved? No. Is it progressing? Yes. Is there a cure? I and about 2.3+m others wish. Anyway, part of my ‘processing’ stuff is that I keep notes. Yip, my memory is far from good. Cognition . So, here are 3 fairly recent ‘notes’ relating to PIP that I still have in my phone for a short blog and how one’s anxiety has been: No escape (1st May) Missed phone calls, a voice message. Joanne ab...